MDQ1

Step-wise protocol for using (Cat. No. MDQ1)

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MDQ1

Sigma

 

Imprint® Methylated DNA Quantification Kit

Description

Frequently Asked QuestionsLive Chat and Frequently Asked Questions are available for this Product.
Features and Benefits• ELISA based format
• Procedure completes in 4 easy to follow steps
• All reagents supplied including control methylated DNA
• Detection limit is 5 ng of fully methylated DNA
• Input DNA may be as low as 10-200 ng
• Procedure completes in 3.5 hours
• 96 well format allows option of studying single samples or high-throughput studies
• May be used with cells, tissues, plasma and other body fluids
General descriptionImprint™ Methylated DNA Quantification technology provides a rapid and reliable method to measure global DNA methylation shifts. The Imprint Methylated DNA Quantification Kit contains all reagents required to detect relative levels of methylated DNA. Up to 200 ng of purified DNA is bound to the wells of the assay strip. The methylated DNA is detected using the Capture and Detection antibodies, then quantified colorimetrically. The amount of methylated DNA present in the sample is proportional to the absorbance measured.
Legal InformationImprint is a registered trademark of Sigma-Aldrich Biotechnology LP and Sigma-Aldrich Co.

Safety

Hazard CodesXn
Risk Statements20/21/22-33
Safety Statements36/37

Components

Kit component only10x Wash Buffer
 DNA Binding Solution
 Methylated Control DNA (50 ng/μL)
 Block Solution
 Capture Antibody
 Detection Antibody
 Developing Solution
 Stop Solution
 8 well Assay Strips

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References

referenceThaler, R., et al., Epigenetic regulation of human buccal mucosa mitochondrial superoxide dismutase gene expression by diet. Br. J. Nutr. 7, 1-7, (2008)
 Suzuki, M., et al., Zebularine-induced reduction in VEGF secretion by HIF-1a degradation in oral squamous cell carcinoma. Molec. Med. Rep. 1, 465-471, (2008)
 Novikova, S.I., et al., Maternal cocaine administration in mice alters DNA methylation and gene expression in hippocampal neurons of neonatal and prepubertal offspring. PLoS ONE 3(4), e1919, (2008)
 Liu, C., et al., Plasma S-adenosylhomocysteine is a better biomarker of atherosclerosis than homocysteine in apolipoprotein E-deficient mice fed high dietary methionine. J. Nutr. 138(2), 311-315, (2008)