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)

The neuregulins

sequencing

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

Elongation of very long chain fatty acid-like (ELOVL) proteins 1-6 are members of the ELO family of proteins

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.