CUL7 Polyclonal Antibody, 100ul Biomatrix Binds directly to the ACTR1A

Binds directly to the ACTR1A subunit of dynactin

Mutations in this gene have been associated with a form of mitochondrial respiratory chain deficiency known as Leigh Syndrome

Carboxypeptidase M encoded by CPM is a membrane-bound arginine/lysine carboxypeptidase

Weakly expressed in kidney

thyroid hormone and vitamin D3 receptors

CUL7 Polyclonal Antibody, 100ul Biomatrix Binds directly to the ACTR1AThe protein encoded by this gene is a component of an E3 ubiquitin protein ligase complex. The encoded protein interacts with TP53, CUL9, and FBXW8 proteins. Defects in this gene are a cause of 3M syndrome type 1 (3M1). Two transcript variants encoding different isoforms have been found for this gene.