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Porcine Gastrin (GAST) ELISA Kit-Competitive

Cat. No.EK3F371

Product TypeAnimal Immunoassay Kits

Size

Product Overview

BioVenic Porcine Gastrin (GAST) ELISA Kit-Competitive is designed for the quantitative determination of Porcine Gastrin (GAST) in serum, plasma, tissue homogenate, cell culture supernatant, cell extract, and other biological fluids using a Competitive ELISA method. For research use only. Sandwich ELISA assay kit targeting Porcine Gastrin (GAST) is available. Please inquiry for more information.

Specifications

Assay Type ELISA-Competitive
Specificity The assay kit is specific for Porcine GAST.
Target Species Swine
Species Reactivity Swine
Detection Range 3.2-20 pg/mL
Reproducibility Intra-Assay: CV < 10%; Inter-Assay: CV < 12%
Assay Time Around 90 min
Sample Requirement Serum, plasma, tissue homogenate, cell culture supernatant, cell extract, and other biological fluids.

Target Information

Gastrin (also known as GAST) is encoded by the GAST gene in pigs. It is a hormone secreted by G-cells in the stomach and duodenum that functions as both a mucosal growth factor and a stimulator of mast and parietal cells. Gastrin binds to cholecystokinin B receptors to stimulate the release of histamines in enterochromaffin-like cells. It induces the insertion of K+/H+ ATPase pumps into the apical membrane of parietal cells, increasing H+ release into the stomach cavity.

Target/Biomarker Porcine GAST
Target Synonym Gastrin; GAST; GAS
Gene ID 445524
UniProt ID P01351

Shipping and Storage

This product is shipped with gel ice packs. It is recommended to store at 2-8 °C (Up to 6 months).

Documents

COA

To request a Certificate of Analysis, please enter the Lot No. in the search box. Note: Certificate of Analysis not available for kits.

The product is for research use only.
Not for commercial, prophylactic, diagnostic, or therapeutic applications.

References

  1. Gonzalez, L. M. et al. Cell lineage identification and stem cell culture in a porcine model for the study of intestinal epithelial regeneration. PloS one. 2013, 8: e66465.
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