AEBP1 Polyclonal Antibody, 20ul Cell Biology Diseases associated with ZDHHC2 include

Diseases associated with ZDHHC2 include hepatocellular carcinoma and locked-in syndrome

and ensures safe operations Maximum RCF of up to 25

Mutations in this gene are associated with the autosomal dominant disorder| encephalopathy| lethal| due to defective mitochondrial and peroxisomal fission (EMPF)

The protein encoded by this gene is a member of the serpin (serine proteinase inhibitor) superfamily

chronic infantile neurological cutaneous and articular (CINCA) syndrome

AEBP1 Polyclonal Antibody, 20ul Cell Biology Diseases associated with ZDHHC2 includeThis gene encodes a member of carboxypeptidase A protein family. The encoded protein may function as a transcriptional repressor and play a role in adipogenesis and smooth muscle cell differentiation. Studies in mice suggest that this gene functions in wound healing and abdominal wall development. Overexpression of this gene is associated with glioblastoma.