MARK2(Phospho Thr596) Polyclonal Antibody, 100ul Live Cell Imaging Defects in this gene are

Defects in this gene are a cause of hereditary coproporphyria (HCP)

Mutations in GYS1 are associated with muscle glycogen storage disease

Featuring a 6-layer glass fiber film filter in natural color

The protein is also partly localized to the nucleus

such as dyskeratosis congenita

MARK2(Phospho Thr596) Polyclonal Antibody, 100ul Live Cell Imaging Defects in this gene areThis gene encodes a member of the Par 1 family of serine threonine protein kinases. The protein is an important regulator of cell polarity in epithelial and neuronal cells, and also controls the stability of microtubules through phosphorylation and inactivation of several microtubule associating proteins. The protein localizes to cell membranes. Multiple transcript variants encoding different isoforms have been found for this gene.