FGF-2 Polyclonal Antibody
¥680.00
Postmeiotic Segregation Increased 2(PMS2) (PT2116) Mouse mAb
活动价：
¥880.00
市场价：¥1280.00
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产品规格：
- 50μL
货号：
FAB2602057
- 产品信息
商品描述
靶点-Target
PMS2
反应性
Human,Mouse,
应用
IHC,ELISA
宿主物种-Host Species
Mouse
同种型-Isotype
IgG1,Kappa
修饰-Modification
Unmodified
MW(Calculated)
96kD
MW(Observed)
110kD
推荐稀释比
IHC 1:50-100;ELISA 1:500-5000
组成
PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
纯化工艺
The antibody was affinity-purified from ascites by affinity-chromatography using specific immunogen.
储存
-15°C to -25°C/1 year(Do not lower than -25°C)
克隆性
Monoclonal
克隆号
PT2116
免疫原
Synthesized peptide derived from human Postmeiotic Segregation Increased 2(PMS2) AA range: 600-700
特异性
The antibody can specifically recognize human PMS2 protein.
基因名称
PMS2 PMSL2
蛋白名称
Postmeiotic Segregation Increased 2(PMS2)
别名
Mismatch repair endonuclease PMS2;DNA mismatch repair protein PMS2;PMS1 protein homolog 2;
Organism-1
Human
基因ID-1
5395
SwissProt-1
P54278
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
细胞定位
Nuclear
