Bio-Connect
WB analysis of various sample lysates using GTX54715 Adenine Nucleotide Translocase 1 antibody. Loading : 25microg per lane
WB analysis of various sample lysates using GTX54715 Adenine Nucleotide Translocase 1 antibody. Loading : 25microg per lane
WB analysis of various sample lysates using GTX54715 Adenine Nucleotide Translocase 1 antibody. Loading : 25microg per lane

Adenine Nucleotide Translocase 1 antibody

GTX54715
GeneTex
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry
Product group Antibodies
ReactivityHuman, Mouse
TargetSLC25A4
Sign in to order and to see your custom pricing.
Large volume orders?
Order with a bulk request

Overview

  • Supplier
    GeneTex
  • Product Name
    Adenine Nucleotide Translocase 1 antibody
  • Delivery Days Customer
    7
  • Application Supplier Note
    WB: 1:500 - 1:2000. ICC/IF: 1:50 - 1:200. *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 ID291
  • Target name
    SLC25A4
  • Target description
    solute carrier family 25 member 4
  • Target synonyms
    AAC1; adenine nucleotide translocator 1 (skeletal muscle); ADP,ATP carrier protein 1; ADP,ATP carrier protein, heart/skeletal muscle; ADP/ATP translocase 1; ANT; ANT 1; ANT1; heart/skeletal muscle ATP/ADP translocator; MTDPS12; MTDPS12A; PEO2; PEO3; PEOA2; solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4; T1
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP12235
  • Protein Name
    ADP/ATP translocase 1
  • Scientific Description
    This gene is a member of the mitochondrial carrier subfamily of solute carrier protein genes. The product of this gene functions as a gated pore that translocates ADP from the cytoplasm into the mitochondrial matrix and ATP from the mitochondrial matrix into the cytoplasm. The protein forms a homodimer embedded in the inner mitochondria membrane. Mutations in this gene have been shown to result in autosomal dominant progressive external opthalmoplegia and familial hypertrophic cardiomyopathy. [provided by RefSeq, Jun 2013]
  • Reactivity
    Human, Mouse
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203