Quick Order |All Online Ordering|Product Catalog Ordering|Oligo Modifications List|Product Info & Literature|Oligo Design Tools/Resources

O6 Methyl dG

O6 Methyl dG

Code : [O6-Me-dG]

Search Modifications Modified Oligos Quick Price Estimate
picture of O6 Methyl dG

Modification : O6 Methyl dG

Catalog Reference Number
Modification Code
5 Prime
3 Prime
Molecular Weight (mw)
Extinction Coeficient (ec)
Technical Info (pdf)
Absorbance MAX
Emission MAX
Absorbance EC

Minor Bases

Catalog NoScalePrice
26-6409-0550 nmol$416.00
26-6409-02200 nmol$416.00
26-6409-011 umol$551.00
26-6409-032 umol$416.00
26-6409-065 umol$2,479.50
26-6409-1010 umol$1,769.00
26-6409-1515 umol$2,211.00
Discounts are available for O6 Methyl dG!
Modification* Discount Price Structure
1 site/order List price
2 sites/order 10% discount
3 sites/order 20% discount
4 sites/order 30% discount
5-9 sites/order 50% discount
10+ sites/order 60% discount
*Exceptions apply

O6-Methyl-deoxyguanosine (O6-Me-dG) is classified as an O-alkyl purine, and O6-Me-dG-modified oligonucleotides are primarily used in studies of the role of DNA alkylating agents in mutagenesis and carcinogenesis, and in studies into possible enzymatic mechanisms involved in repair of DNA alkylation damage. Both in vitro and in vivo, O6-Me-dG DNA lesions are formed by reaction with N-nitrosamines (known carcinogens), particularly those found in tobacco smoke (for example, 4-(methylnitrosamine)-1-(3-pyridyl)-1-butanone (NNK)) (1,2). O6-Me-dG is highly mutagenic due to its strongly mis-pairing characteristics (DNA polymerases preferentially insert thymine opposite O6-Me-dG, leading to G-to-A transitions) (3). Generation of O6-Me-dG lesions in the K-ras proto-oncogene or p53 gene results in activation of the proto-oncogene or inactivation of p53, leading to loss of control over cell growth and cancer (4).O6-Me-dG lesions are repaired by the specialize repair protein O6-alkylguanine DNA alkyltransferase (AGT), which removes the methyl group (as well as other alkyl groups) from O6 via a "suicide" inactivation mechanism, thereby restoring the natural guanine base (5).

1. Hecht, S.S. Tobacco smoke carcinogens and lung cancer. J. Natl. Cancer. Inst. (1999), 91: 1194-1210.
2. Hoffmann, D., Brunnemann, K.D., Prokopczyk, B., Djordjevic, M.V. Tobacco-specific N-nitrosamines and Areca-derived N-nitrosamines: chemistry, biochemistry, carcinogenicity, and relevance to humans. J. Toxicol. Environ, Health (1994), 41: 1-52.
3. Warren,, J.J., Forsberg, L.J., Beese, L.S. The structural basis for the mutagenicity of O6-methyl-guanine lesions. Proc. Natl. Acad. Sci. USA (2006), 103: 19701-19706.
4. Zochbauer-Muller, S., Gazdar, A.F., Minna, J.D.. Molecular pathogenesis of lung cancer. Annual Review of Physiology (2002), 64: 681-708.
5. Zang, H., Fang, Q., Pegg, A.E., Guengerich, F.P. Kinetic analysis of steps in the repair of damaged DNA by human O6-alkylguanine-DNA alkyltransferase. J. Biol. Chem. (2005), 280: 30873-30881.
- O6 Methyl dG

Oligonucleotide Synthesis |  Flourescent Molecular Probes |  Gene Detection Systems |  Tools & Reagents |  Gene Assays |  RNAi
© 2024 Gene Link |  Terms & Conditions |  Licenses |  Privacy Policy |  July 21, 2024 3:13:33 AM