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Multiple fragmentation test

Multiple fragmentation test In this test, a single filament is embedded in a matrix resin and tested under tension until fragmentation into successive shorter lengths is complete and the fibre length has reached equilibrium. ... [Pg.173]

Multiple fragment impact test, propellant. NATO. [Pg.348]

A technique that has revolutionized the field of molecular biology during the last decade is the polymerase chain reaction (PCR). This method, conceived by Kary B. Mullis (1944—) in 1983, involves making multiple copies of fragments of DNA in a short time. Mullis received the 1993 Nobel Prize in chemistry for his work. PCR mimics DNA s natural ability to replicate itself It involves three basic steps conducted at different temperatures. In the first step, a mixture of DNA and other basic PCR ingredients is heated in a test tube to approximately 90°C. At this temperature, the DNA strands unwind. The second step involves lowering the temperature to around 55°C, which allows special enzymes called... [Pg.236]

Now you have to be creative and invent a series of structures that appear to satisfy all the spectroscopic criteria you have so far, and test each structure critically against the spectra. Predict the chemical shifts do they really match Predict all the multiple patterns do they match well Predict the NOEs and mass spectral fragmentation patterns and compare them with the experimental results. Discard any structures that clearly fail a test. Those that pass should be subjected to further, more searching tests. [Pg.7]

Fig. 9.2. Schematic illustration of the (Pa)g-barrel structure. The highly symmetrical structure presumably arose by multiple gene duplication events from a Pa-fragment. This hypothesis was tested using reverse engineering. Bisection of the barrel into two halves yielded correctly folded fragments which, upon heterodimerization, regained parental function. However, further fragmentation awaits experimental exploration. Fig. 9.2. Schematic illustration of the (Pa)g-barrel structure. The highly symmetrical structure presumably arose by multiple gene duplication events from a Pa-fragment. This hypothesis was tested using reverse engineering. Bisection of the barrel into two halves yielded correctly folded fragments which, upon heterodimerization, regained parental function. However, further fragmentation awaits experimental exploration.

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