KO-Validated PMS2 Recombinant Rabbit Monoclonal Antibody
Size:20μL Price:$118
Size:50μL Price:$218
Size:100μL Price:$318
Application:WB,FCM,ICC,IHC-P

Reactivity:Human
Conjugate:Unconjugated
Gene Name:PMS2
SKU: KVAb00099
Detail

Summary

Production Name

KO-Validated PMS2 Recombinant Rabbit Monoclonal Antibody

Description

KD-Validated antibody

Host

Rabbit

Application

WB,FCM,ICC,IHC-P

Reactivity

Human

 

Performance

Conjugation

Unconjugated

Modification

Unmodified

Isotype

Rabbit IgG

Clonality

Rabbit mAb

Form

Liquid

Storage

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

Buffer

Supplied in PBS (pH 7.4) containing 50% glycerol, and 0.02% sodium azide.

Purification

Affinity purification

 

Immunogen

Gene Name

PMS2

Alternative Names

PMS2; PMS1 Homolog 2, Mismatch Repair System Component; HNPCC4; PMS-2; PMSL2; MLH4; PMS1 Homolog 2, Mismatch Repair Protein; Mismatch Repair Endonuclease PMS2; DNA Mismatch Repair Protein PMS2; PMS1 Protein Homolog 2; H_DJ0042M02.9; PMS2 Postmeiotic Segregation Increased 2 (S. Cerevisiae); Postmeiotic Segregation Increased (S. Cerevisiae) 2; PMS2 Postmeiotic Segregation Increased 2; EC 3.1.-.-; LYNCH4; MMRCS4; PMS2CL

Gene ID

5395

SwissProt ID

P54278

 

Application

Dilution Ratio

WB 1:1,000-1:5,000; FC 1:200-1:2,000; ICC 1:100-1:1,000; IHC-P 1:100-1:200

Molecular Weight

Calculated MW: 95.8kDa

 

Background

The protein encoded by this gene is a key component of the mismatch repair system that functions to correct DNA mismatches and small insertions and deletions that can occur during DNA replication and homologous recombination. This protein forms heterodimers with the gene product of the mutL homolog 1 (MLH1) gene to form the MutL-alpha heterodimer. The MutL-alpha heterodimer possesses an endonucleolytic activity that is activated following recognition of mismatches and insertion/deletion loops by the MutS-alpha and MutS-beta heterodimers, and is necessary for removal of the mismatched DNA. There is a DQHA(X)2E(X)4E motif found at the C-terminus of the protein encoded by this gene that forms part of the active site of the nuclease. Mutations in this gene have been associated with hereditary nonpolyposis colorectal cancer (HNPCC; also known as Lynch syndrome) and Turcot syndrome. [provided by RefSeq, Apr 2016]

 

Research Area

Epigenetics and Nuclear Signaling

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