G6PC Antikörper
Kurzübersicht für G6PC Antikörper (ABIN7245446)
Target
Alle G6PC Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
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                                            Produktmerkmale
- Polyclonal Antibody
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                                            Aufreinigung
- Antigen affinity purification
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                                            Immunogen
- Synthetic peptide of human G6PC
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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
- 1.44 mg/mL
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                                            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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    - G6PC (Glucose 6-Phosphatase, Catalytic (G6PC))
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                                            Andere Bezeichnung
- G6PC
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                                            Hintergrund
- Glucose-6-phosphatase (G6Pase) is a multi-subunit integral membrane protein of the endoplasmic reticulum that is composed of a catalytic subunit and transporters for G6P, inorganic phosphate, and glucose. This gene (G6PC) is one of the three glucose-6-phosphatase catalytic-subunit-encoding genes in human: G6PC, G6PC2 and G6PC3. Glucose-6-phosphatase catalyzes the hydrolysis of D-glucose 6-phosphate to D-glucose and orthophosphate and is a key enzyme in glucose homeostasis, functioning in gluconeogenesis and glycogenolysis. Mutations in this gene cause glycogen storage disease type I (GSD1). This disease, also known as von Gierke disease, is a metabolic disorder characterized by severe hypoglycemia associated with the accumulation of glycogen and fat in the liver and kidneys.
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                                            UniProt
- P35575
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                                            Pathways
- Carbohydrate Homeostasis, Cellular Glucan Metabolic Process
 Target
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