兔抗GLRA1多克隆抗体

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. Three transcript variants encoding different isoforms have been found for this gene.

Applications:

ELISA, WB, IHC

Name of antibody:

GLRA1

Immunogen:

Synthetic peptide of human GLRA1

Full name:

glycine receptor, alpha 1

Synonyms：

STHE; HKPX1

SwissProt:

P23415

ELISA Recommended dilution:

2000-5000

IHC positive control:

Human liver cancer

IHC Recommend dilution:

10-50

WB Predicted band size:

53 kDa

WB Positive control:

Human placenta tissue

WB Recommended dilution:

500-2000