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Last updated: 2017/4/23
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NDUFS7 polyclonal antibody

  • Catalog # : PAB17789
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  • Specification
  • Product Description:
  • Rabbit polyclonal antibody raised against synthetic peptide of NDUFS7.
  • Immunogen:
  • A synthetic peptide corresponding to internal of human NDUFS7.
  • Host:
  • Rabbit
  • Reactivity:
  • Human, Mouse, Rat
  • Specificity:
  • This antibody detects endogenous levels of total NDUFS7 protein.
  • Form:
  • Liquid
  • Recommend Usage:
  • Immunohistochemistry (1:50-1:100)
    ELISA (1:40000)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In PBS, pH 7.4 (150mM NaCl, 0.02% sodium azide, 50% glycerol)
  • Storage Instruction:
  • Store at -20°C.
    Aliquot to avoid repeated freezing and thawing.
  • Note:
  • This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
  • Applications
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue using NDUFS7 polyclonal antibody (Cat # PAB17789).
    Peptide "+" means "with peptide blocking".
  • ELISA
  • Application Image
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • enlarge
  • ELISA
  • Gene Information
  • Gene Name:
  • NDUFS7
  • Gene Alias:
  • CI-20KD,FLJ45860,FLJ46880,MGC120002,MY017,PSST
  • Gene Description:
  • NADH dehydrogenase (ubiquinone) Fe-S protein 7, 20kDa (NADH-coenzyme Q reductase)
  • Gene Summary:
  • 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. [provided by RefSeq
  • Other Designations:
  • NADH dehydrogenase [ubiquinone] iron-sulfur protein 7, mitochondrial,NADH-coenzyme Q reductase,NADH-ubiquinone oxidoreductase Fe-S protein 7,NADH:ubiquinone oxidoreductase PSST subunit,complex I, mitochondrial respiratory chain, 20-KD subunit,complex I-20
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