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Protocadherin-15 (PCDH15) Peptide

PCDH15 Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN981439
  • Target See all PCDH15 products
    PCDH15 (Protocadherin-15 (PCDH15))
    Origin
    Human
    Source
    • 1
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Characteristics
    This is a synthetic peptide designed for use in combination with anti-PCDH15 antibody (Catalog #: ARP50153_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.
    Purification
    Purified
  • Application Notes
    Each Investigator should determine their own optimal working dilution for specific applications.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Concentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Handling Advice
    Avoid repeated freeze-thaw cycles.
    Storage
    -20 °C
    Storage Comment
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • 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.

    Alias Symbols: RP11-449J3.2, DFNB23, DKFZp667A1711, USH1F, CDHR15

    Protein Size: 719
    Molecular Weight
    80 kDa
    Gene ID
    65217
    NCBI Accession
    NM_001142763
    UniProt
    A2A3E5
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