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Neural Cell Adhesion Molecule 1 (NCAM1) (C-Term) Peptide

NCAM1 Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN980513

Aperçu rapide pour Neural Cell Adhesion Molecule 1 (NCAM1) (C-Term) Peptide (ABIN980513)

Antigène

CD56 (NCAM1) (Neural Cell Adhesion Molecule 1 (NCAM1))

Origine

Humain

Source

  • 8
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB)
  • Protein Region

    C-Term

    Séquence

    AFFAKSAAIY NPVIYIMMNK QFRNCMLTTI CCGKNPLGDD EASATVSKTE

    Attributs du produit

    This is a synthetic peptide designed for use in combination with anti-NCAM1 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

    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.

    Conseil sur la manipulation

    Avoid repeated freeze-thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Antigène

    CD56 (NCAM1) (Neural Cell Adhesion Molecule 1 (NCAM1))

    Sujet

    Retinitis pigmentosa is an inherited progressive disease which is a major cause of blindness in western communities. It can be inherited as an autosomal dominant, autosomal recessive, or X-linked recessive disorder. In the autosomal dominant form,which comprises about 25 % of total cases, approximately 30 % of families have mutations in the gene encoding the rod photoreceptor-specific protein rhodopsin. This is the transmembrane protein which, when photoexcited, initiates the visual transduction cascade. Defects in this gene are also one of the causes of congenital stationary night blindness.

    Alias Symbols: CD56, MSK39, NCAM

    Protein Interaction Partner: ADRBK1,ARR3,GNGT1,GRK1,GRK5,GRK6,PPP2CA,PRKCA,SAG,ADRBK1,ARR3,GRK1,GRK5,RHO,SAG,UBC

    Protein Size: 348

    Poids moléculaire

    39 kDa

    ID gène

    4684

    NCBI Accession

    NM_181351, NP_851996

    UniProt

    P13591
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