ライフサイエンスコーパス: immunofluorescence

1 and in normal and AE skin biopsy specimens (immunofluorescence).

2 tive muscle fibers, which was verified using immunofluorescence.

3 ogonia, and performed validation studies via immunofluorescence.

4 rizontal cells also transiently exhibit NFIA immunofluorescence.

5 hain reaction followed by immunoblotting and immunofluorescence.

6 l cytoskeletal structure using AFM, SEM, and immunofluorescence.

7 calbindin, as assessed by real-time PCR and immunofluorescence.

8 tic stellate cell activation was detected by immunofluorescence.

9 lymerase chain reaction, immunoblotting, and immunofluorescence.

10 otin nick-end labeling and cleaved caspase 3 immunofluorescence.

11 n, and distribution of hybridized probes and immunofluorescence.

12 ress VIP or VIP receptors were quantified by immunofluorescence.

13 postoperative day 7 by colony formation and immunofluorescence.

14 Human pancreatitis tissues were analyzed by immunofluorescence.

15 thways were investigated by IHC analysis and immunofluorescence.

16 rget proteins are concurrently stained using immunofluorescence.

17 LR and RAMP1 was observed in these areas via immunofluorescence.

18 ated by using real-time quantitative PCR and immunofluorescence.

19 en retrieval to demonstrate monoclonal LC by immunofluorescence.

20 ence of periodontal pathogens using indirect immunofluorescence.

21 to both TUNEL staining and cleaved caspase 3 immunofluorescence.

22 as judged by flow cytometry, Western blot or immunofluorescence.

23 ursor cells (BrdU+/Nestin+) were detected by immunofluorescence.

24 r translocation of NF-kappaB was detected by immunofluorescence.

25 were analyzed using simultaneous multicolor immunofluorescence.

26 turing PAGE, nuclear magnetic resonance, and immunofluorescence.

27 combines ultrathin sectioning of tissue with immunofluorescence allowing precise identification of sm

28 High-resolution imaging of immunofluorescence along the monolayer provided a contin

29 Immunofluorescence also suggested that Ang II reduced su

30 Reciprocal pull-down experiments and immunofluorescence analyses demonstrate that a fraction

31 d quantitative polymerase chain reaction and immunofluorescence analyses of colon tissues from patien

32 Immunofluorescence analyses revealed granular antigen-an

33 Immunofluorescence analyses revealed that PRC1 members a

34 Immunofluorescence analyses showed that MAPKBP1 is not p

35 Immunofluorescence analysis (IFA) and plasma membrane is

36 genomes in productively infected cells, and immunofluorescence analysis confirmed that CDK9, phospho

37 Immunofluorescence analysis demonstrated increased intra

38 Immunofluorescence analysis further demonstrated that ma

39 Furthermore, immunofluorescence analysis in human MS brain tissue sho

40 Finally, immunofluorescence analysis indicates that the efferent

41 double-strand breaks (DSBs) were assessed by immunofluorescence analysis of 53BP1 foci; DSB levels we

42 zones of human brain, as suggested by HUWE1 immunofluorescence analysis of cerebral organoids.

43 Immunofluorescence analysis of human specimens suggested

44 Immunofluorescence analysis of scratch-wounded cells rev

45 Immunofluorescence analysis revealed reduced full-length

46 Immunofluorescence analysis showed that CD8(+) TILs expr

47 Immunofluorescence analysis shows that PDZD11 is localiz

48 including toxicant exposure, immunoblotting, immunofluorescence analysis, tight junction (TJ)-permeab

49 atterns were examined by flow cytometric and immunofluorescence analysis.

50 Using immunofluorescence and ChIP-seq we determine the distrib

51 inase 2 (CDK2) activity followed by endpoint immunofluorescence and computational cell synchronizatio

52 Virus titration, immunofluorescence and confocal laser scanning microscop

53 125 healthy Kenyan children were analysed by immunofluorescence and confocal microscopy to determine

54 sels were assessed ex vivo with quantitative immunofluorescence and correlated with corresponding in

55 We used multiplex immunofluorescence and digital image analysis to examine

56 and increased junction length as revealed by immunofluorescence and electron microscopy reflected cAM

57 By employing confocal immunofluorescence and electron microscopy we investigat

58 Immunofluorescence and electrophysiology data further co

59 mber and cellularity of pancreatic islets by immunofluorescence and FACS.

60 Nur77 protein amounts were assessed by immunofluorescence and flow cytometry in T and B cells i

61 Here, using immunofluorescence and flow cytometry, we show that the

62 Connexin36 immunofluorescence and freeze-fracture replica immunogol

63 Colon tissues were collected and immunofluorescence and histochemical analyses were perfo

64 as type VII collagen expression measured by immunofluorescence and immunoelectron microscopy.

65 In fibrillary GN specimens only, immunofluorescence and immunohistochemistry with an anti

66 s by combining retrograde tract tracing with immunofluorescence and in situ hybridization techniques.

67 LAP+ and LAP- fractions were analyzed by immunofluorescence and microarray.

68 RNA studies and on the cellular level using immunofluorescence and microscopy.

69 Using a combination of immunohistochemistry, immunofluorescence and neural tracing with subunit B of

70 Protein levels were measured by quantitative immunofluorescence and quantitative chromogenic assessme

71 -related proteins and genes, as confirmed by immunofluorescence and RT-qPCR.

72 Immunofluorescence and single-cell RNA sequencing found

73 Live-cell immunofluorescence and super-resolution microscopy of ep

74 Immunofluorescence and total internal reflection fluores

75 Also, by a combination of immunofluorescence and transganglionic tracing following

76 using combinatorial approaches that involved immunofluorescence and transmission electron microscopy,

77 reduced expression of SLC26A6 in duodenum by immunofluorescence and Western blot analysis.

78 Additionally, we confirmed by immunofluorescence and western-blot that rod degeneratio

79 Here, we used neuroanatomical tracing, immunofluorescence, and confocal imaging to demonstrate

80 We combined tissue clearing, 3D-immunofluorescence, and electron tomography (ET) to long

81 drial function; results from immunoblotting, immunofluorescence, and functional assays validated thes

82 rse transcription polymerase chain reaction, immunofluorescence, and immunoblot analyses in Caco-2, H

83 ame patients, and performed gene expression, immunofluorescence, and immunohistochemical analyses.

84 ocal laser and scanning electron microscopy, immunofluorescence, and live-cell imaging, our study sho

85 itative reverse-transcriptase PCR (qRT-PCR), immunofluorescence, and Luminex technology.

86 tome sequencing, ingenuity pathway analysis, immunofluorescence, and nerve elongation, as well as bra

87 combination of in situ hybridization (ISH), immunofluorescence, and PCR for positive-strand and nega

88 ted by immunoprecipitation/Western blotting, immunofluorescence, and proximity ligation assay.

89 lected and analyzed by immunohistochemistry, immunofluorescence, and quantitative polymerase chain re

90 hymal transition (EMT) using flow cytometry, immunofluorescence, and quantitative reverse transcripti

91 and cholesterol and analyzed by immunoblot, immunofluorescence, and reverse transcription quantitati

92 determination of regional activation by Fos immunofluorescence, and RNA sequencing of the basolatera

93 Immunohistochemistry, immunofluorescence, and Western blot were used to valida

94 Studies employing immunofluorescence antibody-based assays reveal no chang

95 development of a simultaneous multi-channel immunofluorescence approach and new algorithms for compu

96 We utilized immunofluorescence approaches to study mTOR cellular dis

97 Viral detection was done by culture, direct immunofluorescence assay (DFA) or polymerase chain react

98 a radiobinding assay, to endomysium using an immunofluorescence assay, and antibodies to a deamidated

99 3-hP2X7R) and underwent Western blotting, an immunofluorescence assay, and radioimmunohistochemistry

100 Immunofluorescence assay, surface proteolysis, and novel

101 al cohort using a novel flow cytometry-based immunofluorescence assay.

102 tosporidium parvum Infection was assessed by immunofluorescence assays and confocal and scanning elec

103 cking of target gene products as assessed by immunofluorescence assays and Western blot analyses.

104 at an early age, while the histological and immunofluorescence assays indicated the presence of prog

105 on, protein-fragment complementation, and co-immunofluorescence assays showed that LH2 and FKBP65 are

106 Indirect immunofluorescence assays that combined monoclonal (oute

107 se chain reaction, immunohistochemistry, and immunofluorescence assays.

108 trophoresis chip thus shows the potential of immunofluorescence based-assay applications to meet diag

109 implications of positive or negative direct immunofluorescence biopsies (DIF) in patients with clini

110 in situ hybridization, immunohistochemistry, immunofluorescence by conventional and spinning disc con

111 Through alanine scanning, immunofluorescence cell staining and co-immunoprecipitat

112 and video microscopy, immunohistochemistry, immunofluorescence, cell viability assays and optical el

113 thways was examined by using flow cytometry, immunofluorescence, coimmunoprecipitation, and gene expr

114 Immunofluorescence comparisons revealed that central exp

115 Immunofluorescence confirmed chemokine expression locali

116 Immunofluorescence/confocal microscopy was used for IL-1

117 Immunofluorescence correctly identified mislocalized or

118 vidual resected tumor samples, determined by immunofluorescence, correlated with the respective (18)F

119 or various cell organelles learned from real immunofluorescence data from the Human Protein Atlas.

120 d the mutant exon 23 in dystrophic mice, and immunofluorescence data supported the restoration of dys

121 can be used to generate synthetic multiplex immunofluorescence data.

122 Double immunofluorescence demonstrated that virtually all ChAT-

123 indistinguishable patients, who have direct immunofluorescence (DIF)-negative biopsies, be excluded

124 on protein, and PilA, as assessed by in situ immunofluorescence, displayed coordinated, unipolar loca

125 Furthermore, MCU immunofluorescence distribution was biased toward the mi

126 Using western blotting, immunofluorescence, ELISA and qRT-PCR, we investigated t

127 Cell surface biotinylation and immunofluorescence experiments in cells expressing the e

128 Immunoprecipitation and immunofluorescence experiments revealed that MUC4beta fo

129 Immunofluorescence experiments show that single-DSBs and

130 We report that RFRP-3 immunofluorescence expression patterns and RFRP-3/GnRH c

131 ied placental macrophages to express CD74 by immunofluorescence, flow cytometry, and RT-PCR.

132 re, we examined all ANA patterns by indirect immunofluorescence for 859 rheumatoid arthritis (RA) pat

133 irmed individuals with AD by Western blot or immunofluorescence for AQP4, amyloid-beta 1-42, and glia

134 Multi-label immunofluorescence for CD163 and Ki-67 confirmed that th

135 We assessed retinal tissues using immunofluorescence for glial fibrillary acidic protein,

136 diacetyl-induced airway damage in mice with immunofluorescence for markers of protein turnover and a

137 essed ex vivo by digital autoradiography and immunofluorescence for microscopic visualization of perf

138 ral fluid culture or PCR, blood culture, and immunofluorescence for P. jirovecii defined microbiologi

139 y a clonogenic assay; apoptosis by Annexin V immunofluorescence; gammaH2AX, Rad51, and HDAC4 by immun

140 and regulatory B cells were visualized with immunofluorescence histology.

141 Traditionally, labeling is achieved by immunofluorescence; however, diffusion of antibody molec

142 ver, in this study we describe two disparate immunofluorescence (IF) experiments that suggest otherwi

143 cation of frameworks for analysing multiplex immunofluorescence image data.

144 ntegrated workflow for analyzing whole-slide immunofluorescence images and tissue microarrays, includ

145 THRIVE was designed with highly multiplexed immunofluorescence images in mind, and, by providing a p

146 Analysis of dual immunofluorescence images indicated a potential perinucl

147 Multiplexed immunofluorescence imaging of formalin-fixed, paraffin-e

148 Immunofluorescence imaging of nsp15 mutant virus-infecte

149 icin protection assays and three-dimensional immunofluorescence imaging.

150 rebellar arteries were labelled for confocal immunofluorescence imaging.

151 elial tissues were collected and analyzed by immunofluorescence, immunohistochemical, and quantitativ

152 ion included hematoxylin and eosin staining, immunofluorescence, immunohistochemistry, picrosirius re

153 We also report anti-Foxo3 immunofluorescence in adult human outer hair cells.

154 DNA double-strand-break levels by gamma-H2AX immunofluorescence in blood lymphocytes.

155 Immunofluorescence in cell culture, quantitative transmi

156 Double immunofluorescence in CIPN rats showed that Nav1.7 was u

157 Using quantitative immunofluorescence in cultured mouse hippocampal neurons

158 of uPA and uPAR were characterized by double immunofluorescence in the inflamed synovium from patient

159 line cores (R2 = 0.83-0.97) by quantitative immunofluorescence in the PD-L1 index tissue microarray.

160 line cores (R2 = 0.83-0.97) by quantitative immunofluorescence in the PD-L1 index tissue microarray.

161 nd qRT-PCR miRNA analyses were combined with immunofluorescence in this study.

162 his finding by cytofluorimetric analysis and immunofluorescence in TUBO-derived tumorspheres and in a

163 Immunofluorescence indicated that podoplanin(+) stromal

164 Immunofluorescence is a highly specific diagnostic test

165 However, sensitivity is limited and immunofluorescence is not suitable as a stand-alone test

166 Three of the MAC-ELISA kits and 1 indirect immunofluorescence kit had comparable performance to the

167 Using immunofluorescence labeling of latent nuclear antigen (L

168 Using immunofluorescence labeling we confirmed the activation

169 Using double-immunofluorescence labeling, we observed the potential c

170 rotein levels, we have developed a quadruple immunofluorescence method to accurately quantify the pre

171 Using immunofluorescence microscopy (IFM), we observed that S.

172 Finally, immunofluorescence microscopy and subcellular fractionat

173 Immunofluorescence microscopy and Western blotting resul

174 Immunofluorescence microscopy and western blotting revea

175 (0, 2 and 6 h) were analysed using confocal immunofluorescence microscopy for fibre type-specific IM

176 17 SCID mice, the bacteria are detectable by immunofluorescence microscopy in neutrophils and macroph

177 sucrose gradient centrifugation and indirect immunofluorescence microscopy indicated that most ROMK p

178 .6 years) were identified using the indirect immunofluorescence microscopy knockout analysis.

179 Unexpectedly, immunofluorescence microscopy localized TbRFT1 to both t

180 ns was confirmed by immunohistochemistry and immunofluorescence microscopy on clinical samples and ti

181 Immunofluorescence microscopy revealed densely packed ch

182 Immunofluorescence microscopy revealed that TIR-1 and JN

183 We examined by immunofluorescence microscopy thoracic aortas from 16 si

184 We utilized quantitative PCR and double immunofluorescence microscopy to determine that both PPA

185 Here, we employed bioinformatic analysis and immunofluorescence microscopy to examine the physiologic

186 bule network was visualized in HeLa cells by immunofluorescence microscopy using Bimolecular Fluoresc

187 These findings were corroborated by immunofluorescence microscopy which demonstrated relativ

188 Immunofluorescence microscopy with anti-peroxisome membr

189 tegrating transcriptomics and antibody-based immunofluorescence microscopy with validation by mass sp

190 g bioluminescence resonance energy transfer, immunofluorescence microscopy, and co-immunoprecipitatio

191 hagosomes was confirmed by Western blotting, immunofluorescence microscopy, and immunoelectron micros

192 eruli at light microscopy, one glomerulus at immunofluorescence microscopy, and one glomerulus at ele

193 essed by scanning electron microscopy (SEM), immunofluorescence microscopy, histochemistry and quanti

194 and proteins were analyzed by using confocal immunofluorescence microscopy, immunoblotting, myelopero

195 Using subcellular fractionation and immunofluorescence microscopy, we observed that PDC-E2 i

196 In the present study, using immunofluorescence microscopy, we show that anaerobiosis

197 s, were confirmed by electron microscopy and immunofluorescence microscopy.

198 MP co-receptor hemojuvelin was visualized by immunofluorescence microscopy.

199 rkers WT1 and synaptopodin, as determined by immunofluorescence microscopy.

200 ellular assembly by immunohistochemistry and immunofluorescence microscopy.

201 and validated with the established method of immunofluorescence microscopy.

202 ild type by immunoblot analysis and confocal immunofluorescence microscopy.

203 ntent and capillarisation using quantitative immunofluorescence microscopy.

204 r exposure to CSF-1 for 2.5 min was shown by immunofluorescence microscopy.

205 Our goal was to validate multiplex immunofluorescence (mIF) panels to apply to formalin-fix

206 Immunofluorescence of human lungs confirmed our in vivo

207 Immunofluorescence of the residual intact internal limit

208 ive and robust method to perform multiplexed immunofluorescence on archived or clinical tissue specim

209 gy of the nuclear envelope was assessed with immunofluorescence on cultured fibroblasts.

210 NETs were visualized by immunofluorescence or quantified by Sytox Green fluoresc

211 ); intestines were collected and analyzed by immunofluorescence, or RNA and protein were collected fr

212 In addition, immunofluorescence provided a result in 55% (39) of case

213 AC cells (reciprocal co-immunoprecipitation, immunofluorescence, proximity ligation, co-capping assay

214 est to diagnose this disease is the indirect immunofluorescence reaction, however two samples of pair

215 ctivity was analyzed by means of microscopy, immunofluorescence, real-time reverse-transcription poly

216 s were more likely to have a negative direct immunofluorescence result than patients with biopsies fr

217 ic pain also showed electrophysiological and immunofluorescence results indicating an increased expre

218 Immunofluorescence results revealed that the CREKA-Lipo-

219 Immunofluorescence results were available within 14 days

220 In addition, immunofluorescence revealed CD8 T cells near virus-infec

221 Immunofluorescence revealed peak infection density in gu

222 Immunofluorescence revealed SGPL1 expression in mouse po

223 transport from the spinal cord combined with immunofluorescence revealed spinal-projecting Galphat-S-

224 Immunofluorescence revealed that EGF-activated EGFR, MEK

225 Immunofluorescence revealed that most of these processes

226 Immunofluorescence revealed the presence of Cx43, the ma

227 Immunofluorescence reveals that cholesterol depletion ab

228 cephalitis virus (JEV), using a high-content immunofluorescence screen.

229 Whole-cell inclusion immunofluorescence serum antibody titers were recorded a

230 We found that periventricular PV-immunofluorescence showed positive correlation to the gr

231 Indirect immunofluorescence showed reduced COL6A5 expression in t

232 Immunofluorescence showed that C5b-9 and C4d deposition

233 Double immunofluorescence showed that neither LPXRFa-immunoreac

234 h a significant increase of lignin and xylan immunofluorescence signal.

235 form to efficiently analyze high-dimensional immunofluorescence signals, we hope to advance these dat

236 age single-molecule FISH in combination with immunofluorescence (smFISH-IF) and determined whether th

237 Immunofluorescence staining against AstA, AT, and TK in

238 f specific ECM proteins was assessed through immunofluorescence staining and colorimetric assay kits.

239 antibodies (MAbs), as determined by indirect immunofluorescence staining and flow-cytometric analysis

240 In the present study, we employed immunofluorescence staining and Western blot analysis to

241 LK-FISH patterns were examined in CTCs using immunofluorescence staining combined with filter-adapted

242 munoblot, electron microscopy, together with immunofluorescence staining for LC3 and p62 indicated an

243 Immunofluorescence staining for macrophages in cross-sec

244 nce were assessed by immunohistochemical and immunofluorescence staining of hearts and aortas.

245 Using combined immunofluorescence staining of SGs markers and COX-2 pro

246 l separation of the TJs of adjacent cells in immunofluorescence staining of the TJ molecules occludin

247 Immunofluorescence staining of ventral prostate tissue f

248 This finding was also validated with immunofluorescence staining on Foxp3(+)CD4(+) and PD-1(+

249 xpression of KCa3.1 in vivo was confirmed by immunofluorescence staining on multinucleated cells at t

250 Immunofluorescence staining revealed a decrease in cathe

251 lfate polyacrylamide gel electrophoresis and immunofluorescence staining to confirm the primary targe

252 Double immunofluorescence staining using antibodies against cho

253 Using triple immunofluorescence staining we tested whether there were

254 Immunofluorescence staining with anti-alpha-tubulin anti

255 In double-label immunofluorescence staining, CD11c+, a marker of myeloid

256 After performing gammaH2AX immunofluorescence staining, DSBs were quantified with a

257 meter macrosections enables simple and rapid immunofluorescence staining, optical clearing, and confo

258 as confirmed in all 3 cell types by means of immunofluorescence staining, RT-PCR, and qRT-PCR, and qR

259 Using immunofluorescence staining, we confirmed the expression

260 ro and in patients with COPD was assessed by immunofluorescence staining, Western blot analysis, and

261 flux, mRNA expression, Western blotting, and immunofluorescence staining.

262 key fibrinolytic molecules was determined by immunofluorescence staining.

263 olute sensitivity when compared to optimized immunofluorescence staining.

264 fluorescence; gammaH2AX, Rad51, and HDAC4 by immunofluorescence staining; HDAC4, Rad51, and ubiquitin

265 Live-cell imaging and immunofluorescence studies demonstrated that the mutant

266 At the tissue level, immunofluorescence studies indicate that MLG epitopes in

267 Combining quantitative PCR analyses with immunofluorescence studies revealed exclusive expression

268 Immunofluorescence studies revealed that the subcellular

269 Finally, flow cytometry and immunofluorescence studies showed that alpha1D protein w

270 In the diagnostic cohort immunofluorescence successfully identified 22 of 25 pati

271 Using the VectraR automated multiparametric immunofluorescence technique, we quantified intratumoral

272 applied ImmunoCAP to measure IgE levels and immunofluorescence techniques to examine epithelial barr

273 In this study, dual immunohistochemical and immunofluorescence techniques were employed to unequivoc

274 Using immunofluorescence technology, activation of MAPKs and A

275 blot analysis and a newly developed indirect immunofluorescence test (IFT).

276 show by single-cell expression profiling and immunofluorescence that SOX7 is broadly expressed across

277 In this study, we showed by immunofluorescence that the target interstitial cells of

278 We also analyzed by double immunofluorescence the relation of this system with othe

279 ential biomarkers, immunohistochemistry, and immunofluorescence, the ex vivo expression of PD-1 and a

280 require endothelial IL-1 receptors, shown by immunofluorescence to be expressed in peritoneal capilla

281 okines; biopsy samples were also analyzed by immunofluorescence to identify sources of IL28 productio

282 CTCs were identified by immunofluorescence using commercially available antibodi

283 Multiple-label immunofluorescence was applied to postmortem sections of

284 Immunofluorescence was performed on patient and mouse sk

285 Immunofluorescence was performed to assess the presence

286 nt RNA-fluorescent in situ hybridization and immunofluorescence), we show here that different genes a

287 Using immunofluorescence, we confirmed the functionality of th

288 es of biochemical cellular fractionation and immunofluorescence, we demonstrate a signal for CD24 in

289 Interestingly, using immunofluorescence, we demonstrated that the GM1 increas

290 By enzyme-linked immunosorbent assay and immunofluorescence, we found that glycophorin A, the mos

291 sing immunoblotting, in situ zymography, and immunofluorescence, we found that LTP induction was asso

292 Western blotting and immunofluorescence were used for evaluating expression o

293 Immunohistochemistry and immunofluorescence were used to determine protein locali

294 and TGF-beta signaling were determined using immunofluorescence, western blot, reverse-transcriptase

295 ons such as transfection, luciferase assays, immunofluorescence, western blotting and virus infection

296 of FAM13A in COPD lungs were assessed using immunofluorescence, Western blotting, and reverse transc

297 Examining SIVE lesions, using double-label immunofluorescence with antibodies against SIV-Gag-p28 a

298 However, conventional immunofluorescence with organic dyes is limited in the n

299 ion standards, similar calibration tools for immunofluorescence with small organic fluorophores are l

300 Through adaptation of the immunofluorescence workflow on FFPE sections milled at h