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Bovine Gamma-Aminobutyric Acid Receptor Subunit Beta-1 (GABRB1) ELISA Kit-Sandwich

Cat. No.EK2F472

Product TypeAnimal Immunoassay Kits

Size

Product Overview

BioVenic Bovine Gamma-Aminobutyric Acid Receptor Subunit Beta-1 (GABRB1) ELISA Kit-Sandwich is designed for the quantitative determination of Bovine Gamma-Aminobutyric Acid Receptor Subunit Beta-1 (GABRB1) in serum, plasma, tissue homogenate, cell culture supernatant, cell extract, and other biological fluids using a Sandwich ELISA method. For research use only.

Specifications

Assay Type ELISA-Sandwich
Specificity The assay kit is specific for Bovine GABRB1.
Target Species Bovine
Species Reactivity Bovine
Reproducibility Intra-Assay: CV < 10%; Inter-Assay: CV < 10%
Assay Time Around 210 min
Sample Requirement Serum, plasma, tissue homogenate, cell culture supernatant, cell extract, and other biological fluids.

Target Information

The beta-1 gamma-aminobutyric acid receptor subunit is another subunit of GABA type A receptors, partnering with GABRA1 and other subunits to form functional receptors. GABRB1 modulates receptor properties and contributes to its activation by GABA. It is found on the postsynaptic membrane of neurons in various brain regions. It is encoded by the bovine gene GABRB1. Research has shown that alcohol consumption increases following mutations in the GABRB1 gene.

Target/Biomarker Bovine GABRB1
Target Synonym Gamma-aminobutyric acid receptor subunit beta-1; GABA;A receptor subunit beta-1
Gene ID 282239
UniProt ID P08220

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. Anstee, Q. M. et al. Mutations in the Gabrb1 gene promote alcohol consumption through increased tonic inhibition. Nature communications. 2013, 4: 2816.
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