产品: MSH2 抗体
货号: DF6257
描述: Rabbit polyclonal antibody to MSH2
应用: WB IHC IF/ICC
文献验证: WB
反应: Human, Mouse, Rat
预测: Pig, Zebrafish, Bovine, Horse, Sheep, Rabbit, Dog, Chicken
蛋白号: P43246
RRID: AB_2838223

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   规格 价格 库存
 50ul RMB¥ 1250 现货
 100ul RMB¥ 2300 现货
 200ul RMB¥ 3000 现货

货期: 当天发货

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产品描述

来源:
Rabbit
应用:
WB 1:500-1:2000, IHC 1:50-1:200, IF/ICC 1:100-500
*The optimal dilutions should be determined by the end user. For optimal experimental results, antibody reuse is not recommended.
*Tips:

WB: 适用于变性蛋白样本的免疫印迹检测. IHC: 适用于组织样本的石蜡(IHC-p)或冰冻(IHC-f)切片样本的免疫组化/荧光检测. IF/ICC: 适用于细胞样本的荧光检测. ELISA(peptide): 适用于抗原肽的ELISA检测.

反应:
Human, Mouse, Rat
克隆:
Polyclonal
特异性:
MSH2 Antibody detects endogenous levels of total MSH2.
RRID:
AB_2838223
引用格式: Affinity Biosciences Cat# DF6257, RRID:AB_2838223.
偶联:
Unconjugated.
纯化:
The antiserum was purified by peptide affinity chromatography using SulfoLink™ Coupling Resin (Thermo Fisher Scientific).
保存:
Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Store at -20 °C. Stable for 12 months from date of receipt.
别名:

展开/折叠

BAT26; COCA 1; COCA1; DNA mismatch repair protein Msh2; FCC 1; FCC1; hMSH2; HNPCC 1; HNPCC; HNPCC1; LCFS2; MSH 2; Msh2; MSH2_HUMAN; MutS homolog 2; MutS homolog 2 colon cancer nonpolyposis type 1; MutS protein homolog 2;

抗原和靶标

免疫原:

A synthesized peptide derived from human MSH2, corresponding to a region within C-terminal amino acids.

基因/基因ID:
描述:
The DNA mismatch repair system (MMR) repairs post-replication DNA, inhibits recombination between non-identical DNA sequences and induces both checkpoint and apoptotic responses following certain types of DNA damage (1). MSH2 (MutS homologue 2) forms the hMutS-α dimer with MSH6 and is an essential component of the mismatch repair process. hMutS-α is part of the BRCA1-associated surveillance complex (BASC), a complex that also contains BRCA1, MLH1, ATM, BLM, PMS2 proteins and the Rad50-Mre11-NBS1 complex (2).Mutations in MSH2 have been found in a large proportion of hereditary non-polyposis colorectal cancer (Lynch Syndrome), the most common form of inherited colorectal cancer in the Western world (3). Mutations have also been associated with other sporadic tumors.

研究领域

· Genetic Information Processing > Replication and repair > Mismatch repair.

· Human Diseases > Drug resistance: Antineoplastic > Platinum drug resistance.

· Human Diseases > Cancers: Overview > Pathways in cancer.   (View pathway)

· Human Diseases > Cancers: Specific types > Colorectal cancer.   (View pathway)

文献引用

1). NLRC5 promotes endometrial carcinoma progression by regulating NF-κB pathway-mediated mismatch repair gene deficiency. Scientific reports, 2024 (PubMed: 38822039) [IF=3.8]

Application: WB    Species: human    Sample: HEC-1B cell

Figure 2 NLRC5 inhibits the expression of MMR genes in EC cells. (A) The correlation between NLRC5 and MSH6, MSH2 in EC was analyzed on GEPIA website. (B) The mRNA expression levels of NLRC5 in HEC-1B and Ishikawa cell lines were examined by qRT-PCR (mean ± SD, n = 3). (C) The protein expression levels of NLRC5 in HEC-1B and Ishikawa cell lines were examined by western blot (mean ± SD, n = 3). (D) The protein expression levels were quantified using the ImageJ software and normalized using β-actin protein levels (mean ± SD, n = 3). The corresponding brightfield images are included in the supplementary material. Data represent mean ± SD, *P 

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