| Product Name | FOXC1 Antibody |
|---|---|
| Description | Rabbit polyclonal antibody to FOXC1 |
| Synonyms | ARA antibody; FKH L7 antibody; FKHL 7 antibody; FKHL7 antibody; Forkhead (Drosophila) like 7 antibody; Forkhead box C1 antibody; Forkhead box protein C1 antibody; Forkhead drosophila homolog like 7 antibody; Forkhead like 7 antibody; Forkhead related activator 3 antibody; Forkhead related protein FKHL7 antibody; Forkhead related transcription factor 3 antibody; Forkhead-related protein FKHL7 antibody; Forkhead-related transcription factor 3 antibody; FOX C1 antibody; FOXC 1 antibody; Foxc1 antibody; FOXC1_HUMAN antibody; FREAC 3 antibody; FREAC-3 antibody; FREAC3 antibody; IGDA antibody; IHG 1 antibody; IHG1 antibody; IRID 1 antibody; IRID1 antibody; Iridogoniodysgenesis type 1 antibody; Myeloid factor delta antibody |
| Host | Rabbit |
| Clonality | Polyclonal |
| Conjugate | Unconjugated |
| Immunogen | Synthetic peptide of human FOXC1 |
| Isotype | IgG |
| Target | FOXC1 |
| Reactivity | Human, Mouse |
| Applications | ELISA, WB |
| Form | Liquid |
| Diluent Buffer | -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol |
| Uniprot | Q12948 |
| Storage | Upon receipt, store at -20°C or -80°C. Avoid repeated freeze. |
| 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. |
| Supplier | Cusabio |
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