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1  via a syringe-based interface mounted on an autosampler.
2 3 freeze-thaw cycles over 3 days, and on the autosampler.
3 servoir containing the IS solution using the autosampler.
4 pt for the transfer of the CE vial to the CE autosampler.
5 g batch sample processing and analysis in an autosampler.
6 utomation of the system using a conventional autosampler.
7 ab-sampling and 24-h-composited samples from autosamplers.
8 itations associated with the speed of common autosamplers.
9 ines and maintenance holes using compositing autosamplers.
10 column-switching system, constructed using 1 autosampler, 2 HPLC pumps, and a 10-port switching valve
11 0.99) and precision (CV < 15%), with short- (autosampler, 4 degrees C) and long-term (freezer, -20 de
12 degree of automation makes the developed EME-autosampler a powerful tool for a wide range of applicat
13 nnel surfaces (such as connection tubing and autosampler) accounted for up to 48% of TE loss.
14 this challenge, we have developed a nanoPOTS autosampler allowing fully automated sample injection fr
15 a 37 degrees C with a temperature-controlled autosampler and column oven.
16 hip, serves functionally as a combination of autosampler and nanoelectrospray ionization source.
17 uch as the stability of lycopene in the HPLC autosampler and the effect of saponification upon lycope
18 nd reagents are delivered by the pump or the autosampler and the reactions can be monitored by the UV
19 f two samples via dual injection ports on an autosampler and two completely independent flowpaths lea
20 (employing a micropump), automated (using an autosampler), and capillary HPLC modes of operation are
21 rocedures from residue methods, placed in an autosampler, and injected directly into a triple quadrup
22 omposed of one binary LC pumping system, one autosampler, and one mass spectrometer.
23 ized transfer vial with a drain port, and an autosampler arm to deliver liquid extract aliquots at de
24  calculation is the contribution made by the autosampler as an example of one type of error that is n
25 ans-lycopene in the HPLC mobile phase in the autosampler at 4 degrees C was determined to be approxim
26 de profile such as the residence time in the autosampler at 4 degrees C, stopping or not stopping the
27 d-catalyzed deamidation during storage in an autosampler at 5 degrees C and (b) a strong chaotropic a
28                  Analytes were stable on the autosampler, at room temperature, at 4 degrees C, and wh
29                                          The autosampler attaches to a standard ABI Procise sequencer
30              We use a prototype microfluidic autosampler, called the "gap sampler", to sequentially m
31                                 The nanoPOTS autosampler can provide analysis throughput of 9.6, 16,
32 rity, processing recovery and matrix effect, autosampler carryover, run size, stability, and data rep
33 , modified Cycle Composer software and a PAL autosampler controlled and operated the ITEX preconditio
34  dansylated derivative into the CTC-PAL Leap autosampler coupled to a Sciex API 4000 mass spectromete
35                                   Using four autosamplers coupled to one chromatographic column and o
36                                       As the autosampler drew sample solution, analytes were extracte
37 -dimension low-pH nanoLC separation using an autosampler equipped with a custom-machined syringe.
38 use of a commercially available multipurpose autosampler equipped with two microsyringes of different
39 shifts and variance in sample loading due to autosampler error.
40  did find minimal carryover contamination in autosampler field controls.
41 se microextraction workflow on the Concept96 autosampler followed by manual coupling of solid-phase m
42 of electro membrane extraction (EME) into an autosampler for high-throughput analysis of samples by E
43  similar to instruments using a conventional autosampler (for Bruker instruments, a BACS) although th
44                            While advances in autosamplers have alleviated some of these drawbacks, sa
45                        We conclude that eDNA autosamplers have potential to improve freshwater biosur
46 oupled to a gas chromatograph with headspace autosampler (HS-GC-MS/MS) was elaborated in this study.
47                                          The autosampler in Biacore 3000 permitted whole cells expres
48               Our strategy is based on rapid autosampler-in-needle-derivatization with p-toluenesulfo
49 the time for the chromatographic run and the autosampler injection sequence.
50 e used in a fully automated mode by using an autosampler injector.
51 into the injection loop using a conventional autosampler (injector) needle pickup from a sample vial.
52 tormwater events at 5 min intervals using an autosampler installed at the residential catchment outle
53 ry columns were interfaced with a commercial autosampler instrument using a novel procedure which all
54 mn length, given the current capabilities of autosampler instrumentation.
55 mn length, given the current capabilities of autosampler instrumentation.
56 es was performed automatically using an HPLC autosampler, involves minimal sample handling, thus mini
57 igh-performance liquid chromatography (HPLC) autosampler is used for automated sample preparation, in
58                                          The autosampler is used in combination with faster Edman cyc
59 ion of bacterial isolates and a computerized autosampler is used to make possible a large number of r
60         In-field performance of GFS equipped autosamplers is demonstrated using ground and streamwate
61  respectively; persistent carryover from the autosampler limited the LOQ achievable.
62  including both the column equilibration and autosampler movement.
63 cluding time for column re-equilibration and autosampler needle washing between each injection.
64  serve as self-powered pre-concentrators and autosamplers of analytes in ambient groundwater and as i
65 s the conversion of plants into self-powered autosamplers of arsenic from their environment.
66           Traditional sampling methods, like autosamplers or grab sampling, are not conducive to quic
67 duced into the OPSI using a widely available autosampler platform utilizing low cost disposable pipet
68                                 A commercial autosampler provides reproducible and unattended sample
69 s involved short-term deployments of an eDNA autosampler (Smith-Root) across a range of riverine habi
70 en 100 and 1000 ng/mL), and determination of autosampler stability (samples were stable for at least
71              Method validation included 24-h autosampler stability and one freeze-thaw cycle stabilit
72 samples when stored for 48 h at 4 degrees C (autosampler stability) and when reanalyzed after storage
73 racy and precision values, recovery studies, autosampler stability, and freeze-thaw stability.
74 o a luer lock adapter connected to a HTC PAL autosampler syringe.
75                                Employing the autosampler system for spatially resolved liquid extract
76 g monolithic column was incorporated into an autosampler system for the online extraction and cleanup
77          We have designed and implemented an autosampler that provides additional sample capacity on
78 rectly from the well plate with a commercial autosampler that was modified with a 10-port valve for c
79 rectly from the well plate with a commercial autosampler that was modified with a 10-port valve for c
80  serially into the capillary reactor from an autosampler, they react in parallel in the capillary rea
81 ple samples to multiple injectors allows the autosampler time to complete its wash cycles and aspirat
82 fully automated with the use of a commercial autosampler unit coupled to an ultrahigh performance liq
83  (GC) analysis by placing the disk into a GC autosampler vial containing 1 mL of N,O-bis(trimethylsil
84 trifuged, the supernate is transferred to an autosampler vial, and 10 microL is injected into the LC-
85 0 pg of protein (330 attomole) loaded in the autosampler vial.
86 emtomole virus particles) were loaded to the autosampler vial.
87 a 100 nM standard following storage in glass autosampler vials and only 1 nM of thiamine was obtained
88 plate setup, was adapted to use 1.5 mL glass autosampler vials instead, which facilitated sampling an
89 peak area was observed) versus polypropylene autosampler vials.
90                          A LEAP Technologies autosampler was customized to perform the automated samp
91 emonstration for single-cell proteomics, the autosampler was first applied to profiling protein expre
92 RSD, <10%; R(2), 0.994) and finally, the EME-autosampler was used to analyze in vitro conversion of m
93 g box designed and constructed in-house, the autosamplers were synchronized with the mass spectromete
94 tor system was established that replaces the autosampler with a four-port, two-position valve equippe
95  technique--the coupling of a headspace (HS) autosampler with a programmed temperature vaporizer (PTV
96                                           An autosampler with an integrated chromatography system was
97 signed to interface directly with commercial autosamplers (with no prior modification), suggesting th