Recombinant Human LOXL3 Protein, His-tagged

This gene encodes a lysyl oxidase, which likely functions as an amine oxidase and plays a role in the formation of crosslinks in collagens and elastin. Deletion of the related gene in mouse causes neonatal mortality with cleft palate, spine deformity, and defects in collagen organization. A mutation in this gene was found in a family with Stickler syndrome.

• Supplier: Creative Biomart
• Product #: LOXL3-277H