NDUFS7 anticorps
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- Antigène Voir toutes NDUFS7 Anticorps
- NDUFS7 (NADH Dehydrogenase (Ubiquinone) Fe-S Protein 7, 20kDa (NADH-Coenzyme Q Reductase) (NDUFS7))
- Reactivité
- Humain, Souris, Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp NDUFS7 est non-conjugé
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Application
- ELISA, Immunohistochemistry (IHC), Western Blotting (WB), Immunofluorescence (IF)
- Immunogène
- NADH dehydrogenase (ubiquinone) Fe-S protein 7, 20kDa (NADH-coenzyme Q reductase)
- Isotype
- IgG
- Top Product
- Discover our top product NDUFS7 Anticorps primaire
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- Indications d'application
- Optimal working dilution should be determined by the investigator.
- Commentaires
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human brain tissue were subjected to SDS PAGE followed by western blot with FNab05634(NDUFS7 antibody) at dilution of 1:500
- Restrictions
- For Research Use only
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- Buffer
- PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Conseil sur la manipulation
- Avoid repeated freeze / thaw cycles.
- Stock
- -20 °C
- Date de péremption
- 12 months
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- Antigène
- NDUFS7 (NADH Dehydrogenase (Ubiquinone) Fe-S Protein 7, 20kDa (NADH-Coenzyme Q Reductase) (NDUFS7))
- Autre désignation
- NDUFS7 (NDUFS7 Produits)
- Synonymes
- anticorps 1010001M04Rik, anticorps CI-20, anticorps CI-20KD, anticorps MY017, anticorps PSST, anticorps NADH dehydrogenase (ubiquinone) Fe-S protein 7, anticorps NADH:ubiquinone oxidoreductase core subunit S7, anticorps Ndufs7, anticorps NDUFS7
- Sujet
- Synonyms:CI-20 Background:This gene encodes a protein that is a subunit of one of the complexes that forms the mitochondrial respiratory chain. This protein is one of over 40 subunits found in complex I, the nicotinamide adenine dinucleotide (NADH):ubiquinone oxidoreductase. This complex functions in the transfer of electrons from NADH to the respiratory chain, and ubiquinone is believed to be the immediate electron acceptor for the enzyme. Mutations in this gene cause Leigh syndrome due to mitochondrial complex I deficiency, a severe neurological disorder that results in bilaterally symmetrical necrotic lesions in subcortical brain regions.
- Poids moléculaire
- 20 kDa
- ID gène
- 374291
- UniProt
- O75251
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