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Analysis of Granulin/GRN by ELISA (CAT#: STEM-MB-1583-LGZ)

Introduction

Granulin (GRN) is encoded in humans by the GRN gene. Its precursor protein-granulin precursor, also known as teratoma cell-derived growth factor. After the signal peptide is cleaved, mature GRN can be produced, and further cleavage can produce many active polypeptides with a molecular weight of 6 kDa. Both peptide and intact GRN regulate cell growth. However, different members of the GRN protein family may exert inhibitory and/or promoting effects on cell growth. Members of the GRN family play important roles in normal development, wound healing, and tumorigenesis. GRN may have cytokine-like activity and play a role in inflammation, wound repair and tissue remodeling. Human liver flukes secrete GRN-like growth hormones that contribute to the development of cholangiocarcinoma. Mutations in the GRN gene can be inherited through autosomal dominant inheritance with high penetrance, producing up to 25% of frontotemporal lobar degeneration.




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, 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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