PLCD1 Polyclonal Antibody, 20ul Peripheral Blood Separation Tube Defects in this gene can

Defects in this gene can be a cause of Brugada Syndrome

and has been shown to form dimers/oligomers through its leucine-zipper motif

The TnI subfamily contains three genes: tnI-skeletal-fast-twitch

Mouse studies suggested an essential role of this protein in spermatogenesis

non-receptor type 1 by PTPN1 is the founding member of the protein tyrosine phosphatase (PTP) family

PLCD1 Polyclonal Antibody, 20ul Peripheral Blood Separation Tube Defects in this gene canThis gene encodes a member of the phospholipase C family. Phospholipase C isozymes play critical roles in intracellular signal transduction by catalyzing the hydrolysis of phosphatidylinositol 4,5 bisphosphate (PIP2) into the second messengers diacylglycerol (DAG) and inositol triphosphate (IP3). The encoded protein functions as a tumor suppressor in several types of cancer, and mutations in this gene are a cause of hereditary leukonychia.