CD56 Polyclonal Antibody, 50ul[BT-AP01573] Organelle Studies Mutations in this gene cause

Mutations in this gene cause hereditary sensory and autonomic neuropathy with spastic paraplegia (HSNSP)

This gene product belongs to the 14-3-3 family of proteins which mediate signal transduction by binding to phosphoserine-containing proteins

susceptibility to Parkinson disease and protection against nicotine dependence

and during mitosis

making it a valuable asset for any lab or research setting

CD56 Polyclonal Antibody, 50ul[BT-AP01573] Organelle Studies Mutations in this gene causeCDC20 appears to act as a regulatory protein interacting with several other proteins at multiple points in the cell cycle. It is required for two microtubule dependent processes, nuclear movement prior to anaphase and chromosome separation.