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Noggin (NOG) (Middle Region) Peptide

NOG Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN980789
  • Antigène Tous les produits NOG
    NOG (Noggin (NOG))
    Protein Region
    Middle Region
    Origine
    Humain
    Source
    • 2
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Séquence
    GGHYDPGFMA TSPPEDRPGG GGGAAGGAED LAELDQLLRQ RPSGAMPSEI
    Attributs du produit
    This is a synthetic peptide designed for use in combination with anti-NOG Antibody(ARP58773_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
  • 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
    NOG (Noggin (NOG))
    Synonymes
    SYM1 Peptide, SYNS1 Peptide, nog-A Peptide, nog1 Peptide, noggin-1 Peptide, noggin Peptide, noggin Peptide, noggin L homeolog Peptide, noggin protein Peptide, NOG Peptide, Nog Peptide, nog.L Peptide, noggin Peptide
    Sujet
    The secreted polypeptide, encoded by this gene, binds and inactivates members of the transforming growth factor-beta (TGF-beta) superfamily signaling proteins, such as bone morphogenetic protein-4 (BMP4). By diffusing through extracellular matrices more efficiently than members of the TGF-beta superfamily, this protein may have a principal role in creating morphogenic gradients. The protein appears to have pleiotropic effect, both early in development as well as in later stages. It was originally isolated from Xenopus based on its ability to restore normal dorsal-ventral body axis in embryos that had been artificially ventralized by UV treatment. The results of the mouse knockout of the ortholog suggest that it is involved in numerous developmental processes, such as neural tube fusion and joint formation. Recently, several dominant human NOG mutations in unrelated families with proximal symphalangism (SYM1) and multiple synostoses syndrome (SYNS1) were identified, both SYM1 and SYNS1 have multiple joint fusion as their principal feature, and map to the same region (17q22) as this gene. All of these mutations altered evolutionarily conserved amino acid residues. The amino acid sequence of this human gene is highly homologous to that of Xenopus, rat and mouse.

    Alias Symbols: SYM1, SYNS1

    Protein Interaction Partner: BMP2,BMP4,BMP5,BMP7,BMP7,NOG

    Protein Size: 232
    Poids moléculaire
    24 kDa
    ID gène
    9241
    NCBI Accession
    NM_005450, NP_005441
    UniProt
    Q13253
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