ACOX2 Polyclonal Antibody, 100ul Lysosome is localized to chromosome 3

is localized to chromosome 3 and the alpha form is localized to chromosome 17

Mutations in THBD are a cause of thromboembolic disease

It then extends each strand from the base-paired region using the opposing overhang as a template

and sgRNA library oligos

Gene Ontology (GO) annotations related to PRSS33 include serine-type endopeptidase activity and serine-type peptidase activity

ACOX2 Polyclonal Antibody, 100ul Lysosome is localized to chromosome 3The product of this gene belongs to the acyl CoA oxidase family. It encodes the branched chain acyl CoA oxidase which is involved in the degradation of long branched fatty acids and bile acid intermediates in peroxisomes. Deficiency of this enzyme results in the accumulation of branched fatty acids and bile acid intermediates and may lead to Zellweger syndrome severe mental retardation and death in children.