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Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2) (C-Term) Peptid

SLC19A2 Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN983844
  • Target Alle SLC19A2 Produkte
    SLC19A2 (Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2))
    Protein Region
    C-Term
    Spezies
    Human
    Quelle
    Synthetic
    Applikation
    Blocking Peptide (BP), Western Blotting (WB)
    Sequenz
    LGLEITTQFL IYASYFALIA VVFLASGAVS VMKKCRKLED PQSSSQVTTS
    Produktmerkmale
    This is a synthetic peptide designed for use in combination with anti-SLC19A2 Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
    Aufreinigung
    Purified
  • Applikationshinweise
    Each Investigator should determine their own optimal working dilution for specific applications.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Konzentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Handhabung
    Avoid repeated freeze-thaw cycles.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    SLC19A2 (Solute Carrier Family 19 (Thiamine Transporter), Member 2 (SLC19A2))
    Synonyme
    SLC19A2 Peptide, TC1 Peptide, THMD1 Peptide, THT1 Peptide, THTR1 Peptide, TRMA Peptide, solute carrier family 19 member 2 Peptide, solute carrier family 19 (thiamine transporter), member 2 Peptide, Slc19a2 Peptide, SLC19A2 Peptide, slc19a2 Peptide
    Hintergrund
    This gene encodes the thiamin transporter protein. Mutations in this gene cause thiamin-responsive megaloblastic anemia syndrome (TRMA), which is an autosomal recessive disorder characterized by diabetes mellitus, megaloblastic anemia and sensorineural deafness.

    Alias Symbols: TC1, THT1, THTR1, TRMA, THMD1

    Protein Size: 497
    Molekulargewicht
    55 kDa
    Gen-ID
    10560
    NCBI Accession
    NM_006996, NP_008927
    UniProt
    O60779
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