RFX6 Antikörper
Kurzübersicht für RFX6 Antikörper (ABIN7246697)
Target
Alle RFX6 Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
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    - 
                                            Produktmerkmale
- Polyclonal Antibody
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                                            Aufreinigung
- Antigen affinity purification
- 
                                            Immunogen
- Fusion protein of human RFX6
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                                            Isotyp
- IgG
 
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    - 
                                            Applikationshinweise
- IHC 1:50-1:300, ELISA 1:5000-1:10000
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                                            Beschränkungen
- Nur für Forschungszwecke einsetzbar
 
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    - 
                                            Format
- Liquid
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                                            Konzentration
- 0.96 mg/mL
- 
                                            Buffer
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
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                                            Konservierungsmittel
- Sodium azide
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                                            Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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                                            Lagerung
- -20 °C
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                                            Informationen zur Lagerung
- Store at -20°C. Avoid freeze / thaw cycles.
 
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    - RFX6 (Regulatory Factor X 6 (RFX6))
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                                            Andere Bezeichnung
- RFX6
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                                            Hintergrund
- The nuclear protein encoded by this gene is a member of the regulatory factor X (RFX) family of transcription factors. Studies in mice suggest that this gene is specifically required for the differentiation of islet cells for the production of insulin, but not for the differentiation of pancreatic polypeptide-producing cells. It regulates the transcription factors involved in beta-cell maturation and function, thus, restricting the expression of the beta-cell differentiation and specification genes. Mutations in this gene are associated with Mitchell-Riley syndrome, which is characterized by neonatal diabetes with pancreatic hypoplasia, duodenal and jejunal atresia, and gall bladder agenesis.
- 
                                            UniProt
- Q8HWS3
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                                            Pathways
- Carbohydrate Homeostasis
 Target
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