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human complement-preserved serum a113  (Quidel)


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    Quidel human complement-preserved serum a113
    Human Complement Preserved Serum A113, supplied by Quidel, 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/product/human+serum+complement+preserved/human+complement/us12162931-708-4-7
    Average 90 stars, based on 1 article reviews
    human complement-preserved serum a113 - by Bioz Stars, 2026-11
    90/100 stars

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    other:

    Article Title: Anti-human claudin 18.2 monoclonal antibody and application thereof
    Article Snippet: The antibody to be tested and the control antibody were diluted with the medium (RPMI1640 medium (Gibco, 11835-030)+1% FBS (Gibco, 10099-141)) to a final concentration of 50 ug/ml, and then diluted 5 times for 8 gradients, and the complement (Quidel, A113) was diluted to a final concentration of 1:50 (V/V).

    Article Title: Properdin binding protein and use thereof
    Article Snippet: Eculizumab (Targetmol, T9915), a recombinant humanized monoclonal antibody against the complement protein C5 was as a control also showed inhibitory ability in the AP pathway, with IC50 of 50 nM.

    Article Title: The Therapeutic Monoclonal Antibody Bamlanivimab Does Not Enhance SARS-CoV-2 Infection by FcR-Mediated Mechanisms
    Article Snippet: Five milliliters of complement from human serum (Quidel, San Diego, CA, USA, A113) was rapidly thawed at 37 °C and six-fold diluted using assay buffer.

    Article Title: Properdin binding protein and use thereof
    Article Snippet: At the same time, human complement-preserved serum (Quidel, A113) was diluted to 20% vol/vol in GVBS-EGTA (1×AP buffer: 0.1% gelatin, 145 mM NaCl, 2.5 mM sodium barbital, pH7.4 with 10 mM Mg/EGTA), incubate on ice for 30 minutes and added (50 μl/well) to the rows of the same 96-well plate such that the final concentration of human serum in each well was 10%.

    Article Title: The Therapeutic Monoclonal Antibody Bamlanivimab Does Not Enhance SARS-CoV-2 Infection by FcR-Mediated Mechanisms.
    Article Snippet: Preparation of Complement Five milliliters of complement from human serum (Quidel, San Diego, CA, USA, A113) was rapidly thawed at 37 ◦C and six-fold diluted using assay buffer.

    CDC Assay:

    Article Title: Human monocarboxylate transporter 1 antibodies and uses thereof
    Article Snippet: ADCC, ADCP and CDC assay plates were gently agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 1 h at 37° C. The stably transfected Jurkat V158 cells or Jurkat H131 cells were diluted to a concentration of 3×106 cells/mL and 50 IL/well was added to the respective ADCC and ADCP assay plates containing the serially diluted test samples and Raji cells, and the plate was mixed by gentle agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 4 hrs at 37° C. Pre-diluted complement from human serum (Quidel A113) was added to the CDC plate (50 μL/well) containing the serially diluted test samples and Raji cells, and the plate was mixed by gentle agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 2 h at 37° C. After incubation, the ADCC, ADCP, and CDC plates were brought to room temperature for 10 minutes followed by addition of 100 μL of One-glo Ex (E8130, Promega) to the ADCC and ADCP assay plates and the Cell-Titer Glo (G7571, Promega) to the CDC assay plates. .. ADCC, ADCP and CDC assay plates were gently agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 1 h at 37° C. The stably transfected Jurkat V158 cells or Jurkat H131 cells were diluted to a concentration of 3×106 cells/mL and 50 IL/well was added to the respective ADCC and ADCP assay plates containing the serially diluted test samples and Raji cells, and the plate was mixed by gentle agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 4 hrs at 37° C. Pre-diluted complement from human serum (Quidel A113) was added to the CDC plate (50 μL/well) containing the serially diluted test samples and Raji cells, and the plate was mixed by gentle agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 2 h at 37° C. After incubation, the ADCC, ADCP, and CDC plates were brought to room temperature for 10 minutes followed by addition of 100 μL of One-glo Ex (E8130, Promega) to the ADCC and ADCP assay plates and the Cell-Titer Glo (G7571, Promega) to the CDC assay plates. ..

    Article Title: Antagonistic CD40 monoclonal antibodies and uses thereof
    Article Snippet: After the incubation, 100 microliters of CellTiter-Glo® (Promega, Madison, WI) was added to each well. .. Twenty-five microliters of human complement (obtained from Quidel; diluted 1:3 with CDC assay medium) was added to each well. .. Percentage of cell viability is plotted for each antibody using Prism v5.01 software from GraphPad Inc.

    Incubation:

    Article Title: Human monocarboxylate transporter 1 antibodies and uses thereof
    Article Snippet: ADCC, ADCP and CDC assay plates were gently agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 1 h at 37° C. The stably transfected Jurkat V158 cells or Jurkat H131 cells were diluted to a concentration of 3×106 cells/mL and 50 IL/well was added to the respective ADCC and ADCP assay plates containing the serially diluted test samples and Raji cells, and the plate was mixed by gentle agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 4 hrs at 37° C. Pre-diluted complement from human serum (Quidel A113) was added to the CDC plate (50 μL/well) containing the serially diluted test samples and Raji cells, and the plate was mixed by gentle agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 2 h at 37° C. After incubation, the ADCC, ADCP, and CDC plates were brought to room temperature for 10 minutes followed by addition of 100 μL of One-glo Ex (E8130, Promega) to the ADCC and ADCP assay plates and the Cell-Titer Glo (G7571, Promega) to the CDC assay plates. .. ADCC, ADCP and CDC assay plates were gently agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 1 h at 37° C. The stably transfected Jurkat V158 cells or Jurkat H131 cells were diluted to a concentration of 3×106 cells/mL and 50 IL/well was added to the respective ADCC and ADCP assay plates containing the serially diluted test samples and Raji cells, and the plate was mixed by gentle agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 4 hrs at 37° C. Pre-diluted complement from human serum (Quidel A113) was added to the CDC plate (50 μL/well) containing the serially diluted test samples and Raji cells, and the plate was mixed by gentle agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 2 h at 37° C. After incubation, the ADCC, ADCP, and CDC plates were brought to room temperature for 10 minutes followed by addition of 100 μL of One-glo Ex (E8130, Promega) to the ADCC and ADCP assay plates and the Cell-Titer Glo (G7571, Promega) to the CDC assay plates. ..

    Article Title: Developing a human monoclonal antibody combination CRM25 to prevent rabies after exposure.
    Article Snippet: This is a PDF file of an article that has undergone enhancements after acceptance, such as the addition of a cover page and metadata, and formatting for readability, but it is not yet the definitive version of record.. This version will undergo additional copyediting, typesetting and review before it is published in its final form, but we are providing this version to give early visibility of the article.. Please note that, during the production process, errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

    Stable Transfection:

    Article Title: Human monocarboxylate transporter 1 antibodies and uses thereof
    Article Snippet: ADCC, ADCP and CDC assay plates were gently agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 1 h at 37° C. The stably transfected Jurkat V158 cells or Jurkat H131 cells were diluted to a concentration of 3×106 cells/mL and 50 IL/well was added to the respective ADCC and ADCP assay plates containing the serially diluted test samples and Raji cells, and the plate was mixed by gentle agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 4 hrs at 37° C. Pre-diluted complement from human serum (Quidel A113) was added to the CDC plate (50 μL/well) containing the serially diluted test samples and Raji cells, and the plate was mixed by gentle agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 2 h at 37° C. After incubation, the ADCC, ADCP, and CDC plates were brought to room temperature for 10 minutes followed by addition of 100 μL of One-glo Ex (E8130, Promega) to the ADCC and ADCP assay plates and the Cell-Titer Glo (G7571, Promega) to the CDC assay plates. .. ADCC, ADCP and CDC assay plates were gently agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 1 h at 37° C. The stably transfected Jurkat V158 cells or Jurkat H131 cells were diluted to a concentration of 3×106 cells/mL and 50 IL/well was added to the respective ADCC and ADCP assay plates containing the serially diluted test samples and Raji cells, and the plate was mixed by gentle agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 4 hrs at 37° C. Pre-diluted complement from human serum (Quidel A113) was added to the CDC plate (50 μL/well) containing the serially diluted test samples and Raji cells, and the plate was mixed by gentle agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 2 h at 37° C. After incubation, the ADCC, ADCP, and CDC plates were brought to room temperature for 10 minutes followed by addition of 100 μL of One-glo Ex (E8130, Promega) to the ADCC and ADCP assay plates and the Cell-Titer Glo (G7571, Promega) to the CDC assay plates. ..

    Transfection:

    Article Title: Human monocarboxylate transporter 1 antibodies and uses thereof
    Article Snippet: ADCC, ADCP and CDC assay plates were gently agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 1 h at 37° C. The stably transfected Jurkat V158 cells or Jurkat H131 cells were diluted to a concentration of 3×106 cells/mL and 50 IL/well was added to the respective ADCC and ADCP assay plates containing the serially diluted test samples and Raji cells, and the plate was mixed by gentle agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 4 hrs at 37° C. Pre-diluted complement from human serum (Quidel A113) was added to the CDC plate (50 μL/well) containing the serially diluted test samples and Raji cells, and the plate was mixed by gentle agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 2 h at 37° C. After incubation, the ADCC, ADCP, and CDC plates were brought to room temperature for 10 minutes followed by addition of 100 μL of One-glo Ex (E8130, Promega) to the ADCC and ADCP assay plates and the Cell-Titer Glo (G7571, Promega) to the CDC assay plates. .. ADCC, ADCP and CDC assay plates were gently agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 1 h at 37° C. The stably transfected Jurkat V158 cells or Jurkat H131 cells were diluted to a concentration of 3×106 cells/mL and 50 IL/well was added to the respective ADCC and ADCP assay plates containing the serially diluted test samples and Raji cells, and the plate was mixed by gentle agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 4 hrs at 37° C. Pre-diluted complement from human serum (Quidel A113) was added to the CDC plate (50 μL/well) containing the serially diluted test samples and Raji cells, and the plate was mixed by gentle agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 2 h at 37° C. After incubation, the ADCC, ADCP, and CDC plates were brought to room temperature for 10 minutes followed by addition of 100 μL of One-glo Ex (E8130, Promega) to the ADCC and ADCP assay plates and the Cell-Titer Glo (G7571, Promega) to the CDC assay plates. ..

    Concentration Assay:

    Article Title: Human monocarboxylate transporter 1 antibodies and uses thereof
    Article Snippet: ADCC, ADCP and CDC assay plates were gently agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 1 h at 37° C. The stably transfected Jurkat V158 cells or Jurkat H131 cells were diluted to a concentration of 3×106 cells/mL and 50 IL/well was added to the respective ADCC and ADCP assay plates containing the serially diluted test samples and Raji cells, and the plate was mixed by gentle agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 4 hrs at 37° C. Pre-diluted complement from human serum (Quidel A113) was added to the CDC plate (50 μL/well) containing the serially diluted test samples and Raji cells, and the plate was mixed by gentle agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 2 h at 37° C. After incubation, the ADCC, ADCP, and CDC plates were brought to room temperature for 10 minutes followed by addition of 100 μL of One-glo Ex (E8130, Promega) to the ADCC and ADCP assay plates and the Cell-Titer Glo (G7571, Promega) to the CDC assay plates. .. ADCC, ADCP and CDC assay plates were gently agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 1 h at 37° C. The stably transfected Jurkat V158 cells or Jurkat H131 cells were diluted to a concentration of 3×106 cells/mL and 50 IL/well was added to the respective ADCC and ADCP assay plates containing the serially diluted test samples and Raji cells, and the plate was mixed by gentle agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 4 hrs at 37° C. Pre-diluted complement from human serum (Quidel A113) was added to the CDC plate (50 μL/well) containing the serially diluted test samples and Raji cells, and the plate was mixed by gentle agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 2 h at 37° C. After incubation, the ADCC, ADCP, and CDC plates were brought to room temperature for 10 minutes followed by addition of 100 μL of One-glo Ex (E8130, Promega) to the ADCC and ADCP assay plates and the Cell-Titer Glo (G7571, Promega) to the CDC assay plates. ..

    Gentle:

    Article Title: Human monocarboxylate transporter 1 antibodies and uses thereof
    Article Snippet: ADCC, ADCP and CDC assay plates were gently agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 1 h at 37° C. The stably transfected Jurkat V158 cells or Jurkat H131 cells were diluted to a concentration of 3×106 cells/mL and 50 IL/well was added to the respective ADCC and ADCP assay plates containing the serially diluted test samples and Raji cells, and the plate was mixed by gentle agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 4 hrs at 37° C. Pre-diluted complement from human serum (Quidel A113) was added to the CDC plate (50 μL/well) containing the serially diluted test samples and Raji cells, and the plate was mixed by gentle agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 2 h at 37° C. After incubation, the ADCC, ADCP, and CDC plates were brought to room temperature for 10 minutes followed by addition of 100 μL of One-glo Ex (E8130, Promega) to the ADCC and ADCP assay plates and the Cell-Titer Glo (G7571, Promega) to the CDC assay plates. .. ADCC, ADCP and CDC assay plates were gently agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 1 h at 37° C. The stably transfected Jurkat V158 cells or Jurkat H131 cells were diluted to a concentration of 3×106 cells/mL and 50 IL/well was added to the respective ADCC and ADCP assay plates containing the serially diluted test samples and Raji cells, and the plate was mixed by gentle agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 4 hrs at 37° C. Pre-diluted complement from human serum (Quidel A113) was added to the CDC plate (50 μL/well) containing the serially diluted test samples and Raji cells, and the plate was mixed by gentle agitation on a plate shaker for 30 seconds at 200 rpm, then incubated for 2 h at 37° C. After incubation, the ADCC, ADCP, and CDC plates were brought to room temperature for 10 minutes followed by addition of 100 μL of One-glo Ex (E8130, Promega) to the ADCC and ADCP assay plates and the Cell-Titer Glo (G7571, Promega) to the CDC assay plates. ..

    CCK-8 Assay:

    Article Title: Developing a human monoclonal antibody combination CRM25 to prevent rabies after exposure.
    Article Snippet: This is a PDF file of an article that has undergone enhancements after acceptance, such as the addition of a cover page and metadata, and formatting for readability, but it is not yet the definitive version of record.. This version will undergo additional copyediting, typesetting and review before it is published in its final form, but we are providing this version to give early visibility of the article.. Please note that, during the production process, errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.



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    Complement Technology Inc complement preserved normal human serum (nhs)
    SAR443809 specifically inhibits AP without inhibiting CP or LP. SAR443809 and its corresponding IgG isotype control were tested in a series of assays to assess their ability to inhibit the different <t>complement</t> pathways. A dose-dilution series of SAR443809 (●) or IgG control antibody (○) were tested in the commercial Wieslab EIA assays for (A) AP, (C) CP, and (D) LP, in which the inhibition of MAC deposition upon pathway specific activation was assessed per manufacturer’s protocol. (B) Antibodies were also tested in AP hemolysis assay. Rabbit erythrocytes were incubated with 10% <t>NHS</t> containing Mg 2+ -EGTA in the presence of varying concentrations of either SAR443809 (●) or the isotype control (○). The extent of hemolysis was quantified using the absorbance of the released hemoglobin in the supernatant. The data reported here is a mean of 3 independent experiments ± standard deviation, for all 4 data sets.
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    SAR443809 specifically inhibits AP without inhibiting CP or LP. SAR443809 and its corresponding IgG isotype control were tested in a series of assays to assess their ability to inhibit the different complement pathways. A dose-dilution series of SAR443809 (●) or IgG control antibody (○) were tested in the commercial Wieslab EIA assays for (A) AP, (C) CP, and (D) LP, in which the inhibition of MAC deposition upon pathway specific activation was assessed per manufacturer’s protocol. (B) Antibodies were also tested in AP hemolysis assay. Rabbit erythrocytes were incubated with 10% NHS containing Mg 2+ -EGTA in the presence of varying concentrations of either SAR443809 (●) or the isotype control (○). The extent of hemolysis was quantified using the absorbance of the released hemoglobin in the supernatant. The data reported here is a mean of 3 independent experiments ± standard deviation, for all 4 data sets.

    Journal: Blood Advances

    Article Title: SAR443809: a selective inhibitor of the complement alternative pathway, targeting complement factor Bb

    doi: 10.1182/bloodadvances.2022009028

    Figure Lengend Snippet: SAR443809 specifically inhibits AP without inhibiting CP or LP. SAR443809 and its corresponding IgG isotype control were tested in a series of assays to assess their ability to inhibit the different complement pathways. A dose-dilution series of SAR443809 (●) or IgG control antibody (○) were tested in the commercial Wieslab EIA assays for (A) AP, (C) CP, and (D) LP, in which the inhibition of MAC deposition upon pathway specific activation was assessed per manufacturer’s protocol. (B) Antibodies were also tested in AP hemolysis assay. Rabbit erythrocytes were incubated with 10% NHS containing Mg 2+ -EGTA in the presence of varying concentrations of either SAR443809 (●) or the isotype control (○). The extent of hemolysis was quantified using the absorbance of the released hemoglobin in the supernatant. The data reported here is a mean of 3 independent experiments ± standard deviation, for all 4 data sets.

    Article Snippet: Complement preserved normal human serum (NHS) was sourced from Complement Technology Inc (Tyler, TX), BioIVT (Westbury, NY), or Innovative Research (Novi, MI).

    Techniques: Control, Inhibition, Activation Assay, Hemolysis Assay, Incubation, Standard Deviation