RALA Polyclonal Antibody, 20ul Serum & Sample Tubes also designated precerebellin 1 or

also designated precerebellin 1 or Cbln1

Mutations in this gene are associated with methylmalonic aciduria and homocystinuria type cblC

Mutations in this gene have been associated with KBG syndrome| which is characterized by macrodontia| distinctive craniofacial features| short stature| skeletal anomalies| global developmental delay| seizures and intellectual disability

It specifically recognizes phosphorylated cyclin-dependent kinase inhibitor 1B (CDKN1B| also referred to as p27 or KIP1) predominantly in S phase and int

touch sensation

RALA Polyclonal Antibody, 20ul Serum & Sample Tubes also designated precerebellin 1 orThe product of this gene belongs to the small GTPase superfamily, Ras family of proteins. GTP binding proteins mediate the transmembrane signaling initiated by the occupancy of certain cell surface receptors. This gene encodes a low molecular mass ras like GTP binding protein that shares about 50% similarity with other ras proteins.