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Shroom Family Member 2 (SHROOM2) (Middle Region) Peptid

SHROOM2 Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN983725
  • Target Alle SHROOM2 Produkte
    SHROOM2 (Shroom Family Member 2 (SHROOM2))
    Protein Region
    Middle Region
    Spezies
    Human
    Quelle
    • 3
    Synthetic
    Applikation
    Blocking Peptide (BP), Western Blotting (WB)
    Produktmerkmale
    This is a synthetic peptide designed for use in combination with anti-SHROOM2 antibody (Catalog #: ARP35054_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
    SHROOM2 (Shroom Family Member 2 (SHROOM2))
    Synonyme
    SHROOM2 Peptide, APXL Peptide, apxl Peptide, shrm2 Peptide, HSAPXL Peptide, 4832440C16 Peptide, Apxl Peptide, C630003H05Rik Peptide, Shrm2 Peptide, shroom family member 2 Peptide, SHROOM2 Peptide, shroom2 Peptide, Shroom2 Peptide
    Hintergrund
    SHROOM2 shares significant similarities with the apical protein from Xenopus laevis which is implicated in amiloride-sensitive sodium channel activity. This gene is a strong candidate gene for ocular albinism type 1 syndrome.The protein encoded by this gene shares significant similarities with the apical protein from Xenopus laevis which is implicated in amiloride-sensitive sodium channel activity. This gene is a strong candidate gene for ocular albinism type 1 syndrome.

    Alias Symbols: APXL, DKFZp781J074, FLJ39277, HSAPXL

    Protein Interaction Partner: YWHAG

    Protein Size: 1616
    Molekulargewicht
    176 kDa
    Gen-ID
    357
    NCBI Accession
    NM_001649, NP_001640
    UniProt
    Q13796
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