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Distal-Less Homeobox 5 (DLX5) (N-Term) Peptide

DLX5 Reactivité: Humain Hôte: Synthetic BP, IHC, WB
N° du produit ABIN975852
  • Antigène Tous les produits DLX5
    DLX5 (Distal-Less Homeobox 5 (DLX5))
    Protein Region
    N-Term
    Origine
    Humain
    Source
    • 6
    Synthetic
    Application
    Blocking Peptide (BP), Immunohistochemistry (IHC), Western Blotting (WB)
    Attributs du produit
    This is a synthetic peptide designed for use in combination with anti-DLX5 antibody (Catalog #: ARP31607_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
    DLX5 (Distal-Less Homeobox 5 (DLX5))
    Synonymes
    SHFM1D Peptide, AI385752 Peptide, RDLX Peptide, X-dll3 Peptide, dll3 Peptide, MGC69418 Peptide, DLX5 Peptide, dlx5 Peptide, dlx4 Peptide, zgc:101787 Peptide, distal-less homeobox 5 Peptide, distal-less homeobox 5 L homeolog Peptide, distal-less homeobox 2b Peptide, distal-less homeobox 5a Peptide, DLX5 Peptide, Dlx5 Peptide, dlx5.L Peptide, dlx5 Peptide, dlx2b Peptide, dlx5a Peptide
    Sujet
    DLX5 is a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene. This protein may play a role in bone development and fracture healing. Mutation in its gene, which is located in a tail-to-tail configuration with another member of the family on the long arm of chromosome 7, may be associated with split-hand/split-foot malformation. This gene encodes a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene. The encoded protein may play a role in bone development and fracture healing. Mutation in this gene, which is located in a tail-to-tail configuration with another member of the family on the long arm of chromosome 7, may be associated with split-hand/split-foot malformation. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

    Alias Symbols: SHFM1D

    Protein Interaction Partner: MAGED1,MSX2,NCOA2,SOX10,SOX8,SPEN,DLX2,DLX5,HOXC8,MSX1,MSX2

    Protein Size: 289
    Poids moléculaire
    32 kDa
    ID gène
    1749
    NCBI Accession
    NM_005221, NP_005212
    UniProt
    P56178
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