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A Bit of History...In the 1960s, melting of double-stranded DNA was monitored by UV absorbance (hyperchromic effect). Analysis required µg amounts of DNA, and often took hours to complete, while samples were slowly heated at rates of 0.1-1.0 ºC/min. Contemporary DNA melting analysis uses fluorescence, and because it is a more sensitive method, it needs only ng amounts of DNA (amounts easily prepared by PCR). Fluorescent DNA melting analysis became popular with the 1997 advent of the real-time PCR instrument LightCycler®. Capillary sample formats and small sample volumes allowed better temperature control and fast melting rates of 0.1-1.0ºC/sec, shortening the melting time to a few minutes. The fluorescence indicator used back in 1997 was the dye SYBR® Green I, a sensitive, convenient dye for real-time monitoring of amplification and melting of amplified products.New to Melting? Watch the High-Resolution Melting Webinar with Dr. Carl Wittwer (Biotechniques, 2017) High-resolution melting analysis is a novel method introduced in 2003. Similar to the LightCycler, this too was a result of collaboration between our lab at the University of Utah and Idaho Technology, Inc (Salt Lake City, UT). The method uses high data-density acquisition, and detects small sequence differences in PCR fragments, just by direct melting. Melting curves can now be used for mutation scanning, sequence matching, and mutliplex genotyping - analyses that traditionally required processing of PCR products by electrophoresis or other non-homogeneous means. Because of its speed and simplicity, popularity of this method is growing. Two inventions were key to high-resolution melting: 1) high-resolution instruments, and 2) novel saturation dyes. To read more, please follow the colored tabs in the navigation bar (top of page) .. Key references Contact us to receive reprints.
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