ライフサイエンスコーパス: flow cytometry

1 emistry), and infiltrating cell populations (flow cytometry).

2 ted transitions across discrete states using flow cytometry.

3 ph nodes, and bone marrow were quantified by flow cytometry.

4 ed using fluorogenic probes, microscopy, and flow cytometry.

5 d cell cycle kinetics were measured by using flow cytometry.

6 was completely C3-dependent, as detected by flow cytometry.

7 d healthy control subjects was analyzed with flow cytometry.

8 ha-stimulated HUVECs and quantified by using flow cytometry.

9 ned via Annexin V/Propidium iodide stain and flow cytometry.

10 an previously reported based on conventional flow cytometry.

11 sis-specific tetramer(+)CD4(+) T cells using flow cytometry.

12 se chain reaction, immunohistochemistry, and flow cytometry.

13 kers and phagocytic ability were assessed by flow cytometry.

14 roducing and non-producing cells purified by flow cytometry.

15 ss using antibody-avid polystyrene beads and flow cytometry.

16 exosomes in epithelial cells was assessed by flow cytometry.

17 Engraftment was assessed by flow cytometry.

18 cocultures were analyzed by using ELISA and flow cytometry.

19 ted from a yeast surface display library via flow cytometry.

20 by nanoparticle tracking analysis (NTA) and flow cytometry.

21 dies by surface plasmon resonance as well as flow cytometry.

22 The expression of CCR7 was determined by flow cytometry.

23 munohistochemistry, electron microscopy, and flow cytometry.

24 rRNA gene-based phylogenetic microarrays and flow cytometry.

25 e molecular composition of human synapses by flow cytometry.

26 y quantitative polymerase chain reaction and flow cytometry.

27 using Western blot, electron microscopy and flow cytometry.

28 vated or injured cells and are detectable by flow cytometry.

29 pressing tumors with immunohistochemistry or flow cytometry.

30 ses of T-cell subsets were measured by using flow cytometry.

31 tly labeled ECL1i in vivo were detected with flow cytometry.

32 ivation of microglial cells were measured by flow cytometry.

33 n an HIV-1-inducible reporter T cell line by flow cytometry.

34 Cell images were acquired with imaging flow cytometry.

35 /AO staining, and cell cycle was analyzed by flow cytometry.

36 peripheral blood DCs was quantified by using flow cytometry.

37 ple sclerosis patients using multiparametric flow cytometry.

38 ns and neutrophil apoptosis were analyzed by flow cytometry.

39 factor expression were assessed by means of flow cytometry.

40 in conjunction with confocal microscopy and flow cytometry.

41 Circulating B cells were characterized by flow cytometry.

42 rasite infection of hepatocyte cell lines by flow cytometry.

43 mma-producing CD4+ T cells, were detected by flow cytometry.

44 culating progenitor cells were enumerated by flow cytometry.

45 ver time in a mouse model of infection using flow cytometry.

46 ulations was evaluated by immunostaining and flow cytometry.

47 ted monocytes (CD14+CD16+) was determined by flow cytometry.

48 s) in lung single-cell preparations by using flow cytometry.

49 vation and histamine release was measured by flow cytometry.

50 en binding and presentation were assessed by flow cytometry.

51 tored immune cell surveillance of the CNS by flow cytometry.

52 the 6 populations of cells were isolated by flow cytometry.

53 ion was assessed by immunohistochemistry and flow cytometry.

54 ated by quantitative PCR, immunoblotting and flow cytometry.

55 nd fenestrated) and open aortic repair using flow cytometry.

56 ymphocytes subsets from cultured blood using flow cytometry.

57 t1 phosphorylation levels were determined by flow cytometry.

58 tochemistry, quantitative RT-PCR, ELISA, and flow cytometry.

59 om NP or tonsil, or after ILC2 coculture, by flow cytometry.

60 ll proliferation and cycle were evaluated by flow cytometry.

61 from allergic patients was analyzed by using flow cytometry.

62 system in the kidney relies predominantly on flow cytometry.

63 d assays and from outgrowth assay readout by flow cytometry.

64 sing 2',7'-dichlorofluorescein diacetate and flow cytometry.

65 were performed by using ELISA, ELISpot, and flow cytometry.

66 and HIV-uninfected controls were analyzed by flow cytometry.

67 comes many limitations of fluorescence-based flow cytometry.

68 ral killer (NK) cell number were measured by flow cytometry.

69 ch were minimal residual disease negative by flow cytometry.

70 and lymph nodes were detected dynamically by flow cytometry.

71 d beta2 integrin adhesion molecules by using flow cytometry.

72 olated from spleen and liver for analysis by flow cytometry.

73 are challenging to distinguish with standard flow cytometry.

74 d antibodies against pan-cytokeratin through flow cytometry.

75 n levels of common endothelial markers using flow cytometry, 3 subpopulations of endothelial cells co

76 disease before CAR-T cells had no disease by flow cytometry after CAR-T cells.

77 specific effector T cells were analyzed with flow cytometry after polyclonal and pathogen-specific st

78 novel use of single cell resolution imaging flow cytometry allowed the visualization and quantificat

79 Imaging flow cytometry also showed that CD1a and CD1d proteins w

80 We then performed flow cytometry analyses in 34 critically injured patient

81 Finally, flow cytometry analyses indicated significantly lower su

82 D We performed whole blood transcriptome and flow cytometry analyses on a total of 70 critically inju

83 transcription polymerase chain reaction, and flow cytometry analyses.

84 Flow cytometry analysis after fluorescent antibody label

85 Flow cytometry analysis indicated the cell cycle was arr

86 ocess of tissue homogenization necessary for flow cytometry analysis introduces bias and results in t

87 Confocal microscopy of kidney sections and flow cytometry analysis of glomerular cells from magneti

88 validated 24 hours after removal of GNPs by flow cytometry analysis of mitochondrial depolarisation.

89 Using flow cytometry analysis of paraffin-embedded colon tissu

90 Flow cytometry analysis of the splenic transitional B ce

91 ing endothelial microvesicles, identified by flow cytometry analysis, and significantly more microves

92 . cruzi infection by confocal microscopy and flow cytometry analysis, showing a high expression in ma

93 rough confocal laser scanning microscopy and flow cytometry analysis, we demonstrated that protein/li

94 Using flow cytometry analysis, we found that erf74 and erf74;e

95 ons in need of high-throughput yet sensitive flow cytometry analysis.

96 counts exhibited excellent correlation with flow cytometry analysis.

97 l types and mediators was performed by using flow cytometry and a multiplex assay with bronchoalveola

98 Flow cytometry and adoptive transfer of purified cells s

99 r cells from liver and blood were studied by flow cytometry and analyzed for responses to cytokine an

100 DBS method demonstrated good agreement with flow cytometry and automated hematology analyzers.

101 Multiparameter flow cytometry and automated image analysis of immunosta

102 e labeled this small molecule with QD620 for flow cytometry and confocal imaging analyses.

103 Flow cytometry and confocal imaging with QD620-IRS furth

104 expression on HNECs were determined by using flow cytometry and confocal microscopy.

105 Cell internalization was studied by flow cytometry and confocal microscopy.

106 ular and cytokine content were quantified by flow cytometry and ELISA, respectively.

107 sthmatic patients and control subjects using flow cytometry and ELISA.

108 immunoglobulin levels were analyzed by using flow cytometry and ELISA.

109 Using intracellular flow cytometry and fluorescence microscopy, we determine

110 ealthy donors was prospectively enrolled for flow cytometry and functional experiments.

111 ines to cytotoxic CD8(+) T cells (CTL) using flow cytometry and gene expression analyses.

112 Flow cytometry and gene expression studies demonstrated

113 terize reprogrammed iCPCs by immunostaining, flow cytometry and gene expression; differentiate iCPCs

114 Repopulation was quantified by flow cytometry and histochemical estimation of dipeptidy

115 Finally, flow cytometry and immunofluorescence studies showed tha

116 at the cellular and tissue levels (n = 6) by flow cytometry and immunohistochemistry.

117 Although expression assays based on flow cytometry and immunostaining have shown that multid

118 ion of differentiated cells is performed via flow cytometry and immunostaining to assess quantitative

119 ric solid tumor cells was tested in vitro by flow cytometry and in vivo by PET/CT imaging and dosimet

120 Using flow cytometry and intracellular cytokine staining after

121 interaction in vitro and in vivo as shown by flow cytometry and intravital imaging.

122 We performed 6-color flow cytometry and linear mixed-effects modeling to defi

123 Flow cytometry and mass cytometry are complementary to e

124 ge of this dual-functionality probe for both flow cytometry and mass cytometry in a mimetic cell mixt

125 ctable podocyte-specific proteins by digital flow cytometry and measured nephrinuria by ELISA.

126 logical and histological studies, as well as flow cytometry and measurements of proinflammatory media

127 nflammation-related genes, monitored by both flow cytometry and microarray analysis.

128 Flow cytometry and microscopy studies revealed no detect

129 Nasal lavage for flow cytometry and nasal swabs for viral PCR were perfor

130 eacted with mouse bone marrow neutrophils by flow cytometry and on spleen sections by immunohistochem

131 Their immunophenotype was assessed by flow cytometry and protein expression; activation of can

132 We enumerated small phytoplankton using flow cytometry and qPCR assays for phylogenetically dist

133 Flow cytometry and quantitative PCR was used to measure

134 ne 2,3-dioxygenase (IDO) were analyzed using flow cytometry and quantitative PCR.

135 nd gene expression patterns were measured by flow cytometry and quantitative polymerase chain reactio

136 ional activity of MRP1 were determined using flow cytometry and SECM, and our findings show that thes

137 Using single-cell flow cytometry and single-molecule RNA-FISH assays, we d

138 evice has been evaluated in combination with flow cytometry and turned out to be around 25% (cells en

139 iched CD1d(hi) CD5(+) B cells were sorted by flow cytometry and were adoptively transferred to recipi

140 der hemodynamic flow conditions coupled with flow cytometry and Western blot analysis to elucidate th

141 cement in TIC marker expression (examined by flow cytometry) and improved tumorsphere formation effic

142 s of inflammation and sepsis, intracellular (flow cytometry) and secreted cytokines (Luminex), were a

143 as for its detection by ELISA, Western blot, flow cytometry, and confocal microscopy.

144 Phenotype of immune cells was analyzed by flow cytometry, and cytokines by enzyme-linked immunosor

145 T cell allogeneic responses were measured by flow cytometry, and diapedesis was assessed using transw

146 Also, mass spectrometry, flow cytometry, and electron microscopy analyses indicat

147 rofiled antigen-responsive cells in PBMCs by flow cytometry, and examined cells in whole blood obtain

148 Using confocal imaging, PCR, flow cytometry, and functional strategies, we addressed

149 pheral blood lymphocyte populations by using flow cytometry, and histologic and ultrastructural analy

150 ections and flat mounts, CD11b-based retinal flow cytometry, and qRT-PCR analysis of key microglia ma

151 We analyzed cell subsets by flow cytometry, and soluble mediators and antibodies by

152 lyzed by ELISA or intracellular staining and flow cytometry, and the expression of muscarinic and nic

153 Enzyme-linked immunosorbent assay (ELISA), flow cytometry, and Western blot are common bioanalytica

154 rter protein fusions are evaluated in ELISA, flow cytometry, and Western blot experiments and compare

155 rse transcription polymerase chain reaction, flow cytometry, and Western blotting-in several nonprost

156 poptosis and efferocytosis by morphology and flow cytometry; and GCS efficacy by apoptosis assays and

157 B-cell subsets were quantified by flow cytometry; annexin-V status identified apoptotic ce

158 cell signaling, such as the western blot and flow cytometry, are limited in three aspects: 1) The per

159 highlights an alternative approach in using flow cytometry as a sensitive method for detecting ZIKV

160 PCs were enumerated by flow cytometry as CD45med(+) blood mononuclear cells exp

161 Analyses by flow cytometry as well as the use of Cldn14-lacZ knock-i

162 tly labelled monomeric detection reagents in flow cytometry, as pull-down ligands to selectively enri

163 Applying a capsid flow cytometry assay, we identified two 2'-C-methyladeno

164 e of CaValpha2delta1, indicated by two-color flow cytometry assays and confocal imaging, and prevente

165 r miR-145 were used in cell permeability and flow cytometry assays for apoptosis and proliferation.

166 characterized by fluorescence microscopy and flow cytometry assays in BXPC-3 and PANC-1 cells, two pa

167 sed apoptosis and cell cycle arrest based on flow cytometry assays.

168 Our flow cytometry-assisted susceptibility test (FAST) metho

169 peripheral blood leucocyte populations using flow cytometry at baseline and after 2 weeks of systemic

170 tiation (CD) proteins used to count cells by flow cytometry, band 3 (CD233), CD71, CD45, and CD41.

171 can be used for both confocal microscopy and flow cytometry based high-throughput quantification of g

172 and Methods A prospective and comprehensive flow cytometry-based immunomonitoring program paralleled

173 acilitate the analysis of LTP, here we use a flow cytometry-based method to track chemically induced

174 MBNL1 locus in HeLa cells and established a flow cytometry-based screening system to identify compou

175 high-throughput neutralization screening and flow cytometry-based sorting of single B cells using HIV

176 of this predicted structure, we developed a flow-cytometry-based assay that measures cytosolic excha

177 We describe a flow-cytometry-based protocol for intracellular mRNA mea

178 ble immunohistochemistry (PCNA-staining) and flow cytometry (BrdU incorporation) revealed that a disc

179 ly offer high fluorescence signal for use in flow cytometry, but also show better performance in mass

180 Flow cytometry can provide high-throughput quantificatio

181 Ts were quantitatively and qualitatively via flow cytometry characterized ex vivo and after culture w

182 ld increase in Ki compared with WT RGS2 in a flow cytometry competition binding assay).

183 Here, we used flow cytometry, confocal microscopy, and pharmacologic a

184 uld increase the concordance between SAB and flow cytometry crossmatch (FCXM) results, thus enabling

185 T cells and dendritic cells were assessed by flow cytometry, cytokines by multiplex enzyme-linked imm

186 ation of the laboratory procedure and of the flow cytometry data analyses, as well as clinical valida

187 ly synthesize low-dimensional projections of flow cytometry data that typically have a high number of

188 od, SANJAY, for visualizing high-dimensional flow cytometry datasets.

189 In this study, transcriptome, flow cytometry, electron microscopy, and immunohistochem

190 Activation was measured by flow cytometry, ELISA of cultured supernatants, and F-ac

191 differentiation were determined by means of flow cytometry, ELISA, and multiplex immunoassay.

192 ers in the airways were assessed by means of flow cytometry, ELISA, Luminex, and immunohistochemistry

193 Flow cytometry experiments confirmed that both peptides

194 In flow cytometry experiments the NPs were twice as bright

195 Using flow cytometry expression of CD38, HLA-DR and PD-1 were

196 g epithelial tissue barrier via multi-colour flow cytometry (FACS).

197 culating phenotypic diversity estimates from flow cytometry (FCM) data of minute amounts of sample.

198 njugates toward GAGs binding was examined by flow cytometry, fluorescence microscopy, and gel electro

199 examined mature human skin-derived MCs using flow cytometry for expression of antigen-presenting mole

200 lar (LG) MK pool (defined by side scatter on flow cytometry) gives rise to a mature high granular (HG

201 chromatography (HPLC), spectrophotometry and flow cytometry have been used to estimate cyt c.

202 e platelets to agonists in vitro assessed by flow cytometry (high-responder donors) are cleared more

203 llows: BAT-CD63 upregulation was assessed by flow cytometry; HR-released histamine was quantified by

204 cardiac-specific heterozygous Bin1 deletion, flow cytometry identified 47% less cBIN1-MPs in plasma,

205 Flow cytometry identified cells expressing CD14 and NRP1

206 High throughput single-cell flow cytometry image analysis following SCI revealed CD2

207 helial to mesenchymal transition (EMT) using flow cytometry, immunofluorescence, and quantitative rev

208 asibility is demonstrated by validation with flow cytometry, immunohistochemistry and single-cell RNA

209 Furthermore, flow cytometry immunophenotyping revealed that rat podoc

210 5 + FOXP3 + CD127dim/-) were evaluated using flow cytometry in 32 patients with cGvHD treated by ECP

211 ensive profiling of cell surface proteins by flow cytometry in naive and primed human PSCs.

212 unts were assessed by immunofluorescence and flow cytometry in T and B cells isolated from human PBMC

213 osinophils were identified by microscopy and flow cytometry in the lungs and paratracheal lymph nodes

214 man leukemia K562 cell line was evaluated by flow cytometry in vitro.

215 Moreover, flow cytometry indicated that cells exited the cell cycl

216 ICCs were studied by flow cytometry, intracellular electrophysiology, isometr

217 Flow cytometry is an optical technique that rapidly meas

218 g strategies currently used in polychromatic flow cytometry is not feasible.

219 High-dimensional flow cytometry is proving to be valuable for the study o

220 y, the differential presence of DPP4 allowed flow cytometry-mediated isolation of senescent cells usi

221 Standardized flow cytometry methods were used to characterize the fol

222 Multicolour Flow Cytometry (MFC) produces multidimensional analytica

223 d SW480 cell survival, which was detected by flow cytometry, MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-di

224 Our immunohistochemical data, combined with flow cytometry (N = 5) which identified a small number o

225 Flow cytometry of both spleen and lymph node samples rev

226 Transcriptome analysis and flow cytometry of IL-17A(+)Foxp3(+) cells indicate that

227 Flow cytometry of intrahepatic T cells isolated from liv

228 Membranous location was confirmed by flow cytometry of viable non-permeabilized cells using a

229 itu hybridization (in situ hybridization and flow cytometry) of primary lymphocytes from patients wit

230 We performed flow cytometry on CD3+Va7.2+CD161+ MAIT cells in blood o

231 residual disease (MRD) levels as measured by flow cytometry on day 28 of induction I.

232 1 clinical trials, and quantified by 4-color flow cytometry or allele-specific oligonucleotide real-t

233 ls and T cells were isolated and analyzed by flow cytometry or cytokine assays.

234 imens were analyzed by means of conventional flow cytometry or cytometry by time-of-flight mass spect

235 plication of MRD assessment techniques, like flow cytometry or polymerase chain reaction-based method

236 ared to be indistinguishable when studied by flow cytometry or qRT-PCR.

237 nic and nicotinic receptors was evaluated by flow cytometry or qRT-PCR.

238 e proteins were selected for confirmation by flow cytometry or Western blot.

239 scription-quantitative PCR, microarrays, and flow cytometry, or indirectly, by the presence of oncoge

240 ng flow-chamber assays, confocal microscopy, flow cytometry, PCR analysis, and proteome array.

241 Flow cytometry provides highly sensitive multiparameter

242 Phase-sensitive flow cytometry (PSFC) is a technique in which fluorescen

243 hway, and kinetics of albumin trafficking by flow cytometry, quantitative confocal microscopy, and an

244 Echocardiography, immunostaining, flow cytometry, quantitative real-time polymerase chain

245 Atomic force microscopy, high-resolution flow cytometry, real-time quantitative RT-PCR, and mass

246 oE, and healthy controls, were analyzed with flow cytometry regarding levels of CD23, CD44, CD54, CRT

247 n on B cells were measured using ELISPOT and flow cytometry, respectively.

248 oimaging, super-resolution microscopies, and flow cytometry reveal almost 100-fold more efficient co-

249 racterization of circulating monocytes using flow cytometry revealed increased chemokine receptor exp

250 Analysis of cell cycle by flow cytometry revealed that inhibition of tumor cell gr

251 Pneumoniae, using flow cytometry, reverse-transcription polymerase chain r

252 Flow cytometry showed about 70% population of dead and c

253 Flow cytometry showed that trastuzumab facilitated uptak

254 By flow cytometry, single cells within these cell lines sim

255 Another strategy is the combination of flow cytometry sorting of antigen-binding B lymphocytes

256 Flow cytometry studies revealed that heparin increased t

257 supplement technology to the microscopy and flow cytometry, the microfluidic deformability sensor wo

258 The phenotype of DC was evaluated by flow cytometry, the production of cytokines was analyzed

259 Despite the analytical prowess of flow cytometry, there are applications where these rates

260 Furthermore, we used flow cytometry to assess inhibition of mIDH2 on hematopo

261 ers, the T cell responses were determined by flow cytometry to be Ag specific.

262 esent the development of rapid methods using flow cytometry to characterize several aspects of the ph

263 The trapped cells were analyzed with flow cytometry to detect apoptosis and pyroptosis; 26% w

264 healthy children (n=20) using multiparameter flow cytometry to detect markers of T cell maturation, e

265 We used flow cytometry to determine the presence of MBL, defined

266 sion tomography imaging, gamma counting, and flow cytometry to evaluate the biodistribution, nanomedi

267 emia, we used high-resolution microscopy and flow cytometry to highlight the heterogeneity of drug ac

268 Utilizing flow cytometry to identify circulating, collagen type 1(

269 We utilized intracellular phospho-flow cytometry to investigate the relationship between M

270 We performed flow cytometry to measure six markers of synaptic subtyp

271 We used flow cytometry to quantify expression of the inhibitory

272 use overexpression studies, mutagenesis, and flow cytometry to show that ICAP1 contains a functional

273 as assessed by detection of virus antigen by flow cytometry together with various hematopoietic cell

274 were analyzed for immune cell composition by flow cytometry, Toll-like receptor (TLR) expression by q

275 sion line and a T-DNA insertion mutant using flow cytometry, transactivation and electrophoretic mobi

276 -induced polyfunctional cellular activity by flow cytometry, transcriptional profiling, epigenetic, a

277 ressed in a cancer cell line was measured by flow cytometry using a fluorescent imaging probe.

278 tory T (Treg)-cell induction was assessed by flow cytometry using a transgenic T-cell transfer model.

279 nying evidence from immunohistochemistry and flow cytometry using antibodies with conformationally se

280 approximately 300 proteins by multiparameter flow cytometry using multiple aneuploid model systems su

281 The high-dimensionality of data generated by flow cytometry usually makes it difficult to visualize.

282 -DQ-gluten tetramer-based assay, we combined flow-cytometry variables in a multiple regression model

283 Flow cytometry was used for the enumeration and characte

284 Polychromatic flow cytometry was used to analyze T-cell activation mar

285 Flow cytometry was used to analyze VEGF-R2 expression in

286 Flow cytometry was used to evaluate bone marrow and sple

287 Flow cytometry was used to examine T-cell development.

288 Flow cytometry was used to measure IFN-gamma, IL-13, IL-

289 By means of imaging flow cytometry, we demonstrate a strong and quick bindin

290 Using flow cytometry, we found that basophils were significant

291 Using imaging flow cytometry, we found that both T. gondii and IL-10 i

292 Here, using immunofluorescence and flow cytometry, we show that the Gfi1(Cre) mice produce

293 aging by confocal microscopy and analysis by flow cytometry, we synthesized derivatives of Taxol link

294 Immunohistochemistry and flow cytometry were used to identify myeloid cells and n

295 , ELISA, western blot, mass spectrometry and flow cytometry were used to screen for autoantibodies, i

296 ational studies, in vitro assays and ex vivo flow-cytometry were performed.

297 eads to loss of gene expression as judged by flow cytometry, Western blot or immunofluorescence.

298 idney tissue, VTEA replicated the results of flow cytometry while providing detailed analysis of the

299 f allergic patients were quantified by using flow cytometry with QuantiBRITE beads and compared with

300 Here we describe a flow cytometry workflow to determine carbapenem suscepti