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scatter plots of the od values obtained from the indirect elisa  (GraphPad Software Inc)

 
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    GraphPad Software Inc scatter plots of the od values obtained from the indirect elisa
    Scatter Plots Of The Od Values Obtained From The Indirect Elisa, supplied by GraphPad Software Inc, 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/scatter plots of the od values obtained from the indirect elisa/product/GraphPad Software Inc
    Average 90 stars, based on 1 article reviews
    scatter plots of the od values obtained from the indirect elisa - by Bioz Stars, 2026-03
    90/100 stars

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    GraphPad Software Inc elisa od values
    Substitution of S982A and L18F weakens the generation of binding antibodies. The area under the <t>curve</t> <t>(AUC)</t> of anti-spike ( A ) and anti-RBD ( B ) IgG induced by the 19 designed groups of DNA immunogens ( n = 3 for each group). The AUC represents the total peak area calculated from <t>ELISA</t> OD values by GraphPad Prism v8. Data were analyzed for statistical significance using the unpaired Student’s t test. Data are shown as the mean with SD in each group. Dotted black lines indicate the limit of quantification (LOQ). * P < 0.05; ** P < 0.01; *** P < 0.001
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    Substitution of S982A and L18F weakens the generation of binding antibodies. The area under the <t>curve</t> <t>(AUC)</t> of anti-spike ( A ) and anti-RBD ( B ) IgG induced by the 19 designed groups of DNA immunogens ( n = 3 for each group). The AUC represents the total peak area calculated from <t>ELISA</t> OD values by GraphPad Prism v8. Data were analyzed for statistical significance using the unpaired Student’s t test. Data are shown as the mean with SD in each group. Dotted black lines indicate the limit of quantification (LOQ). * P < 0.05; ** P < 0.01; *** P < 0.001
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    Immune responses measured at the acute phase after the second dose among BNT162b2 and CoronaVac vaccinees. ( a ) The area under curve (AUC) of anti-Spike and anti-RBD IgG in BNT162b2 (orange) (n=34), CoronaVac (green) (n=28) and non-vaccinated volunteers (grey) (n=16). The AUC represents the total peak area calculated <t>from</t> <t>ELISA</t> OD values by the GraphPad Prism <t>v8.</t> ( b ) Percentage inhibition and IC 50 /IC 90 values against wild type SARS-CoV-2 pseudoviruses in BNT162b2 and CoronaVac vaccinees. ( c ) The neutralization antibody potency index defined by the ratio of IC 50 /AUC of anti-Spike IgG and anti-RBD IgG in BNT162b2 and CoronaVac group. Data showed geometric mean values in each group in a - c . ( d ) Quantified results depict the percentage of RBD, spike and NP-specific IFN-γ + CD4 + T (top) and IFN-γ + CD8 + T (bottom) cells in BNT162b2 (n=33), CoronaVac (n=28) and non-vaccinated volunteers (n=15), respectively. Fresh PBMC were subjected to T cell response measurement by ICS after RBD-, spike- and NP-specific ex vivo peptide pool stimulation, respectively. Numbers under the x-axis in a and d indicate the rate of positive responders. ( e ) The proportions of spike-specific polyfunctional CD4 + T (top) and CD8 + T (bottom) cells were compared in BNT162b2 and CoronaVac-vaccinated responders. After gating on IFN-γ + CD4 + /CD8 + T cells and IFN-γ − CD4 + /CD8 + T cells, single cytokine (IFN-γ + or TNF-α + or IL-2 + only), double cytokines (IFN-γ + TNF-α + or IFN-γ + IL-2 + or TNF-α + IL-2 + ), and triple cytokines (IFN-γ + TNF-α + IL-2 + ) producing cells were analyzed in response to spike-specific ex vivo peptide pool stimulation, respectively. Background-subtracted data was analyzed in all cases in d and e . The bars in D and E indicated median value. ( f ) Phenotypic analysis depicted antigen-specific T cell subsets of BNT162b2 and CoronaVac vaccinees. After gating on IFN-γ + CD4 + or IFN-γ + CD8 + T cells, T cell subsets expressing CCR7 and/or CD45RA were analyzed in response to spike-specific ex vivo peptide pool stimulation. Data were analyzed for statistical significance using Mann-Whitney U test. Dotted black lines indicate the limit of quantification (LOQ). ** P < 0.01, *** P < 0.001, **** P < 0.0001.
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    Image Search Results


    Substitution of S982A and L18F weakens the generation of binding antibodies. The area under the curve (AUC) of anti-spike ( A ) and anti-RBD ( B ) IgG induced by the 19 designed groups of DNA immunogens ( n = 3 for each group). The AUC represents the total peak area calculated from ELISA OD values by GraphPad Prism v8. Data were analyzed for statistical significance using the unpaired Student’s t test. Data are shown as the mean with SD in each group. Dotted black lines indicate the limit of quantification (LOQ). * P < 0.05; ** P < 0.01; *** P < 0.001

    Journal: Cellular and Molecular Immunology

    Article Title: Naturally occurring spike mutations influence the infectivity and immunogenicity of SARS-CoV-2

    doi: 10.1038/s41423-022-00924-8

    Figure Lengend Snippet: Substitution of S982A and L18F weakens the generation of binding antibodies. The area under the curve (AUC) of anti-spike ( A ) and anti-RBD ( B ) IgG induced by the 19 designed groups of DNA immunogens ( n = 3 for each group). The AUC represents the total peak area calculated from ELISA OD values by GraphPad Prism v8. Data were analyzed for statistical significance using the unpaired Student’s t test. Data are shown as the mean with SD in each group. Dotted black lines indicate the limit of quantification (LOQ). * P < 0.05; ** P < 0.01; *** P < 0.001

    Article Snippet: The AUC represents the total peak area calculated from ELISA OD values by GraphPad Prism v8.

    Techniques: Binding Assay, Enzyme-linked Immunosorbent Assay

    Immune responses measured at the acute phase after the second dose among BNT162b2 and CoronaVac vaccinees. ( a ) The area under curve (AUC) of anti-Spike and anti-RBD IgG in BNT162b2 (orange) (n=34), CoronaVac (green) (n=28) and non-vaccinated volunteers (grey) (n=16). The AUC represents the total peak area calculated from ELISA OD values by the GraphPad Prism v8. ( b ) Percentage inhibition and IC 50 /IC 90 values against wild type SARS-CoV-2 pseudoviruses in BNT162b2 and CoronaVac vaccinees. ( c ) The neutralization antibody potency index defined by the ratio of IC 50 /AUC of anti-Spike IgG and anti-RBD IgG in BNT162b2 and CoronaVac group. Data showed geometric mean values in each group in a - c . ( d ) Quantified results depict the percentage of RBD, spike and NP-specific IFN-γ + CD4 + T (top) and IFN-γ + CD8 + T (bottom) cells in BNT162b2 (n=33), CoronaVac (n=28) and non-vaccinated volunteers (n=15), respectively. Fresh PBMC were subjected to T cell response measurement by ICS after RBD-, spike- and NP-specific ex vivo peptide pool stimulation, respectively. Numbers under the x-axis in a and d indicate the rate of positive responders. ( e ) The proportions of spike-specific polyfunctional CD4 + T (top) and CD8 + T (bottom) cells were compared in BNT162b2 and CoronaVac-vaccinated responders. After gating on IFN-γ + CD4 + /CD8 + T cells and IFN-γ − CD4 + /CD8 + T cells, single cytokine (IFN-γ + or TNF-α + or IL-2 + only), double cytokines (IFN-γ + TNF-α + or IFN-γ + IL-2 + or TNF-α + IL-2 + ), and triple cytokines (IFN-γ + TNF-α + IL-2 + ) producing cells were analyzed in response to spike-specific ex vivo peptide pool stimulation, respectively. Background-subtracted data was analyzed in all cases in d and e . The bars in D and E indicated median value. ( f ) Phenotypic analysis depicted antigen-specific T cell subsets of BNT162b2 and CoronaVac vaccinees. After gating on IFN-γ + CD4 + or IFN-γ + CD8 + T cells, T cell subsets expressing CCR7 and/or CD45RA were analyzed in response to spike-specific ex vivo peptide pool stimulation. Data were analyzed for statistical significance using Mann-Whitney U test. Dotted black lines indicate the limit of quantification (LOQ). ** P < 0.01, *** P < 0.001, **** P < 0.0001.

    Journal: EBioMedicine

    Article Title: Waning immune responses against SARS-CoV-2 variants of concern among vaccinees in Hong Kong

    doi: 10.1016/j.ebiom.2022.103904

    Figure Lengend Snippet: Immune responses measured at the acute phase after the second dose among BNT162b2 and CoronaVac vaccinees. ( a ) The area under curve (AUC) of anti-Spike and anti-RBD IgG in BNT162b2 (orange) (n=34), CoronaVac (green) (n=28) and non-vaccinated volunteers (grey) (n=16). The AUC represents the total peak area calculated from ELISA OD values by the GraphPad Prism v8. ( b ) Percentage inhibition and IC 50 /IC 90 values against wild type SARS-CoV-2 pseudoviruses in BNT162b2 and CoronaVac vaccinees. ( c ) The neutralization antibody potency index defined by the ratio of IC 50 /AUC of anti-Spike IgG and anti-RBD IgG in BNT162b2 and CoronaVac group. Data showed geometric mean values in each group in a - c . ( d ) Quantified results depict the percentage of RBD, spike and NP-specific IFN-γ + CD4 + T (top) and IFN-γ + CD8 + T (bottom) cells in BNT162b2 (n=33), CoronaVac (n=28) and non-vaccinated volunteers (n=15), respectively. Fresh PBMC were subjected to T cell response measurement by ICS after RBD-, spike- and NP-specific ex vivo peptide pool stimulation, respectively. Numbers under the x-axis in a and d indicate the rate of positive responders. ( e ) The proportions of spike-specific polyfunctional CD4 + T (top) and CD8 + T (bottom) cells were compared in BNT162b2 and CoronaVac-vaccinated responders. After gating on IFN-γ + CD4 + /CD8 + T cells and IFN-γ − CD4 + /CD8 + T cells, single cytokine (IFN-γ + or TNF-α + or IL-2 + only), double cytokines (IFN-γ + TNF-α + or IFN-γ + IL-2 + or TNF-α + IL-2 + ), and triple cytokines (IFN-γ + TNF-α + IL-2 + ) producing cells were analyzed in response to spike-specific ex vivo peptide pool stimulation, respectively. Background-subtracted data was analyzed in all cases in d and e . The bars in D and E indicated median value. ( f ) Phenotypic analysis depicted antigen-specific T cell subsets of BNT162b2 and CoronaVac vaccinees. After gating on IFN-γ + CD4 + or IFN-γ + CD8 + T cells, T cell subsets expressing CCR7 and/or CD45RA were analyzed in response to spike-specific ex vivo peptide pool stimulation. Data were analyzed for statistical significance using Mann-Whitney U test. Dotted black lines indicate the limit of quantification (LOQ). ** P < 0.01, *** P < 0.001, **** P < 0.0001.

    Article Snippet: The AUC represents the total peak area calculated from ELISA OD values by the GraphPad Prism v8. ( b ) Percentage inhibition and IC 50 /IC 90 values against wild type SARS-CoV-2 pseudoviruses in BNT162b2 and CoronaVac vaccinees. ( c ) The neutralization antibody potency index defined by the ratio of IC 50 /AUC of anti-Spike IgG and anti-RBD IgG in BNT162b2 and CoronaVac group.

    Techniques: Enzyme-linked Immunosorbent Assay, Inhibition, Neutralization, Ex Vivo, Expressing, MANN-WHITNEY

    Baseline characteristics of patients according to EBV antibody levels

    Journal: Cancer Research and Treatment : Official Journal of Korean Cancer Association

    Article Title: Prognostic Value of Serum Epstein-Barr Virus Antibodies and Their Correlation with TNM Classification in Patients with Locoregionally Advanced Nasopharyngeal Carcinoma

    doi: 10.4143/crt.2020.1298

    Figure Lengend Snippet: Baseline characteristics of patients according to EBV antibody levels

    Article Snippet: The EBNA1-IgA and Zta-IgA levels were assessed according to the ELISA OD values according to the manufacturers’ instructions (Shanghai Jining Shiye Co., Ltd., Shanghai, China; Zhongshan Biotechnology Co., Ltd., Zhongshan, China).

    Techniques:

    Correlations between Epstein-Barr virus biomarker levels and the AJCC staging system, eighth edition

    Journal: Cancer Research and Treatment : Official Journal of Korean Cancer Association

    Article Title: Prognostic Value of Serum Epstein-Barr Virus Antibodies and Their Correlation with TNM Classification in Patients with Locoregionally Advanced Nasopharyngeal Carcinoma

    doi: 10.4143/crt.2020.1298

    Figure Lengend Snippet: Correlations between Epstein-Barr virus biomarker levels and the AJCC staging system, eighth edition

    Article Snippet: The EBNA1-IgA and Zta-IgA levels were assessed according to the ELISA OD values according to the manufacturers’ instructions (Shanghai Jining Shiye Co., Ltd., Shanghai, China; Zhongshan Biotechnology Co., Ltd., Zhongshan, China).

    Techniques: Virus, Biomarker Discovery

    Univariable analyses of prognostic factors for the whole cohort of patients with nasopharyngeal carcinoma

    Journal: Cancer Research and Treatment : Official Journal of Korean Cancer Association

    Article Title: Prognostic Value of Serum Epstein-Barr Virus Antibodies and Their Correlation with TNM Classification in Patients with Locoregionally Advanced Nasopharyngeal Carcinoma

    doi: 10.4143/crt.2020.1298

    Figure Lengend Snippet: Univariable analyses of prognostic factors for the whole cohort of patients with nasopharyngeal carcinoma

    Article Snippet: The EBNA1-IgA and Zta-IgA levels were assessed according to the ELISA OD values according to the manufacturers’ instructions (Shanghai Jining Shiye Co., Ltd., Shanghai, China; Zhongshan Biotechnology Co., Ltd., Zhongshan, China).

    Techniques:

    Multivariate analysis of prognostic factors for the whole cohort of patients with nasopharyngeal carcinoma

    Journal: Cancer Research and Treatment : Official Journal of Korean Cancer Association

    Article Title: Prognostic Value of Serum Epstein-Barr Virus Antibodies and Their Correlation with TNM Classification in Patients with Locoregionally Advanced Nasopharyngeal Carcinoma

    doi: 10.4143/crt.2020.1298

    Figure Lengend Snippet: Multivariate analysis of prognostic factors for the whole cohort of patients with nasopharyngeal carcinoma

    Article Snippet: The EBNA1-IgA and Zta-IgA levels were assessed according to the ELISA OD values according to the manufacturers’ instructions (Shanghai Jining Shiye Co., Ltd., Shanghai, China; Zhongshan Biotechnology Co., Ltd., Zhongshan, China).

    Techniques: