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1 and removal of the DEPC-histidine adduct by sodium hydroxide.
2 release agents: puromycin, RNase A/EDTA, and sodium hydroxide.
3 tment with phenyllithium followed by aqueous sodium hydroxide.
4 line conditions using sodium borohydride and sodium hydroxide.
5 chloric acid as well as boiling concentrated sodium hydroxide.
6 ion from solutions of 137Cs dissolved in 1 M sodium hydroxide.
7 ed relative to controls receiving only 0.1 M sodium hydroxide.
8 ed meat sample was extracted with 30 mL of a sodium hydroxide (0.025 M) solution at 100 degrees C for
9 with methyl iodide in the presence of solid sodium hydroxide and can be totally avoided by treating
10 omprises an accelerated digestion step using sodium hydroxide and nitric acid in combination to diges
11 oration were oxidized with hydrogen peroxide/sodium hydroxide and the product alcohols were obtained
12 rom the high-level waste solids with aqueous sodium hydroxide, and then isolates the phosphate by pre
14 utions containing 4 microM PROLI/NO in 0.1 M sodium hydroxide at the rate of 1 nmol.min-1 immediately
15 pobromite (freshly prepared from bromine and sodium hydroxide) at 0 degrees C in 2:5 acetic acid/acet
16 d by treating the carbohydrate with powdered sodium hydroxide before introduction of methyl iodide un
17 njunction with shear force and at an optimal sodium hydroxide concentration we demonstrated a switchl
18 ol/L, 62.11min, 71.23 degrees C and 4.5g for sodium hydroxide concentration, extraction time, tempera
20 te constants (k2) for chemical reaction with sodium hydroxide, did not correlate to k(cat) for CinnAE
24 ation was found with strong alkali exposure (sodium hydroxide>ammonium, calcium hydroxide), even with
26 eaction of epichlorohydrin with concentrated sodium hydroxide in hexane under phase transfer conditio
27 lation reaction with methyl iodide and solid sodium hydroxide in methyl sulfoxide was used for the fi
29 ee hydroxyl group on serine and threonine by sodium hydroxide-induced beta-elimination has not been c
30 r component of sea-salt particles, show that sodium hydroxide is generated upon reaction of deliquesc
32 elimination of the epoxyglycidyl ether with sodium hydroxide may be operative and an alpha deprotona
33 aluated for two extraction methods [methanol/sodium hydroxide (MeOH/NaOH) and methanol/ammonium hydro
34 precipitate forms during N-acetyl-L-cysteine-sodium hydroxide (NALC-NaOH) decontamination, digestion,
35 ndard technique was N-acetyl-L-cysteine with sodium hydroxide (NALC-NaOH) treatment, smear concentrat
36 cal decontamination with N-acetyl-l-cysteine-sodium hydroxide (NALC-NaOH), alone and in combination w
37 Anion-exchange (AE) chromatography using sodium hydroxide (NaOH) and sodium acetate gradients, co
39 ated by the almost 2-fold greater amounts of sodium hydroxide needed to titrate noncatalytic montmori
40 thesized in the laboratory from zeolite A in sodium hydroxide, nitrate, and perrhenate solutions at 9
41 1 eyes) who sustained concomitant accidental sodium hydroxide ocular burns and received appropriate t
42 of FAE-III; (d) the rate of hydrolysis with sodium hydroxide of the methyl esters in general is decr
45 neutral hydroxylamine, hydrochloric acid, or sodium hydroxide released incorporated radiolabel which
47 e aims were to determine whether exposure to sodium hydroxide results in predictable changes in phosp
48 ng effect on the strength and selectivity of sodium hydroxide separation from alkaline aqueous salt s
49 issues of both the strains was determined by sodium hydroxide solubilization METHOD: The affinity of
50 droxide-soluble pectin fraction (DASS), a 1M sodium hydroxide-soluble hemicellulose fraction (1MASS),
51 soluble hemicellulose fraction (1MASS), a 4M sodium hydroxide-soluble hemicellulose fraction (4MASS)
52 ent-soluble pectin fraction (ChSS), a dilute sodium hydroxide-soluble pectin fraction (DASS), a 1M so
53 (grass) and CO2 collected by absorption into sodium hydroxide solution provide excellent time-integra
54 tion of parabens from chloroform into a 50mM sodium hydroxide solution within 10s facilitated their d
60 IS(6x)-HA(3x)-IAA1 proteins was sensitive to sodium hydroxide treatment, indicative of ubiquitin oxye
63 cal fluid extraction (SFE) and purified by a sodium hydroxide wash of the ethyl acetate eluting solve
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