PC-PLD3 Polyclonal Antibody, 20ul Aspirating Pipets that encodes an orphan G

that encodes an orphan G protein-coupled receptor

Defects in MEGF8 are a cause of Carpenter syndrome 2

and sterile solution for 100-1000μl volume

Defects in EP300 are a cause of Rubinstein-Taybi syndrome and may also play a role in epithelial cancer

and has been shown to bind CDC42 in the presence of GTP

PC-PLD3 Polyclonal Antibody, 20ul Aspirating Pipets that encodes an orphan GPLD3 encodes a member of the phospholipase D (PLD) family of enzymes that catalyze the hydrolysis of membrane phospholipids. The phospholipase D family member 3 is a single pass type II membrane protein and contains two PLD phosphodiesterase domains. This protein influences processing of amyloid beta precursor protein. Mutations in this gene are associated with Alzheimer disease risk. Alternatively spliced transcript variants encoding the same protein