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Protocadherin-15 (PCDH15) Peptid

PCDH15 Reaktivität: Säugetier Wirt: Synthetic BP, WB, IHC
Produktnummer ABIN939239
  • Target Alle PCDH15 Produkte
    PCDH15 (Protocadherin-15 (PCDH15))
    Protein-Typ
    Synthetic
    Spezies
    Säugetier
    Quelle
    • 1
    Synthetic
    Applikation
    Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
    Sequenz
    HSIVVQVQCI NKKVGTIIYH EVRIVVRDRN DNSPTFKHES YYATVNELTP
    Produktmerkmale
    A synthetic peptide for use as a blocking control in assays to test for specificity of PCDH15 antibody,
    Alternative Names: PCDH15 control peptide, PCDH15 antibody Blocking Peptide, Anti-PCDH15 Blocking Peptide, Protocadherin 15 Blocking Peptide, RP11-449J3.2 Blocking Peptide, DFNB23 Blocking Peptide, DKFZp667A1711 Blocking Peptide, USH1F Blocking Peptide, PCDH15, PCDH-15, PCDH 15, PCDH-15 Blocking Peptide, PCDH 15 Blocking Peptide
    Aufreinigung
    Serum
  • Applikationshinweise
    Optimal conditions should be determined by the investigator
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
    Buffer
    PBS
    Handhabung
    Avoid repeated freeze/thaw cycles.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20 °C long term.
  • Target
    PCDH15 (Protocadherin-15 (PCDH15))
    Synonyme
    CDHR15 Peptide, DFNB23 Peptide, USH1F Peptide, BB078305 Peptide, ENSMUSG00000046980 Peptide, Gm9815 Peptide, Ush1f Peptide, av Peptide, nmf19 Peptide, protocadherin-15 Peptide, protocadherin related 15 Peptide, protocadherin-15 Peptide, protocadherin 15 Peptide, PCDH15 Peptide, CpipJ_CPIJ005081 Peptide, Pcdh15 Peptide
    Hintergrund
    PCDH15 is a member of the cadherin superfamily. Family members encode integral membrane proteins that mediate calcium-dependent cell-cell adhesion. PCDH15 consists of a signal peptide, 11 extracellular calcium-binding domains, a transmembrane domain and a unique cytoplasmic domain. It plays an essential role in maintenance of normal retinal and cochlear function. Mutations in this gene have been associated with hearing loss, which is consistent with its location at the Usher syndrome type 1F (USH1F) critical region on chromosome 10.
    Molekulargewicht
    80 kDa
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