NDUFS6 Antikörper (AA 29-124)
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- Target Alle NDUFS6 Antikörper anzeigen
- NDUFS6 (NADH Dehydrogenase (Ubiquinone) Fe-S Protein 6, 13kDa (NADH-Coenzyme Q Reductase) (NDUFS6))
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Bindungsspezifität
- AA 29-124
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser NDUFS6 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB)
- Sequenz
- GVRVSPTGEK VTHTGQVYDD KDYRRIRFVG RQKEVNENFA IDLIAEQPVS EVETRVIACD GGGGALGHPK VYINLDKETK TGTCGYCGLQ FRQHHH
- Kreuzreaktivität
- Maus, Ratte
- Produktmerkmale
- Polyclonal Antibodies
- Immunogen
- Recombinant fusion protein containing a sequence corresponding to amino acids 29-124 of human NDUFS6 (NP_004544.1).
- Isotyp
- IgG
- Top Product
- Discover our top product NDUFS6 Primärantikörper
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- Applikationshinweise
- WB,1:500 - 1:2000
- Kommentare
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HIGH QUALITY
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- 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 -20°C. Avoid freeze / thaw cycles.
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- Target
- NDUFS6 (NADH Dehydrogenase (Ubiquinone) Fe-S Protein 6, 13kDa (NADH-Coenzyme Q Reductase) (NDUFS6))
- Andere Bezeichnung
- NDUFS6 (NDUFS6 Produkte)
- Synonyme
- BC059730 antikoerper, IP13 antikoerper, Ip13dis antikoerper, Ndub13 antikoerper, RATIp13dis antikoerper, CI-13kA antikoerper, CI-13kD-A antikoerper, CI13KDA antikoerper, NADH dehydrogenase (ubiquinone) Fe-S protein 6 antikoerper, NADH:ubiquinone oxidoreductase subunit S6 antikoerper, Ndufs6 antikoerper, NDUFS6 antikoerper
- Hintergrund
- This gene encodes a subunit of the NADH:ubiquinone oxidoreductase (complex I), which is the first enzyme complex in the electron transport chain of mitochondria. This complex functions in the transfer of electrons from NADH to the respiratory chain. The subunit encoded by this gene is one of seven subunits in the iron-sulfur protein fraction. Mutations in this gene cause mitochondrial complex I deficiency, a disease that causes a wide variety of clinical disorders, including neonatal disease and adult-onset neurodegenerative disorders.,NDUFS6,CI-13kA,CI-13kD-A,CI13KDA,Cancer,Signal Transduction,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial markers,Oxidative phosphorylation,Neuroscience,Neurodegenerative Diseases,NDUFS6
- Molekulargewicht
- 13 kDa
- Gen-ID
- 4726
- UniProt
- O75380
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