Mismatch Repair Protein 2 (MSH2) (N-Term) Peptide
MSH2
适用: 人
宿主: 合成
BP, WB, IHC
-
- 抗原 See all MSH2 products
- MSH2 (Mismatch Repair Protein 2 (MSH2))
- 蛋白结构域
- N-Term
- 宿主
- 人
-
资源
- 合成
- 应用范围
- Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
- 产品特性
- This is a synthetic peptide designed for use in combination with anti-MSH2 antibody (Catalog #: ARP41351_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- 纯化方法
- Purified
-
-
- 应用备注
- Each Investigator should determine their own optimal working dilution for specific applications.
- 限制
- 仅限研究用
-
- 状态
- Lyophilized
- 溶解方式
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- 浓度
- 1 mg/mL
- 缓冲液
- Final peptide concentration is 1 mg/mL in PBS.
- 注意事项
- Avoid repeated freeze-thaw cycles.
- 储存条件
- -20 °C
- 储存方法
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
-
- 抗原
- MSH2 (Mismatch Repair Protein 2 (MSH2))
- 别名
- COCA1 Peptide, FCC1 Peptide, HNPCC Peptide, HNPCC1 Peptide, LCFS2 Peptide, AI788990 Peptide, wu:fc06b02 Peptide, wu:fc13e09 Peptide, zgc:55333 Peptide, ATMSH2 Peptide, MUTS homolog 2 Peptide, msh2 Peptide, mutS homolog 2 Peptide, mutS homolog 2 (E. coli) Peptide, MUTS homolog 2 Peptide, mutS homolog 2 L homeolog Peptide, MutS protein homolog 2 Peptide, MSH2 Peptide, Msh2 Peptide, msh2 Peptide, msh2.L Peptide
- 背景
-
MSH2 was identified as a locus frequently mutated in hereditary nonpolyposis colon cancer (HNPCC). When cloned, it was discovered to be a human homolog of the E. coli mismatch repair gene mutS, consistent with the characteristic alterations in microsatellite sequences (RER+ phenotype) found in HNPCC. MSH2 was identified as a locus frequently mutated in hereditary nonpolyposis colon cancer (HNPCC). When cloned, it was discovered to be a human homolog of the E. coli mismatch repair gene mutS, consistent with the characteristic alterations in microsatellite sequences (RER+ phenotype) found in HNPCC. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Alias Symbols: COCA1, FCC1, HNPCC, HNPCC1, LCFS2
Protein Interaction Partner: E2F1,E2F1,E2F3,E2F4,BRCA1,EXO1,EXO1,MAX,MSH3,MSH6,MSH6,ATR,ATRIP,BARD1,CHEK2,CREBBP,EXO1,MAX,MSH3,MSH6,PCNA,SMC1A,AIRE,ATM,ATR,ATRIP,BARD1,BLM,BRCA1,BTBD12,CHEK1,CHEK2,EXO1,MAX,MLH1,MRE11A,MSH2,MSH3,MSH6,MYC,NBN,OTUB1,PCNA,PMS2,PTP4A3,RAD50,RFC1
Protein Size: 934 - 分子量
- 105 kDa
- 基因ID
- 4436
- NCBI登录号
- NM_000251, NP_000242
- UniProt
- P43246
-
You are here:
