Anti-MSH2 antibody
5
(4 Reviews)
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(28 Publications)
Rabbit Polyclonal MSH2 antibody. Suitable for IHC-P, ICC/IF, IP, WB and reacts with Mouse, Human samples. Cited in 28 publications. Immunogen corresponding to Synthetic Peptide within Human MSH2 aa 850 to C-terminus.
View Alternative Names
DNA mismatch repair protein Msh2, hMSH2, MutS protein homolog 2, MSH2
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-MSH2 antibody (AB70270)
ICC/IF image of ab70270 stained HepG2 cells. The cells were 4% PFA fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab70270, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MSH2 antibody (AB70270)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human metastatic lymph node (left) and mouse squamous cell carcinoma (right) tissues labelling MSH2 with ab70270 at 1/1000 (1µg/ml) and 1/5000 (0.2µg/ml). Detection : DAB.
- ICC/IF
AbReview45364****
Immunocytochemistry/ Immunofluorescence - Anti-MSH2 antibody (AB70270)
ab70270 staining MSH2 in HeLa cells by ICC/IF (Immunocytochemistry/immunofluorescence). Cells were fixed with paraformaldehyde and permeabilized with 0.5% Triton X-100 in PBS. Samples were incubated with primary antibody (1/500 in PBS) for 1 hour at 22°C. ab150081, an Alexa Fluor® 488-conjugated goat anti-rabbit IgG polyclonal (1/200) was used as the secondary antibody. Counterstained with DAPI.
This image is courtesy of an Abreview submitted by Kirk McManus
- IP
Unknown
Immunoprecipitation - Anti-MSH2 antibody (AB70270)
Immunoprecipitation of HeLa whole cell lysate. Lane 1 : 50µg of input lysate. Lane 2 : HeLa whole cell lysate (1mg) immunoprecipitated with ab70270 at 3µg/mg. Lane 3 : HeLa whole cell lysate immunoprecipitated with control IgG. Samples were subjected to Western blot, analysed with ab70270 at 0.1µg/ml and detected by chemiluminescence with an exposure time of 3 minutes.
All lanes:
Immunoprecipitation - Anti-MSH2 antibody (ab70270)
Predicted band size: 105 kDa
false
- WB
Unknown
Western blot - Anti-MSH2 antibody (AB70270)
All lanes:
Western blot - Anti-MSH2 antibody (ab70270) at 0.1 µg/mL
Lane 1:
HeLa whole cell lysate at 50 µg
Lane 2:
HeLa whole cell lysate at 15 µg
Lane 3:
HeLa whole cell lysate at 5 µg
Lane 4:
Ramos whole cell lysate at 50 µg
Lane 5:
NIH3T3 whole cell lysate at 50 µg
Predicted band size: 105 kDa
Observed band size: 116 kDa
true
Exposure time: 3min
Reactivity data
Product details
Properties and storage information
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Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Components are identified in mismatch repair where MSH2 forms a heterodimer with MSH6 known as the MutSα complex or with MSH3 known as the MutSβ complex. This heterodimerization is critical for the initial steps in the recognition and binding of mismatch errors on the DNA strand. MSH2 complex formation enables it to scan the DNA for errors facilitating the recruitment of additional repair proteins. The activity of MSH2 in these complexes is important in preserving the fidelity of genetic information and prevents mutations that could lead to genomic instability.
Pathways
MSH2 operates within the DNA damage response and repair pathways. The protein is a core component of the mismatch repair pathway which corrects DNA replication errors that elude proofreading activity of DNA polymerases. It interacts with other proteins such as MLH1 and PMS2 forming a synergistic function that amplifies the capacity to recognize and initiate repair of mismatches. The pathway involving MSH2 not only repairs mismatched bases but also plays a role in cell cycle control checkpoints and apoptosis evidencing its pivotal role in maintaining cell cycle integrity.
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Target data
Publications (28)
Recent publications for all applications. Explore the full list and refine your search
Nature aging 5:1739-1749 PubMed40836125
2025
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Epigenetics & chromatin 18:24 PubMed40296143
2025
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Neoplasia (New York, N.Y.) 62:101145 PubMed39985912
2025
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Nature communications 15:8338 PubMed39333076
2024
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Cancer cell international 24:25 PubMed38200495
2024
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Disease models & mechanisms 16: PubMed37395714
2023
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Journal for immunotherapy of cancer 11: PubMed37072347
2023
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Science immunology 8:eade1167 PubMed36961908
2023
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Science advances 9:eadd8564 PubMed36921054
2023
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Journal of immunology (Baltimore, Md. : 1950) 210:369-376 PubMed36603026
2023
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Product promise
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