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GLRA1
Glycine receptor alpha 1STHE
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. [provided by RefSeq, Dec 2015]
Top validated antibodies |
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| Proteintech Group |  17951-1-AP |
4 references | Polyclonal |
WB
EL
FC
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| Novus Biologicals | NB300-113 |
2 references | Polyclonal |
WB
IP
IHC
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| Cusabio Biotech Co., Ltd | CSB-PA009516LA01HU |
Polyclonal |
WB
EL
ICC
IHC
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| GeneTex | GTX106112 |
Polyclonal |
WB
ICC
IHC
|
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| Invitrogen Antibodies | PA5-102668 |
Polyclonal |
WB
ICC
IHC
|
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