NADH Dehydrogenase (Ubiquinone) Fe-S Protein 8, 23kDa (NADH-Coenzyme Q Reductase) (NDUFS8) Peptide
NDUFS8
Reactivity: Mammalian
Host: Synthetic
BP, WB, IHC
Catalog No. ABIN937109
Quick Overview for NADH Dehydrogenase (Ubiquinone) Fe-S Protein 8, 23kDa (NADH-Coenzyme Q Reductase) (NDUFS8) Peptide (ABIN937109)
Target
NDUFS8
(NADH Dehydrogenase (Ubiquinone) Fe-S Protein 8, 23kDa (NADH-Coenzyme Q Reductase) (NDUFS8))
Origin
Mammalian
Source
Synthetic
Application
Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
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Peptide Type
- Synthetic
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Sequence
- CKLCEAICPA QAITIEAEPR ADGSRRTTRY DIDMTKCIYC GFCQEACPVD
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Characteristics
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A synthetic peptide for use as a blocking control in assays to test for specificity of NDUFS8 antibody,
Alternative Names: NDUFS8 control peptide, NDUFS8 antibody Blocking Peptide, Anti-NDUFS8 Blocking Peptide, NADH dehydrogenase, ubiquinone Fe-S protein 8, 23kDa, NADH-coenzyme Q reductase Blocking Peptide, CI23KD Blocking Peptide, TYKY Blocking Peptide, NDUFS8, NDUFS-8, NDUFS 8, NDUFS-8 Blocking Peptide, NDUFS 8 Blocking Peptide -
Purification
- The antibody is affinity-purified from rabbit antiserum by affinity chromatography using epitope-specific immunogen.
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Application Notes
- Optimal conditions should be determined by the investigator
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
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Buffer
- PBS
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Handling Advice
- Avoid repeated freeze/thaw cycles.
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Storage
- -20 °C
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Storage Comment
- Store at -20 °C long term.
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- NDUFS8 (NADH Dehydrogenase (Ubiquinone) Fe-S Protein 8, 23kDa (NADH-Coenzyme Q Reductase) (NDUFS8))
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Background
- This gene encodes a subunit of mitochondrial NADH:ubiquinone oxidoreductase, or Complex I, a multimeric enzyme of the respiratory chain responsible for NADH oxidation, ubiquinone reduction, and the ejection of protons from mitochondria. The encoded protein is involved in the binding of two of the six to eight iron-sulfur clusters of Complex I and, as such, is required in the electron transfer process. Mutations in this gene have been associated with Leigh syndrome.
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Molecular Weight
- 23 kDa
Target
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