GLRA1 Antibody
Product Specifications
Background
The protein encoded by this gene is a subunit of a pentameric inhibitory glycine receptor, which 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. Multiple transcript variants encoding different isoforms have been found.
NCBI Gene ID
2741
Swiss Prot
P23415
Host
Rabbit
Reactivity
Human, Mouse, Rat
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 29-247 of human GLRA1 (NP_000162.2) .
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Neuroscience
Purification
Affinity purification
Positive Control
U-87MG
Concentration
Batch dependent
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Modification
None
Shipping Conditions
Blue Ice
Storage Conditions
Store at -20˚ C. Avoid freeze / thaw cycles.
Product Datasheet
https://www.prosci-inc.com/?datasheet_sku=18-882
Calculated Molecular Weight
Observed: 53kDa
Fragment
IgG
Applications Notes
WB: 1:500 - 1:1000
Symbol
GLRA1
Positive Control 2
U-251MG
Positive Control 3
Mouse testis
Positive Control 4
Mouse brain
Positive Control 5
Rat testis
NCBI Official Name
Glycine receptor, alpha 1
NCBI Organism
Homo sapiens
Other Product Names
GLRA1, STHE, HKPX1
Tested Applications
WB
Physical Properties
Liquid
Curated Selection
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