Author: Sharma, Nidhi; Hoshika, Shuichi; Hutter, Daniel; Bradley, Kevin M.; Benner, Steven A.
Title: Recombinaseâ€Based Isothermal Amplification of Nucleic Acids with Selfâ€Avoiding Molecular Recognition Systems (SAMRS) Cord-id: jm2xpn1w Document date: 2014_9_10
ID: jm2xpn1w
Snippet: Recombinase polymerase amplification (RPA) is an isothermal method to amplify nucleic acid sequences without the temperature cycling that classical PCR uses. Instead of using heat to denature the DNA duplex, RPA uses recombination enzymes to swap singleâ€stranded primers into the duplex DNA product; these are then extended using a strandâ€displacing polymerase to complete the cycle. Because RPA runs at low temperatures, it never forces the system to recreate baseâ€pairs following Watson–Cri
Document: Recombinase polymerase amplification (RPA) is an isothermal method to amplify nucleic acid sequences without the temperature cycling that classical PCR uses. Instead of using heat to denature the DNA duplex, RPA uses recombination enzymes to swap singleâ€stranded primers into the duplex DNA product; these are then extended using a strandâ€displacing polymerase to complete the cycle. Because RPA runs at low temperatures, it never forces the system to recreate baseâ€pairs following Watson–Crick rules, and therefore it produces undesired products that impede the amplification of the desired product, complicating downstream analysis. Herein, we show that most of these undesired side products can be avoided if the primers contain components of a selfâ€avoiding molecular recognition system (SAMRS). Given the precision that is necessary in the recombination systems for them to function biologically, it is surprising that they accept SAMRS. SAMRSâ€RPA is expected to be a powerful tool within the range of amplification techniques available to scientists.
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