MRCK Alpha Polyclonal Antibody, 100ul Cell Dissociation Mutations in this gene cause

Mutations in this gene cause Schwartz-Jampel syndrome type 2

and resides in the golgi apparatus

Cofactor E binds to the cofactor D/beta-tubulin complex

Mutations in this gene are associated with acute myeloid leukemia

including stimulation of monocytes

MRCK Alpha Polyclonal Antibody, 100ul Cell Dissociation Mutations in this gene causeCDC42 binding protein kinase alpha encoded by CDC42BPA is a member of the Serine Threonine protein kinase family. This kinase contains multiple functional domains. Its kinase domain is highly similar to that of the myotonic dystrophy protein kinase (DMPK). This kinase also contains a Rac interactive binding (CRIB) domain, and has been shown to bind CDC42. It may function as a CDC42 downstream effector mediating CDC42 induced peripheral actin