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1 mparable to PCR but without requirement of a thermal cycler.
2 ively compared with that of the conventional thermal cycler.
3 lable kit and a novel method that utilises a thermal cycler.
4 n aluminum boat and then on the block of the thermal cycler.
5 med in an eight-capillary array in a hot-air thermal cycler.
6 during PCR amplification using an analytical thermal cycler.
7 g temperature (from 95 to 20 degrees C) in a thermal cycler.
8 at 37 degrees C, eliminating the need for a thermal cycler.
9 ntamination and lack of the requirement of a thermal cycler.
10 cycle times consistent with traditional PCR thermal cyclers.
11 lliptical pipette tip, a commercial portable thermal cycler, a smartphone, and a portable trans-illum
12 rovolume fluorimeter integrated with a rapid thermal cycler allows both amplification and point mutat
13 a microvolume fluorimeter integrated with a thermal cycler and a PCR-compatible double-stranded DNA
17 tion of more robust formats, improvements in thermal cyclers and labelling and detection methods.
19 ion (PCR) enjoys great popularity, expensive thermal cyclers are required for precise temperature con
22 on, on the other hand, obviates the use of a thermal cycler because reactions occur at a single tempe
23 n the use of a polymer-based continuous flow thermal cycler (CFTC) microchip for Sanger cycle sequenc
26 amplification methods alleviate the need for thermal cyclers; however, they still require continuous
27 each isolate, as generated on two different thermal cyclers, indicated that most of the seeming subs
29 ree emerging technologies: rapid cycling PCR thermal cyclers, peptide nucleic acid (PNA) probes, and
34 ults similar to that of a conventional block thermal cycler with leveling effects observed for amplic
35 onverting a desktop computer into a de facto thermal cycler with software that controls the temperatu
36 icated and evaluated high-throughput kinetic thermal cyclers with 768-reaction capacity for kinetic p