CLCN7 Antikörper
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- Target Alle CLCN7 Antikörper anzeigen
- CLCN7 (Chloride Channel, Voltage-Sensitive 7 (CLCN7))
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser CLCN7 Antikörper ist unkonjugiert
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Applikation
- Immunofluorescence (IF)
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant protein of human CLCN7
- Isotyp
- IgG
- Top Product
- Discover our top product CLCN7 Primärantikörper
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- Applikationshinweise
- IF 1:50 - 1:100
- Kommentare
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Brain, testis, muscle and kidney
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Buffer
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3.
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20C. Avoid freeze / thaw cycles.
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- Target
- CLCN7 (Chloride Channel, Voltage-Sensitive 7 (CLCN7))
- Andere Bezeichnung
- CLCN7 (CLCN7 Produkte)
- Synonyme
- CLC-7 antikoerper, CLC7 antikoerper, OPTA2 antikoerper, OPTB4 antikoerper, PPP1R63 antikoerper, AA409691 antikoerper, AW538136 antikoerper, ClC-7 antikoerper, D17Wsu51e antikoerper, MGC80627 antikoerper, im:7155923 antikoerper, zgc:153490 antikoerper, CLCN7 antikoerper, chloride voltage-gated channel 7 antikoerper, chloride channel, voltage-sensitive 7 antikoerper, chloride channel, voltage-sensitive 7 L homeolog antikoerper, chloride channel 7 antikoerper, chloride channel protein 7 antikoerper, CLCN7 antikoerper, Clcn7 antikoerper, clcn7.L antikoerper, clcn7 antikoerper, CpipJ_CPIJ008618 antikoerper
- Hintergrund
- The product of this gene belongs to the CLC chloride channel family of proteins. Chloride channels play important roles in the plasma membrane and in intracellular organelles. This gene encodes chloride channel 7. Defects in this gene are the cause of osteopetrosis autosomal recessive type 4 (OPTB4), also called infantile malignant osteopetrosis type 2 as well as the cause of autosomal dominant osteopetrosis type 2 (OPTA2), also called autosomal dominant Albers-Schonberg disease or marble disease autosoml dominant. Osteopetrosis is a rare genetic disease characterized by abnormally dense bone, due to defective resorption of immature bone. OPTA2 is the most common form of osteopetrosis, occurring in adolescence or adulthood.
- Molekulargewicht
- 88.679 kDa
- Gen-ID
- 1186
- UniProt
- P51798
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