ライフサイエンスコーパス: ammonium hydroxide

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1 e of solution containing sodium silicate and ammonium hydroxide.

2 7-ketol acetate side chain with aldehyde and ammonium hydroxide.

3 ts denuded of cells by treatment with 0.02 N ammonium hydroxide.

4 ent system consisting of chloroform:methanol:ammonium hydroxide (63:35:5), thereby permitting their s

5 se composed of chloroform:methanol:water:25% ammonium hydroxide (70:30:4:2 v/v/v/v), derivatization w

6 consisted of chloroform:methanol:acetone:25% ammonium hydroxide (75:15:10:1.6 v/v/v/v), derivatizatio

7 age from the solid support with concentrated ammonium hydroxide afforded the boranophosphopeptide and

8 solubilisation in aqua regia or tetramethyl ammonium hydroxide and simple dissolution in diluted HNO

9 ithin 15 min after combining uranyl nitrate, ammonium hydroxide, and hydrogen peroxide in aqueous sol

10 rmal reaction route using cerium nitrate and ammonium hydroxide as reactants.

11 which required deprotection in concentrated ammonium hydroxide at 55 degrees C for 15-18 h.

12 Here, we replace conventional ammonium hydroxide by tetramethylammonium hydroxide (TMA

13 umn introduction of dithiothreitol (DTT) and ammonium hydroxide, each disulfide-containing peptide el

14 etic acid extraction and neutralization with ammonium hydroxide followed by colorimetric detection at

15 n the other hand, in positive ion mode APCI, ammonium hydroxide forms ammonium adducts with carbohydr

16 In the negative ion mode, 50 mM ammonium hydroxide gave the greatest sensitivity for [M

17 holytic buffers, including ammonium formate, ammonium hydroxide, histidine, and arginine.

18 by a short treatment of the support with 5% ammonium hydroxide in methanol at room temperature, with

19 sical protease-serpin complexes (i.e., 1.5 m ammonium hydroxide in the presence of SDS).

20 ol/sodium hydroxide (MeOH/NaOH) and methanol/ammonium hydroxide (MeOH/NH4OH)].

21 in 28-30% NH4OH at 80 degrees C, or <1 h in ammonium hydroxide/methylamine (1:1) (AMA) at 80 degrees

22 a reagents, 2,2'-dipyridyl and tetra-n-butyl ammonium hydroxide (n-Bu4NOH or TBAH), are encapsulated

23 1) 3'-dephosphorylate quickly (9 h in 28-30% ammonium hydroxide (NH4OH) at 55 degrees C, 2 h in 28-30

24 Ammonium hydroxide or acetic acid was added to the mobil

25 U or in the presence of other bases, such as ammonium hydroxide or N-methylmorpholine, the same react

26 akes approximately 6-7 h before the standard ammonium hydroxide overnight incubation.

27 e F digestion was performed in 1:100 diluted ammonium hydroxide overnight.

28 ethacryloyloxy)ethyl dimethyl-(3-sulfopropyl)ammonium hydroxide] (PMEDSAH) that sustains long-term gr

29 ethacryloyloxy)ethyl dimethyl-(3-sulfopropyl)ammonium hydroxide] (PMEDSAH), which sustains long-term

30 The oligosaccharide yield from ammonium hydroxide-PNGase F digestion was better or equa

31 ion of ammonium until the pH reached 7 (with ammonium hydroxide) reduced the p'L,eff to <10(-9) atm a

32 s proposed to place reactive bags containing ammonium hydroxide solution (NH4OH) on the soil surface

33 methyl-1-imidazolyl)borate in a concentrated ammonium hydroxide solution at 85 degrees C.

34 Optimal results were obtained in 1 M ammonium hydroxide solution, in which cleavage is comple

35 was incubated in either phosphate buffer or ammonium hydroxide solutions at 40 and 60 degrees C for

36 >50 years) by removing native RPE cells with ammonium hydroxide to expose the RPE cell basal lamina (

37 ethyl isocyanate followed by aminolysis with ammonium hydroxide to form the desired phosphoramidate.

38 monstrated down to 100 ppb via reaction with ammonium hydroxide to produce the corresponding ammonium

39 ne of two ionization reagents, chloroform or ammonium hydroxide, to aid in ionization.

40 monium formate, ammonium acetate) and bases (ammonium hydroxide, triethylamine) under most conditions

41 f these protecting groups using concentrated ammonium hydroxide varied from 48 h at 55 degrees C to 2

42 [M + H + NH3]+, [M + Na]+, and [M + K]+ when ammonium hydroxide was added to the mobile phase.

43 M + NH3 + H]-, was formed as base peaks when ammonium hydroxide was added to the mobile phase.

44 An alkali wash of 0.3 M ammonium hydroxide was used to solubilize heme from spor

45 Treatment of 18 with ammonium hydroxide yielded diastereoisomeric mixtures of

46 Titration of indole with sodium hydroxide or ammonium hydroxide yields an increasing visible fluoresc

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