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1 of a functional RNA molecule (an aptamer for malachite green).
2 sual and spectrophotometric determination of malachite green.
3 vs) using derivatives of thiazole orange and malachite green.
4 latter via the phosphomolybdate complex with malachite green.
5 ing from the modified ascorbate procedure to malachite green.
6 methods were found to be better choices than malachite green.
7 posure to the cationic triphenylmethane dyes malachite green and brilliant green, tissue culture cell
8 ingerprints between farmed fish treated with malachite green and farmed fish treated with victoria pu
9 , phenol red, calcein, leuco crystal violet, malachite green, and a fluorescent dye for visual detect
10 compared to crystal violet, brilliant green, malachite green, and azure B with decolorization percent
11 nalyses of model dyes (e.g., crystal violet, malachite green, and rhodamine) and pharmaceutical compo
12 , comparing them with the standard CALI dye, malachite green; and we study the relative efficiencies
13                                    Using the malachite green aptamer (MGA) as a model system, we show
14                                      Using a malachite green aptamer as the output, a synthetic trans
15 iRNA, OnRS/Neg (scrambled RNA) and OnRS/MGA (malachite green aptamer)) were readily obtained from 1 l
16 tion, our results demonstrate the ability of malachite green as an excellent SHG-indicator of changes
17 copy using SHG-active antimicrobial compound malachite green as the probe molecule.
18 ontain increased amounts of ATP, whereas the Malachite green assay found elevated levels of free intr
19 substrate were 0.45 mm and 32 nmol/mg/min by malachite green assay, and 0.29 mm and 77 nmol/mg/min by
20 staining, radio-thin-layer chromatography, a malachite green assay, and ELISA.
21 lly characterized SerB2 enzyme and developed malachite green-based high throughput assay system to id
22 , FMN, and theophylline in combinations with malachite green binding aptamer as a signaling domain.
23 ynamics in RNA-small molecule complexes, the malachite green binding aptamer was studied.
24                                    Moreover, malachite green binds beta-arrestin2-GFP coated immunotr
25 ation of a heater dye, a metalloporphyrin or malachite green, bound to different binding sites in the
26 dy is the first to report the degradation of malachite green by P. veronii and the identification of
27                                              Malachite Green dye was used as an analyte to demonstrat
28 inorganic phosphate using Quinaldine red and Malachite green dyes and to the monitoring of alkaline p
29                         This strain degraded malachite green efficiently in a wide range of temperatu
30 nas veronii JW3-6, which was isolated from a malachite green enrichment culture.
31               The relative sensitivities are malachite green > crystal violet > quinaldine red > asco
32 od has been implemented for determination of malachite green in various sea fish samples.
33                                          The malachite green insulin was also covalently labeled with
34                                              Malachite green is a common environmental pollutant that
35                                In our assay, malachite green is used to measure orthophosphate (P(i))
36 ion region was observed in SERI detection of malachite green isothiocyanate (MGITC).
37 detection were established for test analytes malachite green isothiocyanate, 4-aminothiophenol, and R
38 hell nanoparticles in which the Raman label (malachite green isothiocyanate, MGITC) molecules are san
39                        The photochemistry of malachite green leuconitrile (MGCN), basic fuchsin leuco
40  and data processing on the determination of malachite green metabolites in two different organisms,
41                                          The Malachite green method of K. Itaya and M. Ui has adequat
42 sphate precipitation or the phosphomolybdate-malachite green method, this method is more sensitive.
43 ple cyanine (Cy3) donors coupled to a single malachite green (MG) acceptor that fluoresce only when t
44 e present study, the simultaneous removal of malachite green (MG) and auramine-O (AO) dyes from the a
45 ng relies on the activation of the fluorogen Malachite Green (MG) and can be used to label proteins s
46 d Raman studies of two organic chromophores, malachite green (MG) and its ITC derivative (MGITC), tha
47 st strip (dual-ICTS) was developed to detect malachite green (MG) and its metabolite, leucomalachite
48 emiquantitation of the triphenylmethane dye, Malachite Green (MG) and its primary metabolite Leucomal
49                                        Using malachite green (MG) as a model adsorption analyte, a li
50 y useful because it can be combined with the malachite green (MG) assay for inorganic phosphate to fo
51 activating protein is a VL domain that binds malachite green (MG) dye to activate intense fluorescenc
52  using ultrasonication for the adsorption of malachite green (MG) dye.
53              It enhances the fluorescence of malachite green (MG) dyes by a factor of more than 11,00
54 sor for adenosine based on the regulation of malachite green (MG) fluorescence, with comparable sensi
55 BI ligand and of the aptamer recognizing the malachite green (MG) ligand, the orthogonally triggered
56  economical mini-column method for detecting malachite green (MG) residue in fish was developed.
57 f RNA hairpins from the previously described malachite green (MG) RNA aptamer.
58  RNA aptamer that recognizes the chromophore malachite green (MG) with a high level of affinity, and
59 HG) was used to study both the adsorption of malachite green (MG), a positively charged organic dye,
60 he molecular transport of an organic cation, malachite green (MG), across large unilamellar dioleolyp
61 w that the MGA can protect its bound target, malachite green (MG), from oxidation over several days.
62 is B virus ribozyme, siRNA, and aptamers for malachite green (MG), spinach, and streptavidin (STV).
63 hromophore-assisted laser inactivation using malachite green (MG)-tagged antibodies makes it possible
64 tein A/G (pAG) conjugated with the fluorogen malachite green (MG).
65 tively binds to a set of substrates known as malachite green (MG).
66 , and a charged headgroup similar to that in malachite green (MG, 1).
67 ots (QDs), and the acceptor, dextran-binding malachite green (MG-dextran), was conjugated to concanav
68 nto unprecedented analogues of rhodamine and malachite green possessing a central eight-membered ring
69             Each retrieved gel is exposed to malachite green reagent gels differing in acidity and ox
70                                              Malachite green staining demonstrated that spores began
71                                          For malachite green, the calibration graph was linear in the
72 simple method makes it possible to determine malachite green visually in the concentration range 8-30
73                                              Malachite green was selected to optimize the assay becau
74 lybdate complex and subsequent reaction with malachite green, was used to measure the ATPase activity
75 ntermediate products from the degradation of malachite green were identified: leucomalachite green, 4
76                             The acceptor was malachite green which was covalently linked to insulin.
77 veronii JW3-6 could degrade 93.5% of 50 mg/L malachite green within seven days.