GlyRBeta Polyclonal Antibody, 100ul Shaker&Mixing Tryptases comprise a family of

Tryptases comprise a family of trypsin-like serine proteases

and a corresponding pseudogene has been found on chromosome 22

Diseases associated with SEPT2 include gastrointestinal anthrax and acute orbital inflammation

Interacts with RHOT1/Miro-1 and RHOT2/Miro-2

GlyRBeta Polyclonal Antibody, 100ul Shaker&Mixing Tryptases comprise a family ofGLRB encodes the beta subunit of the glycine receptor, which is a pentamer composed of alpha and beta subunits. The receptor functions as a neurotransmitter gated ion channel, which produces hyperpolarization via increased chloride conductance due to the binding of glycine to the receptor. Mutations in this gene cause startle disease, also known as hereditary hyperekplexia or congenital stiff person syndrome, a disease characterized by muscular