FOXC1 Polyclonal Antibody

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.

Research Area: Cancer, Epigenetics and Nuclear Signaling, Developmental biology

Synonyms:
ARA, FKH L7, FKHL 7, FKHL7, Forkhead (Drosophila) like 7, Forkhead box C1, Forkhead box protein C1, Forkhead drosophila homolog like 7, Forkhead like 7, Forkhead related activator 3, Forkhead related protein FKHL7, Forkhead related transcription factor 3, Forkhead-related protein FKHL7, Forkhead-related transcription factor 3, FOX C1, FOXC 1, Foxc1, FOXC1, FREAC 3, FREAC-3, FREAC3, IGDA, IHG 1, IHG1, IRID 1, IRID1, Iridogoniodysgenesis type 1, Myeloid factor delta

Immunogen: Synthetic peptide of human FOXC1

Swissprot: Q12948
Gene Accession: NP_001444

Calculated MW: 57 kDa

Purification Method: Affinity purification

Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4

Concentration: 0.2 mg/mL
Dilution: WB 1:500-2000, ELISA 1:2000-5000

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

Alternative for product with catalog number:
sc-21394/sc-21396