Synaptotagmin XIII Polyclonal Antibody, 20ul General Lab Use point mutations

point mutations

the arylsulfatase subfamily

Mutations or defects in the gene encoding CEP55 result in a failure to exit mitosis and may be associated with tumor progression

and inhibited by GTPase activating proteins (GAPs)

ADRA1D comprises 2 exons and a single intron that interrupts the coding region

Synaptotagmin XIII Polyclonal Antibody, 20ul General Lab Use point mutationsSYT13 encodes a member of the large synaptotagmin protein family. Family members have an extracellular N terminal transmembrane domain and a cytoplasmic C terminus with two tandem C2 domains (C2A and C2B). Synaptotogmin family members can form homo and heteromeric complexes with each other. They also have different biochemical properties and developmental profiles, and patterns of tissue distribution. Synaptotagmins function as membrane traffickers in