TRPM7 Polyclonal Antibody, 20ul Live Cell Imaging CYP20A1 (cytochrome P450 family 20

CYP20A1 (cytochrome P450 family 20 subfamily A member 1) encodes a member of the cytochrome P450 superfamily of enzymes

and H subunit

Mutations in this gene are associated with Jalili syndrome which consists of cone-rod dystrophy and amelogenesis imperfecta

The protein may play a role in tumorigenesis

where it partially colocalizes with the nuclear lamina

TRPM7 Polyclonal Antibody, 20ul Live Cell Imaging CYP20A1 (cytochrome P450 family 20The protein encoded by this gene is both an ion channel and a serine threonine protein kinase. The kinase activity is essential for the ion channel function, which serves to increase intracellular calcium levels and to help regulate magnesium ion homeostasis. Defects in this gene are a cause of amyotrophic lateral sclerosis parkinsonism dementia complex of Guam. Alternative splicing of this gene results in multiple transcript variants.