Postmeiotic Segregation Increased 2(PMS2) Mouse Monoclonal Antibody

Postmeiotic Segregation Increased 2(PMS2) Mouse Monoclonal Antibody

Cat: AMM22040
规格:50μL 价格:¥1200
规格:100μL 价格:¥2150
应用(Application):IHC,ELISA

种属(Reactivity):Human,Mouse
偶联物(Conjugate):Unconjugated
基因名(Gene Name):PMS2 PMSL2

分类: 病理IHC抗体 标签: , , , , , ,

说明书 复制

产品概述

产品名称(Product Name)

Postmeiotic Segregation Increased 2(PMS2) Mouse Monoclonal Antibody

描述(Description)

病理IHC抗体

宿主(Host)

Mouse

应用(Application)

IHC,ELISA

种属反应性(Reactivity)

Human,Mouse

 

产品性能

偶联物(Conjugation)

Unconjugated

修饰(Modification)

Unmodified

同种型(Isotype)

IgG1,Kappa

克隆(Clonality)

Monoclonal

形式(Form)

Liquid

存放说明(Storage)

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

储存溶液(Buffer)

PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA

纯化方式(Purification)

The antibody was affinity-purified from ascites by affinity-chromatography using specific immunogen.

 

免疫原

基因名(Gene Name)

PMS2 PMSL2

别名(Alternative Names)

Mismatch repair endonuclease PMS2;DNA mismatch repair protein PMS2;PMS1 protein homolog 2;

基因ID(Gene ID)

Human:5395

蛋白ID(SwissProt ID)

Human:P54278

 

产品应用

稀释比(Dilution Ratio)

IHC 1:50-100;ELISA 1:500-5000

蛋白分子量(Molecular Weight)

Calculated MW:96kDa,Observed MW:110kDa

 

研究背景

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

 

研究领域

Pathology


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