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IHC-P analysis of human kidney using GTX88043 NDUFS6 antibody, Internal. Antigen retrieval : citrate buffer pH 6 Dilution : 5microg/ml
IHC-P analysis of human kidney using GTX88043 NDUFS6 antibody, Internal. Antigen retrieval : citrate buffer pH 6 Dilution : 5microg/ml
IHC-P analysis of human kidney using GTX88043 NDUFS6 antibody, Internal. Antigen retrieval : citrate buffer pH 6 Dilution : 5microg/ml

NDUFS6 antibody, Internal

GTX88043
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetNDUFS6
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Overview

  • Supplier
    GeneTex
  • Product Name
    NDUFS6 antibody, Internal
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 0.01-0.03microg/ml. IHC-P: 5microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.50 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID4726
  • Target name
    NDUFS6
  • Target description
    NADH:ubiquinone oxidoreductase subunit S6
  • Target synonyms
    CI-13kA; CI13KDA; CI-13kD-A; complex I 13kDa subunit A; complex I, mitochondrial respiratory chain, 13-kD subunit; MC1DN9; NADH dehydrogenase (ubiquinone) Fe-S protein 6, 13kDa (NADH-coenzyme Q reductase); NADH dehydrogenase [ubiquinone] iron-sulfur protein 6, mitochondrial; NADH:ubiquinone oxidoreductase NDUFS6 subunit; NADH-ubiquinone oxidoreductase 13 kDa-A subunit
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDO75380
  • Protein Name
    NADH dehydrogenase [ubiquinone] iron-sulfur protein 6, mitochondrial
  • Scientific Description
    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.[provided by RefSeq, Oct 2009]
  • Reactivity
    Human, Mouse, Rat
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • Adult mesenchymal stem cell ageing interplays with depressed mitochondrial Ndufs6. Zhang Y et al., 2020 Dec 15, Cell Death Dis
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