FOXC1 Polyclonal Antibody
Price:
Size:
200μL
120μL
60μL
20μL
- 宿主: Rabbit
- 反应性: Human;Mouse
- 应用性: WB
Verified Samples |
Verified Samples in WB:Human liver |
Dilution | WB 1:500-2000 |
Clonality | Polyclonal |
Isotype | IgG |
Immunogen | Synthetic peptide of human FOXC1 |
Abbre | FOXC1 |
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 |
Swissprot | |
Calculated MW | 57 kDa |
Cellular Localization | Nucleus. |
Concentration | 0.2 mg/mL |
Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
Buffer | PBS with 0.05% sodium azide and 50% glycerol, PH7.4 |
Purification Method | Affinity purification |
Research Areas | Cancer; Epigenetics and Nuclear Signaling; Developmental biology |
Conjugation | Unconjugated |
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. |
Western Blot analysis of Human normal liver tissue using FOXC1 Polyclonal Antibody at dilution of 1/400
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