PGDH Rabbit Polyclonal Antibody, 100ul Hybridoma Antibody Sequencing |disease:Defects in MMP13 are the

|disease:Defects in MMP13 are the cause of spondyloepimetaphyseal dysplasia type 2 (SEMD2)

Phosphorylation of DMD or UTRN may modulate their affinities for associated proteins

The single FST gene encodes two isoforms

Aberrant expression of this gene in adult tissues is associated with tumorigenesis

PGDH Rabbit Polyclonal Antibody, 100ul Hybridoma Antibody Sequencing |disease:Defects in MMP13 are theThis gene encodes a member of the short chain nonmetalloenzyme alcohol dehydrogenase protein family. The encoded enzyme is responsible for the metabolism of prostaglandins which function in a variety of physiologic and cellular processes such as inflammation. Mutations in this gene result in primary autosomal recessive hypertrophic osteoarthropathy and cranioosteoarthropathy. Multiple transcript variants encoding different isoforms have been found for