| No | Size | Price | Availability | |
| AGP2296-12 | 50ul | 1500.00 | In Stock |  |
| AGP2296-12 | 100ul | 2000.00 | In Stock | |
| Source: | Goat | Gene Id: | 2296 |
| Isotype: | / | Swiss Prot: | Q12948 |
| purity: | Antigen affinity purification |
| 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. [provided by RefSeq |
| Reactivity | Human |
| Tested applications | ELISA |
| Clonality | Polyclonal Antibody |
| Calculated MW | 56.8 kDa |
| Recommended Dilutions | |
| Immunogen | A synthetic peptide corresponding to human FOXC1 |
| Storage | Store at -20°C in Tris saline, pH 7.3 (0.5% BSA, 0.02% sodium azide).Avoid freeze/thaw cycles. |
| Synonym | ARA, FKHL7, FREAC-3, FREAC3, IGDA, IHG1, IRID1 |
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