PMS2 Polyclonal Antibody

Cat.#: 161741

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Product Information

  • Product Name
    PMS2 Polyclonal Antibody
  • Documents
  • Description
    Polyclonal antibody to PMS2
  • Tested applications
    WB, IF, IP
  • Species reactivity
    Human
  • Alternative names
    PMS2 antibody; HNPCC4 antibody; MLH4 antibody; PMS2CL antibody; PMSL2 antibody; mismatch repair endonuclease PMS2 antibody
  • Isotype
    Rabbit IgG
  • Preparation
    Antigen: Recombinant fusion protein containing a sequence corresponding to amino acids 390-670 of human PMS2 (NP_000526.2).
  • Clonality
    Polyclonal
  • Formulation
    PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
  • Storage instructions
    Store at -20℃. Avoid freeze / thaw cycles.
  • Applications
    WB 1:500 - 1:2000
    IF 1:50 - 1:200
    IP 1:20 - 1:50
  • Validations

    Western blot - PMS2 Polyclonal Antibody

    Western blot - PMS2 Polyclonal Antibody

    Western blot analysis of extracts of various cell lines, using PMS2 antibody at 1:1000 dilution.Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution.Lysates/proteins: 25ug per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit .Exposure time: 90s.

    Immunofluorescence - PMS2 Polyclonal Antibody

    Immunofluorescence - PMS2 Polyclonal Antibody

    Immunofluorescence analysis of U2OS cells using PMS2 antibody .

    Immunoprecipitation - PMS2 Polyclonal Antibody

    Immunoprecipitation - PMS2 Polyclonal Antibody

    Immunoprecipitation analysis of 150ug extracts of Jurkat cells using 3ug PMS2 antibody . Western blot was performed from the immunoprecipitate using PMS2 antibody at a dilition of 1:500.

  • Background
    Component of the post-replicative DNA mismatch repair system (MMR). Heterodimerizes with MLH1 to form MutL alpha. DNA repair is initiated by MutS alpha (MSH2-MSH6) or MutS beta (MSH2-MSH3) binding to a dsDNA mismatch, then MutL alpha is recruited to the heteroduplex. Assembly of the MutL-MutS-heteroduplex ternary complex in presence of RFC and PCNA is sufficient to activate endonuclease activity of PMS2. It introduces single-strand breaks near the mismatch and thus generates new entry points for the exonuclease EXO1 to degrade the strand containing the mismatch. DNA methylation would prevent cleavage and therefore assure that only the newly mutated DNA strand is going to be corrected. MutL alpha (MLH1-PMS2) interacts physically with the clamp loader subunits of DNA polymerase III, suggesting that it may play a role to recruit the DNA polymerase III to the site of the MMR. Also implicated in DNA damage signaling, a process which induces cell cycle arrest and can lead to apoptosis in case of major DNA damages.

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"