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Email: info@nsjbio.com
- Tel: 858.663.9055
- Email: info@nsjbio.com
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MutS homolog 6 (MSH6) is a nuclear DNA mismatch repair protein encoded by the MSH6 gene and functions as a key component of the MutSalpha complex together with MSH2. This heterodimer detects base-base mismatches and small insertion-deletion loops that arise during DNA replication, initiating repair mechanisms that maintain genomic stability. MSH6 is widely expressed in proliferating tissues and is particularly abundant in epithelial and hematopoietic cell populations where DNA replication and repair activity are active. Loss or dysfunction of MSH6 disrupts the mismatch repair pathway and contributes to microsatellite instability, a molecular hallmark observed in several cancers including colorectal and endometrial carcinoma associated with Lynch syndrome.
MSH6 Antibody Rabbit Polyclonal for IF is used to visualize intracellular localization of this mismatch repair protein using immunofluorescence microscopy. Because MSH6 functions in monitoring DNA replication fidelity, it localizes primarily within the nucleus where it participates in detection of replication errors and recruitment of downstream repair factors. Immunofluorescence staining typically reveals strong nuclear signal in proliferating cells, reflecting the protein's role in maintaining genomic integrity during the cell cycle. Visualization of MSH6 expression by immunofluorescence enables researchers to examine subcellular distribution patterns, assess protein expression levels within individual cells, and evaluate cellular heterogeneity within cultured cell populations.
Within the mismatch repair pathway, MSH6 forms the MutSalpha complex with MSH2, which recognizes mismatched nucleotides and insertion-deletion loops generated during DNA replication. Following mismatch recognition, the complex recruits downstream repair proteins including MLH1 and PMS2 that coordinate excision and resynthesis of the newly synthesized DNA strand. Proper functioning of this pathway is essential for preventing accumulation of replication-associated mutations and preserving genomic stability. Disruption of MSH6 expression or function therefore contributes to tumorigenesis and has become an important molecular marker in studies of mismatch repair deficiency.
Immunofluorescence-based detection of MSH6 expression provides valuable insight into nuclear localization patterns and cell-to-cell variation in mismatch repair protein abundance. A rabbit polyclonal MSH6 antibody can recognize multiple epitopes within the target protein, which may enhance detection sensitivity in fluorescence microscopy experiments where signal intensity and antigen accessibility can vary depending on fixation or permeabilization conditions. MSH6 antibody reagents are therefore widely used in cell biology and cancer research to study DNA repair pathways, investigate responses to replication stress, and evaluate alterations in mismatch repair proteins across experimental systems.
Optimal dilution of the MSH6 antibody should be determined by the researcher.
Amino acids KAREFEKMNQSLRLFREVCLA from the human protein were used as the immunogen for the MSH6 antibody.
After reconstitution, the MSH6 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
GTBP antibody, G/T mismatch-binding protein antibody, DNA mismatch repair protein MSH6 antibody
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