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1 sults from the Cavidi v1.0, Cavidi v2.0, and Perkin-Elmer, and the Perkin-Elmer Plus external buffers
2 igned column of DNA bases and the underlying Perkin Elmer Applied Biosystems (ABI) fluorescent traces
3 s model 377 (ABI PRISM Linkage Mapping Sets; Perkin Elmer Applied Biosystems), by use of fluorescence
4 lif.), and 16S rRNA gene sequence (MicroSeq; Perkin-Elmer Applied Biosystems Division, Foster City, C
5 y TaqMan PCR on the ABI PRISM 7700 Analyzer (Perkin-Elmer Applied Biosystems, Foster City, Calif.).
6 nto polyacrylamide gels for detection in the Perkin Elmer/Applied Biosystems (PE/ABI) 373 and 377 DNA
7 scence (HTRF(R); Cisbio) and AlphaScreen(R) (Perkin Elmer) assays, an FP-based assay was chosen to sc
8 tive typing system (MicroSeq StaphTrack Kit; Perkin-Elmer Biosystems) based on the sequence analysis
9 e MicroSeq 500 16S bacterial sequencing kit (Perkin-Elmer Biosystems, Foster City, Calif.), which is
10 w fluorogenic probe-based PCR assay (TaqMan; Perkin Elmer Corp./Applied Biosystems, Foster City, Cali
11 e TaqMan LS50B fluorogenic detection system (Perkin-Elmer Corp., Applied Biosystems, Foster City, Cal
12 Fluorogenic probe-based PCR assays (TaqMan; Perkin-Elmer Corp., Applied Biosystems, Foster City, Cal
13 ng fluorescently labeled PCR primers and the Perkin-Elmer DNA sequencer so that unknown-specimen fing
16 v1.0, Cavidi v2.0, and Perkin-Elmer, and the Perkin-Elmer Plus external buffers all correlated well w
17 ectrothermal Atomic Absorption Spectrometry (Perkin Elmer, SIMAA 6000) was developed and validated.
20 microtiter dish with rapid filtration onto a Perkin Elmer unifilter GF/B plate using a Perkin Elmer F
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