Anti-MSH2 抗体 [EPR21017-2] - BSA and Azide free
Anti-MSH2 antibody [EPR21017-2] - BSA and Azide free
- RabMAb
- Recombinant
- KO Validated
- 詳細を見る
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(1 Publication)
Rabbit Recombinant Monoclonal MSH2 antibody. Carrier free. Suitable for WB, ICC/IF, Flow Cyt (Intra), IHC-P and reacts with Mouse, Rat, Human samples. Cited in 1 publication.
別名を表示する
DNA mismatch repair protein Msh2, hMSH2, MutS protein homolog 2, MSH2
- Flow Cyt (Intra)
Lab
Flow Cytometry (Intracellular) - Anti-MSH2 antibody [EPR21017-2] - BSA and Azide free (AB228325)
MSH2 KO HAP1 (MSH2 knockout Human chronic myelogenous leukemia near-haploid cell line, Left) / WT HAP1 (Right) cells were fixed with4% paraformaldehyde and permeabilised with 90% methanol. The cells were incubated with the primary antibody, ab212188 at a 1/6000 dilution (0.01μg) (red line). The secondary antibody used wasGoat anti rabbit IgG (Alexa Fluor® 488, ab150077) at a 1/2000 dilution. The isotype control (black line) antibody wasRabbit monoclonal IgG (ab172730). An unlabelled control without incubation with primary antibody and secondary antibody was also performed (blue line).
90% methanol permeabilisation is recommended. Avoid using TritonX-100 as it may cause non-specific staining.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab212188).
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-MSH2 antibody [EPR21017-2] - BSA and Azide free (AB228325)
Immunohistochemical analysis of paraffin-embedded human testis tissue labeling MSH2 with ab212188 at 1/10000 dilution, followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP). Nuclear staining in human testis was observed (PMID : 10029069). Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is a ready to use Goat Anti-Rabbit IgG H&L (HRP).
Perform heat mediated antigen retrieval using ab93684 (Tris/EDTA buffer, pH 9.0).
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab212188).
関連する標識済み抗体及び組成の異なる製品 (1)
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Anti-MSH2 antibody [EPR21017-2]
Reactivity data
製品の詳細
ab228325 is the carrier-free version of ab212188.
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
出荷温度及び保存条件
製品の状態
精製方法
バッファー組成
出荷温度
短期保存温度
長期保存温度
保管に関する情報
補足情報
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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ターゲットの情報
文献 (1)
Recent publications for all applications. Explore the full list and refine your search
Frontiers in oncology 10:950 PubMed32612954
2020
Applications
Unspecified application
Species
Unspecified reactive species
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