PKCdelta(Phospho-Tyr311) Rabbit Polyclonal Antibody, 100ul Protein Research Defects in PRF1 cause familial

Defects in PRF1 cause familial hemophagocytic lymphohistiocytosis type 2 (HPLH2)

leaving a small fragment termed CLIP (class-II-associated invariant chain peptide)

The early growth response 3 encoded by EGR3 participates in the transcriptional regulation of genes in controling biological rhythm

possibly tissue-specific alternative splicing events

DBI encodes diazepam binding inhibitor

PKCdelta(Phospho-Tyr311) Rabbit Polyclonal Antibody, 100ul Protein Research Defects in PRF1 cause familialProtein kinase C (PKC) is a family of serine and threonine specific protein kinases that can be activated by calcium and the second messenger diacylglycerol. PKC family members phosphorylate a wide variety of protein targets and are known to be involved in diverse cellular signaling pathways. PKC family members also serve as major receptors for phorbol esters a class of tumor promoters. Each member of the PKC family has a specific expression profile