ATS20 Polyclonal Antibody, 20ul Cryopreservation Mutations in this gene are

Mutations in this gene are associated with retinal degenerative diseases including retinitis pigmentosa type 35 (RP35) and cone-rod dystrophy type 10 (CORD10)

Expression of this gene is induced by gamma interferon| and this gene product replaces catalytic subunit 2 (proteasome beta 7 subunit) in the immunoproteasome

is composed of three different subdomains: a four-helix bundle (4H)

The phosphorylation of this protein affects microtubule properties and cell cycle progression

ATS20 Polyclonal Antibody, 20ul Cryopreservation Mutations in this gene areThe protein encoded by this gene is a member of the ADAMTS family of zinc dependent proteases. The encoded protein has a signal peptide that is cleaved to release the mature peptide, which is secreted and found in the extracellular matrix. This protein may be involved in tissue remodeling.