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5x stock elisa plate coating buffer  (Elabscience Biotechnology)


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    Structured Review

    Elabscience Biotechnology 5x stock elisa plate coating buffer
    Schematic representation of the principle of SARS-CoV-2-RBD neutralizing <t>ELISA</t> assay2.2. Assay Optimization
    5x Stock Elisa Plate Coating Buffer, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/5x+stock+elisa+plate+coating+buffer/ELISA+Plate+Coating+Buffer/pmc09288645-235-53-59
    Average 93 stars, based on 4 article reviews
    5x stock elisa plate coating buffer - by Bioz Stars, 2026-09
    93/100 stars

    Images

    1) Product Images from "Application and Validation of SARS-CoV-2 RBD Neutralizing ELISA Assay"

    Article Title: Application and Validation of SARS-CoV-2 RBD Neutralizing ELISA Assay

    Journal: Archives of Razi Institute

    doi: 10.22092/ARI.2021.356677.1890

    Schematic representation of the principle of SARS-CoV-2-RBD neutralizing ELISA assay2.2. Assay Optimization
    Figure Legend Snippet: Schematic representation of the principle of SARS-CoV-2-RBD neutralizing ELISA assay2.2. Assay Optimization

    Techniques Used: Enzyme-linked Immunosorbent Assay

    Standard curve of anti-SARS-COV-2-RBD nAbs for the in-house developed SARS-COV-2-RBD neutralizing ELISA assay
    Figure Legend Snippet: Standard curve of anti-SARS-COV-2-RBD nAbs for the in-house developed SARS-COV-2-RBD neutralizing ELISA assay

    Techniques Used: Enzyme-linked Immunosorbent Assay

    Mean ± standard deviation of OD values of different anti-SARS-COV-2-RBD neutralizing antibody standards generated by the designed neutralizing  ELISA  kit
    Figure Legend Snippet: Mean ± standard deviation of OD values of different anti-SARS-COV-2-RBD neutralizing antibody standards generated by the designed neutralizing ELISA kit

    Techniques Used: Standard Deviation, Generated, Enzyme-linked Immunosorbent Assay, Concentration Assay, Negative Control, Positive Control

    Cut-off value results of the in-house neutralizing  ELISA;  A) Optimized ROC analysis cut-off value of positive and B) Concentration and log concentration limits for the optimal established cut-off in this assay
    Figure Legend Snippet: Cut-off value results of the in-house neutralizing ELISA; A) Optimized ROC analysis cut-off value of positive and B) Concentration and log concentration limits for the optimal established cut-off in this assay

    Techniques Used: Enzyme-linked Immunosorbent Assay, Concentration Assay

    Receiver operating characteristic curve analysis for the optimal cut-off value for detecting the positive anti-SARS-COV-2-RBD neutralizing antibodies using the in-house developed neutralizing ELISA kit
    Figure Legend Snippet: Receiver operating characteristic curve analysis for the optimal cut-off value for detecting the positive anti-SARS-COV-2-RBD neutralizing antibodies using the in-house developed neutralizing ELISA kit

    Techniques Used: Enzyme-linked Immunosorbent Assay

    Serum panels using the in-house designed SARS-COV-2-RBD neutralizing  ELISA  assay; A) Positive control samples for the assay validation and B) Negative control samples for the assay validation
    Figure Legend Snippet: Serum panels using the in-house designed SARS-COV-2-RBD neutralizing ELISA assay; A) Positive control samples for the assay validation and B) Negative control samples for the assay validation

    Techniques Used: Enzyme-linked Immunosorbent Assay, Positive Control, Biomarker Discovery, Negative Control, Concentration Assay

    Agreement of the results between the in-house SARS-COV-2-RBD neutralizing  ELISA  assay and gold standard test at the in-house established cut-off
    Figure Legend Snippet: Agreement of the results between the in-house SARS-COV-2-RBD neutralizing ELISA assay and gold standard test at the in-house established cut-off

    Techniques Used: Enzyme-linked Immunosorbent Assay

    Validation parameters of the in-house SARS-COV-2-RBD neutralizing  ELISA  assay
    Figure Legend Snippet: Validation parameters of the in-house SARS-COV-2-RBD neutralizing ELISA assay

    Techniques Used: Biomarker Discovery, Enzyme-linked Immunosorbent Assay

    Related Articles

    Recombinant:

    Article Title: Application and Validation of SARS-CoV-2 RBD Neutralizing ELISA Assay
    Article Snippet: .. Preparation of Working Human Angiotensin-Converting Enzyme 2 Protein Solution To immobilize the hACE2 protein at 400 ng/well in 100 μl of 1X working Coating Buffer on the microtiter plates wells, a calculated volume from Stock solution vial of Recombinant His-Tag-Human ACE2 protein in a concentration of 2.8 mg/ml (Raybiotech) was diluted immediately before usage with the prepared 1X working coating buffer from 5X stock ELISA Plate Coating Buffer (Elabscience) to a required volume at the appropriate concentration (4 ng/μl), which was determined in the initial experiments. ..

    Article Title: Application and Validation of SARS-CoV-2 RBD Neutralizing ELISA Assay
    Article Snippet: To apply 50 μL of HRP-RBD working solution to fit 10 ng/well, a calculated volume from the prepared HRP-RBD stock solution was diluted with HRP-Conjugate Diluent (Elabscience) to the required volume at the appropriate concentration (0.2 ng/μl), which was determined in the initial experiments. .. To immobilize the hACE2 protein at 400 ng/well in 100 μl of 1X working Coating Buffer on the microtiter plates wells, a calculated volume from Stock solution vial of Recombinant His-Tag-Human ACE2 protein in a concentration of 2.8 mg/ml (Raybiotech) was diluted immediately before usage with the prepared 1X working coating buffer from 5X stock ELISA Plate Coating Buffer (Elabscience) to a required volume at the appropriate concentration (4 ng/μl), which was determined in the initial experiments. ..

    Concentration Assay:

    Article Title: Application and Validation of SARS-CoV-2 RBD Neutralizing ELISA Assay
    Article Snippet: .. Preparation of Working Human Angiotensin-Converting Enzyme 2 Protein Solution To immobilize the hACE2 protein at 400 ng/well in 100 μl of 1X working Coating Buffer on the microtiter plates wells, a calculated volume from Stock solution vial of Recombinant His-Tag-Human ACE2 protein in a concentration of 2.8 mg/ml (Raybiotech) was diluted immediately before usage with the prepared 1X working coating buffer from 5X stock ELISA Plate Coating Buffer (Elabscience) to a required volume at the appropriate concentration (4 ng/μl), which was determined in the initial experiments. ..

    Article Title: Application and Validation of SARS-CoV-2 RBD Neutralizing ELISA Assay
    Article Snippet: To apply 50 μL of HRP-RBD working solution to fit 10 ng/well, a calculated volume from the prepared HRP-RBD stock solution was diluted with HRP-Conjugate Diluent (Elabscience) to the required volume at the appropriate concentration (0.2 ng/μl), which was determined in the initial experiments. .. To immobilize the hACE2 protein at 400 ng/well in 100 μl of 1X working Coating Buffer on the microtiter plates wells, a calculated volume from Stock solution vial of Recombinant His-Tag-Human ACE2 protein in a concentration of 2.8 mg/ml (Raybiotech) was diluted immediately before usage with the prepared 1X working coating buffer from 5X stock ELISA Plate Coating Buffer (Elabscience) to a required volume at the appropriate concentration (4 ng/μl), which was determined in the initial experiments. ..

    Enzyme-linked Immunosorbent Assay:

    Article Title: Application and Validation of SARS-CoV-2 RBD Neutralizing ELISA Assay
    Article Snippet: .. Preparation of Working Human Angiotensin-Converting Enzyme 2 Protein Solution To immobilize the hACE2 protein at 400 ng/well in 100 μl of 1X working Coating Buffer on the microtiter plates wells, a calculated volume from Stock solution vial of Recombinant His-Tag-Human ACE2 protein in a concentration of 2.8 mg/ml (Raybiotech) was diluted immediately before usage with the prepared 1X working coating buffer from 5X stock ELISA Plate Coating Buffer (Elabscience) to a required volume at the appropriate concentration (4 ng/μl), which was determined in the initial experiments. ..

    Article Title: Application and Validation of SARS-CoV-2 RBD Neutralizing ELISA Assay
    Article Snippet: To apply 50 μL of HRP-RBD working solution to fit 10 ng/well, a calculated volume from the prepared HRP-RBD stock solution was diluted with HRP-Conjugate Diluent (Elabscience) to the required volume at the appropriate concentration (0.2 ng/μl), which was determined in the initial experiments. .. To immobilize the hACE2 protein at 400 ng/well in 100 μl of 1X working Coating Buffer on the microtiter plates wells, a calculated volume from Stock solution vial of Recombinant His-Tag-Human ACE2 protein in a concentration of 2.8 mg/ml (Raybiotech) was diluted immediately before usage with the prepared 1X working coating buffer from 5X stock ELISA Plate Coating Buffer (Elabscience) to a required volume at the appropriate concentration (4 ng/μl), which was determined in the initial experiments. ..



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    Elabscience Biotechnology 5x stock elisa plate coating buffer
    Schematic representation of the principle of SARS-CoV-2-RBD neutralizing <t>ELISA</t> assay2.2. Assay Optimization
    5x Stock Elisa Plate Coating Buffer, supplied by Elabscience Biotechnology, 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/5x+stock+elisa+plate+coating+buffer/ELISA+Plate+Coating+Buffer/pmc09288645-235-53-59
    Average 93 stars, based on 1 article reviews
    5x stock elisa plate coating buffer - by Bioz Stars, 2026-09
    93/100 stars
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    Schematic representation of the principle of SARS-CoV-2-RBD neutralizing ELISA assay2.2. Assay Optimization

    Journal: Archives of Razi Institute

    Article Title: Application and Validation of SARS-CoV-2 RBD Neutralizing ELISA Assay

    doi: 10.22092/ARI.2021.356677.1890

    Figure Lengend Snippet: Schematic representation of the principle of SARS-CoV-2-RBD neutralizing ELISA assay2.2. Assay Optimization

    Article Snippet: To immobilize the hACE2 protein at 400 ng/well in 100 μl of 1X working Coating Buffer on the microtiter plates wells, a calculated volume from Stock solution vial of Recombinant His-Tag-Human ACE2 protein in a concentration of 2.8 mg/ml (Raybiotech) was diluted immediately before usage with the prepared 1X working coating buffer from 5X stock ELISA Plate Coating Buffer (Elabscience) to a required volume at the appropriate concentration (4 ng/μl), which was determined in the initial experiments.

    Techniques: Enzyme-linked Immunosorbent Assay

    Standard curve of anti-SARS-COV-2-RBD nAbs for the in-house developed SARS-COV-2-RBD neutralizing ELISA assay

    Journal: Archives of Razi Institute

    Article Title: Application and Validation of SARS-CoV-2 RBD Neutralizing ELISA Assay

    doi: 10.22092/ARI.2021.356677.1890

    Figure Lengend Snippet: Standard curve of anti-SARS-COV-2-RBD nAbs for the in-house developed SARS-COV-2-RBD neutralizing ELISA assay

    Article Snippet: To immobilize the hACE2 protein at 400 ng/well in 100 μl of 1X working Coating Buffer on the microtiter plates wells, a calculated volume from Stock solution vial of Recombinant His-Tag-Human ACE2 protein in a concentration of 2.8 mg/ml (Raybiotech) was diluted immediately before usage with the prepared 1X working coating buffer from 5X stock ELISA Plate Coating Buffer (Elabscience) to a required volume at the appropriate concentration (4 ng/μl), which was determined in the initial experiments.

    Techniques: Enzyme-linked Immunosorbent Assay

    Mean ± standard deviation of OD values of different anti-SARS-COV-2-RBD neutralizing antibody standards generated by the designed neutralizing  ELISA  kit

    Journal: Archives of Razi Institute

    Article Title: Application and Validation of SARS-CoV-2 RBD Neutralizing ELISA Assay

    doi: 10.22092/ARI.2021.356677.1890

    Figure Lengend Snippet: Mean ± standard deviation of OD values of different anti-SARS-COV-2-RBD neutralizing antibody standards generated by the designed neutralizing ELISA kit

    Article Snippet: To immobilize the hACE2 protein at 400 ng/well in 100 μl of 1X working Coating Buffer on the microtiter plates wells, a calculated volume from Stock solution vial of Recombinant His-Tag-Human ACE2 protein in a concentration of 2.8 mg/ml (Raybiotech) was diluted immediately before usage with the prepared 1X working coating buffer from 5X stock ELISA Plate Coating Buffer (Elabscience) to a required volume at the appropriate concentration (4 ng/μl), which was determined in the initial experiments.

    Techniques: Standard Deviation, Generated, Enzyme-linked Immunosorbent Assay, Concentration Assay, Negative Control, Positive Control

    Cut-off value results of the in-house neutralizing  ELISA;  A) Optimized ROC analysis cut-off value of positive and B) Concentration and log concentration limits for the optimal established cut-off in this assay

    Journal: Archives of Razi Institute

    Article Title: Application and Validation of SARS-CoV-2 RBD Neutralizing ELISA Assay

    doi: 10.22092/ARI.2021.356677.1890

    Figure Lengend Snippet: Cut-off value results of the in-house neutralizing ELISA; A) Optimized ROC analysis cut-off value of positive and B) Concentration and log concentration limits for the optimal established cut-off in this assay

    Article Snippet: To immobilize the hACE2 protein at 400 ng/well in 100 μl of 1X working Coating Buffer on the microtiter plates wells, a calculated volume from Stock solution vial of Recombinant His-Tag-Human ACE2 protein in a concentration of 2.8 mg/ml (Raybiotech) was diluted immediately before usage with the prepared 1X working coating buffer from 5X stock ELISA Plate Coating Buffer (Elabscience) to a required volume at the appropriate concentration (4 ng/μl), which was determined in the initial experiments.

    Techniques: Enzyme-linked Immunosorbent Assay, Concentration Assay

    Receiver operating characteristic curve analysis for the optimal cut-off value for detecting the positive anti-SARS-COV-2-RBD neutralizing antibodies using the in-house developed neutralizing ELISA kit

    Journal: Archives of Razi Institute

    Article Title: Application and Validation of SARS-CoV-2 RBD Neutralizing ELISA Assay

    doi: 10.22092/ARI.2021.356677.1890

    Figure Lengend Snippet: Receiver operating characteristic curve analysis for the optimal cut-off value for detecting the positive anti-SARS-COV-2-RBD neutralizing antibodies using the in-house developed neutralizing ELISA kit

    Article Snippet: To immobilize the hACE2 protein at 400 ng/well in 100 μl of 1X working Coating Buffer on the microtiter plates wells, a calculated volume from Stock solution vial of Recombinant His-Tag-Human ACE2 protein in a concentration of 2.8 mg/ml (Raybiotech) was diluted immediately before usage with the prepared 1X working coating buffer from 5X stock ELISA Plate Coating Buffer (Elabscience) to a required volume at the appropriate concentration (4 ng/μl), which was determined in the initial experiments.

    Techniques: Enzyme-linked Immunosorbent Assay

    Serum panels using the in-house designed SARS-COV-2-RBD neutralizing  ELISA  assay; A) Positive control samples for the assay validation and B) Negative control samples for the assay validation

    Journal: Archives of Razi Institute

    Article Title: Application and Validation of SARS-CoV-2 RBD Neutralizing ELISA Assay

    doi: 10.22092/ARI.2021.356677.1890

    Figure Lengend Snippet: Serum panels using the in-house designed SARS-COV-2-RBD neutralizing ELISA assay; A) Positive control samples for the assay validation and B) Negative control samples for the assay validation

    Article Snippet: To immobilize the hACE2 protein at 400 ng/well in 100 μl of 1X working Coating Buffer on the microtiter plates wells, a calculated volume from Stock solution vial of Recombinant His-Tag-Human ACE2 protein in a concentration of 2.8 mg/ml (Raybiotech) was diluted immediately before usage with the prepared 1X working coating buffer from 5X stock ELISA Plate Coating Buffer (Elabscience) to a required volume at the appropriate concentration (4 ng/μl), which was determined in the initial experiments.

    Techniques: Enzyme-linked Immunosorbent Assay, Positive Control, Biomarker Discovery, Negative Control, Concentration Assay

    Agreement of the results between the in-house SARS-COV-2-RBD neutralizing  ELISA  assay and gold standard test at the in-house established cut-off

    Journal: Archives of Razi Institute

    Article Title: Application and Validation of SARS-CoV-2 RBD Neutralizing ELISA Assay

    doi: 10.22092/ARI.2021.356677.1890

    Figure Lengend Snippet: Agreement of the results between the in-house SARS-COV-2-RBD neutralizing ELISA assay and gold standard test at the in-house established cut-off

    Article Snippet: To immobilize the hACE2 protein at 400 ng/well in 100 μl of 1X working Coating Buffer on the microtiter plates wells, a calculated volume from Stock solution vial of Recombinant His-Tag-Human ACE2 protein in a concentration of 2.8 mg/ml (Raybiotech) was diluted immediately before usage with the prepared 1X working coating buffer from 5X stock ELISA Plate Coating Buffer (Elabscience) to a required volume at the appropriate concentration (4 ng/μl), which was determined in the initial experiments.

    Techniques: Enzyme-linked Immunosorbent Assay

    Validation parameters of the in-house SARS-COV-2-RBD neutralizing  ELISA  assay

    Journal: Archives of Razi Institute

    Article Title: Application and Validation of SARS-CoV-2 RBD Neutralizing ELISA Assay

    doi: 10.22092/ARI.2021.356677.1890

    Figure Lengend Snippet: Validation parameters of the in-house SARS-COV-2-RBD neutralizing ELISA assay

    Article Snippet: To immobilize the hACE2 protein at 400 ng/well in 100 μl of 1X working Coating Buffer on the microtiter plates wells, a calculated volume from Stock solution vial of Recombinant His-Tag-Human ACE2 protein in a concentration of 2.8 mg/ml (Raybiotech) was diluted immediately before usage with the prepared 1X working coating buffer from 5X stock ELISA Plate Coating Buffer (Elabscience) to a required volume at the appropriate concentration (4 ng/μl), which was determined in the initial experiments.

    Techniques: Biomarker Discovery, Enzyme-linked Immunosorbent Assay