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Glycoprotein Ib (Platelet), beta Polypeptide (GP1BB) (Middle Region) Peptide

GP1BB Reactivité: Humain Hôte: Synthetic WB, BP
N° du produit ABIN5673247
  • Antigène Tous les produits GP1BB
    GP1BB (Glycoprotein Ib (Platelet), beta Polypeptide (GP1BB))
    Protein Region
    Middle Region
    Origine
    Humain
    Source
    • 1
    • 1
    Synthetic
    Application
    Western Blotting (WB), Blocking Peptide (BP)
    Séquence
    ALRTAHLGAN PWRCDCRLVP LRAWLAGRPE RAPYRDLRCV APPALRGRLL
    Attributs du produit
    This is a synthetic peptide designed for use in combination with anti- GP1BB 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.
  • 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.
    Stock
    -20 °C
    Stockage commentaire
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Antigène
    GP1BB (Glycoprotein Ib (Platelet), beta Polypeptide (GP1BB))
    Synonymes
    BDPLT1 Peptide, BS Peptide, CD42C Peptide, GPIBB Peptide, glycoprotein Ib (platelet), beta polypeptide Peptide, glycoprotein Ib platelet beta subunit Peptide, glycoprotein Ib, beta polypeptide Peptide, GP1BB Peptide, Gp1bb Peptide
    Sujet
    Platelet glycoprotein Ib (GPIb) is a heterodimeric transmembrane protein consisting of a disulfide-linked 140 kD alpha chain and 22 kD beta chain. It is part of the GPIb-V-IX system that constitutes the receptor for von Willebrand factor (VWF), and mediates platelet adhesion in the arterial circulation. GPIb alpha chain provides the VWF binding site, and GPIb beta contributes to surface expression of the receptor and participates in transmembrane signaling through phosphorylation of its intracellular domain. Mutations in the GPIb beta subunit have been associated with Bernard-Soulier syndrome, velocardiofacial syndrome and giant platelet disorder. The 206 amino acid precursor of GPIb beta is synthesized from a 1.0 kb mRNA expressed in plateletes and megakaryocytes. A 411 amino acid protein arising from a longer, unspliced transcript in endothelial cells has been described, however, the authenticity of this product has been questioned. Yet another less abundant GPIb beta mRNA species of 3.5 kb, expressed in nonhematopoietic tissues such as endothelium, brain and heart, was shown to result from inefficient usage of a non-consensus polyA signal in the neighboring upstream gene (SEPT5, septin 5). In the absence of polyadenylation from its own imperfect site, the SEPT5 gene produces read-through transcripts that use the consensus polyA signal of this gene.

    Alias Symbols: BS, CD42C, GPIBB, BDPLT1, GPIbbeta

    Protein Size: 206
    ID gène
    2812
    NCBI Accession
    NM_000407, NP_000398
    UniProt
    P13224
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