分子量：Calculated MW: 51kDa/52kDa
Observed MW: 53kDa

细胞定位：Cell junction, Cell membrane, Multi-pass membrane protein, postsynaptic cell membrane, synapse

稀释方法：WB 1:500 - 1:1000

总结：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.