GPR6 Polyclonal Antibody, 100ul Cell Function Analysis Defects in PPT1 are a

Defects in PPT1 are a cause of infantile neuronal ceroid lipofuscinosis 1 (CLN1

particularly capillaries

Also found in the colon

The protein encoded by this gene belongs to the SMAD| a family of proteins similar to the gene products of the Drosophila gene 'mothers against decapentaplegic' (Mad) and the C

Abnormal recombination between PRKX and a related pseudogene on chromosome Y is a frequent cause of sex reversal disorder in XX males and XY females

GPR6 Polyclonal Antibody, 100ul Cell Function Analysis Defects in PPT1 are aReceptor for the lysosphingolipid sphingosine 1 phosphate (S1P). S1P is a bioactive lysophospholipid that elicits diverse physiological effect on most types of cells and tissues. This receptor mediates its action by association with G proteins that activate a phosphatidylinositol calcium second messenger system.,Belongs to the G protein coupled receptor 1 family.,