MMP2 mouse Monoclonal Antibody(1H1), 50ul Protein Post-translational Modification Mutations in this gene have

Mutations in this gene have been associated with primary ciliary dyskinesia

which may contribute to the pathogenesis

Diseases associated with IFNE include west nile fever

there are multiple processed pseudogenes of RPS19 dispersed through the genome

This gene encodes an FAD-containing enzyme that catalyzes the oxidation of spermine to spermadine and secondarily produces hydrogen peroxide

MMP2 mouse Monoclonal Antibody(1H1), 50ul Protein Post-translational Modification Mutations in this gene haveThis gene is a member of the matrix metalloproteinase (MMP) gene family, that are zinc dependent enzymes capable of cleaving components of the extracellular matrix and molecules involved in signal transduction. The protein encoded by this gene is a gelatinase A, type IV collagenase, that contains three fibronectin type II repeats in its catalytic site that allow binding of denatured type IV and V collagen and elastin. Unlike most MMP family members,