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Protocadherin-15 (PCDH15) Peptide

PCDH15 Reactivity: Mammalian Host: Synthetic BP, WB, IHC
Catalog No. ABIN939239
  • Target See all PCDH15 products
    PCDH15 (Protocadherin-15 (PCDH15))
    Peptide Type
    Synthetic
    Origin
    Mammalian
    Source
    • 1
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
    Sequence
    HSIVVQVQCI NKKVGTIIYH EVRIVVRDRN DNSPTFKHES YYATVNELTP
    Characteristics
    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
    Purification
    Serum
  • 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
    PCDH15 (Protocadherin-15 (PCDH15))
    Synonyms
    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
    Background
    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.
    Molecular Weight
    80 kDa
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