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Illustration of the <t>LF-sVNT</t> protocol and example sensorgrams. (A) First cycle measuring the binding ability of RBD to ACE2 <t>after</t> <t>neutralization.</t> (B) Second cycle measuring the full binding ability of RBD without neutralization. Reproduced with permission from J. Clin. Microbiol. , 2021, 59 , e0019321, 10.1128/JCM.00193-21.
Svnt Commercial Kit Genscript Cpasstm, supplied by GenScript corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Illustration of the <t>LF-sVNT</t> protocol and example sensorgrams. (A) First cycle measuring the binding ability of RBD to ACE2 <t>after</t> <t>neutralization.</t> (B) Second cycle measuring the full binding ability of RBD without neutralization. Reproduced with permission from J. Clin. Microbiol. , 2021, 59 , e0019321, 10.1128/JCM.00193-21.
Cpass™, supplied by GenScript corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Illustration of the <t>LF-sVNT</t> protocol and example sensorgrams. (A) First cycle measuring the binding ability of RBD to ACE2 <t>after</t> <t>neutralization.</t> (B) Second cycle measuring the full binding ability of RBD without neutralization. Reproduced with permission from J. Clin. Microbiol. , 2021, 59 , e0019321, 10.1128/JCM.00193-21.
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Illustration of the <t>LF-sVNT</t> protocol and example sensorgrams. (A) First cycle measuring the binding ability of RBD to ACE2 <t>after</t> <t>neutralization.</t> (B) Second cycle measuring the full binding ability of RBD without neutralization. Reproduced with permission from J. Clin. Microbiol. , 2021, 59 , e0019321, 10.1128/JCM.00193-21.
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Illustration of the <t>LF-sVNT</t> protocol and example sensorgrams. (A) First cycle measuring the binding ability of RBD to ACE2 <t>after</t> <t>neutralization.</t> (B) Second cycle measuring the full binding ability of RBD without neutralization. Reproduced with permission from J. Clin. Microbiol. , 2021, 59 , e0019321, 10.1128/JCM.00193-21.
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GenScript corporation svnt kit (cpass™
Illustration of the <t>LF-sVNT</t> protocol and example sensorgrams. (A) First cycle measuring the binding ability of RBD to ACE2 <t>after</t> <t>neutralization.</t> (B) Second cycle measuring the full binding ability of RBD without neutralization. Reproduced with permission from J. Clin. Microbiol. , 2021, 59 , e0019321, 10.1128/JCM.00193-21.
Svnt Kit (Cpass™, supplied by GenScript corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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GenScript corporation surrogate virus neutralization test cpasstm
Comparisons of immunization profiles between the mother and both twins.
Surrogate Virus Neutralization Test Cpasstm, supplied by GenScript corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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The serology test results of 0–7, 8–14, 15–21, 22–28 days after symptom onset were compared (lateral axis), respectively. Each dot represents one tested specimen and the vertical axis represents the %inhibition of <t>SARS-CoV-2</t> <t>NAbs</t> tested by <t>sVNT.</t> The dash line represents the cutoff at 20% inhibition. The horizontal lines indicates the median interquartile range (IQR). The p values were calculated from two-tailed test.
Svnt Assay (Cpass™, supplied by GenScript corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Sensitivity of the different serological tests and cut-offs used based on the final serum panels. Values between brackets represent 95 % confidence intervals on the estimations.
Surrogate Virus Neutralization Test (Svnt, Genscript Cpasstm), supplied by GenScript corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Illustration of the LF-sVNT protocol and example sensorgrams. (A) First cycle measuring the binding ability of RBD to ACE2 after neutralization. (B) Second cycle measuring the full binding ability of RBD without neutralization. Reproduced with permission from J. Clin. Microbiol. , 2021, 59 , e0019321, 10.1128/JCM.00193-21.

Journal: Chemical Science

Article Title: Diagnostics and analysis of SARS-CoV-2: current status, recent advances, challenges and perspectives

doi: 10.1039/d2sc06665c

Figure Lengend Snippet: Illustration of the LF-sVNT protocol and example sensorgrams. (A) First cycle measuring the binding ability of RBD to ACE2 after neutralization. (B) Second cycle measuring the full binding ability of RBD without neutralization. Reproduced with permission from J. Clin. Microbiol. , 2021, 59 , e0019321, 10.1128/JCM.00193-21.

Article Snippet: Michiels et al. compared the sVNT commercial kit (GenScript cPassTM) with a live virus neutralization assay and Luminex multiplex immunoassay (MIA), and studied two different cohorts using these three methods.

Techniques: Binding Assay, Neutralization

Comparisons of immunization profiles between the mother and both twins.

Journal: Vaccines

Article Title: Placental Transfer Immunity to the Newborns in a Twin Pregnant Women Vaccinated with Heterologous CoronaVac-ChAdOx1

doi: 10.3390/vaccines11010116

Figure Lengend Snippet: Comparisons of immunization profiles between the mother and both twins.

Article Snippet: Additionally, serum-neutralizing antibodies against wild-type and delta (B.1.617.2) variants were determined using a surrogate virus neutralization test (cPassTM, GenScript, Piscataway, NJ, USA) according to the manufacturer’s instruction with modifications.

Techniques: Neutralization, Activity Assay, Inhibition

The serology test results of 0–7, 8–14, 15–21, 22–28 days after symptom onset were compared (lateral axis), respectively. Each dot represents one tested specimen and the vertical axis represents the %inhibition of SARS-CoV-2 NAbs tested by sVNT. The dash line represents the cutoff at 20% inhibition. The horizontal lines indicates the median interquartile range (IQR). The p values were calculated from two-tailed test.

Journal: PLoS ONE

Article Title: Early detection of neutralizing antibodies against SARS-CoV-2 in COVID-19 patients in Thailand

doi: 10.1371/journal.pone.0246864

Figure Lengend Snippet: The serology test results of 0–7, 8–14, 15–21, 22–28 days after symptom onset were compared (lateral axis), respectively. Each dot represents one tested specimen and the vertical axis represents the %inhibition of SARS-CoV-2 NAbs tested by sVNT. The dash line represents the cutoff at 20% inhibition. The horizontal lines indicates the median interquartile range (IQR). The p values were calculated from two-tailed test.

Article Snippet: Blood specimens from patients with PCR-confirmed COVID-19 were tested for NAbs against SARS-CoV-2 antibodies using sVNT assay (cPassTM, GenScript USA), according to the manufacturer’s instructions.

Techniques: Inhibition, Two Tailed Test

Every dot represents one tested specimen and the vertical axis represents the %inhibition of SARS-CoV-2 NAbs tested by sVNT. The dashed line represents the cutoff at 20% inhibition. The horizontal lines indicate the median interquartile range (IQR). The p values were calculated from two-tailed test.

Journal: PLoS ONE

Article Title: Early detection of neutralizing antibodies against SARS-CoV-2 in COVID-19 patients in Thailand

doi: 10.1371/journal.pone.0246864

Figure Lengend Snippet: Every dot represents one tested specimen and the vertical axis represents the %inhibition of SARS-CoV-2 NAbs tested by sVNT. The dashed line represents the cutoff at 20% inhibition. The horizontal lines indicate the median interquartile range (IQR). The p values were calculated from two-tailed test.

Article Snippet: Blood specimens from patients with PCR-confirmed COVID-19 were tested for NAbs against SARS-CoV-2 antibodies using sVNT assay (cPassTM, GenScript USA), according to the manufacturer’s instructions.

Techniques: Inhibition, Two Tailed Test

Every dot represents one tested specimen and the vertical axis represents the %inhibition of SARS-CoV-2 NAbs tested by sVNT. The dashed line represents the cutoff at 20% inhibition. The horizontal lines indicate the median interquartile range (IQR). The p values were calculated from two-tailed test.

Journal: PLoS ONE

Article Title: Early detection of neutralizing antibodies against SARS-CoV-2 in COVID-19 patients in Thailand

doi: 10.1371/journal.pone.0246864

Figure Lengend Snippet: Every dot represents one tested specimen and the vertical axis represents the %inhibition of SARS-CoV-2 NAbs tested by sVNT. The dashed line represents the cutoff at 20% inhibition. The horizontal lines indicate the median interquartile range (IQR). The p values were calculated from two-tailed test.

Article Snippet: Blood specimens from patients with PCR-confirmed COVID-19 were tested for NAbs against SARS-CoV-2 antibodies using sVNT assay (cPassTM, GenScript USA), according to the manufacturer’s instructions.

Techniques: Inhibition, Two Tailed Test

Sensitivity of the different serological tests and cut-offs used based on the final serum panels. Values between brackets represent 95 % confidence intervals on the estimations.

Journal: Journal of Virological Methods

Article Title: Evaluation of a surrogate virus neutralization test for high-throughput serosurveillance of SARS-CoV-2

doi: 10.1016/j.jviromet.2021.114228

Figure Lengend Snippet: Sensitivity of the different serological tests and cut-offs used based on the final serum panels. Values between brackets represent 95 % confidence intervals on the estimations.

Article Snippet: Here, we performed an independent evaluation of a commercially available surrogate virus neutralization test (sVNT, GenScript cPassTM) that can be done without biosafety level 3 containment in less than 2 h. When using the cVNT and a Luminex multiplex immunoassay (MIA) as reference, the sVNT obtained a sensitivity of 94 % (CI 90–96 %) on a panel of 317 immune sera that were obtained from hospitalized and mild COVID-19 cases from Belgium and a sensitivity of 88 % (CI 81–93 %) on a panel of 184 healthcare workers from the Democratic Republic of Congo.

Techniques: Luminex

Correlations between the percentage of inhibition measured by the surrogate viral neutralisation test (sVNT) and the log(dilution factors or signal-to-noise ratio) for the conventional viral neutralization test (cVNT) or the Luminex multiplex immunological assay (MIA) as calculated by the nonparametric Spearman correlation test (r s ). Seropositivity cut-off levels for the sVNT are indicated by the dashed grey lines at 20 or 30 % inhibition. Negative samples on the cVNT or MIA were not included in these figures.

Journal: Journal of Virological Methods

Article Title: Evaluation of a surrogate virus neutralization test for high-throughput serosurveillance of SARS-CoV-2

doi: 10.1016/j.jviromet.2021.114228

Figure Lengend Snippet: Correlations between the percentage of inhibition measured by the surrogate viral neutralisation test (sVNT) and the log(dilution factors or signal-to-noise ratio) for the conventional viral neutralization test (cVNT) or the Luminex multiplex immunological assay (MIA) as calculated by the nonparametric Spearman correlation test (r s ). Seropositivity cut-off levels for the sVNT are indicated by the dashed grey lines at 20 or 30 % inhibition. Negative samples on the cVNT or MIA were not included in these figures.

Article Snippet: Here, we performed an independent evaluation of a commercially available surrogate virus neutralization test (sVNT, GenScript cPassTM) that can be done without biosafety level 3 containment in less than 2 h. When using the cVNT and a Luminex multiplex immunoassay (MIA) as reference, the sVNT obtained a sensitivity of 94 % (CI 90–96 %) on a panel of 317 immune sera that were obtained from hospitalized and mild COVID-19 cases from Belgium and a sensitivity of 88 % (CI 81–93 %) on a panel of 184 healthcare workers from the Democratic Republic of Congo.

Techniques: Inhibition, Neutralization, Luminex, Multiplex Assay