ライフサイエンスコーパス: stable isotope labeling

1 movement of small molecules in plants using stable isotope labeling.

2 ific modifications of a protein using in-gel stable isotope labeling.

3 investigated by PAGE, mass spectrometry, and stable isotope labeling.

4 n of lipids in monolayers and bilayers using stable isotope labeling.

5 on is achieved through the use of whole-cell stable isotope labeling.

6 m Lumbricus rubellus were investigated using stable isotope labeling.

7 e combined with experiments that incorporate stable isotope labeling.

8 se of a chronic-administration protocol with stable-isotope labeling.

9 We have used stable isotope labeling ((15)N) of E. coli RNA in conjun

10 (PSII) chlorophyll and proteins, a combined stable isotope labeling (15N)/mass spectrometry method w

11 Using stable isotope labeling along with a two-step strategy f

12 We tested Census with stable-isotope labeling analyses as well as label-free a

13 nitor microbial mineralization using reverse stable isotope labeling analysis (RIL) of dissolved inor

14 r of NAT, which was further confirmed by the stable isotope labeling analysis using deuterated acetat

15 Subsequent stable isotope labeling analysis using deuterated ethano

16 We used a combination of stable isotope labeling and arteriovenous difference mea

17 monstrate whole-plant metabolic profiling by stable isotope labeling and combustion isotope-ratio mas

18 In vivo stable isotope labeling and computer-assisted metabolic

19 aves using stable isotope labeling (isobaric stable isotope labeling and isotope-coded affinity tags)

20 Here we used stable isotope labeling and isotopomer analysis to trace

21 y detection are typically conducted by using stable isotope labeling and label-free quantitation appr

22 g immobilization sites on a protein based on stable isotope labeling and MALDI-TOF mass spectrometry.

23 Using metabolic stable isotope labeling and mass spectrometry, we demons

24 The combination of stable isotope labeling and molecular network generation

25 the phosphorylation of these sites by using stable isotope labeling and MS(2) analysis.

26 Using stable isotope labeling and proteomics, we identified a

27 The aim of the present study was to combine stable isotope labeling and tandem mass spectrometry for

28 Using stable isotope labeling and tandem mass spectrometry, we

29 hromatography-mass spectrometry coupled with stable isotope labeling and the accurate mass and time t

30 able of large-scale proteome profiling using stable isotope labeling and the determination of >5 prot

31 ough the one-carbon metabolic pathway, using stable-isotope labeling and detection of lysine methylat

32 d, conformational changes and dynamics using stable-isotope labeling and mass spectrometry (CDSiL-MS)

33 erformed on whole cells and cell walls using stable-isotope labeling and rotational-echo double-reson

34 analyze PDH-deficient parasites using rapid stable-isotope labeling and show that PDH does not appre

35 Using a novel combination of stable-isotope labeling and tandem mass spectrometry, we

36 rotein, molecular homology modeling, in vivo stable isotope labeling, and transient expression in pet

37 P rhesus monkeys in conjunction with in vivo stable-isotope-labeling, and dose-dependently reduced ne

38 A novel stable isotope labeling approach using (15)N and (18)O w

39 gestion exchange a convenient and affordable stable isotope labeling approach.

40 A novel stable-isotope labeling approach for identification of p

41 iplexed quantification methods, specifically stable isotope labeling approaches such as isobaric tags

42 by (13)C-MFA advanced methods for measuring stable-isotope labeling are needed.

43 This protocol is compatible with stable isotope labeling at the protein and peptide level

44 quantification can be achieved by performing stable isotope labeling by amino acids in cell culture (

45 Using stable isotope labeling by amino acids in cell culture (

46 Super-stable isotope labeling by amino acids in cell culture (

47 By using stable isotope labeling by amino acids in cell culture (

48 We combined stable isotope labeling by amino acids in cell culture (

49 quantitation methods of biomolecules such as stable isotope labeling by amino acids in cell culture (

50 In this study, we adapted stable isotope labeling by amino acids in cell culture (

51 Using Stable Isotope Labeling by Amino acids in Cell culture (

52 ns were quantified by using the differential stable isotope labeling by amino acids in cell culture (

53 issue culture ((1)N/(1)N metabolic labeling, stable isotope labeling by amino acids in cell culture (

54 The method is based on stable isotope labeling by amino acids in cell culture (

55 Stable isotope labeling by amino acids in cell culture (

56 ass spectrometry combined with the method of stable isotope labeling by amino acids in cell culture (

57 A two-state stable isotope labeling by amino acids in cell culture (

58 d phosphoproteomics that incorporates triple stable isotope labeling by amino acids in cell culture (

59 ed approaches-microarray gene expression and stable isotope labeling by amino acids in cell culture (

60 We developed a stable isotope labeling by amino acids in cell culture (

61 Through comparative stable isotope labeling by amino acids in cell culture (

62 iphosphate (ATP) affinity probe coupled with stable isotope labeling by amino acids in cell culture (

63 this RNA structure, we used a combination of stable isotope labeling by amino acids in cell culture (

64 Additionally, by comparing the stable isotope labeling by amino acids in cell culture (

65 titative proteomic data, including data from stable isotope labeling by amino acids in cell culture a

66 Stable isotope labeling by amino acids in cell culture a

67 Proteomics analysis was carried out using stable isotope labeling by amino acids in cell culture c

68 Stable isotope labeling by amino acids in cell culture e

69 Stable isotope labeling by amino acids in cell culture f

70 uantified in vivo by mass spectrometry using stable isotope labeling by amino acids in cell culture m

71 s paper, we describe systematic quantitative stable isotope labeling by amino acids in cell culture p

72 Quantitative proteomics based on stable isotope labeling by amino acids in cell culture s

73 of gene expression was revealed using pulsed stable isotope labeling by amino acids in cell culture t

74 We used a modified version of stable isotope labeling by amino acids in cell culture t

75 ed by modifying the widely used technique of stable isotope labeling by amino acids in cell culture t

76 We further performed stable isotope labeling by amino acids in cell culture t

77 To clarify these issues, we used dynamic stable isotope labeling by amino acids in cell culture t

78 Proteins, extracted from a SILAC (stable isotope labeling by amino acids in cell culture)

79 s was determined using a quantitative SILAC (stable isotope labeling by amino acids in cell culture)-

80 proteins, we conducted a family-wide SILAC (stable isotope labeling by amino acids in cell culture)-

81 SILAC (stable isotope labeling by amino acids in cell culture)-

82 ing mass spectrometry-based technologies and stable isotope labeling by amino acids in cell culture,

83 Stable isotope labeling by amino acids in cell culture,

84 n complexes and analyzed their components by stable isotope labeling by amino acids in cell culture-b

85 In a stable isotope labeling by amino acids in cell culture-b

86 In combination with the use of the stable isotope labeling by amino acids in cell culture-b

87 Using stable isotope labeling by amino acids in cell culture-b

88 Using stable isotope labeling by amino acids in cell culture-m

89 Furthermore, using stable isotope labeling by amino acids in culture (SILAC

90 proteomic analyses of deletion strains using stable isotope labeling by amino acids in culture identi

91 er physiological light-dark conditions using stable isotope labeling by amino acids quantitative MS.

92 Stable isotope labeling by essential nutrients in cell c

93 This methodology of stable isotope labeling by essential nutrients in cell c

94 The goal of the present study was to use a stable-isotope labeling by amino acids in cell culture (

95 eukocyte life span estimates on the basis of stable isotope labeling can vary up to 10-fold among lab

96 ed magnetic beads, in conjunction with (18)O stable isotope labeling catalyzed by both trypsin and PN

97 ulfate depletion of the serum, an affordable stable isotope labeling chemistry for samples with a lar

98 The application of stable isotope labeling combined with SRM can overcome m

99 We utilized a recently developed method of stable-isotope labeling combined with cerebrospinal flui

100 investigate this disparity, we generated new stable isotope labeling data in healthy adult subjects u

101 ts were measured in vivo using a pulse-chase stable isotope labeling experiment.

102 heterogeneity, (3) and isotopic shifts from stable isotope labeling experiments are identified and a

103 The FFC algorithm is able to integrate stable isotope labeling experiments into the analysis an

104 Stable isotope labeling experiments show that, after MeJ

105 Stable isotope labeling experiments showed that ADT1 sup

106 d to further define this proposed synthesis, stable isotope labeling experiments were performed with

107 Here, we describe the use of stable isotope-labeling experiments for studying metabol

108 able of analyzing untargeted LC/MS data from stable isotope-labeling experiments.

109 ributions (MID) is of great significance for stable isotope-labeling experiments.

110 Metabolic flux analysis based on stable-isotope labeling experiments and analysis of mass

111 ease solubility and ionization, and utilizes stable isotope labeling for MS1 level identification of

112 h to differential metabolomics that involves stable isotope labeling for relative quantification as p

113 Mass spectrometry-based stable isotope labeling has become a key technology for

114 n and post-translational modifications using stable isotope labeling has been achieved, but insights

115 In the present work, a stable isotope labeling HPLC-ESI(+)-MS/MS approach was e

116 investigated by a novel methodology based on stable isotope labeling HPLC-ESI(+)-MS/MS.

117 The stable isotope labeling HPLC-ESI-MS/MS approach describe

118 In the work presented here, a stable isotope labeling HPLC-ESI-MS/MS approach was empl

119 combines a photo-cross-linking strategy with stable isotope labeling in cell culture (SILAC)-based qu

120 This stable isotope labeling in cell culture method enables t

121 show by blue-native gel electrophoresis and stable isotope labeling in cell culture proteomics that

122 used protein mass spectrometry with dynamic stable isotope labeling in cell culture to achieve a pro

123 by the AACT/SILAC (amino acid-coded tagging/stable isotope labeling in cell culture)-based quantitat

124 been greatly propelled by the development of stable isotope labeling in cell cultures (SILAC), a set

125 ificantly, PAF-C purifications combined with stable isotope labeling in cells (SILAC) quantitation fo

126 ghput quantitative studies using (16)O/(18)O stable isotope labeling in combination with the accurate

127 We conclude that stable isotope labeling in healthy humans is consistent

128 ere, we describe use of quantitative in vivo stable isotope labeling in mammals to accurately compare

129 strategy for brain proteomics called SILAM (Stable Isotope Labeling in Mammals).

130 issue in plant biology, we developed SILIP (stable isotope labeling in planta) using tomato plants (

131 We made use of stable isotope labeling in tissue culture (SILAC) to ide

132 thod to measure carbohydrate composition and stable-isotope labeling in algal biomass using gas chrom

133 yrosine protein immunoprecipitation step and stable-isotope labeling, in a single experiment, we iden

134 Stable isotope labeling is central to NMR studies of nuc

135 nthesis/degradation ratio mass spectrometry, stable isotope labeling is employed to calculate a relat

136 A new method for proteolytic stable isotope labeling is introduced to provide quantit

137 Stable isotope labeling is the state of the art techniqu

138 st proteomes of fully developed leaves using stable isotope labeling (isobaric stable isotope labelin

139 A stable isotope labeling kinetics experiment in NHPs was

140 report the translation of the human in vivo stable-isotope-labeling kinetics (SILK) method to a rhes

141 uthentic metabolite standards via the use of stable isotope labeling, liquid chromatography mass spec

142 uencing, global untargeted metabolomics, and stable isotope labeling mass spectrometry to identify me

143 Stable-isotope-labeling mass spectrometry involves the a

144 - and K-ras-derived DNA sequences by using a stable isotope labeling-mass spectrometry approach recen

145 To address this issue, a new stable isotope labeling method that targets tyrosine res

146 hod described here provides the first direct stable-isotope labeling method to definitely detect phos

147 Here we describe an improved stable-isotope labeling method using a phosphoprotein is

148 phoresis techniques, metabolic labeling, and stable isotope labeling methods to name only a few.

149 Stable isotope-labeling methods, coupled with novel tech

150 Stable isotope labeling-multiple reaction monitoring mas

151 Using stable isotope labeling of amino acids in a cell culture

152 e-enriched fractions, which were compared by stable isotope labeling of amino acids in cell culture (

153 is after SII stimulation using a strategy of stable isotope labeling of amino acids in cell culture (

154 s of pulmonary origin using the technique of stable isotope labeling of amino acids in cell culture (

155 en the development and implementation of the stable isotope labeling of amino acids in cell culture (

156 cycline-inducible RTA expression and applied stable isotope labeling of amino acids in cell culture (

157 abeling approaches such as isobaric tags and stable isotope labeling of amino acids in cell culture (

158 pled isotope-coded affinity tag, and coupled stable isotope labeling of amino acids in cell culture e

159 We used the stable isotope labeling of amino acids in cell culture p

160 1 KO mice in combination with in vivo pulsed stable isotope labeling of amino acids in cell culture p

161 roteins were screened by quantitative SILAC (stable isotope labeling of amino acids in cell culture)

162 sequencing)-based transcriptomics and SILAC (stable isotope labeling of amino acids in cell culture)-

163 Using a SILAC (stable isotope labeling of amino acids in cell culture)-

164 Using stable isotope labeling of amino acids in culture (SILAC

165 Stable isotope labeling of an intracellular chemical pre

166 measures three states simultaneously through stable isotope labeling of cells with amino acids in cel

167 Stable isotope labeling of CNS proteins can be utilized

168 elopment, we have established conditions for stable isotope labeling of cultured embryos under steady

169 o a solid support using hydrazide chemistry, stable isotope labeling of glycopeptides and the specifi

170 Surprisingly, results obtained with stable isotope labeling of mammals revealed that, in viv

171 Differential (18)O/(16)O stable isotope labeling of peptides that relies on enzym

172 We report an enzymatic strategy for "stable isotope labeling of phosphonates in extract" (SIL

173 improved methods for chemical and metabolic stable isotope labeling of proteins and peptides.

174 Stable isotope labeling of small-molecule metabolites (e

175 Differential stable isotope labeling of the ClpPRS complex with iTRAQ

176 and kinetic information without the need for stable isotope labeling of the molecules of interest.

177 By coupling our methodology with stable-isotope labeling of amino acids in cell culture (

178 noncanonical amino acid tagging (BONCAT) and stable-isotope labeling of amino acids in cell culture (

179 uantitative measurements can be performed by stable-isotope labeling of the peptides in the reductive

180 technologies with respect to the methods for stable isotope labeling, process automation and data pro

181 In this work an improved stable isotope labeling protocol for nucleic acids is in

182 ve proteomics, thanks to the availability of stable-isotope labeling reagents.

183 exchange between bound and free ligand or on stable isotope labeling, relying instead on a tert-butyl

184 Stable-isotope labeling reveals that even severely aggre

185 echniques, along with a judiciously designed stable isotope labeling scheme, to measure atomistic-res

186 Peptide quantitation based on stable isotope labeling showed that the surfactant induc

187 ids remodeled by the parasite cytoplasm, and stable isotope labeling shows some apicoplast lipids are

188 Stable isotope labeling (SIL) techniques have the potent

189 In addition, stable-isotope labeling simplified identification of the

190 In addition, a stable isotope-labeling step can be included to modify c

191 The use of stable isotope labeling strategies that are adaptable to

192 This dogma was recently challenged by stable isotope labeling studies with heavy water, which

193 a protein isoform analysis method utilizing stable isotope labeling tandem mass spectrometry (SILT M

194 Here, we used a stable isotope labeling technique ((18)O and (2)H) to de

195 Here, we applied a stable isotope-labeling technique in combination with ma

196 We also employed a stable-isotope labeling technique to illuminate high-pri

197 Stable isotope labeling techniques for quantitative top-

198 We used two stable isotope-labeling techniques to identify kinetical

199 roughput in quantitative proteomics that use stable-isotope labeling techniques combined with high-re

200 Finally, we show using stable isotope labeling that in an embryonic mouse cell

201 has been made thanks to the introduction of stable isotope labeling, the state-of-the-art technique

202 dimethylsulfonium moiety of SMM was shown by stable isotope labeling to be incorporated as a unit int

203 We applied stable isotope labeling to detect source-specific iron b

204 The approach was enhanced with stable isotope labeling to overcome ambiguities in deter

205 hod that relies on phosphatase treatment and stable-isotope labeling to determine absolute stoichiome

206 We further used stable-isotope labeling to trace the metabolic dynamics

207 titative protein profiling based on in vitro stable isotope labeling, two-dimensional polyacrylamide

208 with high sensitivity, we developed cysteine-stable isotope labeling using amino acids in cell cultur

209 d degreening were determined by differential stable-isotope labeling using formaldehyde.

210 we describe an integrated approach combining stable isotope labeling, various protein enrichment and

211 We utilized stable isotope labeling with amino acids (SILAC) in PTEC

212 beling technique, NeuCode (neutron encoding) stable isotope labeling with amino acids in cell culture

213 ed for this study was generated using SILAC (Stable Isotope Labeling with Amino acids in Cell culture

214 tion mass spectrometry and quantification by Stable Isotope Labeling with Amino Acids in Cell Culture

215 Using stable isotope labeling with amino acids in cell culture

216 teasome's composition in samples prepared by stable isotope labeling with amino acids in cell culture

217 Using stable isotope labeling with amino acids in cell culture

218 By dissecting the SlyA regulon using stable isotope labeling with amino acids in cell culture

219 ased on quantitative mass spectrometry using stable isotope labeling with amino acids in cell culture

220 escribes an integrated approach that couples stable isotope labeling with amino acids in cell culture

221 obtained on 462 proteins by using the SILAC (stable isotope labeling with amino acids in cell culture

222 Mass spectrometry-SILAC (stable isotope labeling with amino acids in cell culture

223 photyrosine profiling method with 'spike-in' stable isotope labeling with amino acids in cell culture

224 n adherent and non-adherent conditions using stable isotope labeling with amino acids in cell culture

225 We coupled cell fractionation with stable isotope labeling with amino acids in cell culture

226 ssisted affinity purification), coupled with stable isotope labeling with amino acids in cell culture

227 e analysis of the TIM23 interactome based on stable isotope labeling with amino acids in cell culture

228 hitis virus (IBV) N protein was mapped using stable isotope labeling with amino acids in cell culture

229 Using stable isotope labeling with amino acids in culture (SIL

230 proximity-labeled proteins were analyzed by stable isotope labeling with amino acids in culture (SIL

231 In this paper, we describe a stable isotope labeling with amino acids in culture-base

232 Stable isotope labeling with d0- and d4-succinic anhydri

233 Stable isotope labeling with multiple reaction monitorin

234 Our approach in combining stable isotope labeling with NanoSIMS and TEM imaging ca

235 adecynoic acid (17-ODYA) in combination with stable-isotope labeling with amino acids in cell culture

236 We adapted stable-isotope labeling with amino acids in cell culture