NDUFS7 antibody
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- Target See all NDUFS7 Antibodies
- NDUFS7 (NADH Dehydrogenase (Ubiquinone) Fe-S Protein 7, 20kDa (NADH-Coenzyme Q Reductase) (NDUFS7))
- Reactivity
- Human, Mouse, Rat
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This NDUFS7 antibody is un-conjugated
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Application
- ELISA, Immunohistochemistry (IHC), Western Blotting (WB), Immunofluorescence (IF)
- Immunogen
- NADH dehydrogenase (ubiquinone) Fe-S protein 7, 20kDa (NADH-coenzyme Q reductase)
- Isotype
- IgG
- Top Product
- Discover our top product NDUFS7 Primary Antibody
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- Application Notes
- Optimal working dilution should be determined by the investigator.
- Comment
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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
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Handling Advice
- Avoid repeated freeze / thaw cycles.
- Storage
- -20 °C
- Expiry Date
- 12 months
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- Target
- NDUFS7 (NADH Dehydrogenase (Ubiquinone) Fe-S Protein 7, 20kDa (NADH-Coenzyme Q Reductase) (NDUFS7))
- Alternative Name
- NDUFS7 (NDUFS7 Products)
- Synonyms
- 1010001M04Rik antibody, CI-20 antibody, CI-20KD antibody, MY017 antibody, PSST antibody, NADH dehydrogenase (ubiquinone) Fe-S protein 7 antibody, NADH:ubiquinone oxidoreductase core subunit S7 antibody, Ndufs7 antibody, NDUFS7 antibody
- Background
- 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.
- Molecular Weight
- 20 kDa
- Gene ID
- 374291
- UniProt
- O75251
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