| 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, Mouse, Zebrafish | 
| Tested applications | WB IHC ELISA ChIP | 
| Clonality | Polyclonal Antibody | 
| Calculated MW | 56.8 kDa | 
| Recommended Dilutions | 
                                     WB 1-1.5 ug/mL 
                                    IHC 3-5 ug/mL 
                                    
                                    
                                    
                                    
                                    
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| Immunogen | A synthetic peptide corresponding to C-terminus of 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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