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A real-time polymerase chain reaction (real-time PCR, or qPCR when used quantitatively) is a laboratory technique of molecular biology based on the polymerase chain reaction (PCR). It monitors the amplification of a targeted DNA molecule during the PCR (i.e., in real time), not at its end, as in conventional PCR. Real-time PCR can be used ...
A strip of eight PCR tubes, each containing a 100 μL reaction mixture Placing a strip of eight PCR tubes into a thermal cycler. The polymerase chain reaction (PCR) is a method widely used to make millions to billions of copies of a specific DNA sample rapidly, allowing scientists to amplify a very small sample of DNA (or a part of it) sufficiently to enable detailed study.
The addition−fragmentation chain-transfer process was first reported in the early 1970s. [3] However, the technique was irreversible, so the transfer reagents could not be used to control radical polymerization at this time. For the first few years addition−fragmentation chain-transfer was used to help synthesize end-functionalized polymers.
One of the key characteristics of a living polymerization is that the chain termination and transfer reactions are essentially eliminated from the four elementary reactions of chain-growth polymerization leaving only initiation and (chain) propagation reactions. A key characteristic of living polymerization is that the rate of initiation ...
Living cationic polymerization is a living polymerization technique involving cationic propagating species. [1] [2] It enables the synthesis of very well defined polymers (low molar mass distribution) and of polymers with unusual architecture such as star polymers and block copolymers and living cationic polymerization is therefore as such of commercial and academic interest.
Chain-growth polymerization or chain-growth polymerisation is a polymerization technique where monomer molecules add onto the active site on a growing polymer chain one at a time. [1] There are a limited number of these active sites at any moment during the polymerization which gives this method its key characteristics.
Digital polymerase chain reaction (digital PCR, DigitalPCR, dPCR, or dePCR) is a biotechnological refinement of conventional polymerase chain reaction methods that can be used to directly quantify and clonally amplify nucleic acids strands including DNA, cDNA, or RNA.
Repeated applications of polymerase could lead to a chain reaction of replication for a specific segment of the genome – PCR. Later in 1983 Mullis began to test his idea. His first experiment [2] did not involve thermal cycling – he hoped that the polymerase could perform continued replication on its own. Later experiments that year ...