<p>In the sandwich ELISA assay format, the wells were coated with E1 mG2a/hG3 as a capture. Ten different healthy subjects’ sera were used at different dilutions and spiked with 14c10 hG1. Each graph is representative of the average of at least two independent experiments. Error bars represent the SEM.</p
<p>Each bar represents the mean value ±SD of one experiment performed in triplicate.</p
<p>Binding ELISA testing subject 16Ms plasma against normal human plasma and four monoclonal antibod...
Electrophoretic methods to detect, characterize and quantify M-proteins play an important role in th...
<p>(A) Schematics showing the difference in the hinge structure between mG2a and mG2a/hG3. (B) 12% S...
<p>Cohort sera samples from three time points (T0, T6 and T12) were analyzed by ELISA to detect IgG2...
<p>sE-Cad level was measured by ELISA and was normalized to reflect the secretion of 10<sup>7</sup> ...
<p>A) Polyclonal antibody versus monoclonal antibody end point titration (17 nM to 0.016 nM) using E...
<p>The levels of aberrantly glycosylated IgA1 in culture supernatant of B lymphocytes were detected ...
<p>(A) Positive controls (CI, CII), High- (H), Low- (L) titer NMO sera and MS sera were tested using...
<p>DAS-ELISA had a detection limit of 1 × 10<sup>3</sup> CFU/mL (OD<sub>450</sub> = 0.26, column 3) ...
<p>Monoclonal <b>A</b>) SA and <b>B</b>) GST antibodies were titrated in SA- or GST coated ELISA. Th...
<p>Mean serum concentration of C3201-HSA in low and high dose groups determined by specific sandwich...
<p>Plates were coated with purified soluble E1 or E2 glycoprotein or NS3 of HCV as antigen to detect...
The detection limit is one of the most important performance parameters for bioanalytical techniques...
<p>Sera used in this study were incubated with the recombinant E-ectodomain protein (lineage 1). Mea...
<p>Each bar represents the mean value ±SD of one experiment performed in triplicate.</p
<p>Binding ELISA testing subject 16Ms plasma against normal human plasma and four monoclonal antibod...
Electrophoretic methods to detect, characterize and quantify M-proteins play an important role in th...
<p>(A) Schematics showing the difference in the hinge structure between mG2a and mG2a/hG3. (B) 12% S...
<p>Cohort sera samples from three time points (T0, T6 and T12) were analyzed by ELISA to detect IgG2...
<p>sE-Cad level was measured by ELISA and was normalized to reflect the secretion of 10<sup>7</sup> ...
<p>A) Polyclonal antibody versus monoclonal antibody end point titration (17 nM to 0.016 nM) using E...
<p>The levels of aberrantly glycosylated IgA1 in culture supernatant of B lymphocytes were detected ...
<p>(A) Positive controls (CI, CII), High- (H), Low- (L) titer NMO sera and MS sera were tested using...
<p>DAS-ELISA had a detection limit of 1 × 10<sup>3</sup> CFU/mL (OD<sub>450</sub> = 0.26, column 3) ...
<p>Monoclonal <b>A</b>) SA and <b>B</b>) GST antibodies were titrated in SA- or GST coated ELISA. Th...
<p>Mean serum concentration of C3201-HSA in low and high dose groups determined by specific sandwich...
<p>Plates were coated with purified soluble E1 or E2 glycoprotein or NS3 of HCV as antigen to detect...
The detection limit is one of the most important performance parameters for bioanalytical techniques...
<p>Sera used in this study were incubated with the recombinant E-ectodomain protein (lineage 1). Mea...
<p>Each bar represents the mean value ±SD of one experiment performed in triplicate.</p
<p>Binding ELISA testing subject 16Ms plasma against normal human plasma and four monoclonal antibod...
Electrophoretic methods to detect, characterize and quantify M-proteins play an important role in th...