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

Analysis of PRLR by ELISA (CAT#: STEM-MB-1585-LGZ)

Introduction

The prolactin receptor (PRLR) is a cytokine receptor, encoded by a gene located on chromosome 5p13-14, that interacts with prolactin as a transmembrane receptor. PRLR includes an extracellular domain that binds prolactin, a transmembrane domain, and a cytoplasmic domain. PRLR is widely expressed in mammary gland, placenta, kidney, liver and pancreas, and it can be activated by growth hormone (GH) and human placental lactogen (hPL) in addition to prolactin. Studies have shown that the abnormality of PRLR is closely related to the pathogenesis and prognosis of certain tumors, especially breast cancer. The specific combination with PRLR can stimulate the growth of breast cancer cells, and some antagonists that can combine with PRLR but not form dimers can inhibit the growth of breast cancer cells. Several isoforms of PRLR exist, among which the soluble PRLR cannot transduce prolactin signaling.




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