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Invitrogen™ PMS2/PMS2CL Polyclonal Antibody

Rabbit Polyclonal Antibody

Supplier:  Invitrogen™ PA5106710

Catalog No. PIPA5106710


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Description

Description

Antibody detects endogenous levels of total PMS2/PMS2CL.

Mismatch DNA repair in bacteria is carried out by the MutL, MutH, and MutS proteins. The MutS protein initially binds to mismatched DNA. This is followed by binding of the MutH endonuclease and MutL to form a complex that carries out excision repair. The hMSH2 gene specifies a MutS homologue and hMLH1, hPMS1, and hPMS2 encode MutL homologs. Mutations in these genes are associated with hereditary nonpolyposis colon cancer (HNPCC), one of the most common hereditary diseases in man. As with the bacterial system, HNPCC is characterized by frequent microsatellite mutations that arise by somatic mutation due to a replication error (RER+) phenotype. Both hPMS1 and hPMS2 are mutated in the germline of HNPCC patients. Although the exact function of MutL and its homologs has yet to be determined, it is known that a complex of PMS2 and MLH1 (MutLa) from HeLa cells can complement a deficiency of MLH1 in hypermutable H6 colorectal tumor cells.
TRUSTED_SUSTAINABILITY
Specifications

Specifications

PMS2/PMS2CL
Polyclonal
Unconjugated
PMS2CL
DNA mismatch repair protein PMS2; H_DJ0042M02.9; HNPCC4; mismatch repair endonuclease PMS2; MLH4; PMS1 homolog 2, mismatch repair protein; PMS1 homolog 2, mismatch repair system component; PMS1 protein homolog 2; PMS2; PMS2 C-terminal like pseudogene; PMS2 postmeiotic segregation increased 2; PMS2CL; PMS2P13; PMSL2; postmeiotic segregation increased 2 nirs variant 6
Rabbit
Affinity Chromatography
RUO
441194, 5395
-20°C
Liquid
Immunohistochemistry (Paraffin), Western Blot, Immunocytochemistry
1 mg/mL
PBS with 50% glycerol and 0.02% sodium azide; pH 7.4
P54278, Q68D20
PMS2, PMS2CL
A synthesized peptide derived from human PMS2CL(Accession Q68D20), corresponding to amino acid residues D124-C174.
100 μL
Primary
Human
Antibody
IgG
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