GLRA1 / Unconjugated / 2B9
Product Details
| Description | GLRA1 - glycine receptor, alpha 1 (startle disease/hyperekplexia, stiff man syndrome) (2B9) | |
|---|---|---|
| Conjugate | Unconjugated | |
| Clone | 2B9 | |
| Target Species | Human | |
| Applications | ELISA, WB | |
| Supplier | Novus Biologicals | |
| Catalog # | Sign in to view product details, citations, and spectra | |
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About GLRA1
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]
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]
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227 GLRA1 antibodies from over 12 suppliers available with over 16 conjugates.
