Anti-PMS2 antibody (620-670) (STJ502562)

SPECIFICATIONS
ClonalityPolyclonal
HostRabbit
ConjugationUnconjugated
IsotypeIgG
ImmunogenSynthetic peptide taken within amino acid region 620-670 on human Mismatch Repair endonuclease PMS2 protein.
STJ502562-100
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General Information

Short DescriptionRabbit polyclonal antibody anti-PMS2 (620-670) is suitable for use in ELISA, Immunohistochemistry, Immunoprecipitation and Western Blot research applications.
ApplicationsELISA/IHC/IP/WB
HostRabbit
ReactivityHuman/Monkey
NoteSTRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.

Product Properties

ClonalityPolyclonal
IsotypeIgG
ConjugationUnconjugated
Concentration0.65-0.69 ยตg/ยตl
PurificationAffinity Purified
Dilution RangeWB: 1:500-1:1, 000
DB: 1:20, 000-1:50, 000
ELISA: 1:20, 000-1:50, 000
IP: 1:200
IHC: 1:100
FormulationContains Tris, HCl/Glycine buffer pH 7.4-7.8, 30% Glycerol and 0.5% BSA, along with cryo-protective agents, Hepes, and long-term preservatives (0.02% Sodium Azide).
Storage InstructionStore at-20ยฐC for long term storage. Avoid freeze-thaw cycles.

Target Information

ImmunogenSynthetic peptide taken within amino acid region 620-670 on human Mismatch Repair endonuclease PMS2 protein.
Immunogen Region620-670

Additional Info

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-MSH6) 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.

Information sourced from Uniprot.org

Citations

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