Rabbit Polyclonal antibody to Glycine Receptor alpha 1The 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.[provided by RefSeq, Mar 2009]
Immunogen
A synthetic peptide of human GLRA1
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
IHC-PWB
WB: 1:500 - 1:200. IHC: 1:50 - 1:100:
Species Reactivity
HumanMouse
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Gene Synonyms
GLRA1 HKPX1 glycine receptor alpha 1 STHE
Target
Glycine Receptor alpha 1
Molecular Weight(MW)
53 kDa (note)
Application
Application
IHC-P analysis of human esophagus cancer tissue using Glycine Receptor alpha 1 antibody.
Application
WB analysis of extracts from various cell lines using Glycine Receptor alpha 1 antibody.
Application Notes
WB: 1:500 - 1:200. IHC: 1:50 - 1:100:
Additional Information
Form
Liquid
Storage Instructions
Store at -20°C (regular) or -80°C (long term). Avoid freeze / thaw cycles.