LETM1 Rabbit Polyclonal Antibody, 100ul Purification Each member of the PKC

Each member of the PKC family has a specific expression profile and is believed to play distinct roles in cells

while the HLH domain facilitates the mono- and heterodimeric interactions required for efficient DNA binding

and it also acts as a tumor suppressor

a major controlling element of neutrophil elastase activity

This gene encodes a dual-specificity phosphatase that associates with polyribosomes

LETM1 Rabbit Polyclonal Antibody, 100ul Purification Each member of the PKCThis gene encodes a protein that is localized to the inner mitochondrial membrane. The protein functions to maintain the mitochondrial tubular shapes and is required for normal mitochondrial morphology and cellular viability. Mutations in this gene cause Wolf Hirschhorn syndrome a complex malformation syndrome caused by the deletion of parts of the distal short arm of chromosome 4. Related pseudogenes have been identified on chromosomes 8 15 and 19.