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Gel: 8%SDS-PAGE, Lysate: 40 ug, Lane 1-2: 231 cells, Jurkat cells, Primary antibody: CSB-PA999557(NDUFAF1 Antibody) at dilution 1/500, Secondary antibody: Goat anti rabbit IgG at 1/8000 dilution, Exposure time: 20 seconds
Gel: 8%SDS-PAGE, Lysate: 40 ug, Lane 1-2: 231 cells, Jurkat cells, Primary antibody: CSB-PA999557(NDUFAF1 Antibody) at dilution 1/500, Secondary antibody: Goat anti rabbit IgG at 1/8000 dilution, Exposure time: 20 seconds
Gel: 8%SDS-PAGE, Lysate: 40 ug, Lane 1-2: 231 cells, Jurkat cells, Primary antibody: CSB-PA999557(NDUFAF1 Antibody) at dilution 1/500, Secondary antibody: Goat anti rabbit IgG at 1/8000 dilution, Exposure time: 20 seconds

NDUFAF1 Antibody

Research Use Only
CSB-PA999557
Cusabio
ApplicationsWestern Blot, ELISA
Product group Antibodies
ReactivityHuman
TargetNDUFAF1
Price on request
Packing Size
Large volume orders?
Order with a bulk request

Overview

  • Supplier
    Cusabio
  • Product Name
    NDUFAF1 Antibody
  • Delivery Days Customer
    20
  • Applications
    Western Blot, ELISA
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID51103
  • Target name
    NDUFAF1
  • Target description
    NADH:ubiquinone oxidoreductase complex assembly factor 1
  • Target synonyms
    CGI65; CGI-65; CIA30; complex I intermediate-associated protein 30, mitochondrial; MC1DN11; NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, assembly factor 1; NADH dehydrogenase (ubiquinone) complex I, assembly factor 1; NADH-ubiquinone oxidoreductase 1 alpha subcomplex, assembly factor 1
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ9Y375
  • Protein Name
    Complex I intermediate-associated protein 30, mitochondrial
  • Scientific Description
    This gene encodes a complex I assembly factor protein. Complex I (NADH-ubiquinone oxidoreductase) catalyzes the transfer of electrons from NADH to ubiquinone (coenzyme Q) in the first step of the mitochondrial respiratory chain, resulting in the translocation of protons across the inner mitochondrial membrane. The encoded protein is required for assembly of complex I, and mutations in this gene are a cause of mitochondrial complex I deficiency. Alternatively spliced transcript variants have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 19.
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C
  • UNSPSC
    12352203