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1 ion of I2 with subsequent analysis by liquid scintillation counting.
2 intravenous administration and up to 48 h by scintillation counting.
3 yer chromatography, and quantified by liquid scintillation counting.
4 cally added (65)Zn and subsequent whole-body scintillation counting.
5 sotope retention was monitored by whole-body scintillation counting.
6 nce liquid chromatography and quantitated by scintillation counting.
7 ioactivity of each fraction is determined by scintillation counting.
8 concentrations in the whole brain by liquid scintillation counting.
9 ing levels of [3H]thymidine incorporation by scintillation counting.
10 ed conjugate present is determined by liquid scintillation counting.
11 try and validated by whole-body potassium-40 scintillation counting.
12 sing radiolabeled substrate, extraction, and scintillation counting.
13 rophoretic separation and autoradiography or scintillation counting.
14 H-thymidine into nuclear DNA as monitored by scintillation counting.
15 ed by quantitative autoradiography and gamma-scintillation counting.
16 and radiolabel incorporation was assayed by scintillation counting.
17 remained at specified times was measured by scintillation counting.
18 ransported protein was quantitated by liquid scintillation counting.
19 substrate and the radioactivity measured by scintillation counting.
20 portions of lenses were determined by liquid scintillation counting.
21 aper and the radioactivity was determined by scintillation counting.
22 ts were quantified by metabolic labeling and scintillation counting.
23 radiometric measurement of trapped 14CO2 by scintillation counting.
24 ctivity concentration was measured by liquid scintillation counting.
25 labeled products and their identification by scintillation counting.
26 cid precipitation of the protein followed by scintillation counting.
27 ed by quantitative autoradiography, TLC, and scintillation counting.
28 n each sample is less than that required for scintillation counting.
29 unoprecipitation by HPLC with on-line liquid scintillation counting.
30 ody scintigraphy, autoradiography, and gamma scintillation counting.
31 hy, the 3H activity was determined by liquid scintillation counting.
32 tography (HPLC) with detection by continuous scintillation counting.
33 abeled DNA to the bead-immobilized enzyme by scintillation counting.
34 r, both as FeSO4, was measured by whole-body scintillation counting 13 d after oral administration.
35 as isolated, purified and analyzed by liquid scintillation counting, (2)H- or (13)C NMR or selective
36 ed with X-ray film and quantitated by liquid scintillation counting after extraction from the gels.
37 into the proteins, was quantitated by liquid scintillation counting after gel solubilization by H2O2.
38 Labelled peptides were detected by on-line scintillation counting after immunoprecipitation and HPL
39 bel into the fusion proteins was measured by scintillation counting after sodium dodecyl sulfate-poly
40 at five time points in tissue extracts using scintillation counting and 13C nuclear magnetic resonanc
41 olabeled chemical in conjunction with liquid scintillation counting and accelerator mass spectrometry
42 in food samples using ultra low-level liquid scintillation counting and alpha-particle spectrometry.
46 (1, 3, 7, 14, and 35 days) were analyzed by scintillation counting and HPLC to characterize the phar
47 on by mixed, undefined cultures using liquid scintillation counting and liquid chromatography with ra
48 both control and ARF rats, as detected using scintillation counting and whole-body ARG (10.56 +/- 1.0
49 d couples solid phase extraction with liquid scintillation counting, and scintillating anion exchange
51 ed by quantitative autoradiography and gamma-scintillation counting at 24 h after CED, 47.4% of the i
52 n from vinegar used in preparation of liquid scintillation counting cocktails for measurements of low
55 radiolabeled receptor-antibody complexes and scintillation counting enabled quantitation of the subty
56 tric approach using industry-standard liquid scintillation counting equipment that can both identify
57 values, measured experimentally using liquid scintillation counting, fit very well the expected value
58 wet chemistry digestion technique and liquid scintillation counting for (14)C activity measurements.
60 aphy-mass spectrometry, (13)C- and (1)H-NMR, scintillation counting, HPLC, gas chromatography-flame i
62 nstituted enzyme mixture, followed by liquid scintillation counting, indicated that [14C]-8-MOP bindi
64 specific elapsed time intervals using liquid scintillation counting (LSC) for nanomolar concentration
73 in-agarose beads) and quantitative analysis (scintillation counting) of only the biotinylated glycope
74 , and the supernatant was measured by liquid scintillation counting prior to injection on the HPLC to
77 as empirically determined by HPLC and liquid scintillation counting to be 24.4 Ci/mmol, approximately
78 tometrically, and cathepsin D (CD) by liquid scintillation counting using [14C] hemoglobin as substra
79 eins on a glass fiber filter for analysis by scintillation counting, was designed to be fast and accu
80 merit similar to those obtained with liquid scintillation counting were achieved by exploiting a sim
81 amples with 3H activities measured by liquid scintillation counting were utilized to develop and vali
83 se vial were calibrated using 4pibeta liquid scintillation counting with 3H-standard efficiency traci
84 h replaces the traditional radiolabeling and scintillation counting with fluorescent staining and dig
85 opriate region of the gel followed by liquid scintillation counting yields an isotope ratio which ref
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