GLRA1 蛋白
(Glycine Receptor, alpha 1 (GLRA1))
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.[provided by RefSeq, Mar 2009].
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6 results
GLRA1
宿主: 人
宿主: HEK-293 Cells
Synthetic Nanodisc
ELISA, Imm, cryo-EM, PhD, SPR
GLRA1
宿主: 人
宿主: 大肠杆菌（E. Coli）
Recombinant
Greater than 90 % as determined by SDS-PAGE.
ELISA, WB
Aliases for GLRA1 蛋白
glycine receptor alpha 1 (GLRA1) 蛋白glycine receptor, alpha 1 (Glra1) 蛋白
glycine receptor, alpha 1 (glra1) 蛋白
glycine receptor, alpha 1 subunit (Glra1) 蛋白
B230397M16Rik 蛋白
GLYRA1 蛋白
HKPX1 蛋白
nmf11 蛋白
oscillator 蛋白
ot 蛋白
spasmodic 蛋白
spd 蛋白
STHE 蛋白
[a]Z1 蛋白
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