ライフサイエンスコーパス: tissue extract

1 radioactive, sensitive assay of MCD in crude tissue extract.

2 ed considerably more versican in the injured tissue extract.

3 with unrelated proteins in an unfractionated tissue extract.

4 lex biological samples, such as a mouse lung tissue extract.

5 the response of metabolite ions in rat brain tissue extract.

6 r demonstrated to assign molecules in a worm tissue extract.

7 ological samples, such as serum, plasma, and tissue extracts.

8 ions from the separation of complex neuronal tissue extracts.

9 nd cyclin A as determined by Western blot of tissue extracts.

10 for analyzing telomerase activity in cell or tissue extracts.

11 ysis of metabolites in biological fluids and tissue extracts.

12 dependent pterin ring reduction was found in tissue extracts.

13 tic tool of the antioxidant capacity in leaf tissue extracts.

14 rin in alpha-actinin immunoprecipitates from tissue extracts.

15 esearch studies using relevant biofluids and tissue extracts.

16 properties of granuloma-inducing sarcoidosis tissue extracts.

17 undance was detected in primary colon cancer tissue extracts.

18 n vivo spectrum were confirmed in studies of tissue extracts.

19 y can be immunodepleted from prostate cancer tissue extracts.

20 oid of 3-OST-1 enzyme activity in plasma and tissue extracts.

21 nzyme activity peaked at 12 h in hippocampal tissue extracts.

22 adenosine, even in complex mixtures such as tissue extracts.

23 of D-AKAP2 was characterized by using mouse tissue extracts.

24 e, and sesquiterpenes are detectable only in tissue extracts.

25 idized to oxindole-3-acetic acid by Zea mays tissue extracts.

26 lysates, hepatic subcellular fractions, and tissue extracts.

27 xogenously to supernatant fluids of the null tissue extracts.

28 imultaneously quantify these biomolecules in tissue extracts.

29 rate of synthesis of glutathione in cell and tissue extracts.

30 the mutant allele in total RNA derived from tissue extracts.

31 action of SATB1 and CDP in several different tissue extracts.

32 fication of dTPP II activity from Drosophila tissue extracts.

33 idases from both human cell lysate and mouse tissue extracts.

34 n assay to search for regulators in cell and tissue extracts.

35 rocessing were present in seven of seven AAA tissue extracts.

36 ve proform in all tumor cell lines and tumor tissue extracts.

37 used them to identify authentic proteins in tissue extracts.

38 red by analysis of glutamate enrichment from tissue extracts.

39 measurement of glutamate C4 enrichment from tissue extracts.

40 ns was confirmed by Western blot analysis of tissue extracts.

41 72 recognize a >200-kDa protein in cell and tissue extracts.

42 activity in murine macrophage and human lung tissue extracts.

43 ms are translated as proteins in human brain tissue extracts.

44 ectroscopically quantified in cell and tumor tissue extracts.

45 t FOXC1 to directly classify BLBC types from tissue extracts.

46 of monoglyceride regioisomers directly from tissue extracts.

47 nt from results obtained using HPLC-MS/MS of tissue extracts.

48 with amino acids, orphan ligands, serum, and tissue extracts.

49 rformed with excellent recovery in different tissue extracts.

50 d cleavage of its in vivo substrate titin in tissue extracts.

51 es screening of the FFA composition in crude tissue extracts.

52 chromatography (LC)-MS/MS results from brain tissue extracts.

53 d to assess gene and protein expression from tissue extracts.

54 substances and other peroxidases present in tissue extracts.

55 y characterized in liver, brain, and adipose tissue extracts.

56 cromolecular complexes directly from cell or tissue extracts.

57 ilar substrate specificity in worm and mouse tissue extracts.

58 detect endogenous SphK activity in cell and tissue extracts.

59 to endogenous protein complexes from animal tissue extracts.

60 pidly measured in minimally prepared cell or tissue extracts.

61 easure the amounts of these species in brain tissue extracts.

62 fic cleavage was confirmed by digestion with tissue extracts.

63 lipid mass spectral profiles from crude lung tissue extracts.

64 in tumors and by (1)H MRS in cell and tumor tissue extracts.

65 t message for ERG2 and 3 in whole myometrial tissue extracts.

66 antibody in a variety of cultured cells and tissue extracts.

67 of apoptosis in live mice, whole organs and tissue extracts.

68 bstantial levels of IGF-1:TTC in spinal cord tissue extracts.

69 sugar phosphate standards into complex plant tissue extracts.

70 the pellet after low speed centrifugation of tissue extracts.

71 n account for all such activity in mammalian tissues extracts.

72 trated increased CCR5 protein in hippocampal tissue extracts 32 hours after lesioning.

73 We have isolated from tissue extracts a distinct and abundant mammalian Pol II

74 ercent signal recovery in concentrated plant tissue extract, allowing for quantitative detection with

75 e by NMR and show that CoA, when oxidized in tissue extract, also forms the same disulfide metabolite

76 Forty-one percent of the tissue extracts, amplified by the PCR reacted positively

77 st existing tools using a human glioblastoma tissue extract and illustrate its ability to automatical

78 de cocktail was spiked into a complex native tissue extract and quantified by unscheduled multiple re

79 recognized multiple bands of 240-110 kDa in tissue extracts and collagenous bands of 150-140 kDa in

80 profiling procedures involve the analysis of tissue extracts and consequently lack cellular or subcel

81 End-stage ADPKD renal tissue extracts and cyst fluids were assayed for time-de

82 azine induced HIF-1alpha and VEGF protein in tissue extracts and elevated plasma VEGF levels.

83 Their effects were evaluated in muscle tissue extracts and freshly dissociated SM cells.

84 ge of terpenoid metabolites in complex plant tissue extracts and is independent of retention time, ab

85 This study was performed on medial tissue extracts and primary cultures of VSMCs of human t

86 o enzymes could be coimmunoprecipitated from tissue extracts and proposed functional interactions bet

87 Immunoprecipitation analysis of tissue extracts and proximity ligation assays in dissoci

88 ear magnetic resonance (NMR) spectroscopy of tissue extracts and steady-state isotopomer analyses.

89 two parts: the preparation of cell cytosolic/tissue extracts and the detection of total glutathione (

90 is stably associated with other proteins in tissue extracts and the first nuclear receptor shown to

91 S experiments performed using methanol/water tissue extracts and up to 50% coverage in comparison wit

92 The results were confirmed in tissue extracts and were in line with the predictions ma

93 esent a systematic analysis of a sample set (tissue extracts), and the utility of a simple correlatio

94 When applied to human urine samples, kidney tissue extract, and plasma, the WADE technique allowed f

95 Both HO-1 and HO-2 were present in the IAS tissue extracts, and both enzymes were localized in the

96 ctins, is present in numerous cell lines and tissue extracts, and is expressed on the cell surface.

97 ve PRMT1 activity from RAT1 extracts, murine tissue extracts, and purified rat liver FDH preparations

98 xidants on recombinant proteins and cell and tissue extracts, and the efficiencies of the alkylating

99 oreover, in contrast to earlier views, MT in tissue extracts appears to be less stable than T.

100 Tissue extracts are treated with subunit-specific probes

101 d activity-profiling approach in which whole tissue extracts are used to directly identify optimal pe

102 prepared by seeded growth from frontal lobe tissue extracts, are similar in the two cases but with s

103 t, kidney, brain, liver, and skeletal muscle tissue extracts as examples.

104 ysically associated with each other in maize tissue extracts, as demonstrated by reciprocal coimmunop

105 The assay is useful with crude tissue extracts, as demonstrated by the determination of

106 MSA can be measured in tissue extracts at 0.04 nmol (equivalent to 2 microM).

107 K, which is ubiquitously expressed in normal tissue extracts but is absent from many tumor cell lines

108 thiopropyl resin was employed to debulk the tissue extract by selectively removing a substantial fra

109 osis confirmed by histological analysis from tissue extracted by endoscopic retrograde cholangiopancr

110 osomal DNA fragmentation was investigated in tissue extracts by agarose gel electrophoresis.

111 hange factor, in neuronal cells and in brain tissue extracts by co-immunoprecipitation and co-localiz

112 ntification of hundreds of lipids species in tissue extracts by direct-infusion MS, localization of l

113 between immunohistochemistry and analysis of tissue extracts by enzyme immunoassay.

114 Analysis of lung washings and colon tissue extracts by Western blotting in the unreduced sta

115 A complete reduced folate pool analysis of a tissue extract can be obtained in less than 2 h once a s

116 However, coeluting components in tissue extracts can interfere with ionization at the int

117 metabolite analysis, enzyme assays with WRC tissue extracts, cloning, and functional characterizatio

118 uent mortality in exposure experiments using tissue extracts, coelomic fluid and effluent water from

119 using activity-guided fractionation of mouse tissue extracts combined with untargeted metabolomics an

120 teady-state (13)C-NMR isotopomer analysis of tissue extracts confirmed that flux rates through PDH, a

121 High resolution 13C NMR spectra of tissue extracts confirmed that the exogenous lactate did

122 e of approximately 8-kDa was also evident in tissue extracts containing the 225-kDa form.

123 RA synovial tissue extracts demonstrated elevated levels of MMP-9 an

124 Analysis of ischemic wound tissue extracts demonstrated significantly reduced expre

125 dostatin levels in either serum or carcinoma tissue extracts did not change in cathepsin S- or cystat

126 Inhibition of seeding initiated by brain tissue extracts differed among donors with different tau

127 leveraged direct proteomic analysis of tumor tissue extracts, differential feature selection characte

128 In Western blot analyses of whole-tissue extracts, Egr-1 protein levels were shown to be i

129 -LC-MS analysis of a proteolytic digest of a tissue extract, equivalent to a sample size of approxima

130 ological samples of interest (urine, plasma, tissue extracts, etc.), which requires evaluating the ro

131 Northern hybridization and immunoblotting of tissue extracts found keratocan distribution to be more

132 versal of the pH of an adult rat hippocampal tissue extract from 10.5 to 7.4 led to an almost complet

133 our multimodal workflow was applied to brain tissue extracted from a Sprague-Dawley rat dosed with a

134 genes, was found to be coexpressed mainly in tissue extracted from breast and ovarian cancers, but al

135 tical neurons treated with Abeta or cortical tissue extracts from 12-month-old APPswe/PS1dE9 transgen

136 nanograms of SF per milligram of protein) in tissue extracts from 166 breast cancers and correlated t

137 t detect the BK or JC polyomaviruses in lung tissue extracts from 33 patients with IPF by using real-

138 I-MS approach was successfully used on tumor tissue extracts from a K-ras transgenic mouse model of l

139 ptide sequencing from complex neuroendocrine tissue extracts from a marine model organism, Callinecte

140 we studied adipogenesis by liver and adipose tissue extracts from a polar bear and three synthetic mi

141 ently activated by native proteases in aorta tissue extracts from ApoE(-)/(-), but not from normal mi

142 rin-B co-immunoprecipitates with InsP(3)R in tissue extracts from brain, heart, and lung.

143 v antibodies to inhibit the seeding by brain tissue extracts from different donors with tauopathies v

144 Tissue extracts from FDH(+/+), FDH(+/-), and FDH(-/-) mi

145 t protein in raw plasma samples and in brain tissue extracts from healthy individuals and post mortem

146 against recombinant serine proteases and in tissue extracts from healthy mice and from models of inf

147 ect and purify the lumican core protein from tissue extracts from human donors 6 to 89 years of age.

148 e protease responsible for processing Shh in tissue extracts from human stomach.

149 -DNA excision activity as judged by assay of tissue extracts from knockout mice as well as by the res

150 Ex vivo measurements of tissue extracts from liver, kidney, and tumor indicated

151 Tissue extracts from Minpp1-deficient mice lacked detect

152 ermine the GL-3 concentrations in plasma and tissue extracts from normal individuals and patients and

153 atasets of serum, urine, cortex, and stomach tissue extracts from the rats were analysed by multivari

154 Tissue extracts from the RV of 20 patients were assayed

155 Reaction rates with tissue extracts from two grasses were linear for at leas

156 een applied to cells grown in culture and to tissue extracts from young and old animals.

157 lecular mass of 28 kD on western analysis of tissue extracts from zinnia, forsythia (Forsythia suspen

158 STR2-EGFP, or AdEGFP as well as ex vivo with tissues extracted from mice.

159 oxide dismutase and catalase were assayed in tissue extracts generated from fresh human trabecular me

160 NP tissue extracts had significantly more anti-basement mem

161 ed proteomic analyses performed on cartilage tissue extracts identified the serine protease HtrA1/PRS

162 y, and direct applicability to biofluids and tissue extracts impart great promise for the discovery a

163 Screening of tissue extracts in a cell line engineered to overexpress

164 nd cellular fibronectin mRNAs in whole-liver tissue extracts in both models.

165 duced AMPK phosphorylation at Thr172 in lung tissue extracts, increased protein content and cell coun

166 Tissue extracts incubated with reduced thioredoxin are t

167 sis of D2 ubiquitination driven by different tissue extracts indicated that D2 ubiquitination in the

168 n of ABBP-1 from an active apoB mRNA editing tissue extract inhibits its editing activity.

169 on of a P450 enzyme system with cofactor and tissue extract is done under a mixture of (18)O(2)/(16)O

170 rometry analyses of neuropeptides in complex tissue extracts is not due to neuropeptides being below

171 t the low pH used for peptide isolation from tissue extracts, is even more active than QL9 in cytotox

172 e detected on immunoblots of mouse cytosolic tissue extracts; it was most highly expressed in spleen,

173 s from contact lenses, had no equivalents in tissue-extracted mucins.

174 cal production of antibodies was measured in tissue extracts, nasal lavage fluid, and sera by using m

175 OSM expression was measured in tissue extracts, nasal secretions, and bronchoalveolar l

176 precipitates with the beta(2)-AR in cell and tissue extracts, nucleating a signaling complex that inc

177 Myocardial tissue extracts obtained 24 hours after CCPA treatment w

178 A was detected in all animals from pulmonary tissue extracts obtained at necropsy.

179 legans, but has not been detected in several tissue extracts of Mus musculus.

180 An ELISA of tissue extracts of normal prostate, high-grade prostatic

181 demonstrated with heart and hindlimb muscle tissue extracts of rats infused with [2,4,6,8-13C4]-octa

182 cyclododecadiene, while in liver and adipose tissues extracts only a single monohydroxy-pentabromocyc

183 y known phosphoinositide present in cell and tissue extracts or produced in kinase and phosphatase as

184 n for distinguishing these isozymes in crude tissue extracts or subcellular fractions; that is, activ

185 tinal opacification that evolves as upstream tissues extract oxygen to the detriment of tissues downs

186 induced DNA damage in mouse liver and testis tissue extracts prepared at regular intervals over the c

187 Therefore tissue extracts prepared for chemical analysis are not a

188 utility of the assay was demonstrated using tissue extracts prepared from a group of taxonomically d

189 ectrometry (LC-MS/MS) lipidomics analysis of tissue extracts prepared using two different procedures:

190 nd mass spectrometry analysis of Gb4Cer from tissue extracts remains challenging.

191 iated apoB mRNA editing activity of in vitro tissue extracts requires the presence of Hsp70/ABBP-2.

192 Western blotting of tissue extracts revealed a diffuse smear with a mean siz

193 Northern analysis of rat tissue extracts showed that rat msrA mRNA is present in

194 Analysis of tissue extracts spiked with steroids revealed that most

195 mum catalytic activity of aconitase in total tissue extracts, suggesting that a cytosolic isoform of

196 de (oxidized + reduced forms) was noted from tissue extracts, suggesting that the loss in contrast as

197 ion-PCR analysis of RNA isolated from rabbit tissue-extracted T. pallidum additionally showed that tp

198 Putrescine is found in tissue extracts that contain sea lamprey alarm cue, and

199 show that IAA-RP (i) is present in brain and tissue extracts that exhibit I-R activity; (ii) is prese

200 Although both MMP were detected in tissue extracts, the differences in expression levels an

201 In some lung tissue extracts, the eicosanoid metabolites 5-oxo-eicosa

202 In whole-tissue extracts, the expression of IL-32 protein was sig

203 the physiological range and the metabolizing tissues extract their required oxygen from blood at a lo

204 Furthermore, the assay can be also used on tissue extracts to analyze the in vivo pharmacokinetics

205 normalized to the DNA content of the various tissue extracts to approximate normalization to the numb

206 assess the metabolites found in biofluids or tissue extracts to define a metabolic profile that descr

207 56 PCR-based assays performed robotically on tissue extracts to determine simultaneously the presence

208 led casein, meat myofibrillar and connective tissue extracts to explore their effects on meat structu

209 e and measure the viscoelastic properties of tissue extracts to provide the first force-velocity curv

210 plant systems (Soybean Glycine max) and leaf tissue extracts (Tococa spp.).

211 TSG-6 was present in arthritic joint tissue extracts together with the heavy chains of inter-

212 ngly, only a six-line signal was detected in tissue extracts under these conditions.

213 BA, glutamate and glutamine were assessed in tissue extracts using (13)C-edited (1)H nuclear magnetic

214 Analysis of the tissue extracts using acid precipitation demonstrated th

215 ds on processed and stained liver tissues or tissue extracts using current standard analytical techni

216 ations in different lipid classes present in tissue extracts using electrospray ionization (ESI) and

217 which was confirmed by parallel analysis of tissue extracts using electrospray-ionization MS.

218 avior of Gbeta(5), RGS7, RGS9, and Galpha in tissue extracts using immunoprecipitation and convention

219 ication of endogenous substrates of P450s in tissue extracts using metabolomic and isotopic labeling

220 spartate was measured at five time points in tissue extracts using scintillation counting and 13C nuc

221 Accumulation of cAMP in the tissue extract was determined by radioimmunoassay (RIA).

222 and cyclic adenosine monophosphate (cAMP) in tissue extracts was measured by radioimmunoassay, IP3 pr

223 melanogenic activities of individual adipose tissue extracts was noted.

224 Using this method to fractionate soluble tissue extracts, we identified the muscle isoform of pho

225 phonate referred to as FP-biotin, with crude tissue extracts, we quickly and with high sensitivity de

226 The sample detection limits in in vivo tissue extracts were 100 pg and 5 pg on-column for LC/MS

227 Tissue extracts were also analyzed by MALDI wide-isolati

228 Culture media, digestion supernatants, and tissue extracts were assayed for sulfated glycosaminogly

229 The KCa stimulatory effects of target tissue extracts were blocked by a neutralizing pan-TGFbe

230 As samples, both model proteins and tissue extracts were employed.

231 Tissue extracts were examined for ERK activation by phos

232 Murine tissue extracts were found to contain pepstatin-inhibita

233 Tissue extracts were found to influence the LC-MS/MS res

234 Mitochondria, adult cardiomyocytes, and tissue extracts were isolated from the left ventricle (L

235 ogenous nitrotyrosine-containing proteins in tissue extracts were poor substrates.

236 Tissue extracts were prepared and analyzed for protease

237 teral nephrectomy was performed and cortical tissue extracts were prepared.

238 striatal tissue was homogenized to generate tissue extracts which were added to E14.5 ventral mesenc

239 level in single living cell, cell lysate and tissue extract with high sensitivity.

240 d investigated the function of TSLP in nasal tissue extracts with a bioassay based on activation of h

241 nd less ROS in their roots apices (tested in tissue extracts with Amplex Red).

242 of FDH activity in RAT1 cells and in murine tissue extracts with antibody to FDH does not diminish t

243 ted to be useful in identifying reactions in tissue extracts with orphan human P450s.

244 ith wide-isolation MS/MS for analysis of the tissue extracts with scan-by-scan COC-to-COC-d(3) normal

245 of HNA and HNE were confirmed by spiking the tissue extracts with synthetic metabolites and finally b

246 SDE1 biomarkers for citrus greening in plant tissue extracts with the dynamic range over three orders

247 Incubation of human brain postmortem tissue extracts with urocortin and urotensin resulted in

248 s telomerase detection in mammalian cell and tissue extracts with very low telomerase activity levels

249 vo sequencing of neuropeptides directly from tissue extract without any genomic information.