FREAC3 polyclonal, anti-human, mouse

Background:
This gene 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 anomaly.

Synonyms: ARA, IGDA, IHG1, FKHL7, IRID1, RIEG3, FREAC3, FREAC-3

Cellular Location: Nucleus

Immunogen:
A synthetic peptide of human FOXC1

Gene Symbol: FOXC1

Gene ID: 2296

Swiss prot: Q12948

Calculated MW: 57 kDa

Recommended dilution:
WB 1:500-2000

Purity:
Affinity purification

Storage Buffer:
Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.

Storage:
Store at -20℃. Avoid freeze / thaw cycles.