Stathmin-3 Polyclonal Antibody, 100ul Apoptosis & Autophagy The DPC localizes to the

The DPC localizes to the sarcolemma and its disruption is associated with various forms of muscular dystrophy

Recessive mutations in this gene have been associated with a hereditary form of spastic paraparesis (HSP)

This gene likely encodes a member of the secernin family of proteins

CSN-dependent phosphorylation of TP53 and JUN promotes and protects degradation by the Ubl system

subcellular location:Translocates to the cytoplasm on phosphorylation where it binds binding to YWHAZ

Stathmin-3 Polyclonal Antibody, 100ul Apoptosis & Autophagy The DPC localizes to theSTMN3 encodes Stathmin 3 which is a member of the stathmin protein family. Members of this protein family form a complex with tubulins at a ratio of 2 tubulins for each stathmin protein. Microtubules require the ordered assembly of alpha and beta tubulins, and formation of a complex with stathmin disrupts microtubule formation and function. A pseudogene of this gene is located on chromosome 22. Alternative splicing results in multiple transcript