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PR Domain Containing 16 (PRDM16) (Middle Region) Peptide

PRDM16 Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN982174

Aperçu rapide pour PR Domain Containing 16 (PRDM16) (Middle Region) Peptide (ABIN982174)

Antigène

PRDM16 (PR Domain Containing 16 (PRDM16))

Origine

Humain

Source

  • 3
Synthetic

Application

Blocking Peptide (BP), Western Blotting (WB)
  • Protein Region

    Middle Region

    Séquence

    LNHTQDAKLP SPLGNPALPL VSAVSNSSQG TTAAAGPEEK FESRLEDSCV

    Attributs du produit

    This is a synthetic peptide designed for use in combination with anti-PRDM16 Antibody(ARP33260_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

    PRDM16 (PR Domain Containing 16 (PRDM16))

    Sujet

    The reciprocal translocation t(1,3)(p36,q21) occurs in a subset of myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). This gene is located near the 1p36.3 breakpoint and has been shown to be specifically expressed in the t(1:3)(p36,q21)-positive MDS/AML. The protein encoded by this gene is a zinc finger transcription factor and contains an N-terminal PR domain. The translocation results in the overexpression of a truncated version of this protein that lacks the PR domain, which may play an important role in the pathogenesis of MDS and AML. Alternatively spliced transcript variants encoding distinct isoforms have been reported.

    Alias Symbols: KIAA1675, MEL1, PFM13

    Protein Interaction Partner: INADL

    Protein Size: 1275

    Poids moléculaire

    140 kDa

    ID gène

    63976

    NCBI Accession

    NM_022114, NP_071397

    UniProt

    Q9HAZ2
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