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P Protein (OCA2) (Middle Region) Peptid

OCA2 Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN981085
  • Target Alle OCA2 Produkte
    OCA2 (P Protein (OCA2))
    Protein Region
    Middle Region
    Spezies
    Human
    Quelle
    • 2
    Synthetic
    Applikation
    Blocking Peptide (BP), Western Blotting (WB)
    Produktmerkmale
    This is a synthetic peptide designed for use in combination with anti-OCA2 antibody (Catalog #: ARP44255_P050). 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
    OCA2 (P Protein (OCA2))
    Synonyme
    D7H15S12 Peptide, D7Icr28RN Peptide, D7Nic1 Peptide, p Peptide, BEY Peptide, BEY1 Peptide, BEY2 Peptide, BOCA Peptide, D15S12 Peptide, EYCL Peptide, EYCL2 Peptide, EYCL3 Peptide, HCL3 Peptide, P Peptide, PED Peptide, SHEP1 Peptide, OCA2 Peptide, P protein Peptide, oculocutaneous albinism II Peptide, OCA2 melanosomal transmembrane protein Peptide, P Peptide, p Peptide, Oca2 Peptide, OCA2 Peptide, oca2 Peptide
    Substanzklasse
    Viral Protein
    Hintergrund
    OCA2 is believed to be an integral membrane protein involved in small molecule transport, specifically tyrosine - a precursor of melanin. Mutations in the gene encoding OCA2 result in type 2 oculocutaneous albinism.This gene encodes the human homologue of the mouse p (pink-eyed dilution) gene. The encoded protein is believed to be an integral membrane protein involved in small molecule transport, specifically tyrosine - a precursor of melanin. Mutations in this gene result in type 2 oculocutaneous albinism. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

    Alias Symbols: BOCA, D15S12, EYCL3, P, PED, BEY, BEY1, BEY2, EYCL, HCL3, EYCL2, SHEP1

    Protein Size: 838
    Molekulargewicht
    93 kDa
    Gen-ID
    4948
    NCBI Accession
    NM_000275, NP_000266
    UniProt
    Q04671
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