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Fibrillin 1 (FBN1) Peptide

FBN1 Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN976704
  • Antigène Tous les produits Fibrillin 1 (FBN1)
    Fibrillin 1 (FBN1)
    Origine
    Humain
    Source
    • 5
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Attributs du produit
    This is a synthetic peptide designed for use in combination with anti-FBN1 antibody (Catalog #: ARP37969_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
    Fibrillin 1 (FBN1)
    Synonymes
    FBN1 Peptide, ACMICD Peptide, ECTOL1 Peptide, FBN Peptide, GPHYSD2 Peptide, MASS Peptide, MFS1 Peptide, OCTD Peptide, SGS Peptide, SSKS Peptide, WMS Peptide, WMS2 Peptide, AI536462 Peptide, B430209H23 Peptide, Fib-1 Peptide, Tsk Peptide, fibrillin 1 Peptide, FBN1 Peptide, Fbn1 Peptide
    Sujet
    FBN1 is a member of the fibrillin family. FBN1 is a large, extracellular matrix glycoprotein that serve as a structural component of 10-12 nm calcium-binding microfibrils. These microfibrils provide force bearing structural support in elastic and nonelastic connective tissue throughout the body. Mutations in this gene are associated with Marfan syndrome, isolated ectopia lentis, autosomal dominant Weill-Marchesani syndrome, MASS syndrome, and Shprintzen-Goldberg craniosynostosis syndrome.

    Alias Symbols: FBN, SGS, WMS, MASS, MFS1, OCTD, SSKS, WMS2, ACMICD, GPHYSD2

    Protein Interaction Partner: FBLN2,CALR,DCN,ELN,FBLN2,FBN2,HSPG2,LTBP1,MFAP2,MFAP5,MYOC,VCAN,ELN,FBLN2,MFAP2,MYOC,VCAN

    Protein Size: 195
    Poids moléculaire
    21 kDa
    ID gène
    2200
    NCBI Accession
    NM_000138
    UniProt
    Q75N89
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