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GLRB
Glycine receptor betaThis gene encodes the beta subunit of the glycine receptor, which is a pentamer composed of alpha and beta subunits. The receptor functions as a neurotransmitter-gated ion channel, which produces hyperpolarization via increased chloride conductance due to the binding of glycine to the receptor. Mutations in this gene cause startle disease, also known as hereditary hyperekplexia or congenital stiff-person syndrome, a disease characterized by muscular rigidity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]
Top validated antibodies |
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| Invitrogen Antibodies |  MA5-31741 |
Monoclonal |
WB
EL
ICC
FC
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| Proteintech Group | 15371-1-AP |
2 references | Polyclonal |
WB
EL
IHC
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| Novus Biologicals | NBP2-61774 |
Monoclonal |
WB
EL
ICC
FC
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| antibodies-online | ABIN5683576 |
Monoclonal |
WB
EL
ICC
IHC
FC
|
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| LSBio | LS-C816437 |
Polyclonal |
WB
IP
IHC
|
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