Your search returned products across suppliers with conjugation options.

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. Mul... Read more
 

Verification

Prior to displaying your results, please confirm you are a real person.

By continuing, you agree to the FluoroFinder Terms and Conditions.

Selected products
Remove all from compare list