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

NCAM1 Reaktivität: Human Wirt: Synthetic BP, WB
Produktnummer ABIN980513

Kurzübersicht für Neural Cell Adhesion Molecule 1 (NCAM1) (C-Term) Peptid (ABIN980513)

Target

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

Spezies

Human

Quelle

  • 8
Synthetic

Applikation

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

    C-Term

    Sequenz

    AFFAKSAAIY NPVIYIMMNK QFRNCMLTTI CCGKNPLGDD EASATVSKTE

    Produktmerkmale

    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.

    Aufreinigung

    Purified
  • Applikationshinweise

    Each Investigator should determine their own optimal working dilution for specific applications.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Konzentration

    1 mg/mL

    Buffer

    Final peptide concentration is 1 mg/mL in PBS.

    Handhabung

    Avoid repeated freeze-thaw cycles.

    Lagerung

    -20 °C

    Informationen zur Lagerung

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

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

    Hintergrund

    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

    Molekulargewicht

    39 kDa

    Gen-ID

    4684

    NCBI Accession

    NM_181351, NP_851996

    UniProt

    P13591
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