コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 lt to identify the charge variants in a cIEF electropherogram.
2 diagonal in a reconstructed two-dimensional electropherogram.
3 rate spots that fall off the diagonal in the electropherogram.
4 dard deviation of under 5% for the total ion electropherogram.
5 surface was fit to a set of 20 spots in each electropherogram.
6 electropherogram to generate a contour plot electropherogram.
7 g 40% relative standard deviation across the electropherogram.
8 d producing the equivalent of a conventional electropherogram.
9 of 0.28 in the conventional one-dimensional electropherogram.
10 spectra of each of the eluting peaks in the electropherogram.
11 antibody charge variants observed in a cIEF electropherogram.
12 were calculated from their peak areas in the electropherogram.
13 sing peak areas generated from extracted ion electropherograms.
14 exes with DNA, giving distorted peaks in the electropherograms.
15 imaging system are converted to conventional electropherograms.
16 y separated experimentally in the form of an electropherogram, achieving a separation resolution of 1
17 tetrapeptide was obtained directly from the electropherogram and used in the calculation of the DNA-
19 Historically, SHAPE data was collected on electropherograms and change in structure was evaluated
20 to deconvolute the components present in the electropherograms and classify the quinoa varieties acco
21 ontactless conductivity detection (CE-C(4)D) electropherograms and interference-free electrospray ion
22 in silico by using computer-simulated NECEEM electropherograms and then applied it to experimental de
23 ts the data quality and repeatability of the electropherograms, and we demonstrate an automatic hando
25 entified in eight parallel channels when the electropherograms are compared with that of the standard
26 y axes should be changed when the time scale electropherograms are modified to get the distributions.
29 affinity to these motifs is observed in the electropherograms as a change in peak width, which when
30 samples were found to produce representative electropherograms as a single hand-dissected brain sampl
33 lecules should generate very narrow peaks in electropherograms, because longitudinal diffusion was th
35 obility of each DNA extension product in the electropherogram coded the SNPs without the use of a siz
40 erotonin-related analytes from a single-cell electropherogram demonstrates the performance of such a
42 localized to the nucleus was detected on the electropherogram following laser-mediated disruption of
50 upole system provided acceptable ion current electropherograms from fmole levels from analytical stan
52 upole system provided acceptable ion current electropherograms from subpicomole levels of the targete
53 odel is validated by its application for the electropherograms from the diffusion path of a set of pr
54 apillary electrophoresis based on time-scale electropherograms generally uses time-corrected peak are
56 ber information from standard dye-terminator electropherograms has been little explored, yet this tec
57 s the N-glycan, the peak disappears from the electropherogram, identifying the N-glycan structure.
58 ples analyzed directly, producing a detailed electropherogram in only 120 s on a microfabricated glas
60 unsubstituted rhodamine terminators produced electropherograms in which weak G peaks are observed aft
61 ass detector, all the peaks in the total ion electropherograms, including some totally or partially u
63 oated silica capillary, and the shape of the electropherogram indicated the efficiency is limited by
65 much more relevant to change the time-scale electropherograms into mass relative distribution of the
66 o-dimensional correlation CE, a conventional electropherogram is spread into two dimensions through c
68 encing cause background noise in fluorescent electropherograms, leading to errors in sequence determi
69 e migration order and spacing of peaks in CE electropherograms measured under the same conditions.
74 hows the presence of additional peaks in the electropherogram of the cancer patient that could be ass
75 use of this integrated microfluidic device, electropherograms of amino acids from individual Jurkat
76 k attributable to dopamine was identified in electropherograms of brain microdialysate samples obtain
81 his combination resulted in the most uniform electropherogram profiles, superior to those produced by
86 n time was between 2 and 3% for selected ion electropherograms (SIEs) generated for six ions; median
87 /reTOFMS combination, resulting in total ion electropherograms similar to those obtained using UV abs
88 ver 60 additional peaks were detected in the electropherograms, suggesting the potential for monitori
90 sfully identify components seen in UV or LIF electropherograms, thereby expanding the capability of C
92 This finding was attributed to the use of electropherograms to detect artifacts such as aggregator
93 quired to perform the variable change on the electropherogram was developed with an emphasis on the f
94 d CE separation efficiency for the SIM CE/MS electropherograms was determined to be 2860 plates (peak
95 >90% increase in area under the curve of the electropherograms was observed with the interface compar
96 Additional properties exhibited in the CE electropherograms were also explained using the computer
98 ragments were precisely sized (+/-1 bp), and electropherograms were generated for each genome with Ge
100 d the monitoring of overlapping peaks in the electropherogram when newly formed products resulting fr
101 B using the new device produced a CE-ESI-MS electropherogram with a signal-to-noise ratio of over 10
104 of the PCR products were determined from the electropherogram without using a calibration plot and cu