FoxC1/2 Polyclonal Antibody, 20ul Pipette Micro Tips reducing the research

reducing the research

Mutations in CACNA2D1 can cause cardiac deficiencies

The full-length nature of some variants has not been determined

The Ab hydrolase domain containing (ABHD) gene subfamily is comprised of 15 mostly uncharacterized members

Cut like homeobox 1 encoded by CUX1 is a member of the homeodomain family of DNA binding proteins

FoxC1/2 Polyclonal Antibody, 20ul Pipette Micro Tips reducing the researchFOXC1 belongs to the forkhead family of transcription factors which is characterized by a distinct DNA binding forkhead domain. The specific function of this gene has not yet been determined; however, it has been shown to play a role in the regulation of embryonic and ocular development. Mutations in this gene cause various glaucoma phenotypes including primary congenital glaucoma, autosomal dominant iridogoniodysgenesis anomaly, and Axenfeld Rieger