PC-PLD2 Polyclonal Antibody, 20ul Plasma Defects in this gene are

Defects in this gene are a cause of retinitis pigmentosa autosomal recessive (ARRP) disease

ITIH1 encodes a member of the inter-alpha-trypsin inhibitor family of proteins

Knockout mouse studies show defects in the formation of vertebrae and ribs that also involve cartilage formation in these structures

based on the presence or absence of the SH3 (Src homology 3) domain

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PC-PLD2 Polyclonal Antibody, 20ul Plasma Defects in this gene areThe protein encoded by PLD2 (phospholipase D2) catalyzes the hydrolysis of phosphatidylcholine to phosphatidic acid and choline. The activity of the encoded enzyme is enhanced by phosphatidylinositol 4,5 bisphosphate and ADP ribosylation factor 1. This protein localizes to the peripheral membrane and may be involved in cytoskeletal organization, cell cycle control, transcriptional regulation, and or regulated secretion. Two transcript variants