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Analysis of Tie1/TIE/JTK14 by ELISA (CAT#: STEM-MB-1577-LGZ)

Introduction

Tyrosine protein kinase receptor Tie1 is a single transmembrane type I membrane protein, belonging to the protein kinase superfamily, tyrosine protein kinase family and Tie subfamily. Tie1 has three EGF-like domains, three fibronectin type III domains, two immunoglobulin like C2-type domains, and one protein kinase domain. Tie1 is a cell surface protein specifically expressed in endothelial cells; however, studies have shown that it can also be expressed in immature hematopoietic cells and platelets. Tie1 is essential for the survival and growth of microvascular endothelial cells during the capillary emergence phase of vascular development. Tie1 up-regulates the cell adhesion molecules VCAM-1, E-selectin, and ICAM-1 through a p38-dependent mechanism. The expression of Tie1 enhances the adhesion of monocyte derived immune cells to endothelial cells. Tie1 has a pro-inflammatory effect and plays an important role in inflammatory diseases of the endothelium such as atherosclerosis.




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

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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