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WB analysis of various sample lysates using GTX33351 NDUFV1 antibody. Dilution : 1:1000 Loading : 25microg per lane
WB analysis of various sample lysates using GTX33351 NDUFV1 antibody. Dilution : 1:1000 Loading : 25microg per lane
WB analysis of various sample lysates using GTX33351 NDUFV1 antibody. Dilution : 1:1000 Loading : 25microg per lane

NDUFV1 antibody

GTX33351
GeneTex
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry
Product group Antibodies
TargetNDUFV1
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Overview

  • Supplier
    GeneTex
  • Product Name
    NDUFV1 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500 - 1:2000. ICC/IF: 1:50 - 1:100. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoFluorescence, Western Blot, ImmunoCytoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID4723
  • Target name
    NDUFV1
  • Target description
    NADH:ubiquinone oxidoreductase core subunit V1
  • Target synonyms
    CI-51K, CI51KD, MC1DN4, UQOR1, NADH dehydrogenase [ubiquinone] flavoprotein 1, mitochondrial, NADH dehydrogenase (ubiquinone) flavoprotein 1, 51kDa, NADH-ubiquinone oxidoreductase 51 kDa subunit, complex I 51 kda subunit, complex I 51kDa subunit, complex I, mitochondrial respiratory chain, mitochondrial NADH dehydrogenase ubiquinone flavoprotein 1, mitochondrial NADH:ubiquinone oxidoreductase 51 kda subunit
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP49821
  • Protein Name
    NADH dehydrogenase [ubiquinone] flavoprotein 1, mitochondrial
  • Scientific Description
    The mitochondrial respiratory chain provides energy to cells via oxidative phosphorylation and consists of four membrane-bound electron-transporting protein complexes (I-IV) and an ATP synthase (complex V). This gene encodes a 51 kDa subunit of the NADH:ubiquinone oxidoreductase complex I; a large complex with at least 45 nuclear and mitochondrial encoded subunits that liberates electrons from NADH and channels them to ubiquinone. This subunit carries the NADH-binding site as well as flavin mononucleotide (FMN)- and Fe-S-biding sites. Defects in complex I are a common cause of mitochondrial dysfunction; a syndrome that occurs in approximately 1 in 10,000 live births. Mitochondrial complex I deficiency is linked to myopathies, encephalomyopathies, and neurodegenerative disorders such as Parkinsons disease and Leigh syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Oct 2009]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203