ライフサイエンスコーパス: ninhydrin

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1 the most traditional detection methods uses ninhydrin, a chemical that reacts with amino acids in th

2 roperoxides, vitamin K, ubiquinone, juglone, ninhydrin, alloxan, dehydroascorbate, DTNB, lipoic acid/

3 tterionic radical condensation products from ninhydrin and nitrogen-containing solvents may represent

4 e approaches: (i) a quantitative fluorescent ninhydrin assay for free lysine, (ii) matrix-assisted la

5 The use of the fluorescent ninhydrin assay to quantitatively detect free lysine hyd

6 ple, sensitive, and quantitative fluorescent ninhydrin assay, and results were confirmed by MALDI-TOF

7 anogens) in plants was studied using a novel ninhydrin-based spectrophotometric micromethod.

8 ent results due to the nonspecificity of the ninhydrin color reaction.

9 The ninhydrin-cyanide system obeys Beer's law in the range f

10 visualized using either standard procedures (ninhydrin development) or SIMS, and therefore the protoc

11 technique requiring twice the amount as the ninhydrin/GC/IRMS method.

12 In the second method (ninhydrin/GC/IRMS) the CO2 was purified by on-line GC.

13 (NIR) fluorescent polymers and then embedded ninhydrin into the Pdot matrix.

14 This new approach for using ninhydrin is combined with an optimized extraction proto

15 at the chromophore, i.e., the product of the ninhydrin-like reaction showing the blue color, is depro

16 EB) and 1,2-DATT (or AETT) could result from ninhydrin-like reactions, rather than the formation of p

17 ped by sequential four-component reaction of ninhydrin, malononitrile, primary amines, and dialkyl ac

18 In this study a ninhydrin method for measuring the total protein content

19 esent a modified approach to the traditional ninhydrin method.

20 uded 950 micrograms (leucine equivalents) of ninhydrin-positive material per day and 870 micrograms (

21 -carboxy-methylcysteine to the generation of ninhydrin-reacting components having the chromatographic

22 of arginase activity based on the ornithine-ninhydrin reaction.

23 liberation of carbon dioxide (CO2) using the ninhydrin reaction.

24 tent of tissue hydrolysates is presented.The ninhydrin reagent is stable at room temperature for up t

25 The conditions for ninhydrin reagent preparation were discussed.

26 The ninhydrin techniques require microgram quantities of leu

27 Ninhydrin (the fingerprint developing agent) spontaneous

28 Ninhydrin undergoes an unprecedented condensation reacti

29 ric estimation of the liberated proline with ninhydrin using acidic media and heat.

30 sed on photometric detection of ammonia with ninhydrin, was developed to study urease activity.

31 was observed in the condensation reaction of ninhydrin with 2-amino-N-phenylbenzamide derivatives hav

32 nalogous to that observed in the reaction of ninhydrin with amino acids to yield Ruhemann's Purple, t

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