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Cadherin 23 (CDH23) (N-Term) Peptide

CDH23 Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN2184165
  • Antigène Tous les produits CDH23
    CDH23 (Cadherin 23 (CDH23))
    Protein Region
    N-Term
    Origine
    Humain
    Source
    • 5
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Séquence
    DHQGVITRKV NIQVGDVNDN APTFHNQPYS VRIPENTPVG TPIFIVNATD
    Attributs du produit
    This is a synthetic peptide designed for use in combination with anti-CDH23 Antibody. 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
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    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.
    Conseil sur la manipulation
    Avoid repeat freeze-thaw cycles.
    Stock
    -20 °C
    Stockage commentaire
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Antigène
    CDH23 (Cadherin 23 (CDH23))
    Synonymes
    4930542A03Rik Peptide, USH1D Peptide, ahl Peptide, ahl1 Peptide, bob Peptide, bus Peptide, mdfw Peptide, nmf112 Peptide, nmf181 Peptide, nmf252 Peptide, sals Peptide, v Peptide, CDHR23 Peptide, W Peptide, cadherin 23 (otocadherin) Peptide, cadherin related 23 Peptide, cadherin-related 23 Peptide, Cdh23 Peptide, CDH23 Peptide
    Sujet
    This gene is a member of the cadherin superfamily, whose genes encode calcium dependent cell-cell adhesion glycoproteins. The encoded protein is thought to be involved in stereocilia organization and hair bundle formation. The gene is located in a region containing the human deafness loci DFNB12 and USH1D. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of this cadherin-like gene. Alternative splice variants encoding different isoforms have been described.

    Alias Symbols: CDHR23, USH1D

    Protein Size: 406
    Poids moléculaire
    44 kDa
    ID gène
    64072
    NCBI Accession
    NM_001171932, NP_001165403
    UniProt
    A5D6V9
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