GLRA1 Primary Antibody
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.
Purified recombinant fragment of human GLRA1 (AA: extra 29-154) expressed in E. Coli.
Purified antibody in PBS with 0.05% sodium azide
4°C; -20°C for long term storage
Figure 1: Black line: Control Antigen (100 ng);Purple line: Antigen (10ng); Blue line: Antigen (50 ng); Red line:Antigen (100 ng)
Figure 2:Western blot analysis using GLRA1 mAb against human GLRA1 (AA: extra 29-154) recombinant protein. (Expected MW is 40.3 kDa)
Figure 3:Western blot analysis using GLRA1 mAb against HEK293 (1) and GLRA1 (AA: extra 29-154)-hIgGFc transfected HEK293 (2) cell lysate.
For Research Use Only. Not for use in diagnostic procedures.