PMS2 Monoklonaler Antikörper

PMS2 Monoklonal Antikörper für WB, ELISA

Wirt / Isotyp

Maus / IgG2a

Getestete Reaktivität

human, Maus, Ratte

Anwendung

WB, ELISA

Konjugation

Unkonjugiert

Publikationen(6)

CloneNo.

1G4E6

Kat-Nr. : 66075-1-Ig

Synonyme

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



Geprüfte Anwendungen

Erfolgreiche Detektion in WBA431-Zellen, HeLa-Zellen

Empfohlene Verdünnung

AnwendungVerdünnung
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

Veröffentlichte Anwendungen

WBSee 6 publications below

Produktinformation

66075-1-Ig bindet in WB, ELISA PMS2 und zeigt Reaktivität mit human, Maus, Ratten

Getestete Reaktivität human, Maus, Ratte
In Publikationen genannte Reaktivitäthuman
Wirt / Isotyp Maus / IgG2a
Klonalität Monoklonal
Typ Antikörper
Immunogen PMS2 fusion protein Ag12661
Vollständiger Name PMS2 postmeiotic segregation increased 2 (S. cerevisiae)
Berechnetes Molekulargewicht 862 aa, 96 kDa
Beobachtetes Molekulargewicht 100 kDa
GenBank-ZugangsnummerBC093921
Gene symbol PMS2
Gene ID (NCBI) 5395
Konjugation Unkonjugiert
Form Liquid
Reinigungsmethode Protein-A-Reinigung
Lagerungspuffer PBS with 0.02% sodium azide and 50% glycerol
LagerungsbedingungenBei -20°C lagern. Nach dem Versand ein Jahr lang stabil Aliquotieren ist bei -20oC Lagerung nicht notwendig. 20ul Größen enthalten 0,1% BSA.

Hintergrundinformationen

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).

Protokolle

PRODUKTSPEZIFISCHE PROTOKOLLE
WB protocol for PMS2 antibody 66075-1-IgProtokoll herunterladen
STANDARD-PROTOKOLLE
Klicken Sie hier, um unsere Standardprotokolle anzuzeigen

Publikationen

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

Rezensionen

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)