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Analysis of Angiotensinogen/AGT/SerpinA8 by ELISA (CAT#: STEM-MB-1575-LGZ)

Introduction

Angiotensinogen (AGT), also known as SerpinA8, is a member of the serine protease inhibitor family. AGT is an alpha-2-globulin that is constitutionally produced by the liver and released into the bloodstream. AGT is an essential component of renin-angiotensin system and an effective blood pressure regulator. AGT can be cleaved into three chains: angiotensin-1, angiotensin-2, and angiotensin-3. Absence of AGT is associated with essential hypertension and tubular hypoplasia. Several serine protease inhibitors (antithrombin, maspin, pigment epithelium-derived factors, and kallistatin) have recently been shown to have anti-angiogenic activity, indicating a common mechanism for endothelial cell proliferation and migration. AGT and its renin cleavage products are also angiogenic inhibitors in the range of plasma concentrations observable in vitro and in vivo.




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

Alcoholic hepatitis; chronic myeloid leukemia; intermediate coronary syndrome; systemic scleroderma (multiple); and type 2 diabetes mellitus.

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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