QuickDetect™ Secretory IgA (Mouse) ELISA Kit

Immunoglobulin A (IgA) has two subclasses (IgA1 and IgA2) and can be produced as a monomeric as well as a dimeric form. The IgA dimeric form is the most prevalent and is also called secretory IgA (sIgA). sIgA is the main immunoglobulin found in mucous secretions, including tears, saliva, sweat, colostrum and secretions from the genitourinary tract, gastrointestinal tract, prostate and respiratory epithelium. It is also found in small amounts in blood. The secretory component of sIgA protects the immunoglobulin from being degraded by proteolytic enzymes, thus sIgA can survive in the harsh gastrointestinal tract environment and provide protection against microbes that multiply in body secretions. BioVision’s sIgA ELISA kit is a sandwich ELISA assay for the quantitative measurement of sIgA in Mouse serum, plasma and cell culture supernatants in 90 minutes. The density of color is proportional to the amount of sIgA captured from the samples.

Alternate Name: N/A

Tag Line: A rapid sandwich ELISA kit for the quantitative measurement of secretory IgA in mouse serum, plasma, urine, cell culture supernatant, tissue homogenate and other biological fluid

Summary: • Detection method- Absorbance (450 nm) • Species reactivity- mouse • Application- quantitative measurement of IgA in mouse serum, plasma, urine, cell culture samples, tissue samples

Detection Method: Absorbance (450 nm)

Sample Type: Serum, plasma, urine, cell culture samples, biological fluid.

Species Reactivity: Mouse

Applications: This ELISA kit is used for quantitative measurement of IgA in mouse serum, plasma, urine, cell culture samples, biological fluid.

Features & Benefits: Easy, convenient and time-saving method to measure the level of IgA in mouse Serum, plasma, urine, cell culture samples, biological fluid. Detection Range: 30 - 2000 pg/ml Sensitivity: < 6 pg/ml Assay Precision: Intra-Assay: CV < 10%; Inter-Assay: CV < 12% (CV (%) = SD/mean X 100) Cross Reactivity: No significant cross-reactivity or interference between this analyte and its analogues was observed.