Tel:
+49 (0)241 95 163 153
Fax:
+49 (0)241 95 163 155
E-Mail:
orders@anticorps-enligne.fr

T-Box 5 (TBX5) Peptide

TBX5 Reactivité: Humain Hôte: Synthetic BP, WB, IHC
N° du produit ABIN984848
  • Antigène Tous les produits T-Box 5 (TBX5)
    T-Box 5 (TBX5)
    Origine
    Humain
    Source
    • 2
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
    Attributs du produit
    This is a synthetic peptide designed for use in combination with anti-TBX5 antibody (Catalog #: ARP33403_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
    T-Box 5 (TBX5)
    Synonymes
    TBX5 Peptide, tbx-5 Peptide, xtbx-5 Peptide, xtbx5 Peptide, tbx5 Peptide, HOS Peptide, tbx5.1 Peptide, zTbx5 Peptide, zf-tbx5 Peptide, T-box 5 Peptide, T-box 5 L homeolog Peptide, T-box 5a Peptide, TBX5 Peptide, tbx5 Peptide, tbx5.L Peptide, Tbx5 Peptide, tbx5a Peptide
    Sujet
    TBX5 is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. This gene is closely linked to related family member T-box 3 (ulnar mammary syndrome) on human chromosome 12. The encoded protein may play a role in heart development and specification of limb identity. Mutations in this gene have been associated with Holt-Oram syndrome, a developmental disorder affecting the heart and upper limbs. Several transcript variants encoding different isoforms have been described for this gene.

    Alias Symbols: HOS

    Protein Interaction Partner: GATA4,NKX2-5,GATA4,NKX2-5

    Protein Size: 518
    Poids moléculaire
    58 kDa
    ID gène
    6910
    NCBI Accession
    NM_000192, NP_000183
    UniProt
    Q99593
Vous êtes ici:
Support technique