PRRX2 Polyclonal Antibody, 100ul Cryopreservation Alternate transcriptional splice variants

Alternate transcriptional splice variants

This gene encodes a type II membrane protein that belongs to the ITM2 family

RCF:21380×g

The gene mutations are associated with mulibrey (muscle-liver-brain-eye) nanism| an autosomal recessive disorder that involves several tissues of mesodermal origin

pathway:Pigment biosynthesis

PRRX2 Polyclonal Antibody, 100ul Cryopreservation Alternate transcriptional splice variantsThe DNA associated protein encoded by this gene is a member of the paired family of homeobox proteins. Expression is localized to proliferating fetal fibroblasts and the developing dermal layer, with downregulated expression in adult skin. Increases in expression of this gene during fetal but not adult wound healing suggest a possible role in mechanisms that control mammalian dermal regeneration and prevent formation of scar response to wounding. The