Stathmin-3 Polyclonal Antibody, 100ul Apoptosis & Autophagy Recessive mutations in this gene

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

Among its related pathways are Metabolism and Immune System

hereditary sensory

The product of CAMK2G is a gamma chain

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

Stathmin-3 Polyclonal Antibody, 100ul Apoptosis & Autophagy Recessive mutations in this geneSTMN3 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