CD56 Polyclonal Antibody, 100ul[BT-AP01819] Multi-Layer Cell Culture System Mutations and deletions in NKX2-1

Mutations and deletions in NKX2-1 are associated with benign hereditary chorea

MEF2 polypeptide C

At least two transcript variants have been identified for CKS1B

Mutations in this gene can cause X-chromosomal non-specific mental retardation

The presence of this domain is thought to target these proteins to membrane lipids through interaction with phospholipids in the membrane

CD56 Polyclonal Antibody, 100ul[BT-AP01819] Multi-Layer Cell Culture System Mutations and deletions in NKX2-1KIT encodes the human homolog of the proto oncogene c kit. C kit was first identified as the cellular homolog of the feline sarcoma viral oncogene v kit. This protein is a type 3 transmembrane receptor for MGF (mast cell growth factor, also known as stem cell factor). Mutations in this gene are associated with gastrointestinal stromal tumors, mast cell disease, acute myelogenous lukemia, and piebaldism. Multiple transcript variants encoding different