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>   首页   >   产品   >   流式抗体   >   未偶联流式验证抗体   >   Anti-MSH2 Antibody   

Anti-MSH2 Antibody

     
  • 1 - Anti-MSH2 Antibody AP95954
    Western blot analysis of MSH2 expression in Hela (A), NIH/3T3 (B), A549 (C), A431 (D) whole cell lysates. (Predicted band size: 105 kD; Observed band size: 105 kD)
  • 19 - Anti-MSH2 Antibody AP95954
    Immunohistochemical analysis of MSH2 staining in human cervical cancer formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
  • 3 - Anti-MSH2 Antibody AP95954
    Immunofluorescent analysis of MSH2 staining in Hela cells. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a hidified chamber. Cells were washed with PBST and incubated with an AF488-conjugated secondary antibody (green) in PBS at room temperature in the dark. Phalloidin - AF594 was used to stain Actin filaments (red). DAPI was used to stain the cell nuclei (blue).
  • 4 - Anti-MSH2 Antibody AP95954
    Flow cytometric analysis of HeLa cells using Anti-MSH2 Antibody (green) and negative control (red).
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Product Information
Application
  • Applications Legend:
  • E=ELISA
  • WB=Western Blotting
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB, IHC, FC, IF/IC
Primary Accession P43246
Reactivity Human, Mouse
Host Mouse
Clonality Monoclonal
Calculated MW 104743 Da
Additional Information
Gene ID 4436
Other Names DNA mismatch repair protein Msh2; hMSH2; MutS protein homolog 2
Target/Specificity Recombinant fusion protein of human MSH2 expressed in E. Coli
Dilution WB~~WB (1/500 - 1/1000)
IHC~~1:100~500
FC~~FC (1/100 - 1/200)
IF/IC~~N/A
Format Mouse IgG1. Liquid in PBS, pH 7.3, 30% glycerol, and 0.01% sodium azide.
StorageStore at -20 °C.Stable for 12 months from date of receipt

For Research Use Only. Not For Use In Diagnostic Procedures.

Protein Information
Name MSH2
Function Component of the post-replicative DNA mismatch repair system (MMR). Forms two different heterodimers: MutS alpha (MSH2-MSH6 heterodimer) and MutS beta (MSH2-MSH3 heterodimer) which binds to DNA mismatches thereby initiating DNA repair. When bound, heterodimers bend the DNA helix and shields approximately 20 base pairs. MutS alpha recognizes single base mismatches and dinucleotide insertion-deletion loops (IDL) in the DNA. MutS beta recognizes larger insertion-deletion loops up to 13 nucleotides long. After mismatch binding, MutS alpha or beta forms a ternary complex with the MutL alpha heterodimer, which is thought to be responsible for directing the downstream MMR events, including strand discrimination, excision, and resynthesis. Recruits DNA helicase MCM9 to chromatin which unwinds the mismatch containing DNA strand (PubMed:26300262). ATP binding and hydrolysis play a pivotal role in mismatch repair functions. The ATPase activity associated with MutS alpha regulates binding similar to a molecular switch: mismatched DNA provokes ADP-->ATP exchange, resulting in a discernible conformational transition that converts MutS alpha into a sliding clamp capable of hydrolysis-independent diffusion along the DNA backbone. This transition is crucial for mismatch repair. MutS alpha may also play a role in DNA homologous recombination repair. In melanocytes may modulate both UV-B-induced cell cycle regulation and apoptosis.
Cellular Location Nucleus. Chromosome
Tissue Location Ubiquitously expressed.
Research Areas
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