FOXC1 Polyclonal Antibody
| 规格： | / 20μL / 60μL / 120μL / 200μL |
| 价格： | / ￥420 / ￥1010 / ￥1640 / ￥2365 |
货号：E-AB-17316
宿主: Rabbit
反应性: H,M
应用: WB
Overview
| Synonyms | ARA,FKH L7,FKHL 7,FKHL7,Forkhead (Drosophila) like 7,Forkhead box C1,Forkhead box protein C1,Forkhead drosophila homolog like 7,Forkhead like 7,Forkhead related activator 3,Forkhead related protein FKHL7,Forkhead related transcription factor 3,Forkhead-related protein FKHL7,Forkhead-related transcription factor 3,FOX C1,FOXC 1,Foxc1,FOXC1,FREAC 3,FREAC-3,FREAC3,IGDA,IHG 1,IHG1,IRID 1,IRID1,Iridogoniodysgenesis type 1,Myeloid factor delta,FOXC1抗体 |
| Swissprot | Q12948 |
| Source | Rabbit |
| Reactivity | Human,Mouse |
| Immunogen | Synthetic peptide of human FOXC1 |
| Application | WB(Detection kit: E-IR-R304) |
| Recommended dilution | WB,,1:500-2000; |
| Concentration | 0.2mg/mL |
| Clonality | Polyclonal |
Properties
| Cellular localization | Nucleus. |
| Tissue specificity | Expressed in all tissues and cell lines examined. |
| Isotype | IgG |
| Purification | Affinity purification |
| Conjugation | Unconjugated |
| Storage instructions | Store at -20℃. Avoid freeze / thaw cycles. |
| Storage buffer | PBS with 0.05% sodium azide, 50% glycerol, PH7.3 |
| 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. |
