ライフサイエンスコーパス: immunofluorescence

1 ot bind human or mouse epidermis by indirect immunofluorescence.

2 phy, whereas TAM burden was determined using immunofluorescence.

3 various proteins within NPs was assessed by immunofluorescence.

4 nation was compared with autoradiography and immunofluorescence.

5 aepithelial leukocytes, and tissue multiplex immunofluorescence.

6 expanding retinal network, as determined by immunofluorescence.

7 muscle, and thinner varicose axons with less immunofluorescence.

8 ribe analysis using quantitative single-cell immunofluorescence.

9 an hepatocytes (PHH) by Western blotting and immunofluorescence.

10 A array analysis, in situ hybridization, and immunofluorescence.

11 ines are screened by immunoprecipitation and immunofluorescence.

12 s were tested for IgE and IgG4 binding using immunofluorescence.

13 qPCR, flow cytometry, Western blotting, and immunofluorescence.

14 ers for each target was also confirmed using immunofluorescence.

15 CD47 receptor binding was demonstrated by immunofluorescence.

16 Immunohistochemistry, immunofluorescence, 15-PGDH activity assays, and in situ

17 Immunofluorescence against DA revealed immunoreactivity

18 Finally, immunofluorescence also showed ERICH3 colocalization wit

19 ts were contextualized through multispectral immunofluorescence analyses and evaluating putative cell

20 quantitative real-time PCR, immunoblot, and immunofluorescence analyses confirmed that MRP3 (multidr

21 Single-gene RT-qPCR, immunoblot, and immunofluorescence analyses confirmed that MRP3, which w

22 Histological and immunofluorescence analyses indicate abnormal organelle

23 Immunofluorescence analyses of patient fibroblasts revea

24 tation, immunoblotting, gene expression, and immunofluorescence analyses, we report that CD40 ligatio

25 sion electron microscopy, immunoblotting and immunofluorescence analyses, we studied the protective e

26 cted and analyzed by immunohistochemical and immunofluorescence analyses.

27 e polymerase chain reaction, immunoblot, and immunofluorescence analyses.

28 A full optoPlate-96 experiment with immunofluorescence analysis can be performed within ~24

29 Immunofluorescence analysis characterized the mutant phe

30 Furthermore, single-cell immunofluorescence analysis demonstrated reciprocal expr

31 Immunofluorescence analysis indicated similar results fo

32 Immunofluorescence analysis localized PHIP to the leadin

33 epidermolytic ichthyosis was observed by the immunofluorescence analysis of correctly gene-edited sin

34 Immunofluorescence analysis of MDA-MB-231 ADAM15A expres

35 Surprisingly, confocal immunofluorescence analysis of P. murina-infected mouse

36 Immunofluorescence analysis of skin rash, lungs, lymph n

37 Immunofluorescence analysis of the occipital cortex show

38 or specificity, followed by Western blot and immunofluorescence analysis on islets from 10 and 12 don

39 le-exome and RNA sequencing, integrated with immunofluorescence analysis, to uncover the immunogenomi

40 1 application under immunohistochemistry and immunofluorescence analysis.

41 ised and was detected in complex with P27 by immunofluorescence and co-immunoprecipitation, respectiv

42 Immunofluorescence and coimmunoprecipitation studies rev

43 We used immunofluorescence and confocal microscopy analysis to i

44 Using immunofluorescence and confocal microscopy, we determine

45 Immunofluorescence and electron microscopy of Drosophila

46 Immunofluorescence and electron microscopy were largely

47 ic material in this specimen, and subsequent immunofluorescence and enzyme-linked immunosorbant assay

48 of congenic mouse strains permits the use of immunofluorescence and flow cytometry-based methodologie

49 Colonoids were analyzed by immunofluorescence and for ion transport.

50 asurement, transmission electron microscopy, immunofluorescence and genetic analyses, and high-speed

51 Biopsies from patients were analyzed by immunofluorescence and histochemical analyses.

52 rtalized lung cancer cell lines via indirect immunofluorescence and immunoblotting, respectively.

53 By immunofluorescence and immunoelectron microscopy, dynami

54 Meanwhile, histological immunofluorescence and immunohistochemical analyses reve

55 We collected gastric tissues and performed immunofluorescence and immunohistochemical analyses to s

56 Immunofluorescence and immunohistochemistry examinations

57 body has been extensively used in fixed cell immunofluorescence and immunohistochemistry.

58 The same tissues were analyzed by indirect immunofluorescence and immunoperoxidase assays using the

59 s to IP by combining retrograde tracing with immunofluorescence and in situ hybridization techniques.

60 Flow cytometry, immunofluorescence and murine cytokinesis-block micronuc

61 scription of the antioxidant response genes (immunofluorescence and nuclear RNA sequencing) were inve

62 ker epithelial expression was measured using immunofluorescence and quantified using the H score (MMP

63 aying auditory signals to the brain, we used immunofluorescence and quantitative image analysis to ex

64 ldown, and coimmunoprecipitation assays, and immunofluorescence and scanning electron microscopy anal

65 Biliary senescence was determined by immunofluorescence and senescence-associated beta-galact

66 Here, using several human cell lines, immunofluorescence and structured illumination microscop

67 Using immunofluorescence and tracing experiments, we found tha

68 llowing LD-STZ treatment was validated using immunofluorescence and transgenic animals expressing NF-

69 This was in concurrence with immunofluorescence and ultrastructure analysis of murine

70 Immunofluorescence and Western blot confirmed PTH1R expr

71 ds, leading to a larger quantity of CD44 (by immunofluorescence) and a higher production of collagen

72 ys was demonstrated by immunohistochemistry, immunofluorescence, and electron microscopy, while singl

73 s, MitoTracker-based mitochondrial analysis, immunofluorescence, and high-throughput coregulator anal

74 nd colon tissues were analyzed by histology, immunofluorescence, and immunoblots.

75 , GFAP) were examined using gene expression, immunofluorescence, and in silico modeling approaches in

76 n of neuronal tracing, immunohistochemistry, immunofluorescence, and in situ hybridization, we charac

77 biased receptomics, transcriptomic analyses, immunofluorescence, and in situ hybridization, we found

78 were collected and analyzed by histology and immunofluorescence, and mesenchymal cells were isolated.

79 tion, and differentiation by flow cytometry, immunofluorescence, and organoid assays.

80 ament compartment as shown by fractionation, immunofluorescence, and proximity ligation assays.

81 LAT1 expression (quantitative real-time PCR, immunofluorescence, and RNA sequencing), its interaction

82 estern blotting, qPCR, immunohistochemistry, immunofluorescence, and transcriptional profiling for mR

83 protein overexpression, quantitative RT-PCR, immunofluorescence, and various biochemical assays, we f

84 Using high speed video microscopy-, immunofluorescence-, and in situ hybridization analyses,

85 nor serum samples were evaluated by indirect immunofluorescence antibody assay to identify immunoglob

86 Surface assays, such as ELISA and immunofluorescence, are nothing short of ubiquitous in b

87 lidated, high-resolution digital microscopic immunofluorescence assay (IFA) that incorporates beta-ca

88 and analyzed for Cryptosporidium by qPCR and immunofluorescence assay (IFA).

89 ng infectivity assays, quantitative PCR, and immunofluorescence assay approaches, we have further cha

90 The gold standard test is an immunofluorescence assay utilizing whole cell antigens,

91 Immunofluorescence assay was used to detect CpEF1alpha w

92 ared and validated with a reference clinical immunofluorescence assay, confirming an excellent correl

93 Immunofluorescence assays (IFA) specific for double-stra

94 s from qRT-PCR were compared with those from immunofluorescence assays (IFA).

95 -Rad Laboratories, Hercules, CA) and matched immunofluorescence assays (IFAs; MBL Bion, Des Plaines,

96 eplication-transcription conflicts and using immunofluorescence assays and DNA combing approaches, we

97 Using immunofluorescence assays and Western blotting during in

98 Indirect immunofluorescence assays confirmed 17 of them interacte

99 observation questions the reliability of LC3-immunofluorescence assays in cells with compromised auto

100 In immunofluorescence assays, host MUC13 protein expression

101 on, replicon DNA replication and whole virus immunofluorescence assays.

102 th CD spectroscopy, atomic force microscopy, immunofluorescence-based imaging, and various biochemica

103 , lacking a spatial context, and traditional immunofluorescence, capturing only two to six molecular

104 ssues were analyzed by immunohistochemistry, immunofluorescence, cell viability, apoptosis assays, an

105 ity ligation assay, immunoprecipitation, and immunofluorescence, concordant with CFTR correction.

106 Moreover, proteomics and immunofluorescence confirmed the presence of major vesic

107 Immunofluorescence confocal microscopy of differentiated

108 ng on LAM (n = 4) and control (n = 7) lungs, immunofluorescence confocal microscopy, ELISA, and aptam

109 esis, electrophysiological measurements, and immunofluorescence confocal microscopy, we addressed whe

110 sing human and murine cell lines, along with immunofluorescence, confocal microscopy, endocytosis, PL

111 ney biopsies, with or without IgG by routine immunofluorescence, contain Gd-IgA1-specific IgG autoant

112 aracterization with immunohistochemistry and immunofluorescence demonstrated membranes to be negative

113 ty to the target, we carried out an indirect immunofluorescence detection assay of GNPs-antiENaC boun

114 We quantitatively analyzed immunofluorescence distribution of oxidative damage mark

115 ere imaged by multiple modalities, including immunofluorescence, electron microscopy and second harmo

116 copy findings in all autopsies and performed immunofluorescence, electron microscopy, and in situ hyb

117 Immunofluorescence, ELISA, and electron microscopy were

118 o nascent polypeptide chains, anti-puromycin immunofluorescence enables visualization of nascent prot

119 te transporter 2 (Vglut2) gene, coupled with immunofluorescence experiments against tyrosine hydroxyl

120 A series of immunofluorescence experiments confirmed NIPAL1's magnes

121 Immunofluorescence experiments indicate that the vast ma

122 Immunofluorescence experiments with CHIKV replicase with

123 d corresponding CEC density were analyzed by immunofluorescence flat mount-staining.

124 pecifically in the telomeres, ChIP, telomere immunofluorescence, fluorescence in situ hybridization (

125 Indeed, immunofluorescence/fluorescence in situ hybridization (i

126 and cardiac tissues was assessed by indirect immunofluorescence, fluorescent in situ hybridization an

127 Immunohistochemistry/immunofluorescence for CD1a, CD3, CD28, CD40, CD69, CD80

128 OSB between 11 and 15 weeks of gestation by immunofluorescence for established neuronal and neural p

129 ues were stained by immunohistochemistry and immunofluorescence for immune cell markers and tumor arc

130 hematoxylin-eosin staining for overt damage, immunofluorescence for necroptosis, and Sirius red/fast

131 Immunofluorescence for transforming growth factor-beta(1

132 iology approach that integrates results from immunofluorescence, G4 ligands, heme-affinity reagents,

133 37 degrees C, cell phenotype was assessed by immunofluorescence, gene and protein expression, and pro

134 Retrograde tracing plus triple-label immunofluorescence identified fewer bulbospinal non-C1 n

135 n in near-real time returns inferred virtual immunofluorescence (IF) images that estimate the underly

136 2019 (COVID-19) pandemic, we detected a new immunofluorescence (IF) pattern in serum autoantibody (a

137 solated by DEP chip and subjected to on-chip immunofluorescence (IF) staining to determine the concen

138 ulin A (IgA) A and immunoglobulin G indirect immunofluorescence (IIF) on human salt-split skin and th

139 The immunofluorescence images further showed that TMPRSS2 wa

140 roteomes based on the systematic analysis of immunofluorescence images of 12 073 proteins in the Huma

141 morphometric and molecular analyses, such as immunofluorescence imaging and single cell RNA sequencin

142 multimodal, in situ, mass spectrometry, and immunofluorescence imaging for the characterization of n

143 The use of postanalysis immunofluorescence imaging from the same tissue confirme

144 lls and evaluate their opsin expression from immunofluorescence imaging tiles spanning roughly 6 mm a

145 without disruption of Crt) were analyzed by immunofluorescence, immunoblots, and/or quantitative rev

146 pressed in T84 cells, which were analyzed by immunofluorescence, immunoblots, high-performance liquid

147 Here, using HEK 293T cells and immunofluorescence, immunoblotting, RNAi, subcellular fr

148 lyzed using multimodal nonlinear microscopy, immunofluorescence, immunohistochemistry, and quantitati

149 Immunoblotting, immunofluorescence, immunohistochemistry, and ribonucleo

150 Endocytosis inhibitors, immunofluorescence, immunoprecipitation, and knockdown s

151 munohistochemistry, and tissue clarification immunofluorescence in mouse and human.

152 Here, by using immunofluorescence in mouse tissue, we investigated the

153 g immunoprecipitation, Western blotting, and immunofluorescence in NIH/3T3 cells transfected with wil

154 Proteasome inhibitors increased SLC26A9 immunofluorescence in primary human bronchial epithelial

155 TPBG immunofluorescence in RBCs was strongly altered by the l

156 Immunofluorescence, in situ hybridization, and confocal

157 rocessing/presentation pathways decrease and immunofluorescence indicates a depletion of innate and a

158 On the basis of immunofluorescence, infected cell types included CD68(+)

159 ed to accurately quantify tumour buds across immunofluorescence labelled whole slide images from 100

160 o PBB3 fluorescence and phospho-tau antibody immunofluorescence labelling of brain sections of chroni

161 Herein, using immunofluorescence, live-cell imaging, and MS-based anal

162 Immunofluorescence localization experiments revealed tha

163 l barrier function was assessed by analyzing immunofluorescence localization of TJ proteins, mucosal

164 activation markers via immunohistochemistry, immunofluorescence, Luminex assay, ELISA, UniCAP, fluore

165 , kinase assays, co-immunoprecipitation, and immunofluorescence measures of signaling, we more specif

166 .1 trafficking, as shown by Western blot and immunofluorescence microcopy analysis.

167 long with several biochemical approaches and immunofluorescence microscopy analyses, we sought to inv

168 reparations were used in vitro to assess, by immunofluorescence microscopy and Alizarin red staining,

169 By using immunofluorescence microscopy and EM, we also demonstrat

170 Immunofluorescence microscopy and expression of GFP-fuse

171 Immunofluorescence microscopy and flow cytometry reveale

172 biochemical assays and approaches, including immunofluorescence microscopy and FRET analyses, we demo

173 in beta and ADAM proteases could be shown by immunofluorescence microscopy and immunoprecipitation ex

174 alpha- and beta-cells using 3-D confocal and immunofluorescence microscopy and orthogonal analyses.

175 on of tissue-associated bacteria, histology, immunofluorescence microscopy and scanning electron micr

176 Here, we use coimmunoprecipitation and immunofluorescence microscopy approaches to ask whether

177 Immunofluorescence microscopy deciphered an early-stage

178 Functional studies and immunofluorescence microscopy experiments in multiple ce

179 evidence for the proposed mechanism includes immunofluorescence microscopy experiments showing co-occ

180 However, routine immunofluorescence microscopy fails to detect IgG in man

181 We next used immunofluorescence microscopy imaging, flow cytometry an

182 Immunofluorescence microscopy in CXCR4-expressing cells

183 interaction with the P protein, as shown by immunofluorescence microscopy of cells expressing differ

184 Immunofluorescence microscopy revealed a redistribution

185 Western blot and immunofluorescence microscopy revealed the presence of N

186 analysis, immunoblotting, HEK293 cells, and immunofluorescence microscopy to identify a histidine-co

187 Immunofluorescence microscopy was used to characterize (

188 Immunofluorescence microscopy was used to determine if p

189 Here using RNAi, endogenous epitope tagging, immunofluorescence microscopy, and 3D-structured illumin

190 Using MALDI-2 and StxB-based immunofluorescence microscopy, Gb3Cer and Gb4Cer were ma

191 Fluorescence microscopy, in particular immunofluorescence microscopy, has been used extensively

192 nuclide-treated patients are quantifiable by immunofluorescence microscopy, using phosphorylation of

193 Using immunofluorescence microscopy, we determined that Vpu is

194 Using immunofluorescence microscopy, we observed that although

195 ficking, as demonstrated by Western blot and immunofluorescence microscopy.

196 )F4/80(+)NOS2(+) cells by flow cytometry and immunofluorescence microscopy.

197 pilin PpdD, as shown by shearing assays and immunofluorescence microscopy.

198 s validated by aptamer screening, ELISA, and immunofluorescence microscopy.

199 As and cells were analyzed by immunoblot and immunofluorescence microscopy.

200 terocolitis and measured levels of S100A8 by immunofluorescence microscopy.

201 assays, genome editing, flow cytometry, and immunofluorescence microscopy.

202 tathione S-transferase pulldown experiments, immunofluorescence, molecular modeling, and docking expe

203 images of phospho-myosin light chain (pMLC) immunofluorescence, moreover, revealed stiffness-depende

204 rous AT-related CeL transcripts, and we used immunofluorescence (n = 3) and tract-tracing (n = 2) met

205 as assessed histologically (H/E staining and immunofluorescence of CD45 and Ly6G).

206 By immunofluorescence of differentiated mouse podocytes (MP

207 ser microdissection experiments, and in situ immunofluorescence of murine adipose fat pads.

208 Finally, CFD and immunofluorescence on human intracranial aneurysms showe

209 Serum AHAs and AIDAs were tested by indirect immunofluorescence on human myocardium and skeletal musc

210 xpression of selected genes was validated by immunofluorescence on retinal wholemounts and cryosectio

211 RNA sequencing, flow cytometry, immunoblots, immunofluorescence, or reverse transcription polymerase

212 Using immunofluorescence, our study is the first to demonstrat

213 MID group, 6 patients changed their apparent immunofluorescence phenotype between monotypic and polyt

214 e serum and skin of AD patients by ELISA and immunofluorescence, respectively.

215 Training dataset measurements of immunofluorescence retina nuclear layers disclosed no si

216 Immunofluorescence revealed MreB is most abundant at neg

217 Immunofluorescence revealed prelabeled MAPC cells in the

218 Finally, immunofluorescence reveals that coexpression of all thre

219 ing recovery of one IAV isolate confirmed by immunofluorescence, reverse transcriptase quantitative P

220 Here, using several approaches, including immunofluorescence, RNA immunoprecipitation and methylat

221 We used histologic, immunofluorescence, RNA sequencing, and metabolic assays

222 Immunofluorescence showed albumin leakage from blood ves

223 Immunofluorescence showed ERICH3 colocalization with 5-H

224 Immunofluorescence showed that HIF-1alpha deletion in NT

225 Immunofluorescence showed the lack of plakoglobin in the

226 Duplex immunofluorescence slides stained for E-cadherin and vim

227 n, and surface plasmon resonance assays; and immunofluorescence, small-angle X-ray scattering, and MS

228 scopy (d(SL max) = 4.1 mm +/- 0.9 mm) and by immunofluorescence staining (d(IF max) = 4.7 mm +/- 1.1

229 and M2 TAMs were identified using multiplex immunofluorescence staining and a tumor cell-TAM proximi

230 Immunofluorescence staining and confocal microscopy reve

231 We demonstrate by immunofluorescence staining and immunoblotting the prese

232 In addition, immunofluorescence staining and RT-PCR showed downregula

233 caveolae regulated by flow were analyzed by immunofluorescence staining and transmission electron mi

234 al and morphometrical analysis combined with immunofluorescence staining and ultrastructural analysis

235 Thereafter, we used immunofluorescence staining and western blot to test the

236 Furthermore, immunofluorescence staining of capsular bags for the fib

237 Immunofluorescence staining of cross-sections and flat-m

238 Immunofluorescence staining of CXCR5 and CXCL13 in combi

239 ression analyses and estrogen receptor (ESR) immunofluorescence staining of esophageal biopsy specime

240 Immunofluorescence staining of NK cells was performed on

241 Immunofluorescence staining on human RCC samples demonst

242 Immunofluorescence staining revealed a relatively high a

243 Immunofluorescence staining revealed central coherent co

244 Immunofluorescence staining revealed that the virus prev

245 Immunofluorescence staining reveals that COP1 preferenti

246 Double immunofluorescence staining showed that CC2D1A is expres

247 Double immunofluorescence staining showed that orexin is locali

248 hy, F-actin binding and bundling assays, and immunofluorescence staining to evaluate F-actin alignmen

249 e accomplish this by combining DESI-MSI with immunofluorescence staining using specific cell-type mar

250 Concordantly, NRF2 immunofluorescence staining was decreased in patient cor

251 omputed tomography scanning, histologic, and immunofluorescence staining were conducted to evaluate h

252 Immunoassay and immunofluorescence staining were performed for IL6 and p

253 verse-phase protein arrays, western blot and immunofluorescence staining were used to evaluate the ef

254 protein in HCSC and MCSC was examined using immunofluorescence staining, and corneal rubbing was app

255 with high-throughput studies, live imaging, immunofluorescence staining, fluorescent in situ hybridi

256 ate the expression pattern of PDLIM1 through immunofluorescence staining, immunoblots, subcellular fr

257 on were assessed with DAPI staining and Ki67 immunofluorescence staining, respectively.

258 and elastin in airway and cystic walls using immunofluorescence staining, we found that the thickness

259 with flow cytometry, RT-PCR, MultiPlex, and immunofluorescence staining.

260 zen tissue sections in a manner analogous to immunofluorescence staining.

261 and female mice using PCR, Western blot, and immunofluorescence staining.

262 latively high quantum yields, and utility in immunofluorescence staining.

263 bule length is shortened, as demonstrated by immunofluorescence staining.

264 stroma-poor regions, which was confirmed by immunofluorescence staining.

265 hairdressers and 1 patient with ACD by using immunofluorescence staining.

266 eaction and protein expression visualized by immunofluorescence stainings.

267 ivity, we performed electrophysiological and immunofluorescence studies on hiPSC-derived cerebrocorti

268 Immunofluorescence studies revealed TBC1D8B presence in

269 disease is established by kidney biopsy and immunofluorescence studies to identify the monotypic imm

270 Using tissue immunofluorescence studies, we also report that the expr

271 stigate the mediators of itch in SD using an immunofluorescence study on patient lesions focusing on

272 stiffness-dependent differences in alpha-SMA immunofluorescence, suggesting that a stiff microenviron

273 PGNMID can change its apparent clonality by immunofluorescence supporting oligoclonal immune respons

274 col is implemented using tissue-based cyclic immunofluorescence (t-CyCIF) as an imaging platform, the

275 Using in situ hybridization and immunofluorescence techniques, we showed that PROX1 is e

276 egies alongside mass cytometry and multiplex immunofluorescence techniques.

277 using flow cytometry and identified through immunofluorescence that professional antigen-presenting

278 We used flow cytometry, histology, and immunofluorescence to characterize CD8 effector memory T

279 le-brain optical clearing and multiple-label immunofluorescence to create a comprehensive and quantit

280 Here we use western blotting and immunofluorescence to examine the effects of multiple ac

281 SI-MS imaging were used for H&E staining and immunofluorescence to identify different histological re

282 tative location of pF(L) , with RNAScope and immunofluorescence to identify the neurochemical phenoty

283 from some mice and analyzed by histology and immunofluorescence to quantify mast cells and expression

284 gement was assessed by confocal anti-tubulin immunofluorescence to quantify microtubule bundling in i

285 rom mice and human patients were analyzed by immunofluorescence to verify findings at the protein lev

286 Therefore, immunofluorescence tomography is a powerful new tool to

287 a microbe was serendipitously visualized by immunofluorescence was analyzed using the same method, b

288 Immunofluorescence was performed for vimentin, N-cadheri

289 ansplants was measured in recipient mice and immunofluorescence was performed on the retrieved transp

290 By using immunofluorescence, we confirm that PLK4 is localized to

291 Using immunofluorescence, we found that BCL-xL protein express

292 Hi-C) analysis, chromatin binding assays and immunofluorescence, we show that, by telophase, condensi

293 By in situ hybridization and immunofluorescence, we showed that Cnrip1, Plek and Ppp3

294 Western blot and immunofluorescence were performed for MTOC and triglycer

295 Flow cytometry, immunocytochemistry, immunofluorescence, Western blot, and RT-PCR were perfor

296 Using real-time quantitative PCR, immunofluorescence, Western blotting, and both chromogen

297 on human ALS brain sections in comparison to immunofluorescence with Iba1 and GFAP.

298 Immunofluorescence with validated antibodies revealed th

299 gle-cell RNA sequencing, flow cytometry, and immunofluorescence, with IL-5Ralpha function determined

300 es were collected and analyzed by histology, immunofluorescence, xMAP, and reverse-transcription poly