ライフサイエンスコーパス: malachite green

1 of a functional RNA molecule (an aptamer for malachite green).

2 vs) using derivatives of thiazole orange and malachite green.

3 latter via the phosphomolybdate complex with malachite green.

4 ing from the modified ascorbate procedure to malachite green.

5 methods were found to be better choices than malachite green.

6 posure to the cationic triphenylmethane dyes malachite green and brilliant green, tissue culture cell

7 , comparing them with the standard CALI dye, malachite green; and we study the relative efficiencies

8 Using the malachite green aptamer (MGA) as a model system, we show

9 Using a malachite green aptamer as the output, a synthetic trans

10 iRNA, OnRS/Neg (scrambled RNA) and OnRS/MGA (malachite green aptamer)) were readily obtained from 1 l

11 substrate were 0.45 mm and 32 nmol/mg/min by malachite green assay, and 0.29 mm and 77 nmol/mg/min by

12 staining, radio-thin-layer chromatography, a malachite green assay, and ELISA.

13 lly characterized SerB2 enzyme and developed malachite green-based high throughput assay system to id

14 , FMN, and theophylline in combinations with malachite green binding aptamer as a signaling domain.

15 ynamics in RNA-small molecule complexes, the malachite green binding aptamer was studied.

16 Moreover, malachite green binds beta-arrestin2-GFP coated immunotr

17 ation of a heater dye, a metalloporphyrin or malachite green, bound to different binding sites in the

18 Malachite Green dye was used as an analyte to demonstrat

19 inorganic phosphate using Quinaldine red and Malachite green dyes and to the monitoring of alkaline p

20 The relative sensitivities are malachite green > crystal violet > quinaldine red > asco

21 The malachite green insulin was also covalently labeled with

22 In our assay, malachite green is used to measure orthophosphate (P(i))

23 ion region was observed in SERI detection of malachite green isothiocyanate (MGITC).

24 detection were established for test analytes malachite green isothiocyanate, 4-aminothiophenol, and R

25 hell nanoparticles in which the Raman label (malachite green isothiocyanate, MGITC) molecules are san

26 The photochemistry of malachite green leuconitrile (MGCN), basic fuchsin leuco

27 The Malachite green method of K. Itaya and M. Ui has adequat

28 sphate precipitation or the phosphomolybdate-malachite green method, this method is more sensitive.

29 ple cyanine (Cy3) donors coupled to a single malachite green (MG) acceptor that fluoresce only when t

30 ng relies on the activation of the fluorogen Malachite Green (MG) and can be used to label proteins s

31 d Raman studies of two organic chromophores, malachite green (MG) and its ITC derivative (MGITC), tha

32 emiquantitation of the triphenylmethane dye, Malachite Green (MG) and its primary metabolite Leucomal

33 Using malachite green (MG) as a model adsorption analyte, a li

34 y useful because it can be combined with the malachite green (MG) assay for inorganic phosphate to fo

35 activating protein is a VL domain that binds malachite green (MG) dye to activate intense fluorescenc

36 It enhances the fluorescence of malachite green (MG) dyes by a factor of more than 11,00

37 sor for adenosine based on the regulation of malachite green (MG) fluorescence, with comparable sensi

38 economical mini-column method for detecting malachite green (MG) residue in fish was developed.

39 RNA aptamer that recognizes the chromophore malachite green (MG) with a high level of affinity, and

40 HG) was used to study both the adsorption of malachite green (MG), a positively charged organic dye,

41 he molecular transport of an organic cation, malachite green (MG), across large unilamellar dioleolyp

42 w that the MGA can protect its bound target, malachite green (MG), from oxidation over several days.

43 is B virus ribozyme, siRNA, and aptamers for malachite green (MG), spinach, and streptavidin (STV).

44 hromophore-assisted laser inactivation using malachite green (MG)-tagged antibodies makes it possible

45 tein A/G (pAG) conjugated with the fluorogen malachite green (MG).

46 , and a charged headgroup similar to that in malachite green (MG, 1).

47 ots (QDs), and the acceptor, dextran-binding malachite green (MG-dextran), was conjugated to concanav

48 Malachite green staining demonstrated that spores began

49 Malachite green was selected to optimize the assay becau

50 lybdate complex and subsequent reaction with malachite green, was used to measure the ATPase activity

51 The acceptor was malachite green which was covalently linked to insulin.