FoxC1/2 Polyclonal Antibody, 20ul Pipette Micro Tips and it may also mediate

and it may also mediate both cell proliferation and cell death

reducing the research

Mutations in CACNA2D1 can cause cardiac deficiencies

Each domain contains two cysteines

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

FoxC1/2 Polyclonal Antibody, 20ul Pipette Micro Tips and it may also mediateFOXC1 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