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1 site polarity with modifier addition (0.9 mM ammonium acetate).
2 lutions of intermediate salt content (150 mM ammonium acetate).
3  with external countercurrent flow of 2.5 mM ammonium acetate.
4 uctures and single-strand controls in 100 mM ammonium acetate.
5  following 24-hour and 48-hour withdrawal of ammonium acetate.
6 on with subsequent one-pot condensation with ammonium acetate.
7 oteins using MS-compatible concentrations of ammonium acetate.
8 propanol in the ratio of 85:15:33 with 0.01% ammonium acetate.
9 om chalcones, beta-dicarbonyl compounds, and ammonium acetate.
10 cuum centrifuge, and reconstituted in 200 mM ammonium acetate.
11 acetonitrile plus 0.1% formic acid and 25 mM ammonium acetate.
12 sed of CO2/methanol solvent with addition of ammonium acetate.
13  6-aminopyrimidine in acetic acid containing ammonium acetate.
14 nt elution with a mobile phase consisting of ammonium acetate 0.05 M and acetonitrile at 25 degrees C
15 y medium (acetonitrile/water 1:1 v/v, 5.0 mM ammonium acetate, 0.75 vol % acetic acid) and was oxidiz
16 t for injection was found to be a mixture of ammonium acetate 2 mM/acetonitrile (60/40 ; v/v).
17                                              Ammonium acetate (5 mM) was added to the mobile phase to
18 phases containing acetonitrile and additives ammonium acetate (90:10, v/v, pH 6.1) or formate (90:10,
19       Rats given a long-term diet of 20 g/dL ammonium acetate (AmAc) in rat chow or 0.1% iodoacetamid
20  its utility, the predominant "buffer" used, ammonium acetate (AmAc) with pK(a) values of 4.75 for ac
21 urification or storage buffer, often aqueous ammonium acetate (AmAc).
22 istribution of BSA is narrow (+14 to +18) in ammonium acetate (AmmAc), whereas it is much broader (+1
23 f sample flow rate and various electrolytes (ammonium acetate, ammonium bicarbonate, ammonium formate
24          We compared three volatile buffers (ammonium acetate, ammonium bicarbonate, and ammonium for
25 er sized capillaries for complexes in 100 mM ammonium acetate and 100 mM triethylammonium acetate and
26       The HILIC mobile phase contained 25 mM ammonium acetate and allowed identifying impurities at l
27 plexes were analyzed in solutions containing ammonium acetate and selected trialkylamines or diaminoa
28 , we treated Suwannee River NOM (SRNOM) with ammonium acetate and sodium cyanoborohydride to convert
29 om readily available 2-alkynylbenzamides and ammonium acetate and takes place under mild reaction con
30                         The concentration of ammonium acetate and the cone voltage are major factors
31 )-ones with enamines (generated in situ from ammonium acetate and the corresponding methylaryl(hetary
32 wo protic ionic liquids, (bis(2-hydroxyethyl)ammonium acetate and triethylammonium acetate).
33 th molecular masses in the 5-76 kDa range in ammonium acetate and triethylammonium bicarbonate are in
34 ion, as did neutral salts (ammonium formate, ammonium acetate) and bases (ammonium hydroxide, triethy
35 bromoarylaldehydes and terminal alkynes with ammonium acetate, and a variety of substituted isoquinol
36 ally, we examined HEPES, Tris, MES, citrate, ammonium acetate, and phosphate-buffered saline (PBS) an
37               For example, 20 mM HEPES, MES, ammonium acetate, and Tris are found to consume 1 mM hyp
38 ew approach is based on the use of 0.3 mol/L ammonium acetate as a representative salt of a weak acid
39  and aromatic/heteroaromatic aldehydes using ammonium acetate as an ideal promoter under neat conditi
40                                     By using ammonium acetate as the dialysis buffer, it was also fou
41 embrane proteins in nanodiscs simply require ammonium acetate as the mobile phase.
42 s of benzoxazole derivatives from catechols, ammonium acetate as the nitrogen source, and aldehydes (
43                                           An ammonium acetate assisted gold-catalyzed cascade cycliza
44 tomosis, anesthetized rats were infused with ammonium acetate at 33 degrees, 35 degrees, and 37 degre
45  interactions were effectively avoided using ammonium acetate at ionic strengths above 0.1 M.
46 s a self-coating reagent in conjunction with ammonium acetate at pH approximately 7.4, narrow capilla
47              For example, in the presence of ammonium acetate, at low flow rates, lower charge states
48 bile phase of acetonitrile, formic acid, and ammonium acetate, at pH 3.6.
49 tic capillary coating in combination with an ammonium acetate-based electrolyte at physiological pH e
50                                              Ammonium acetate buffer (0.5 M) was associated with the
51 le for at least 8 days after the addition of ammonium acetate buffer (pH 5.5).
52                       Spraying the sample in ammonium acetate buffer (pH 7) using a jet stream source
53 ns of poly(ethylene glycol) (PEG) in a 10 mM ammonium acetate buffer are electrosprayed, and the maxi
54 ted the IMP 241 bivalent hapten-peptide with ammonium acetate buffer at pH 4-5 and eluted the (68)Ga
55 2A-peptide can be labeled with 64Cu in 0.1 M ammonium acetate buffer in 2 h at 95 degrees C.
56  requires the incubation of 64CuCl2 in 0.1 M ammonium acetate buffer with the TETA-peptide for 30 min
57 environment (0.01 M dithiothreitol in pH 7.0 ammonium acetate buffer), the PLCys features resembled i
58 e identified as: 30-min reaction time, 0.5 M ammonium acetate buffer, pH 7-7.5 and 37 degrees C.
59 umab, and trastuzumab emtansine with a 50 mM ammonium acetate buffer, this new hydrophilic chromatogr
60  filter and by dialysis into a 10 mM aqueous ammonium acetate buffer.
61 unretained while the NPs are separated by an ammonium acetate buffered methanol-water eluent, compati
62  mobile phase system was found comparable to ammonium acetate buffers in application to ACE chromatog
63 high concentrations of sodium, as opposed to ammonium acetate buffers.
64 equipment, and its consumables are primarily ammonium acetate buffers.
65  report here that addition of high levels of ammonium acetate can improve analyte signal in aqueous e
66 th a gradient elution by using methanol -5mM ammonium acetate containing formic acid (pH 3.5).
67       DLPs were transferred to 10 mM aqueous ammonium acetate, electrosprayed into the gas phase, con
68 ically labeled amines by using (15)N-labeled ammonium acetate, facilitating the identification of rea
69  15.2 muL, a maximum concentration of 200 mM ammonium acetate flowing at 0.25 mL/min was converted in
70 es in C2C12 murine myotubes to withdrawal of ammonium acetate following 24-hour exposure to 10 mM amm
71           Diluting the lysed blood sample in ammonium acetate for a minimum of 6 h before injecting t
72 novel technique employs a mobile phase 50 mM ammonium acetate for high sensitivity in MS and elution
73   NaAc is more inhibitory than potassium and ammonium acetate for Z. mobilis and the combination of e
74 tivated carbohydrates, oxoacetonitriles, and ammonium acetate gave densely functionalized pyrroles in
75                 After generator elution, the ammonium acetate generator eluent (15-20 mL) is passed t
76  small volume ( approximately 500 muL) of an ammonium acetate/HCl (pH 4.5) solution suitable for dire
77  MBq of (44)Sc in a volume of 200-400 muL of ammonium acetate/HCl solution (1 M, pH 3.5-4.0) within 1
78 th neutral, hydrophilic coating, using 50 mM ammonium acetate in 20% methanol (pH 3.1) as the backgro
79 umn as the stationary phase and 8 mmol L(-1) ammonium acetate in 22%v/v methanol solution (pH 4) as t
80 ong anion exchange column eluted with 100 mM ammonium acetate in 50:50 (v/v) acetonitrile/water was i
81 patible mobile phase consisting of 20 mmol/L ammonium acetate in a 1:1 water-acetonitrile mixture.
82 se column using a linear gradient of 5-20 mM ammonium acetate in a mobile phase consisting of hexane,
83 itive mobile-phase strategy (formic acid and ammonium acetate in aqueous and organic phase, respectiv
84                         A key role played by ammonium acetate in chemoselectivity has been examined.
85 tic aldehydes with 2,2'-dipyridyl ketone and ammonium acetate in hot acetic acid provides ready acces
86 emic form by employing indole-isonitrile and ammonium acetate in the Ugi 4-center-3-component reactio
87   Moreover, relative to ammonium formate and ammonium acetate in water-rich methanol modifier, the am
88 ueous solution buffered to pH 6.8 with 20 mM ammonium acetate, in the DT IM-MS instrument, each buffe
89 M to approximately 0.35 mM by an intravenous ammonium acetate infusion.
90 to its respective acid or base, for example, ammonium acetate into acetic acid.
91                                              Ammonium acetate is a commonly used additive, despite it
92                                              Ammonium acetate is widely used in native mass spectrome
93 er series: no denaturation was induced using ammonium acetate (kosmotropic), whereas ammonium formate
94  7 rotavirus types so far studied in aqueous ammonium acetate may be a special feature of this electr
95 st for the ester deacylation reactions under ammonium acetate mediated condition.
96  in the presence of aliphatic acetates under ammonium acetate mediated condition.
97 wed by dilution (10 times) with a mixture of ammonium acetate:methanol (50:50, v/v).
98  the mobile phase consisting of 10mM aqueous ammonium acetate:methanol:acetonitrile (50:30:20; v/v/v)
99 ica column with a gradient of methanol-water-ammonium acetate mixture as a modifier.
100                                              Ammonium acetate (NH(4)Ac) is a widely used solvent addi
101  3-bromopropenals, benzoylacetonitriles, and ammonium acetate (NH(4)OAc).
102 tassium acetate (KAc), NH4Cl, (NH4)2SO4, and ammonium acetate (NH4Ac) mixed with or without 100 micro
103                  Negative mode ionization in ammonium acetate offers the advantage of charge reductio
104     Four groups received either a continuous ammonium acetate or control infusion; half of the animal
105  subsequent amine incorporation using either ammonium acetate or HMDS.
106 The optimum method was developed using 10 mM ammonium acetate pH 2.5 and acetonitrile in a gradient m
107                Using a mobile phase of 0.2 M ammonium acetate (pH 6.9), several proteins (i.e., myogl
108  were found at a potential of about 1.1 V in ammonium acetate (pH 7.0) and 1.25 V in ammonium hydroge
109 yzed using a background electrolyte of 25 mM ammonium acetate (pH 8.0) containing increasing concentr
110 at washing with ammonium formate, pH 6.4, or ammonium acetate, pH 6.7, significantly increases signal
111 d is based on phenol extraction coupled with ammonium acetate precipitation, and the second is based
112 nvolves the desalting of nucleic acids using ammonium acetate precipitation, followed by characteriza
113                                              Ammonium acetate represents a gentler droplet environmen
114 ore, murine C2C12 myotubes were treated with ammonium acetate resulting in intracellular concentratio
115 ith a 10 to 60% N-propanol gradient in 0.1 M ammonium acetate, resulting in the elution of LF from th
116 tions combined simultaneous pH gradient with ammonium acetate salt gradient elution modes.
117                  We demonstrate that a 25 mM ammonium acetate solution adjusted to the proper pH can
118  when 2.5% sulfolane was mixed with a 200 mM ammonium acetate solution containing the protein when th
119 ing acid-denatured myoglobin with an aqueous ammonium acetate solution to increase solution pH result
120 tion is lowered (from 7.0 to 5.4, in a 20 mM ammonium acetate solution) and may be related to in vivo
121 nds acquired at 260 nm wavelength in aqueous ammonium acetate solution.
122 eneity, and structure of POPC-PDs in aqueous ammonium acetate solutions at pH 4.8 and 6.8 were invest
123 n myohemerythrin from peanut worm in aqueous ammonium acetate solutions from ~15 to 92 degrees C.
124                             The use of these ammonium acetate solutions permits direct MALDI-MS analy
125 ing unfolded proteins are mixed with aqueous ammonium acetate solutions to increase the solution pH a
126 thus, enabling simulated droplets containing ammonium acetate that form experimentally observed (de)p
127                           In the presence of ammonium acetate, the two intermediate compounds undergo
128 improvement in S/N is obtained by adding 8 M ammonium acetate to aqueous solutions of cytochrome c wi
129 imary and secondary aryl alcohols along with ammonium acetate to form pyridine scaffolds via catalyti
130 mately 7 and 11, respectively, by adding 7 M ammonium acetate to the solution.
131 salts, such as phosphate-buffered saline and ammonium acetate, to eluents enhances the suitability of
132 te to sodium acetate, potassium acetate, and ammonium acetate tolerances.
133 e radiopharmacy labeling conditions in 0.5 M ammonium acetate was 17-148 min at pH 6.5, but it was on
134                            For example, when ammonium acetate was replaced with acetic acid in the sh
135 recipitation by alkaline phenol and methanol/ammonium acetate was the choice for protein extraction.
136 K-Gel ODS-100V column using a mixture of 5mM ammonium acetate water solution and methanol as a mobile
137                                           An ammonium acetate water/acetonitrile binary gradient was
138  acetate following 24-hour exposure to 10 mM ammonium acetate were complemented by in vivo studies in
139 ns soluble in chloroform/methanol containing ammonium acetate were first extracted from lyophilized m
140 tetramer (human) in aqueous solution (150 mM ammonium acetate) were investigated using a variable tem
141                      Buffered eluents (0.1 M ammonium acetate) were necessary to stabilize 4-alpha-rh
142 ng sulfonamides were heated in a solution of ammonium acetate, which yielded imidazo[2,1-a]isoindolon
143  (100 mm x 2.1 mm d.i. x 1.7 um) column with ammonium acetate with 0.01% of trifluoroacetic acid as e
144 BE-nMS reveals that mobile phases containing ammonium acetate with lauryl-dimethylamine oxide are mos
145 onium acetate and for streptavidin in 200 mM ammonium acetate with no charge reduction.

 
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