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FOXC1 Antibody

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)].
FOXC1
forkhead box C1
Forkhead box protein C1
:  ARA FKHL7 forkhead box C1 protein 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 More... Less...
Product
Specifications
Ordering Information
Human
IP, IHC
Between 275 and 325
$339
$99
Human
WB, IP, IHC
Between 375 and 425
$339
$229
$99
Human
WB, IP, IHC
Includes: 1 each of A303-519A and A303-520A
$472
Includes: 1 each of A303-519A and A303-520A