GLRA1 polyclonal, anti-human, mouse, rat

Background:
The protein encoded by this gene is a subunit of a pentameric inhibitory glycine receptor. The receptor mediates postsynaptic inhibition in the central nervous system. Defects in this gene are a cause of startle disease (STHE), also known as hereditary hyperekplexia or congenital stiff-person syndrome. Two transcript variants encoding different isoforms have been found for this gene.

Synonyms: STHE, HKPX1

Cellular Location: Cytoplasm

Immunogen:
A synthetic peptide of human GLRA1

Gene Symbol: GLRA1

Gene ID: 2741

Swiss prot: P23415

Calculated MW: 53 kDa

Recommended dilution:
WB 1:500-2000, IHC 1:25-100,

Purity:
Affinity purification

Storage Buffer:
Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.

Storage:
Store at -20℃. Avoid freeze / thaw cycles.