Unlock Exclusive Discounts & Flash Sales! Click Here to Join the Deals on Every Wednesday!

Analysis of IGFBP-7 / MAC25 / PSF by ELISA (CAT#: STEM-MB-1552-LGZ)

Introduction

The insulin-like growth factor (IGF) binding protein superfamily consists of six high-affinity IGf-binding proteins (IGFBP) and at least four other low-affinity binding proteins, called igFBP-associated proteins (IGFBP-RP). IGFBP7 is a low-affinity IGF-binding protein that plays an integral role in regulating insulin-like growth factor (IGF) action in a variety of cell types, including stimulation of prostacycline production and cell adhesion. Some IGFBPs may also have intrinsic biological activity independent of their ability to bind to IGF proteins. IGFBP7 levels have been linked to the development of cancer. Loss of IGFBP7 expression is associated with poor survival and tumor chemotherapy resistance in many cancer types. IGFBP7 has also been identified as a biomarker of cell cycle arrest in human acute kidney injury and as a prognostic indicator for the development of early acute kidney injury.




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
Advertisement