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human plasma  (Boster Bio)


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    Structured Review

    Boster Bio human plasma
    Human Plasma, supplied by Boster Bio, used in various techniques. Bioz Stars score: 90/100, based on 17 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human plasma/product/Boster Bio
    Average 90 stars, based on 17 article reviews
    human plasma - by Bioz Stars, 2026-02
    90/100 stars

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    Figure 2 ELISA validation of three serum biomarkers using an independent cohort and their correlation with clinical indices. (A–C) A cohort of 80 serum samples: 30 healthy controls (HC, green) and 50 patients with lupus nephritis (LN, red) were tested by ELISA for the levels of ICAM2, <t>TIMP1</t> and THBS1. (D) The discriminatory abilities of the three serum markers were assessed in distinguishing patients with LN from HCs using receiver operating characteristic (ROC) curve analysis. (E–K) The correlation of ELISA-assayed serum ICAM2 levels with clinical indices in LN. r denotes Spearman’s correlation coefficient. ****p<0.0001. AUC, area under the curve.
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    Image Search Results


    Figure 2 ELISA validation of three serum biomarkers using an independent cohort and their correlation with clinical indices. (A–C) A cohort of 80 serum samples: 30 healthy controls (HC, green) and 50 patients with lupus nephritis (LN, red) were tested by ELISA for the levels of ICAM2, TIMP1 and THBS1. (D) The discriminatory abilities of the three serum markers were assessed in distinguishing patients with LN from HCs using receiver operating characteristic (ROC) curve analysis. (E–K) The correlation of ELISA-assayed serum ICAM2 levels with clinical indices in LN. r denotes Spearman’s correlation coefficient. ****p<0.0001. AUC, area under the curve.

    Journal: Lupus science & medicine

    Article Title: Proteomics uncovers ICAM2 (CD102) as a novel serum biomarker of proliferative lupus nephritis.

    doi: 10.1136/lupus-2024-001446

    Figure Lengend Snippet: Figure 2 ELISA validation of three serum biomarkers using an independent cohort and their correlation with clinical indices. (A–C) A cohort of 80 serum samples: 30 healthy controls (HC, green) and 50 patients with lupus nephritis (LN, red) were tested by ELISA for the levels of ICAM2, TIMP1 and THBS1. (D) The discriminatory abilities of the three serum markers were assessed in distinguishing patients with LN from HCs using receiver operating characteristic (ROC) curve analysis. (E–K) The correlation of ELISA-assayed serum ICAM2 levels with clinical indices in LN. r denotes Spearman’s correlation coefficient. ****p<0.0001. AUC, area under the curve.

    Article Snippet: Serum samples for TIMP1 (CUSABIO, Catalogue No CSB- E08003h, Wuhan, China) and THBS1 (CUSABIO, Catalogue No CSB- E08763h, Wuhan, China) were diluted 1:100 and 1:400, respectively, whereas the ICAM2 (BOSTER, Catalogue No EK0999, Peachtree Corners, Georgia) ELISA assays used serum at 1:5 dilution.

    Techniques: Enzyme-linked Immunosorbent Assay, Biomarker Discovery

    Journal: iScience

    Article Title: Human monocyte-derived macrophages shift subcellular metalloprotease activity depending on their activation state

    doi: 10.1016/j.isci.2024.111171

    Figure Lengend Snippet:

    Article Snippet: Human MMP-9/TIMP-1 DuoSet ELISA , R&D Systems , Cat # DY1449.

    Techniques: Plasmid Preparation, Recombinant, Knock-Out, Blocking Assay, Staining, Antibody Labeling, Reverse Transcription, Lysis, Protease Inhibitor, Enzyme-linked Immunosorbent Assay, Fractionation, Cell Culture, Software, Flow Cytometry, Fluorescence, Spectrophotometry

    Journal: iScience

    Article Title: Human monocyte-derived macrophages shift subcellular metalloprotease activity depending on their activation state

    doi: 10.1016/j.isci.2024.111171

    Figure Lengend Snippet:

    Article Snippet: Human TIMP-1 DuoSet ELISA , R&D Systems , Cat #DY970.

    Techniques: Plasmid Preparation, Recombinant, Knock-Out, Blocking Assay, Staining, Antibody Labeling, Reverse Transcription, Lysis, Protease Inhibitor, Enzyme-linked Immunosorbent Assay, Fractionation, Cell Culture, Software, Flow Cytometry, Fluorescence, Spectrophotometry

    Journal: iScience

    Article Title: Human monocyte-derived macrophages shift subcellular metalloprotease activity depending on their activation state

    doi: 10.1016/j.isci.2024.111171

    Figure Lengend Snippet:

    Article Snippet: MMP-12 (Human MMP-12 ELISA, Cat # EH327RB, Invitrogen), ADAM-9 (Human ADAM-9 DuoSet ELISA, Cat # DY939, R&D Systems), TIMP-1 (Human TIMP-1 DuoSet ELISA, Cat # DY970, R&D Systems), TIMP-2 (Human TIMP-2 DuoSet ELISA, Cat # DY971, R&D Systems), MMP-9/TIMP-1 complex (Human MMP-9/TIMP-1 DuoSet ELISA, Cat # DY1449, R&D Systems), Cystatin C (Human Cystatin C DuoSet ELISA, Cat # DY1196, R&D Systems), Cathepsin D (Human Cathepsin D DuoSet ELISA, Cat # DY1014, R&D Systems), Serpin E1 (Human Serpin E1 DuoSet ELISA, Cat # DY1786, R&D Systems), Tumor Necrosis Factor alpha (TNF-α) (Human TNF-alpha DuoSet ELISA, Cat # DY210, R&D Systems), IL-1β (Human IL-1 beta DuoSet ELISA, Cat # DY201, R&D Systems), IL-6 (Human IL-6 DuoSet ELISA, Cat # DY206, R&D Systems) and CCL-18 (Human CCL18/PARC DuoSet ELISA, Cat # DY394, R&D Systems) concentrations were measured by sandwich ELISA according to the manufacturer’s protocols.

    Techniques: Plasmid Preparation, Recombinant, Knock-Out, Blocking Assay, Staining, Antibody Labeling, Reverse Transcription, Lysis, Protease Inhibitor, Enzyme-linked Immunosorbent Assay, Fractionation, Cell Culture, Software, Flow Cytometry, Fluorescence, Spectrophotometry