Rabbit anti-FOXC1 Antibody
Catalog #
FOXC1
Human
IHC
,IP
Rabbit
Polyclonal
Whole IgG
between 275 and 325
IgG
Unconjugated
Antigen Affinity Purified
Product Details
Human
Human
2 - 8 °C
1 year from date of receipt
Forkhead box C1 (FOXC1) belongs to the forkhead family of transcription factors which is characterized by a distinct DNA-binding forkhead domain. The specific function of FOXC1 has not yet been determined; however, the gene has been shown to play a role in the regulation of embryonic and ocular development. Mutations in the FOXC1 gene cause various glaucoma phenotypes including primary congenital glaucoma, autosomal dominant iridogoniodysgenesis anomaly, and Axenfeld-Rieger anomaly.[taken from NCBI Entrez Gene (Gene ID: 2296)].
Alternate Names
ARA; ASGD3; FKHL7; forkhead box C1 protein; forkhead box protein C1; forkhead, drosophila, homolog-like 7; forkhead/winged helix-like transcription factor 7; forkhead-related activator 3; forkhead-related protein FKHL7; forkhead-related transcription factor 3; FREAC3; FREAC-3; IGDA; IHG1; IRID1; myeloid factor-delta; RIEG3
Applications