CD55 Polyclonal Antibody, 100ul[BT-AP01928] Filtration This gene encodes a member

This gene encodes a member of the Wiskott-Aldrich syndrome (WAS) protein family

Mutations in this gene are associated with McArdle disease (myophosphorylase deficiency)| a glycogen storage disease of muscle

which forms a complex with CDK4 or CDK6

Cdk proteins work in concert with the cyclins to phosphorylate key substrates involved in each phase of cell cycle progression

The encoded protein contains a C-terminal caspase activation and recruitment domain (CARD)

CD55 Polyclonal Antibody, 100ul[BT-AP01928] Filtration This gene encodes a memberGGT7 is a member of a gene family that encodes enzymes involved in both the metabolism of glutathione and in the transpeptidation of amino acids. Changes in the activity of gamma glutamyltransferase may signal preneoplastic or toxic conditions in the liver or kidney. The gamma glutamyltransferase 7 encoded by GGT7 consists of a heavy and a light chain, and it can interact with CT120, a plasma membrane associated protein that is possibly involved in