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MagNA Pure Compact Instrument
For general laboratory use.
MagNA Pure LC 2.0 Instrument
For general laboratory use.
LightCycler® 480 Instrument II
Rapid high-throughput, plate-based real-time PCR amplification and detection instrument.
For life science research only. Not for use in diagnostic procedures.
LightCycler® 480 Block Kit 96 Silver
Easily interchangeable 96-well thermal block cycler unit for the LightCycler® 480 Instrument.
For life science research only. Not for use in diagnostic procedures.
LightCycler® 480 Block Kit 384 Silver
Easily interchangeable 384-well thermal block cycler unit for the LightCycler® 480 Instrument.
For life science research only. Not for use in diagnostic procedures.
Methylation-sensitive high-resolution melting
Nature Protocols, 3, 1903 - 1908
Methylation-sensitive high-resolution melting
Nature Protocols, 3, 1903 - 1908
Detection of seagull meat in meat mixtures using Real-time PCR analysis
Food Control, 34, 1, 47 - 49
Detection of seagull meat in meat mixtures using Real-time PCR analysis
Food Control, 34, 1, 47 - 49
Specific Amplification of Difficult PCR Products from Small Amounts of DNA Using FastStart Taq DNA Polymerase
High Pure PCR Cleanup Micro Kit
Add more flexibility to nucleic acid purification - quickly and efficiently purify products from PCR and other reactions.
Mutation Detection Using Multi-color Detection on the LightCycler System
The LightCycler System is a powerful tool for amplifying and quantitating PCR products in a very short time (Wittwer et al. 1997). By using melting curve analysis, the system also provides a unique and innovative approach for the detection of single nucleotide polymorphisms.
Quantitative PCR by Continuous Fluorescence Monitoring of a Double Strand DNA-Specific Binding Dye
A simple method for quantitative PCR using the LightCyclerTM and the dsDNA binding dye SYBR® Green I Dye is demonstrated. The method has a dynamic range of at least six orders of magnitude and a sensitivity of a single copy per reaction. Two methods for removing the confounding signal from nonspecific amplification products are described. The method is suitable for both DNA and RNA quantification.
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Confirm the presence of a specific target, with high-specificity qualitative detection using products from the Roche workflow.
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