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Solute Carrier Family 25 (Mitochondrial Carrier, Graves Disease Autoantigen), Member 16 (SLC25A16) Peptide

SLC25A16 Reactivity: Mammalian Host: Synthetic BP, WB, IHC
Catalog No. ABIN940083
  • Target See all SLC25A16 products
    SLC25A16 (Solute Carrier Family 25 (Mitochondrial Carrier, Graves Disease Autoantigen), Member 16 (SLC25A16))
    Peptide Type
    Synthetic
    Origin
    Mammalian
    Source
    • 3
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
    Sequence
    KTTVAPLDRV KVLLQAHNHH YKHLGVFSAL RAVPQKEGFL GLYKGNGAMM
    Characteristics
    A synthetic peptide for use as a blocking control in assays to test for specificity of SLC25 A16 antibody,
    Alternative Names: SLC25A16 control peptide, SLC25A16 antibody Blocking Peptide, Anti-SLC25A16 Blocking Peptide, Solute Carrier Family 25 Member 16 Blocking Peptide, D10S105E Blocking Peptide, GDA Blocking Peptide, GDC Blocking Peptide, HGT.1 Blocking Peptide, MGC39851 Blocking Peptide, ML7 Blocking Peptide, hML7 Blocking Peptide, SLC25A16, SLCA16-25, SLCA16 25, SLCA16-25 Blocking Peptide, SLCA16 25 Blocking Peptide
  • Application Notes
    Optimal conditions should be determined by the investigator
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
    Buffer
    PBS
    Handling Advice
    Avoid repeated freeze/thaw cycles.
    Storage
    -20 °C
    Storage Comment
    Store at -20 °C long term.
  • Target
    SLC25A16 (Solute Carrier Family 25 (Mitochondrial Carrier, Graves Disease Autoantigen), Member 16 (SLC25A16))
    Background
    SLC25A16 is a protein that contains three tandemly repeated mitochondrial carrier protein domains. The protein is localized in the inner membrane and facilitates the rapid transport and exchange of molecules between the cytosol and the mitochondrial matrix space. SLC25A16 gene has a possible role in Graves' disease.
    Molecular Weight
    36 kDa
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