PRKX Polyclonal Antibody, 100ul Reservoirs Mutations in this gene are

Mutations in this gene are associated with congenital stationary night blindness type 2B

these enzymes offer bold action and challenge the norms of DNA manipulation

|subunit:When phosphorylated| interacts directly with the PIK3R1 subunit of phosphoinositide 3-kinase and the SH2 domains of GRB2| GRAP| GRAP2| PLCG1 and PLCG2

This protein localizes to the peripheral membrane and may be involved in cytoskeletal organization

This gene belongs to a family of genes that encode an isolated SCAN domain

PRKX Polyclonal Antibody, 100ul Reservoirs Mutations in this gene arePRKX (protein kinase, X linked) encodes a serine threonine protein kinase that has similarity to the catalytic subunit of cyclic AMP dependent protein kinases. The encoded protein is developmentally regulated and may be involved in renal epithelial morphogenesis. This protein may also be involved in macrophage and granulocyte maturation. Abnormal recombination between PRKX and a related pseudogene on chromosome Y is a frequent cause of sex reversal