This protein forms a homohexameric complex that interacts with a variety of cofactors and extracts ubiquitinated proteins from lipid membranes or protein complexes. Mutations in this gene cause IBMPFD (inclusion body myopathy with paget disease of bone and frontotemporal dementia), ALS (amyotrophic lateral sclerosis) and Charcot-Marie-Tooth disease in human patients.

Aliases：    p97; TERA; CDC48; FTDALS6    

Entrez GeneID：    7415    

Swissprot :   P55072    

WB Predicted band size：    89.3kDa    

Host/Isotype：    Mouse IgG1    

Species Reactivity：    Human, Mouse    

Immunogen：    Purified recombinant fragment of human VCP (AA:707-806) expressed in Mammalian system    

WB    1/500 - 1/2000    

IF/ICC    1/200 - 1/1000    

FCM    1/200 - 1/400    

ELISA    1/10000