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Analysis of Apolipoprotein AII/Apo A2 by ELISA (CAT#: STEM-MB-1565-LGZ)

Introduction

Apolipoprotein AII (Apo A2) is the second largest APolipoprotein in human plasma high density lipoprotein (HDL) after Apo A1, and is the most hydrophilic among exchangeable APolipoproteins. Apo A2 is synthesized by the liver and small intestine and exists in plasma as a monomer or dimer. The Apo A2 gene consists of four exons and three introns. Four exons encode the 5' -terminal untranslated region, propeptide, a short n-terminal domain, and a C-terminal domain composed of a variable number of lipid binding androgynous helices. Apo A2 can stabilize HDL structure and affect HDL metabolism by binding lipids. The role of Apo A2 in lipid metabolism and atherosclerosis shows important clinical significance. Apo A2 levels are associated with increased atherosclerotic susceptibility, free fatty acid levels, body fat, and insulin resistance.




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

Diabetes Mellitus, Metabonomics

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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