MMP-8 Polyclonal Antibody, 100ul Custom DNA Oligos This gene encodes a member

This gene encodes a member of the dual specificity protein kinase family

The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms

The gene is deleted in Williams-Beuren syndrome| a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11

PGBD1 belongs to the subfamily of piggyBac transposable element derived (PGBD) genes

Mutations in this gene cause nephronophthisis (NPHP)| an autosomal recessive kidney disease characterized by tubular basement membrane disruption| interstitial lymphohistiocytic cell infiltration| and development of cysts at the corticomedullary border of the kidneys

MMP-8 Polyclonal Antibody, 100ul Custom DNA Oligos This gene encodes a memberMMP8 encodes a member of the matrix metalloproteinase (MMP) family of proteins. These proteins are involved in the breakdown of extracellular matrix in embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Proteolysis at different sites on this protein results in multiple active forms of the enzyme with distinct N termini. This protein functions in the degradation of type I, II