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real-time surface plasmon resonance (spr) based biacore t200 biosensor  (Biacore)

 
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    Biacore real-time surface plasmon resonance (spr) based biacore t200 biosensor
    Real Time Surface Plasmon Resonance (Spr) Based Biacore T200 Biosensor, supplied by Biacore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/real-time surface plasmon resonance (spr) based biacore t200 biosensor/product/Biacore
    Average 90 stars, based on 1 article reviews
    real-time surface plasmon resonance (spr) based biacore t200 biosensor - by Bioz Stars, 2026-02
    90/100 stars

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    Affinity analysis of the designed antibodies. ( A ) Initial affinity screening of designed antibodies binding to Aβ1-42 oligomers and AL fibrils, respectively, by ELISA. For each experiment, control group using PBS incubated with Aβ1-42 oligomers or AL fibrils was carried out. Experiments were performed three times, and each sample was run in triplicate. Data are expressed as mean ± SEM. M1–M30: different designed mutants; wild-type: crenezumab; control: PBS. ( B ) SPR profile of a direct comparison of wild-type (WT) and mutant (M5) binding to Aβ42 oligomers and AL fibrils using the Biacore <t>T200.</t> ( C ) Further affinity analysis of M5, M10, and M29 mutants binding to Aβ1-42 oligomers and AL fibrils, respectively, by Biacore T200.
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    Affinity analysis of the designed antibodies. ( A ) Initial affinity screening of designed antibodies binding to Aβ1-42 oligomers and AL fibrils, respectively, by ELISA. For each experiment, control group using PBS incubated with Aβ1-42 oligomers or AL fibrils was carried out. Experiments were performed three times, and each sample was run in triplicate. Data are expressed as mean ± SEM. M1–M30: different designed mutants; wild-type: crenezumab; control: PBS. ( B ) SPR profile of a direct comparison of wild-type (WT) and mutant (M5) binding to Aβ42 oligomers and AL fibrils using the Biacore T200. ( C ) Further affinity analysis of M5, M10, and M29 mutants binding to Aβ1-42 oligomers and AL fibrils, respectively, by Biacore T200.

    Journal: International Journal of Molecular Sciences

    Article Title: Re-Engineering Therapeutic Anti-Aβ Monoclonal Antibody to Target Amyloid Light Chain

    doi: 10.3390/ijms25031593

    Figure Lengend Snippet: Affinity analysis of the designed antibodies. ( A ) Initial affinity screening of designed antibodies binding to Aβ1-42 oligomers and AL fibrils, respectively, by ELISA. For each experiment, control group using PBS incubated with Aβ1-42 oligomers or AL fibrils was carried out. Experiments were performed three times, and each sample was run in triplicate. Data are expressed as mean ± SEM. M1–M30: different designed mutants; wild-type: crenezumab; control: PBS. ( B ) SPR profile of a direct comparison of wild-type (WT) and mutant (M5) binding to Aβ42 oligomers and AL fibrils using the Biacore T200. ( C ) Further affinity analysis of M5, M10, and M29 mutants binding to Aβ1-42 oligomers and AL fibrils, respectively, by Biacore T200.

    Article Snippet: Based on the ELISA assay results, eight engineered antibodies were screening out for further binding affinity verification using a surface plasmon resonance (SPR)-based assay on Biacore T200 instruments.

    Techniques: Binding Assay, Enzyme-linked Immunosorbent Assay, Incubation, Comparison, Mutagenesis