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Solute Carrier Family 45, Member 2 (SLC45A2) Peptide

SLC45A2 Reactivity: Mammalian Host: Synthetic BP, WB, IHC
Catalog No. ABIN939366
  • Target See all SLC45A2 products
    SLC45A2 (Solute Carrier Family 45, Member 2 (SLC45A2))
    Peptide Type
    Synthetic
    Origin
    Mammalian
    Source
    • 1
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
    Sequence
    IGWTAFLSNM LFFTDFMGQI VYRGDPYSAH NSTEFLIYER GVEVGCWGFC
    Characteristics
    A synthetic peptide for use as a blocking control in assays to test for specificity of SLC45 A2 antibody,
    Alternative Names: SLC45A2 control peptide, SLC45A2 antibody Blocking Peptide, Anti-SLC45A2 Blocking Peptide, Solute Carrier Family 45 Member 2 Blocking Peptide, 1A1 Blocking Peptide, AIM1 Blocking Peptide, MATP Blocking Peptide, SLC45A2, SLCA2-45, SLCA2 45, SLCA2-45 Blocking Peptide, SLCA2 45 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
    SLC45A2 (Solute Carrier Family 45, Member 2 (SLC45A2))
    Synonyms
    SLC45A2 Peptide, matp Peptide, aim1 Peptide, im:7138762 Peptide, MGC114950 Peptide, 1A1 Peptide, AIM1 Peptide, MATP Peptide, OCA4 Peptide, SHEP5 Peptide, Aim-1 Peptide, Aim1 Peptide, Dbr Peptide, Matp Peptide, blanc-sale Peptide, bls Peptide, uw Peptide, solute carrier family 45 member 2 Peptide, solute carrier family 45, member 2 Peptide, solute carrier family 45 member 2 L homeolog Peptide, SLC45A2 Peptide, slc45a2 Peptide, slc45a2.L Peptide, Slc45a2 Peptide
    Background
    SLC45A2 is a melanocyte differentiation antigen that is expressed in a high percentage of melanoma cell lines. A similar sequence gene in medaka, 'B,' encodes a transporter that mediates melanin synthesis. Mutations in this gene are a cause of oculocutaneous albinism type 4.
    Molecular Weight
    51 kDa
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