PKN Polyclonal Antibody, 100ul Serum Defects in this gene are

Defects in this gene are a cause of Walker-Warburg syndrome (WWS)

Deficiency in this protein (B-cell linker)has also been shown in some cases of pre-B acute lymphoblastic leukemia

filopodia motility and probably synapse formation

also known as ALS2CR16 (amyotrophic lateral sclerosis 2 chromosomal region candidate gene 16 protein) or ALS2CR17

PKN Polyclonal Antibody, 100ul Serum Defects in this gene areThe protein encoded by PKN1 (protein kinase N1) belongs to the protein kinase C superfamily. This kinase is activated by Rho family of small G proteins and may mediate the Rho dependent signaling pathway. This kinase can be activated by phospholipids and by limited proteolysis. The 3 phosphoinositide dependent protein kinase 1 (PDPK1 PDK1) is reported to phosphorylate this kinase, which may mediate insulin signals to the actin cytoskeleton. The