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Analysis of IGFBP-5 by ELISA (CAT#: STEM-MB-1527-LGZ)

Introduction

IGFBP-5 is the most conserved protein in the IGFBPs family, and acts as a major regulator to regulate cell growth and development. Exist in blood in the form of IGF-IGFBP-ALS (acid labie subunit) trimer, the role of this trimer is to transport and prolong the half-life of IGFs, and regulate the concentration of IGFs in blood. The activation of IGFBP5 and the occurrence and development of tumors By observing the research trends in recent years, it is not difficult to find that the research on IGFBP-5 in the scientific community mainly focuses on the impact on the occurrence and development of tumors.




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

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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