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Description
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. [provided by RefSeq
Specifications
Specifications
| Antigen | FOXC1 |
| Applications | ELISA, Western Blot |
| Classification | Monoclonal |
| Clone | 1E11 |
| Conjugate | Unconjugated |
| Description | Mouse monoclonal antibody raised against a full length recombinant FOXC1. |
| Formulation | PBS with no preservative; pH 7.4 |
| Gene | FOXC1 |
| Gene Accession No. | NM_001453 |
| Gene Alias | ARA/FKHL7/FREAC-3/FREAC3/IGDA/IHG1/IRID1 |
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