Product Pathways - Cell Cycle / Checkpoint
MYH (D13D4) Rabbit mAb #6248
PhosphoSitePlus® protein, site, and accession data: MUTYH
| Applications | Reactivity | Sensitivity | MW (kDa) | Isotype |
|---|---|---|---|---|
| W | H | Endogenous | 55 | Rabbit IgG |
Applications Key:
W=Western Blotting
Reactivity Key:
H=Human
Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.
Protocols
- 6248:
- Western Blotting
Specificity / Sensitivity
MYH (D13D4) Rabbit mAb recognizes endogenous levels of total MYH protein.
Source / Purification
Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues near the carboxy terminus of human MYH protein.
Western Blotting
Western blot analysis of extracts from various cell lines using MYH (D13D4) Rabbit mAb.
Background
Base excision repair (BER) proteins catalyze the removal of incorrect or damaged bases, including oxidized bases, from DNA. N-glycosylases specific to a given lesion remove the incorrect base as the first step in BER. MYH is the mammalian ortholog of E. coli MutY, a DNA glycosylase that catalyzes the removal of 8-oxoG:A mismatches (1). Several MYH isoforms have been detected in human cells localizing to either the nucleus or the mitochondria (2). MYH interacts with DNA repair proteins and localizes to DNA damage foci after oxidative damage (3). Research studies have shown that mutations in the corresponding MYH gene are associated with human gastric (4) and colorectal (5-7) cancers.
- Slupska, M.M. et al. (1996) J Bacteriol 178, 3885-92.
- Ohtsubo, T. et al. (2000) Nucleic Acids Res 28, 1355-64.
- Shi, G. et al. (2006) Biochem J 400, 53-62.
- Kobayashi, K. et al. (2008) Anticancer Res 28, 215-21.
- Bai, H. et al. (2007) Cancer Lett 250, 74-81.
- Pope, M.A. et al. (2005) DNA Repair (Amst) 4, 315-25.
- Wooden, S.H. et al. (2004) Cancer Lett 205, 89-95.
Application References
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For Research Use Only. Not For Use In Diagnostic Procedures.
