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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.
In chain-growth (or chain) polymerization, the only chain-extension reaction step is the addition of a monomer to a growing chain with an active center such as a free radical, cation, or anion. Once the growth of a chain is initiated by formation of an active center, chain propagation is usually rapid by addition of a sequence of monomers.
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.
Instead an active propagating radical interchanges its role with a latent radical in a dormant complex. The activation of one polymer chain means the deactivation of another polymer chain. If the exchange process is much faster than the polymerisation rate (k p), effectively all polymer chains grow at the same rate. Because the large polymer ...
RAFT is a degenerative chain transfer process and is free radical in nature. RAFT agents contain di- or tri-thiocarbonyl groups, and it is the reaction with an initiator, usually AIBN, that creates a propagating chain or polymer radical. This polymer chain then adds to the C=S and leads to the formation of a stabilized radical intermediate.
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.
During polymerization, a polymer spends most of its time in increasing its chain length, or propagating. After the radical initiator is formed, it attacks a monomer (Figure 11). [8] In an ethene monomer, one electron pair is held securely between the two carbons in a sigma bond. The other is more loosely held in a pi bond. The free radical uses ...
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