Anticorps Monoclonal anti-PMS2

PMS2 Monoclonal Antibody for WB, ELISA

Hôte / Isotype

Mouse / IgG2a

Réactivité testée

Humain, rat, souris

Applications

WB, ELISA

Conjugaison

Non conjugué

Publications(6)

CloneNo.

1G4E6

N° de cat : 66075-1-Ig

Synonymes

1G4E6, EC:3.1.-.-, HNPCC4, PMS1 protein homolog 2, PMS2CL



Applications testées

Résultats positifs en WBcellules A431, cellules HeLa

Dilution recommandée

ApplicationDilution
Western Blot (WB)WB : 1:500-1:2000
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, check data in validation data gallery

Applications publiées

WBSee 6 publications below

Informations sur le produit

66075-1-Ig cible PMS2 dans les applications de WB, ELISA et montre une réactivité avec des échantillons Humain, rat, souris

Réactivité Humain, rat, souris
Réactivité citéeHumain
Hôte / Isotype Mouse / IgG2a
Clonalité Monoclonal
Type Anticorps
Immunogène PMS2 Protéine recombinante Ag12661
Nom complet PMS2 postmeiotic segregation increased 2 (S. cerevisiae)
Masse moléculaire calculée 862 aa, 96 kDa
Poids moléculaire observé 100 kDa
Numéro d’acquisition GenBankBC093921
Symbole du gène PMS2
Identification du gène (NCBI) 5395
Conjugaison Non conjugué
Forme Liquide
Méthode de purification Purification par protéine A
Tampon de stockage PBS with 0.02% sodium azide and 50% glycerol
Conditions de stockageStocker à -20°C. Stable pendant un an après l'expédition. L'aliquotage n'est pas nécessaire pour le stockage à -20oC Les 20ul contiennent 0,1% de BSA.

Informations générales

PMS2, also named as PMSL2, belongs to the DNA mismatch repair mutL/hexB family. It is a component of the post-replicative DNA mismatch repair system (MMR). It heterodimerizes with MLH1 to form MutL alpha. MulL 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. It also implicated in DNA damage signaling, a process which induces cell cycle arrest and can lead to apoptosis in case of major DNA damages. (PMID: 16873062, PMID: 18206974) Defects in PMS2 are the cause of hereditary non-polyposis colorectal cancer type 4 (HNPCC4). Defects in PMS2 are a cause of mismatch repair cancer syndrome (MMRCS).

Protocole

Product Specific Protocols
WB protocol for PMS2 antibody 66075-1-IgDownload protocol
Standard Protocols
Click here to view our Standard Protocols

Publications

SpeciesApplicationTitle
humanWB

Mol Carcinog

The mechanism of RGS5 regulating gastric cancer mismatch repair protein

Authors - Zhenwei Yang
humanWB

Sci Rep

Mismatch repair proteins play a role in ATR activation upon temozolomide treatment in MGMT-methylated glioblastoma.

Authors - Sachita Ganesa
humanWB

Mol Genet Genomic Med

PMS2 germline mutation c.943C>T (p.Arg315*)-induced Lynch syndrome-associated ovarian cancer.

Authors - Xiaoqing Guo
humanWB

Cell Mol Biol Lett

MRE11A: a novel negative regulator of human DNA mismatch repair

Authors - Demin Du
humanWB

Drug Resist Updat

Intercellular adhesion molecule-1 suppresses TMZ chemosensitivity in acquired TMZ-resistant gliomas by increasing assembly of ABCB1 on the membrane

Authors - Xin Zhang
humanWB

Cell Rep

Phosphorylation of SIRT7 by ATM causes DNA mismatch repair downregulation and adaptive mutability during chemotherapy

Authors - Lianhui Sun

Avis

The reviews below have been submitted by verified Proteintech customers who received an incentive for providing their feedback.


FH

Daniela (Verified Customer) (03-17-2022)

Bands in WB and IF staining were both aspecific.

  • Applications: Western Blot, Immunofluorescence
  • Primary Antibody Dilution: 1:1000 for WB; 1:100 for IF
  • Cell Tissue Type: Gastric mouse organoids and oesophageal cancer cell line
PMS2 Antibody Western Blot,Immunofluorescence validation (1:1000 for WB; 1:100 for IF dilution) in Gastric mouse organoids and oesophageal cancer cell line (Cat no:66075-1-Ig)
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