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WB analysis of human heart lysate using GTX88036 NDUFS7 antibody, Internal. Dilution : 0.1microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of human heart lysate using GTX88036 NDUFS7 antibody, Internal. Dilution : 0.1microg/ml Loading : 35microg protein in RIPA buffer
WB analysis of human heart lysate using GTX88036 NDUFS7 antibody, Internal. Dilution : 0.1microg/ml Loading : 35microg protein in RIPA buffer

NDUFS7 antibody, Internal

GTX88036
GeneTex
ApplicationsWestern Blot
Product group Antibodies
ReactivityHuman
TargetNDUFS7
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Overview

  • Supplier
    GeneTex
  • Product Name
    NDUFS7 antibody, Internal
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1-3microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.50 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID374291
  • Target name
    NDUFS7
  • Target description
    NADH:ubiquinone oxidoreductase core subunit S7
  • Target synonyms
    CI-20; CI-20KD; complex I 20kDa subunit; complex I, mitochondrial respiratory chain, 20-KD subunit; complex I-20kD; MC1DN3; MY017; NADH dehydrogenase (ubiquinone) Fe-S protein 7, 20kDa (NADH-coenzyme Q reductase); NADH dehydrogenase [ubiquinone] iron-sulfur protein 7, mitochondrial; NADH:ubiquinone oxidoreductase PSST subunit; NADH-coenzyme Q reductase; NADH-ubiquinone oxidoreductase 20 kDa subunit; PSST; PSST subunit
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDO75251
  • Protein Name
    NADH dehydrogenase [ubiquinone] iron-sulfur protein 7, mitochondrial
  • Scientific Description
    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, Jul 2008]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203