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MutL Homolog 1 (MLH1) (Middle Region) Peptide

MLH1 Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN5671688
  • Antigène Tous les produits MLH1
    MLH1 (MutL Homolog 1 (MLH1))
    Protein Region
    Middle Region
    Origine
    Humain
    Source
    • 3
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Séquence
    AAKNQSLEGD TTKGTSEMSE KRGPTSSNPR KRHREDSDVE MVEDDSRKEM
    Attributs du produit
    This is a synthetic peptide designed for use in combination with anti- MLH1 Antibody. 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.
  • Indications d'application
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Stock
    -20 °C
    Stockage commentaire
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Antigène
    MLH1 (MutL Homolog 1 (MLH1))
    Synonymes
    CG11482 Peptide, Dmel\\CG11482 Peptide, dmlh-1 Peptide, dmlh1 Peptide, zgc:66301 Peptide, MLH1 Peptide, LOC100232198 Peptide, 1110035C23Rik Peptide, AI317206 Peptide, AI325952 Peptide, AI561766 Peptide, COCA2 Peptide, FCC2 Peptide, HNPCC Peptide, HNPCC2 Peptide, hMLH1 Peptide, mutL homolog 1 Peptide, CG11482 gene product from transcript CG11482-RB Peptide, mutL homolog 1 S homeolog Peptide, mutL homolog 1, colon cancer, nonpolyposis type 2 (E. coli) Peptide, DNA mismatch repair protein Mlh1 Peptide, MLH1 Peptide, Mlh1 Peptide, mlh1.S Peptide, mlh1 Peptide, LOC588545 Peptide
    Sujet
    This gene was identified as a locus frequently mutated in hereditary nonpolyposis colon cancer (HNPCC). It is a human homolog of the E. coli DNA mismatch repair gene mutL, consistent with the characteristic alterations in microsatellite sequences (RER+phenotype) found in HNPCC. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional transcript variants have been described, but their full-length natures have not been determined.

    Alias Symbols: FCC2, COCA2, HNPCC, hMLH1, HNPCC2

    Protein Size: 515
    ID gène
    4292
    NCBI Accession
    NM_000249, NP_000240
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