Product Pathways - Cell Cycle / Checkpoint
MLH1 (4C9C7) Mouse mAb #3515
PhosphoSitePlus® protein, site, and accession data: MLH1
| Applications | Reactivity | Sensitivity | MW (kDa) | Isotype |
|---|---|---|---|---|
| W IP IF-IC F | H Mk | Endogenous | 85 | Mouse IgG1 |
Applications Key:
W=Western Blotting
IP=Immunoprecipitation
IF-IC=Immunofluorescence (Immunocytochemistry)
F=Flow Cytometry
Reactivity Key:
H=Human
Mk=Monkey
Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.
Protocols
Specificity / Sensitivity
MLH1 (4C9C7) Mouse mAb detects endogenous levels of total MLH1 protein.
Source / Purification
Monoclonal antibody is produced by immunizing animals with truncated recombinant MBP-MLH1.
Western Blotting
Western blot analysis of extracts from various cell types using MLH1 (4C9C7) Mouse mAb.
IP
MLH1 was immunoprecipitated from HeLa cell lysates using MLH1 (4C9C7) Mouse mAb. Western blot was performed using the same antibody. Lane 1 is 5% input.
Flow Cytometry
Flow cytometric analysis of IGROV-1 cells (red) and Jurkat cells (blue) using MLH1 (4C9C7) Mouse mAb.
Background
Mismatch repair (MMR), a conserved process that involves correcting errors made during DNA synthesis, is crucial to the maintenance of genomic integrity. MLH1 is the human homologue of the E. coli MMR gene mutL. MMR requires recognition of a base mismatch or insertion/deletion loop by a MutS homolog followed by recruitment of a MutL heterodimeric complex consisting of MLH1 and PMS1 (MutL-γ), PMS2 (MutL-α) or MLH3 (MutL-γ). Other factors required for MMR in eukaryotes are EXO1, PCNA, RFC, RPA, DNA polymerases and DNA ligase (reviewed in 1). Inactivation of the MLH1 gene causes genome instability and predisposition to cancer (2-5). The MLH1 gene is frequently mutated in hereditary nonpolyposis colon cancer (HNPCC) (6). MLH1 also plays a role in meiotic recombination (7).
- Modrich, P. (2006) J Biol Chem 281, 30305-9.
- Seng, T.J. et al. (2008) Br J Cancer 99, 375-82.
- Harley, I. et al. (2008) Gynecol Oncol 109, 384-7.
- Mao, G. et al. (2008) J Biol Chem 283, 3211-6.
- Hubner, R.A. and Houlston, R.S. (2007) J Natl Cancer Inst 99, 1490; author reply 1490-1.
- Vasen, H.F. (2005) Fam Cancer 4, 219-25.
- Argueso, J.L. et al. (2003) Mol Cell Biol 23, 873-86.
Application References
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For Research Use Only. Not For Use In Diagnostic Procedures.