×
For best experience we recommend to activate Javascript in your browser.
GLRA1 antibody
GLRA1
Reactivity: Human, Mouse, Rat
WB, ELISA, IHC
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-GLRA1 Antibody
(hide)
Target
See all GLRA1 Antibodies
GLRA1
(Glycine Receptor, alpha 1 (GLRA1))
Reactivity
All reactivities for GLRA1 antibodies
Human, Mouse, Rat
Host
All hosts for GLRA1 antibodies
Rabbit
Clonality
All clonalities for GLRA1 antibodies
Polyclonal
Conjugate
All conjugates for GLRA1 antibodies
This GLRA1 antibody is un-conjugated
Application
All applications for GLRA1 antibodies
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
Characteristics
Polyclonal Antibody
Purification
Affinity purification
Immunogen
Synthetic peptide of human GLRA1
Isotype
IgG
Top Product
Discover our top product GLRA1 Primary Antibody
Alternatives
(show)
Application Details
(hide)
Application Notes
WB 1:500-1:2000, IHC 1:25-1:100
Restrictions
For Research Use only
Handling
(hide)
Format
Liquid
Concentration
0.2 mg/mL
Buffer
PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for GLRA1
(hide)
Target
GLRA1
(Glycine Receptor, alpha 1 (GLRA1))
Alternative Name
GLRA1 (GLRA1 Products )
Synonyms
GLYRA1 antibody, HKPX1 antibody, STHE antibody, [a]Z1 antibody, B230397M16Rik antibody, nmf11 antibody, oscillator antibody, ot antibody, spasmodic antibody, spd antibody, glycine receptor alpha 1 antibody, glycine receptor, alpha 1 antibody, glycine receptor, alpha 1 subunit antibody, GLRA1 antibody, Glra1 antibody, glra1 antibody
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.
Molecular Weight
53 kDa
NCBI Accession
NP_000162
UniProt
P23415
Pathways
Synaptic Membrane
Recently viewed
(hide)