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Distal-Less Homeobox 5 (DLX5) Peptid

DLX5 Reaktivität: Human Wirt: Synthetic BP, IHC, WB
Produktnummer ABIN975853
  • Target Alle DLX5 Produkte
    DLX5 (Distal-Less Homeobox 5 (DLX5))
    Spezies
    Human
    Quelle
    • 6
    Synthetic
    Applikation
    Blocking Peptide (BP), Immunohistochemistry (IHC), Western Blotting (WB)
    Produktmerkmale
    This is a synthetic peptide designed for use in combination with anti-DLX5 antibody (Catalog #: ARP32867_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.
    Aufreinigung
    Purified
  • Applikationshinweise
    Each Investigator should determine their own optimal working dilution for specific applications.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Konzentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Handhabung
    Avoid repeated freeze-thaw cycles.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target
    DLX5 (Distal-Less Homeobox 5 (DLX5))
    Synonyme
    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
    Hintergrund
    DLX5 is a member of a homeobox transcription factor family. DLX5 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.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.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.

    Alias Symbols: SHFM1D

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

    Protein Size: 289
    Molekulargewicht
    31 kDa
    Gen-ID
    1749
    NCBI Accession
    NM_005221, NP_005212
    UniProt
    P56178
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