C1QT5 Polyclonal Antibody, 20ul Immune Cell Analysis has been defined for this

has been defined for this gene

Mutations in this gene are the cause of several cardiomyopathies and keratodermas| including skin fragility-woolly hair syndrome

Acyl-Coenzyme A oxidase 3 also know as pristanoyl -CoA oxidase (ACOX3)is involved in the desaturation of 2-methyl branched fatty acids in peroxisomes

It participates in apoptosis signaling through highly specific protein-protein homophilic interactions

C1QT5 Polyclonal Antibody, 20ul Immune Cell Analysis has been defined for thisThis gene encodes a member of a family of proteins that function as components of basement membranes and may play a role in cell adhesion. Mutations in this gene have been associated with late onset retinal degeneration. The protein may be encoded by either a bicistronic transcript including sequence from the upstream membrane frizzled related protein gene (MFRP), or by a monocistronic transcript expressed from an internal promoter.