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Analysis of MICA by ELISA (CAT#: STEM-MB-1523-LGZ)

Introduction

MHC Class I polypeptide-related Sequence A is a protein encoded by the MICA gene in humans. MICA is minimally expressed in normal cells, but is often expressed or shed in epithelial tumors and can be induced by bacterial and viral infections. In recent years, the activation pathway of NKG2D receptor represented by MICA and the mutual regulatory mechanism between the two have received extensive attention in the research fields of tumor immunity, autoimmunity and anti-infection immunity. This membrane protein molecule can bind to the NKG2D receptor on the surface of NK cells, thus activating the killing activity of NK cells. The identification of MICA involves tumor surveillance, viral infections, and autoimmune diseases. The distribution characteristics of MICA gene were related to geographical and population factors, and the distribution frequency of alleles was different among different populations.




Principle

Enzyme-linked immunosorbent assay (ELISA) is an enzyme-labeled solid phase immunoassay technique. Its basic principle is to bind the antigen (or antibody) to the solid phase carrier, and the antigen (or antibody) and a certain enzyme link to enzyme labeled antigen (or antibody). During detection, the sample to be tested and the enzymic antigen (or antibody) react with the antigen (or antibody) on the solid phase carrier according to certain procedures, and then remove the unreacted part by washing method. After adding the substrate, the substrate is catalyzed by the enzyme on the solid phase carrier to produce colored substances. Through qualitative or quantitative detection of the amount of colored products, the content of the substance to be measured in the sample can be determined.

Applications

Oncology & Cancer, Immunology/Inflammation

Procedure

1. Add standards or samples to each well and incubate.
2. Pour off the liquid in the well, biotinylated antibody working solution and incubate.
3. Add enzyme conjugate working solution and incubate.
4. Add substrate TMB and incubate.
5. Add stop solution and measure OD value.
6. Calculation of results.

Materials

• Sample Type: Serum, plasma, cell culture supernatant and other biological samples
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