NDUFS6 antibody (AA 29-124)
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- Target See all NDUFS6 Antibodies
- NDUFS6 (NADH Dehydrogenase (Ubiquinone) Fe-S Protein 6, 13kDa (NADH-Coenzyme Q Reductase) (NDUFS6))
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Binding Specificity
- AA 29-124
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This NDUFS6 antibody is un-conjugated
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Application
- Western Blotting (WB)
- Sequence
- GVRVSPTGEK VTHTGQVYDD KDYRRIRFVG RQKEVNENFA IDLIAEQPVS EVETRVIACD GGGGALGHPK VYINLDKETK TGTCGYCGLQ FRQHHH
- Cross-Reactivity
- Mouse, Rat
- Characteristics
- Polyclonal Antibodies
- Immunogen
- Recombinant fusion protein containing a sequence corresponding to amino acids 29-124 of human NDUFS6 (NP_004544.1).
- Isotype
- IgG
- Top Product
- Discover our top product NDUFS6 Primary Antibody
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- Application Notes
- WB,1:500 - 1:2000
- Comment
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HIGH QUALITY
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- PBS with 0.02 % sodium azide,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.
- Storage
- -20 °C
- Storage Comment
- 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))
- Alternative Name
- NDUFS6 (NDUFS6 Products)
- Synonyms
- BC059730 antibody, IP13 antibody, Ip13dis antibody, Ndub13 antibody, RATIp13dis antibody, CI-13kA antibody, CI-13kD-A antibody, CI13KDA antibody, NADH dehydrogenase (ubiquinone) Fe-S protein 6 antibody, NADH:ubiquinone oxidoreductase subunit S6 antibody, Ndufs6 antibody, NDUFS6 antibody
- Background
- 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
- Molecular Weight
- 13 kDa
- Gene ID
- 4726
- UniProt
- O75380
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