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biotinylated trem2  (Sino Biological)


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    Structured Review

    Sino Biological biotinylated trem2
    Biotinylated Trem2, supplied by Sino Biological, used in various techniques. Bioz Stars score: 94/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/biotinylated+trem2/Human+TREM-2+Protein+(ECD%2C+His+%26+AVI+Tag)%2C+Biotinylated/pm41604675-227-0-5
    Average 94 stars, based on 6 article reviews
    biotinylated trem2 - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    Binding Assay:

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a first-in-class dual-function TREM2 modulator: Receptor activation and shedding inhibition.
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5 % Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: Structure-Based Virtual Screening Identifies TREM2-Targeted Small Molecules that Enhance Microglial Phagocytosis
    Article Snippet: of EN020 to human TREM2 protein was assessed using surface plasmon resonance (SPR) on a Biacore 8K system (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084- H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, 0.5% Surfactant P20, pH 7.4) to a level of 4,343 ± 399 RU. .. Prior to immobilization, the chip surface was conditioned with three 1- minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU. .. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Generated:

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a first-in-class dual-function TREM2 modulator: Receptor activation and shedding inhibition.
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5 % Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: Structure-Based Virtual Screening Identifies TREM2-Targeted Small Molecules that Enhance Microglial Phagocytosis
    Article Snippet: of EN020 to human TREM2 protein was assessed using surface plasmon resonance (SPR) on a Biacore 8K system (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084- H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, 0.5% Surfactant P20, pH 7.4) to a level of 4,343 ± 399 RU. .. Prior to immobilization, the chip surface was conditioned with three 1- minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU. .. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Biomarker Discovery:

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a first-in-class dual-function TREM2 modulator: Receptor activation and shedding inhibition.
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5 % Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: Structure-Based Virtual Screening Identifies TREM2-Targeted Small Molecules that Enhance Microglial Phagocytosis
    Article Snippet: of EN020 to human TREM2 protein was assessed using surface plasmon resonance (SPR) on a Biacore 8K system (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084- H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, 0.5% Surfactant P20, pH 7.4) to a level of 4,343 ± 399 RU. .. Prior to immobilization, the chip surface was conditioned with three 1- minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU. .. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Derivative Assay:

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a first-in-class dual-function TREM2 modulator: Receptor activation and shedding inhibition.
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5 % Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: Structure-Based Virtual Screening Identifies TREM2-Targeted Small Molecules that Enhance Microglial Phagocytosis
    Article Snippet: of EN020 to human TREM2 protein was assessed using surface plasmon resonance (SPR) on a Biacore 8K system (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084- H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, 0.5% Surfactant P20, pH 7.4) to a level of 4,343 ± 399 RU. .. Prior to immobilization, the chip surface was conditioned with three 1- minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU. .. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Concentration Assay:

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a first-in-class dual-function TREM2 modulator: Receptor activation and shedding inhibition.
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5 % Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: Structure-Based Virtual Screening Identifies TREM2-Targeted Small Molecules that Enhance Microglial Phagocytosis
    Article Snippet: of EN020 to human TREM2 protein was assessed using surface plasmon resonance (SPR) on a Biacore 8K system (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084- H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, 0.5% Surfactant P20, pH 7.4) to a level of 4,343 ± 399 RU. .. Prior to immobilization, the chip surface was conditioned with three 1- minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU. .. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Negative Control:

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a first-in-class dual-function TREM2 modulator: Receptor activation and shedding inhibition.
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5 % Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: Structure-Based Virtual Screening Identifies TREM2-Targeted Small Molecules that Enhance Microglial Phagocytosis
    Article Snippet: of EN020 to human TREM2 protein was assessed using surface plasmon resonance (SPR) on a Biacore 8K system (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084- H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, 0.5% Surfactant P20, pH 7.4) to a level of 4,343 ± 399 RU. .. Prior to immobilization, the chip surface was conditioned with three 1- minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU. .. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Positive Control:

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a first-in-class dual-function TREM2 modulator: Receptor activation and shedding inhibition.
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5 % Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: Structure-Based Virtual Screening Identifies TREM2-Targeted Small Molecules that Enhance Microglial Phagocytosis
    Article Snippet: of EN020 to human TREM2 protein was assessed using surface plasmon resonance (SPR) on a Biacore 8K system (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084- H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, 0.5% Surfactant P20, pH 7.4) to a level of 4,343 ± 399 RU. .. Prior to immobilization, the chip surface was conditioned with three 1- minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU. .. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Standard Deviation:

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a first-in-class dual-function TREM2 modulator: Receptor activation and shedding inhibition.
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5 % Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: Structure-Based Virtual Screening Identifies TREM2-Targeted Small Molecules that Enhance Microglial Phagocytosis
    Article Snippet: of EN020 to human TREM2 protein was assessed using surface plasmon resonance (SPR) on a Biacore 8K system (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084- H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, 0.5% Surfactant P20, pH 7.4) to a level of 4,343 ± 399 RU. .. Prior to immobilization, the chip surface was conditioned with three 1- minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU. .. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Fluorescence:

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a first-in-class dual-function TREM2 modulator: Receptor activation and shedding inhibition.
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5 % Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: Structure-Based Virtual Screening Identifies TREM2-Targeted Small Molecules that Enhance Microglial Phagocytosis
    Article Snippet: of EN020 to human TREM2 protein was assessed using surface plasmon resonance (SPR) on a Biacore 8K system (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084- H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, 0.5% Surfactant P20, pH 7.4) to a level of 4,343 ± 399 RU. .. Prior to immobilization, the chip surface was conditioned with three 1- minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU. .. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    In Vitro:

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a first-in-class dual-function TREM2 modulator: Receptor activation and shedding inhibition.
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5 % Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: Structure-Based Virtual Screening Identifies TREM2-Targeted Small Molecules that Enhance Microglial Phagocytosis
    Article Snippet: of EN020 to human TREM2 protein was assessed using surface plasmon resonance (SPR) on a Biacore 8K system (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084- H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, 0.5% Surfactant P20, pH 7.4) to a level of 4,343 ± 399 RU. .. Prior to immobilization, the chip surface was conditioned with three 1- minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU. .. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Activity Assay:

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a first-in-class dual-function TREM2 modulator: Receptor activation and shedding inhibition.
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5 % Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: Structure-Based Virtual Screening Identifies TREM2-Targeted Small Molecules that Enhance Microglial Phagocytosis
    Article Snippet: of EN020 to human TREM2 protein was assessed using surface plasmon resonance (SPR) on a Biacore 8K system (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084- H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, 0.5% Surfactant P20, pH 7.4) to a level of 4,343 ± 399 RU. .. Prior to immobilization, the chip surface was conditioned with three 1- minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU. .. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Control:

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a first-in-class dual-function TREM2 modulator: Receptor activation and shedding inhibition.
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5 % Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: Structure-Based Virtual Screening Identifies TREM2-Targeted Small Molecules that Enhance Microglial Phagocytosis
    Article Snippet: of EN020 to human TREM2 protein was assessed using surface plasmon resonance (SPR) on a Biacore 8K system (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084- H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, 0.5% Surfactant P20, pH 7.4) to a level of 4,343 ± 399 RU. .. Prior to immobilization, the chip surface was conditioned with three 1- minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU. .. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Size-exclusion Chromatography:

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a first-in-class dual-function TREM2 modulator: Receptor activation and shedding inhibition.
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5 % Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: Structure-Based Virtual Screening Identifies TREM2-Targeted Small Molecules that Enhance Microglial Phagocytosis
    Article Snippet: of EN020 to human TREM2 protein was assessed using surface plasmon resonance (SPR) on a Biacore 8K system (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084- H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, 0.5% Surfactant P20, pH 7.4) to a level of 4,343 ± 399 RU. .. Prior to immobilization, the chip surface was conditioned with three 1- minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU. .. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Purification:

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a first-in-class dual-function TREM2 modulator: Receptor activation and shedding inhibition.
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5 % Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: Structure-Based Virtual Screening Identifies TREM2-Targeted Small Molecules that Enhance Microglial Phagocytosis
    Article Snippet: of EN020 to human TREM2 protein was assessed using surface plasmon resonance (SPR) on a Biacore 8K system (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084- H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, 0.5% Surfactant P20, pH 7.4) to a level of 4,343 ± 399 RU. .. Prior to immobilization, the chip surface was conditioned with three 1- minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU. .. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Comparison:

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a first-in-class dual-function TREM2 modulator: Receptor activation and shedding inhibition.
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5 % Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: Structure-Based Virtual Screening Identifies TREM2-Targeted Small Molecules that Enhance Microglial Phagocytosis
    Article Snippet: of EN020 to human TREM2 protein was assessed using surface plasmon resonance (SPR) on a Biacore 8K system (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084- H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, 0.5% Surfactant P20, pH 7.4) to a level of 4,343 ± 399 RU. .. Prior to immobilization, the chip surface was conditioned with three 1- minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU. .. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Two Tailed Test:

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a first-in-class dual-function TREM2 modulator: Receptor activation and shedding inhibition.
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5 % Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: Structure-Based Virtual Screening Identifies TREM2-Targeted Small Molecules that Enhance Microglial Phagocytosis
    Article Snippet: of EN020 to human TREM2 protein was assessed using surface plasmon resonance (SPR) on a Biacore 8K system (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084- H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, 0.5% Surfactant P20, pH 7.4) to a level of 4,343 ± 399 RU. .. Prior to immobilization, the chip surface was conditioned with three 1- minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU. .. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Western Blot:

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a first-in-class dual-function TREM2 modulator: Receptor activation and shedding inhibition.
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5 % Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: Structure-Based Virtual Screening Identifies TREM2-Targeted Small Molecules that Enhance Microglial Phagocytosis
    Article Snippet: of EN020 to human TREM2 protein was assessed using surface plasmon resonance (SPR) on a Biacore 8K system (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084- H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, 0.5% Surfactant P20, pH 7.4) to a level of 4,343 ± 399 RU. .. Prior to immobilization, the chip surface was conditioned with three 1- minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU. .. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Expressing:

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a first-in-class dual-function TREM2 modulator: Receptor activation and shedding inhibition.
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5 % Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: Structure-Based Virtual Screening Identifies TREM2-Targeted Small Molecules that Enhance Microglial Phagocytosis
    Article Snippet: of EN020 to human TREM2 protein was assessed using surface plasmon resonance (SPR) on a Biacore 8K system (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084- H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, 0.5% Surfactant P20, pH 7.4) to a level of 4,343 ± 399 RU. .. Prior to immobilization, the chip surface was conditioned with three 1- minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU. .. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Over Expression:

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a first-in-class dual-function TREM2 modulator: Receptor activation and shedding inhibition.
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5 % Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: Structure-Based Virtual Screening Identifies TREM2-Targeted Small Molecules that Enhance Microglial Phagocytosis
    Article Snippet: of EN020 to human TREM2 protein was assessed using surface plasmon resonance (SPR) on a Biacore 8K system (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084- H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, 0.5% Surfactant P20, pH 7.4) to a level of 4,343 ± 399 RU. .. Prior to immobilization, the chip surface was conditioned with three 1- minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU. .. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Phospho-proteomics:

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a first-in-class dual-function TREM2 modulator: Receptor activation and shedding inhibition.
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5 % Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: Structure-Based Virtual Screening Identifies TREM2-Targeted Small Molecules that Enhance Microglial Phagocytosis
    Article Snippet: of EN020 to human TREM2 protein was assessed using surface plasmon resonance (SPR) on a Biacore 8K system (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084- H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, 0.5% Surfactant P20, pH 7.4) to a level of 4,343 ± 399 RU. .. Prior to immobilization, the chip surface was conditioned with three 1- minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU. .. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Activation Assay:

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a first-in-class dual-function TREM2 modulator: Receptor activation and shedding inhibition.
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5 % Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: Structure-Based Virtual Screening Identifies TREM2-Targeted Small Molecules that Enhance Microglial Phagocytosis
    Article Snippet: of EN020 to human TREM2 protein was assessed using surface plasmon resonance (SPR) on a Biacore 8K system (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084- H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, 0.5% Surfactant P20, pH 7.4) to a level of 4,343 ± 399 RU. .. Prior to immobilization, the chip surface was conditioned with three 1- minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU. .. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Ligand Binding Assay:

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a first-in-class dual-function TREM2 modulator: Receptor activation and shedding inhibition.
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5 % Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: Structure-Based Virtual Screening Identifies TREM2-Targeted Small Molecules that Enhance Microglial Phagocytosis
    Article Snippet: of EN020 to human TREM2 protein was assessed using surface plasmon resonance (SPR) on a Biacore 8K system (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084- H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, 0.5% Surfactant P20, pH 7.4) to a level of 4,343 ± 399 RU. .. Prior to immobilization, the chip surface was conditioned with three 1- minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU. .. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Residue:

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a first-in-class dual-function TREM2 modulator: Receptor activation and shedding inhibition.
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5 % Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: Structure-Based Virtual Screening Identifies TREM2-Targeted Small Molecules that Enhance Microglial Phagocytosis
    Article Snippet: of EN020 to human TREM2 protein was assessed using surface plasmon resonance (SPR) on a Biacore 8K system (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084- H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, 0.5% Surfactant P20, pH 7.4) to a level of 4,343 ± 399 RU. .. Prior to immobilization, the chip surface was conditioned with three 1- minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU. .. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Inhibition:

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a first-in-class dual-function TREM2 modulator: Receptor activation and shedding inhibition.
    Article Snippet: The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).The interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8 K instrument (Cytiva).. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5 % Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4343 ± 399 RU.. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: Structure-Based Virtual Screening Identifies TREM2-Targeted Small Molecules that Enhance Microglial Phagocytosis
    Article Snippet: of EN020 to human TREM2 protein was assessed using surface plasmon resonance (SPR) on a Biacore 8K system (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084- H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, 0.5% Surfactant P20, pH 7.4) to a level of 4,343 ± 399 RU. .. Prior to immobilization, the chip surface was conditioned with three 1- minute injections of 1 M NaCl in 50 mM NaOH.

    Article Title: As48, a First-in-Class Dual-Function TREM2 Modulator: Receptor Activation and Shedding Inhibition
    Article Snippet: interaction between As48 and the human TREM2 protein was evaluated using surface plasmon resonance (SPR) on a Biacore 8K instrument (Cytiva). .. Biotinylated TREM2 (Cat. No. 11084-H49H-B, Sino Biological) was immobilized on an SA Sensor Chip (Cytiva) in PBS-P buffer (0.2 M phosphate buffer, 27 mM KCl, 1.37 M NaCl, and 0.5% Surfactant P20, pH 7.4; Cytiva) to a response level of RU 4,343 ± 399 RU. .. Before protein immobilization, the chip surface was conditioned with three 1-minute injections of 1 M NaCl in 50 mM NaOH.



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    R&D Systems goat anti human biotinylated trem2 detection antibody
    (A) Schematic of siRNA transfection of iMG. Cells were transfected 24 hours after iMG plating. After an additional 24 hours, cells were incubated with 2 μg/mL of pHrodo-labeled oligomerized amyloid (1-42) and imaged over a 20-hour window. (B) Confocal fluorescence images of iMG assessed for internalization of pHrodo-oligomerized amyloid beta treated as in (A). Digital phase contrast was used to visualize iMG. Images are stitched from four 20X images. Scale bar represents 400 μm. (C) Normalized intensity of internalized pHrodo-oligomerized amyloid beta in iMG per hour. Data are normalized to mock transfected control. (D) Normalized intensity of internalized pHrodo-oligomerized amyloid beta in iMG at endpoint. Data are normalized to mock transfected control. (E) RNA isolated from iMG 24 hours after transfection was used to quantify the percent CD33 mRNA expression by qPCR. (F) Change in <t>TREM2</t> secretion in conditioned media from iMG was quantified 24 hours after transfection by MSD. (G) Protein lysates isolated from iMG 24 hours after transfection were used to quantify percent SYK phosphorylation by AlphaLISA. Data represent mean ± SEM using one-way ANOVA with uncorrected Fisher’s LSD (D) and Dunnett’s multiple comparison test (E-G). Data points (n-numbers) are plotted on each bar graph and scatter plot each representing an independent experimental replicate. Line plots are representative of three independent experimental replicates (C).
    Goat Anti Human Biotinylated Trem2 Detection Antibody, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/biotinylated+trem2/Human+TREM2+Biotinylated+Antibody/pm41435829-741-11-17
    Average 93 stars, based on 1 article reviews
    goat anti human biotinylated trem2 detection antibody - by Bioz Stars, 2026-10
    93/100 stars
      Buy from Supplier

    93
    R&D Systems trem2
    (A) Schematic of siRNA transfection of iMG. Cells were transfected 24 hours after iMG plating. After an additional 24 hours, cells were incubated with 2 μg/mL of pHrodo-labeled oligomerized amyloid (1-42) and imaged over a 20-hour window. (B) Confocal fluorescence images of iMG assessed for internalization of pHrodo-oligomerized amyloid beta treated as in (A). Digital phase contrast was used to visualize iMG. Images are stitched from four 20X images. Scale bar represents 400 μm. (C) Normalized intensity of internalized pHrodo-oligomerized amyloid beta in iMG per hour. Data are normalized to mock transfected control. (D) Normalized intensity of internalized pHrodo-oligomerized amyloid beta in iMG at endpoint. Data are normalized to mock transfected control. (E) RNA isolated from iMG 24 hours after transfection was used to quantify the percent CD33 mRNA expression by qPCR. (F) Change in <t>TREM2</t> secretion in conditioned media from iMG was quantified 24 hours after transfection by MSD. (G) Protein lysates isolated from iMG 24 hours after transfection were used to quantify percent SYK phosphorylation by AlphaLISA. Data represent mean ± SEM using one-way ANOVA with uncorrected Fisher’s LSD (D) and Dunnett’s multiple comparison test (E-G). Data points (n-numbers) are plotted on each bar graph and scatter plot each representing an independent experimental replicate. Line plots are representative of three independent experimental replicates (C).
    Trem2, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/biotinylated+trem2/Human+TREM2+Biotinylated+Antibody/pm41435829-718-83-86
    Average 93 stars, based on 1 article reviews
    trem2 - by Bioz Stars, 2026-10
    93/100 stars
      Buy from Supplier

    Image Search Results


    (A) Schematic of siRNA transfection of iMG. Cells were transfected 24 hours after iMG plating. After an additional 24 hours, cells were incubated with 2 μg/mL of pHrodo-labeled oligomerized amyloid (1-42) and imaged over a 20-hour window. (B) Confocal fluorescence images of iMG assessed for internalization of pHrodo-oligomerized amyloid beta treated as in (A). Digital phase contrast was used to visualize iMG. Images are stitched from four 20X images. Scale bar represents 400 μm. (C) Normalized intensity of internalized pHrodo-oligomerized amyloid beta in iMG per hour. Data are normalized to mock transfected control. (D) Normalized intensity of internalized pHrodo-oligomerized amyloid beta in iMG at endpoint. Data are normalized to mock transfected control. (E) RNA isolated from iMG 24 hours after transfection was used to quantify the percent CD33 mRNA expression by qPCR. (F) Change in TREM2 secretion in conditioned media from iMG was quantified 24 hours after transfection by MSD. (G) Protein lysates isolated from iMG 24 hours after transfection were used to quantify percent SYK phosphorylation by AlphaLISA. Data represent mean ± SEM using one-way ANOVA with uncorrected Fisher’s LSD (D) and Dunnett’s multiple comparison test (E-G). Data points (n-numbers) are plotted on each bar graph and scatter plot each representing an independent experimental replicate. Line plots are representative of three independent experimental replicates (C).

    Journal: bioRxiv

    Article Title: Increased CD33 levels tune activation and function of induced human microglial cells through inhibition of the TREM2 pathway

    doi: 10.64898/2026.01.28.701050

    Figure Lengend Snippet: (A) Schematic of siRNA transfection of iMG. Cells were transfected 24 hours after iMG plating. After an additional 24 hours, cells were incubated with 2 μg/mL of pHrodo-labeled oligomerized amyloid (1-42) and imaged over a 20-hour window. (B) Confocal fluorescence images of iMG assessed for internalization of pHrodo-oligomerized amyloid beta treated as in (A). Digital phase contrast was used to visualize iMG. Images are stitched from four 20X images. Scale bar represents 400 μm. (C) Normalized intensity of internalized pHrodo-oligomerized amyloid beta in iMG per hour. Data are normalized to mock transfected control. (D) Normalized intensity of internalized pHrodo-oligomerized amyloid beta in iMG at endpoint. Data are normalized to mock transfected control. (E) RNA isolated from iMG 24 hours after transfection was used to quantify the percent CD33 mRNA expression by qPCR. (F) Change in TREM2 secretion in conditioned media from iMG was quantified 24 hours after transfection by MSD. (G) Protein lysates isolated from iMG 24 hours after transfection were used to quantify percent SYK phosphorylation by AlphaLISA. Data represent mean ± SEM using one-way ANOVA with uncorrected Fisher’s LSD (D) and Dunnett’s multiple comparison test (E-G). Data points (n-numbers) are plotted on each bar graph and scatter plot each representing an independent experimental replicate. Line plots are representative of three independent experimental replicates (C).

    Article Snippet: Briefly, streptavidin-coated small spot MSD plates (Meso Scale Diagnostics, Rockville, MD) were coated with Biotinylated goat anti-human TREM2 polyclonal antibody (R&D Systems) used as a capture antibody for 1.5 hours with agitation at 600 rpm.

    Techniques: Transfection, Incubation, Labeling, Fluorescence, Control, Isolation, Expressing, Phospho-proteomics, Comparison

    (A) Schematic of AAV6-mediated transduction of iMG. Cells were transduced with an MOI of 125000 at the time of plating. On day 3, cells were incubated with 2 μg/mL of pHrodo-labeled oligomerized amyloid (1-42) and imaged over a 20-hour window. (B) Protein lysates isolated from iMG 72 hours after transduction were used to quantify percent CD33 protein expression by MSD. Data are normalized to no AAV6 transduction control. (C) Confocal fluorescence images of iMG assessed for internalization of pHrodo-oligomerized amyloid beta treated as in (A). Digital phase contrast was used to visualize iMG. Images are stitched from four 20X images. Scale bar represents 400 μm. (D) Normalized intensity of internalized pHrodo-oligomerized amyloid beta in iMG transduced with or without AAV6-CD33 or AAV6-mCherry per hour. Data are normalized to no AAV6 transduction control. (E) Normalized intensity of internalized pHrodo-oligomerized amyloid beta in iMG transduced with or without AAV6-CD33 or AAV6-mCherry at endpoint. Data are normalized to no AAV6 transduction control. (F) TREM2 secretion in conditioned media was quantified from iMG 72 hours after transduction by MSD. (G)(left) Percent change in TREM2 secretion in conditioned media was quantified from HMC3 cells 48 hours after transduction with increasing AAV6-CD33 concentrations by MSD. Data are represented as a percent change relative to dose-matched AAV6-mCherry. (right) TREM2 secretion in conditioned media was quantified from HMC3 cells 48 hours after transduction of AAV6-CD33 by MSD. (MOI = 250000). (H) Protein lysates isolated from HMC3 cells 48 hours after transduction were used to quantify percent full length TREM2 protein expression by MSD. (MOI = 250000). Data represent mean ± SEM using one-way ANOVA with post-hoc Tukey’s multiple comparisons test (B), with uncorrected Fisher’s LSD (E), with post-hoc Dunnett multiple comparisons test (F, G) and one-tailed unpaired t-test (H). Data points (n-numbers) are plotted on each bar graph and scatter plot each representing an independent experimental replicate. Line plots represent three independent experimental replicates (D, G).

    Journal: bioRxiv

    Article Title: Increased CD33 levels tune activation and function of induced human microglial cells through inhibition of the TREM2 pathway

    doi: 10.64898/2026.01.28.701050

    Figure Lengend Snippet: (A) Schematic of AAV6-mediated transduction of iMG. Cells were transduced with an MOI of 125000 at the time of plating. On day 3, cells were incubated with 2 μg/mL of pHrodo-labeled oligomerized amyloid (1-42) and imaged over a 20-hour window. (B) Protein lysates isolated from iMG 72 hours after transduction were used to quantify percent CD33 protein expression by MSD. Data are normalized to no AAV6 transduction control. (C) Confocal fluorescence images of iMG assessed for internalization of pHrodo-oligomerized amyloid beta treated as in (A). Digital phase contrast was used to visualize iMG. Images are stitched from four 20X images. Scale bar represents 400 μm. (D) Normalized intensity of internalized pHrodo-oligomerized amyloid beta in iMG transduced with or without AAV6-CD33 or AAV6-mCherry per hour. Data are normalized to no AAV6 transduction control. (E) Normalized intensity of internalized pHrodo-oligomerized amyloid beta in iMG transduced with or without AAV6-CD33 or AAV6-mCherry at endpoint. Data are normalized to no AAV6 transduction control. (F) TREM2 secretion in conditioned media was quantified from iMG 72 hours after transduction by MSD. (G)(left) Percent change in TREM2 secretion in conditioned media was quantified from HMC3 cells 48 hours after transduction with increasing AAV6-CD33 concentrations by MSD. Data are represented as a percent change relative to dose-matched AAV6-mCherry. (right) TREM2 secretion in conditioned media was quantified from HMC3 cells 48 hours after transduction of AAV6-CD33 by MSD. (MOI = 250000). (H) Protein lysates isolated from HMC3 cells 48 hours after transduction were used to quantify percent full length TREM2 protein expression by MSD. (MOI = 250000). Data represent mean ± SEM using one-way ANOVA with post-hoc Tukey’s multiple comparisons test (B), with uncorrected Fisher’s LSD (E), with post-hoc Dunnett multiple comparisons test (F, G) and one-tailed unpaired t-test (H). Data points (n-numbers) are plotted on each bar graph and scatter plot each representing an independent experimental replicate. Line plots represent three independent experimental replicates (D, G).

    Article Snippet: Briefly, streptavidin-coated small spot MSD plates (Meso Scale Diagnostics, Rockville, MD) were coated with Biotinylated goat anti-human TREM2 polyclonal antibody (R&D Systems) used as a capture antibody for 1.5 hours with agitation at 600 rpm.

    Techniques: Transduction, Incubation, Labeling, Isolation, Expressing, Control, Fluorescence, One-tailed Test

    (A) Schematic of the TREM2-CD33 pathway. CD33 inhibition acts on SYK activation, upstream of microglial activation pathways AKT, ERK, p38, and JNK. (B) Protein lysates isolated from THP-1 monocytes 48 hours after transduction were used to quantify percent SYK phosphorylation by MSD. (MOI = 31250) (C) 48 hours post-transduction, THP-1 cells (MOI = 31250) were treated with increasing concentrations of TREM2-targeting antibody agonist (0-10 μg/mL). After 5 minutes, protein lysates were isolated and used to quantify percent SYK phosphorylation by MSD. (D) 48-hours post-transduction of increasing concentrations of AAV6-CD33 (MOI = 0-31250), THP-1 cells were treated with a TREM2-targeting antibody agonist (2.5 ug/mL). After 5 minutes, protein lysates were isolated and used to quantify percent SYK phosphorylation by MSD. (E) Percent AKT and GSK3β phosphorylation was quantified from HMC3 cell lysates 48 hours after transduction of AAV6-CD33, quantified by MSD and ELISA, respectively. (F) Percent ERK and p38-MAPK phosphorylation was quantified from HMC3 cell lysates 48 hours after transduction of AAV6-CD33, quantified by ELISA. (G) Percent JNK phosphorylation was quantified from HMC3 cell lysates 48 hours after transduction of AAV6-CD33, quantified by ELISA. (H) (left to right) Percent expression of secreted IL10, IL1β, TNFα, and IL6 in conditioned media from HMC3 cells 24 hours after LPS challenge and 48 hours after transduction of AAV6-CD33 was quantified by MSD. Data represent mean ± SEM using one-tailed unpaired t-test (A, E-G), and two-way ANOVA using uncorrected Fisher’s LSD with a single pooled variance (H). Data points (n-numbers) are plotted on each bar graph and scatter plot each representing an independent experimental replicate. Line plots are representative of three and two independent experimental replicates (C, D, respectively).

    Journal: bioRxiv

    Article Title: Increased CD33 levels tune activation and function of induced human microglial cells through inhibition of the TREM2 pathway

    doi: 10.64898/2026.01.28.701050

    Figure Lengend Snippet: (A) Schematic of the TREM2-CD33 pathway. CD33 inhibition acts on SYK activation, upstream of microglial activation pathways AKT, ERK, p38, and JNK. (B) Protein lysates isolated from THP-1 monocytes 48 hours after transduction were used to quantify percent SYK phosphorylation by MSD. (MOI = 31250) (C) 48 hours post-transduction, THP-1 cells (MOI = 31250) were treated with increasing concentrations of TREM2-targeting antibody agonist (0-10 μg/mL). After 5 minutes, protein lysates were isolated and used to quantify percent SYK phosphorylation by MSD. (D) 48-hours post-transduction of increasing concentrations of AAV6-CD33 (MOI = 0-31250), THP-1 cells were treated with a TREM2-targeting antibody agonist (2.5 ug/mL). After 5 minutes, protein lysates were isolated and used to quantify percent SYK phosphorylation by MSD. (E) Percent AKT and GSK3β phosphorylation was quantified from HMC3 cell lysates 48 hours after transduction of AAV6-CD33, quantified by MSD and ELISA, respectively. (F) Percent ERK and p38-MAPK phosphorylation was quantified from HMC3 cell lysates 48 hours after transduction of AAV6-CD33, quantified by ELISA. (G) Percent JNK phosphorylation was quantified from HMC3 cell lysates 48 hours after transduction of AAV6-CD33, quantified by ELISA. (H) (left to right) Percent expression of secreted IL10, IL1β, TNFα, and IL6 in conditioned media from HMC3 cells 24 hours after LPS challenge and 48 hours after transduction of AAV6-CD33 was quantified by MSD. Data represent mean ± SEM using one-tailed unpaired t-test (A, E-G), and two-way ANOVA using uncorrected Fisher’s LSD with a single pooled variance (H). Data points (n-numbers) are plotted on each bar graph and scatter plot each representing an independent experimental replicate. Line plots are representative of three and two independent experimental replicates (C, D, respectively).

    Article Snippet: Briefly, streptavidin-coated small spot MSD plates (Meso Scale Diagnostics, Rockville, MD) were coated with Biotinylated goat anti-human TREM2 polyclonal antibody (R&D Systems) used as a capture antibody for 1.5 hours with agitation at 600 rpm.

    Techniques: Inhibition, Activation Assay, Isolation, Transduction, Phospho-proteomics, Enzyme-linked Immunosorbent Assay, Expressing, One-tailed Test