ライフサイエンスコーパス: immunocytochemistry

1 calreticulin (immunoblot, mass spectrometry, immunocytochemistry).

2 Further verification was performed using immunocytochemistry.

3 RNA and plasmid constructs, and analyzed by immunocytochemistry.

4 abbits and confirmed to be myofibroblasts by immunocytochemistry.

5 e in flow cytometry, immunofluorescence, and immunocytochemistry.

6 philic marker MPO in human neutrophils using immunocytochemistry.

7 the intact rat brain by electron microscopy immunocytochemistry.

8 sue organization and biomarker expression by immunocytochemistry.

9 urity, as confirmed by electrophysiology and immunocytochemistry.

10 es showing compatibility of OligoFISSEQ with immunocytochemistry.

11 protein was detected by Western blotting and immunocytochemistry.

12 r of co-localization with mitochondria using immunocytochemistry.

13 etected and identified by immunoblotting and immunocytochemistry.

14 stigated with in vitro electrophysiology and immunocytochemistry.

15 (GLUT1) in oligodendrocytes was assessed by immunocytochemistry.

16 uals via flow cytometry, immunoblotting, and immunocytochemistry.

17 ssues from these animals were analyzed using immunocytochemistry.

18 immunoblot assay, immunohistochemistry, and immunocytochemistry.

19 Purity and phenotype was confirmed with immunocytochemistry.

20 ursor protein (beta-APP-IAT) and RMO14 (NFC) immunocytochemistry.

21 mpared to that in untreated control cells by immunocytochemistry.

22 ystem and of its subcellular localization by immunocytochemistry.

23 ing in situ hybridization, real-time PCR and immunocytochemistry.

24 INtec p16(INK4a) cytology (mtm laboratories) immunocytochemistry.

25 Endosomal TLR3 in hPDL cells was observed by immunocytochemistry.

26 ssing circadian clock proteins in the SCN by immunocytochemistry.

27 tein levels by Western blot and quantitative immunocytochemistry.

28 rf2 subcellular localization was assessed by immunocytochemistry.

29 re analyzed by Western blot and double label immunocytochemistry.

30 rat using electron microscopic dual-labeling immunocytochemistry.

31 lar localization of PKCdelta was examined by immunocytochemistry.

32 (pmTOR), as assessed by Western blotting and immunocytochemistry.

33 GDNF localization was examined by immunocytochemistry.

34 on in male rats and gerbils as seen with Fos immunocytochemistry.

35 BSA by enzyme-linked immunosorbent assay and immunocytochemistry.

36 idimensional time-lapse video microscopy and immunocytochemistry.

37 ed the effects on cell differentiation using immunocytochemistry.

38 ylase in situ hybridization, and parvalbumin-immunocytochemistry.

39 Y13 was confirmed by quantitative RT-PCR and immunocytochemistry.

40 gh-resolution light and electron microscopic immunocytochemistry.

41 t shock on the localization of melanopsin by immunocytochemistry.

42 itro is confirmed both by flow cytometry and immunocytochemistry.

43 n and were all vimentin-positive as shown by immunocytochemistry.

44 Of 3413 bone marrow specimens examined by immunocytochemistry, 104 (3.0%) were positive for tumors

45 Using immunocytochemistry, a proximity ligation assay, and co-

46 nervation by medium spiny neuron axons using immunocytochemistry, activity-dependent labeling, and el

47 ts was assessed by Western-blot analysis and immunocytochemistry after 8 and 20weeks of diabetes.

48 Here, we combined retrograde tracing with immunocytochemistry against tyrosine hydroxylase (TH) or

49 tase activity, scratch assay cell migration, immunocytochemistry alpha-smooth muscle actin (alpha-SMA

50 Electron microscopy, gene expression, and immunocytochemistry analyses provided evidence that impa

51 hrough reciprocal coimmunoprecipitations and immunocytochemistry analyses the association between Gly

52 Western blot and immunocytochemistry analysis for alphaSMA were also perf

53 Accordingly, immunocytochemistry analysis showed that NKCC2 and OS9 c

54 Immunocytochemistry analysis shows that SR1848 induces r

55 Using immunocytochemistry and a blinded scoring system, we obs

56 Immunocytochemistry and biochemical fractionation studie

57 mGluR-LTD in wild-type and Fmr1 KO mice and immunocytochemistry and biotinylation assay to study rel

58 Neurones and astrocytes were identified by immunocytochemistry and by stimulation; 3-4 muM L-glutam

59 Neuronal survival was examined using immunocytochemistry and cell counting.

60 Using immunocytochemistry and cellular quantification analyses

61 Immunocytochemistry and confocal imaging of primary hipp

62 We performed single cell electrophysiology, immunocytochemistry and confocal microscopy and suggest

63 era toxin beta (CTB) in the VTA, fluorescent immunocytochemistry and confocal microscopy were used to

64 In addition, immunocytochemistry and electron microscopy revealed a s

65 localized in hippocampal post-synapses, with immunocytochemistry and electron microscopy revealing co

66 Immunocytochemistry and electron microscopy were utilize

67 Importantly, functional analysis with immunocytochemistry and electrophysiological recordings

68 ing classic neuroanatomical methods, such as immunocytochemistry and electrophysiology.

69 ts were consistent with ZO-1 and VE-cadherin immunocytochemistry and expression of claudin-5, which w

70 The immunocytochemistry and flow cytometry analyses on diffe

71 Immunocytochemistry and flow cytometry showed that F302L

72 ies by western blotting, immunofluorescence, immunocytochemistry and flow cytometry.

73 Immunocytochemistry and hydroethidine-based detection of

74 Intracellular IL-26 was detected using immunocytochemistry and immunocytofluorescence.

75 ied proteins have a number of uses including immunocytochemistry and immunoprecipitation of the modif

76 By using immunocytochemistry and mass dye fills, we characterized

77 In a second step, a combination of immunocytochemistry and mass spectrometric profiling of

78 Harvested tissue was processed for immunocytochemistry and prepared by ultrathin series sec

79 Immunocytochemistry and proximity ligation assays reveal

80 Immunocytochemistry and qPCR analyses on freshly isolate

81 s by western blotting, immunohistochemistry, immunocytochemistry and quantitative PCR for components

82 hout TGF-beta1 inhibitor were evaluated with immunocytochemistry and real-time polymerase chain react

83 cholangiocyte cultures (SMCCs and LMCCs) by immunocytochemistry and real-time polymerase chain react

84 immunohistochemistry, in situ hybridization, immunocytochemistry and RT PCR, we show that the morphol

85 ite fragmentation and focal swelling by both immunocytochemistry and scanning electron microscopy.

86 Immunocytochemistry and subcellular fractionation gave c

87 ficed and corneal nerves were examined using immunocytochemistry and three-dimensional volumetric ana

88 ta and SDOCT examinations were correlated to immunocytochemistry and transmission electron microscopy

89 Immunocytochemistry and Western blot analysis determinin

90 Epha2 distribution was examined using immunocytochemistry and Western blot analysis.

91 Immunocytochemistry and western blot studies showed that

92 a down-regulation of E-cadherin expression (immunocytochemistry and western blot); these changes wer

93 of alpha-smooth muscle actin was analyzed by immunocytochemistry and western blot.

94 s) resembling EndoMT were monitored by qPCR, immunocytochemistry and western blots.

95 escence mainly determined NO production, and immunocytochemistry and Western blotting evaluated Src a

96 E2 increased Cav1.2alpha (immunocytochemistry) and mRNA (RT-PCR) levels but did no

97 rough a combination of protein biochemistry, immunocytochemistry, and both in vivo and in vitro elect

98 CA IV expression in oocytes was confirmed by immunocytochemistry, and CA IV activity measured by mass

99 Based on atomic force microscopy, immunocytochemistry, and chemical analyses, we propose t

100 techniques, including reporter gene assays, immunocytochemistry, and ChIP-qPCR we show here, to the

101 vel interactors validated by bioinformatics, immunocytochemistry, and coimmunoprecipitation.

102 using bioinformatics, Western blotting (WB), immunocytochemistry, and coimmunoprecipitation.

103 rse-transcriptase polymerase chain reaction, immunocytochemistry, and confocal imaging from striatum.

104 qPCR, Western immunoblotting, immunocytochemistry, and ELISA immunoassay were utilized

105 cificity and bioactivity via immunoblotting, immunocytochemistry, and flow cytometric analysis.

106 divided into types according to morphology, immunocytochemistry, and function.

107 subunits were evaluated by quantitative PCR, immunocytochemistry, and immunohistochemistry.

108 rse transcriptase-polymerase chain reaction, immunocytochemistry, and in vivo transplantation.

109 parasites since those driven by bioimaging, immunocytochemistry, and neuropeptide biochemistry 20-30

110 alidating fibroblast cells by morphology and immunocytochemistry, and optimizing culture conditions b

111 We used in situ hybridization, immunocytochemistry, and pharmacology to identify the ka

112 found (using TaqMan RT-PCR, immunoblotting, immunocytochemistry, and proteome analysis) that the EAA

113 nalysis of progenitors using flow cytometry, immunocytochemistry, and qRT-PCR showed high neuralizati

114 Validation based on beta-amyloid load by immunocytochemistry, and replication with fibrillar beta

115 Injected cells were localized by fluorescent immunocytochemistry, and the degree of retinal vascular

116 confocal microscopy, Western blot analysis, immunocytochemistry, and the fear conditioning test.

117 interference and phase-contrast microscopy, immunocytochemistry, and transmission electron microscop

118 CD11b, F4/80 immunocytochemistry, and TUNEL assay were used to examin

119 last transformation, using quantitative PCR, immunocytochemistry, and Western blot.

120 p11 expression using in situ hybridization, immunocytochemistry, and whole-tissue volume imaging.

121 tic marker expression were monitored by PCR, immunocytochemistry, and/or flow cytometry.

122 e actin (alphaSMA), fibronectin, and F-actin immunocytochemistry, and/or immunoblotting.

123 By immunocytochemistry, antibody AF1-003 recognizes a small

124 Immunocytochemistry assays demonstrated that these chann

125 The subcellular fractionation and immunocytochemistry assays indicated that the R310/311A

126 monocytes as judged by Western blotting and immunocytochemistry assays.

127 The present investigation used immunocytochemistry at the electron microscopic level to

128 In the present investigation, immunocytochemistry at the electron microscopic level wa

129 structures using human retinal sections and immunocytochemistry at the fovea level.

130 rons for a variety of applications including immunocytochemistry, biochemical studies, shRNA-mediated

131 This study combined NO imaging, immunocytochemistry, biochemistry, and molecular biology

132 Abeta and beta-amyloid precursor protein by immunocytochemistry, but no [3H]PiB binding.

133 were localized on the same sections used for immunocytochemistry by autofluorescence and polarized li

134 ur ex vivo model of tissue contraction using immunocytochemistry, chemical inhibitors, and small inte

135 Immunocytochemistry, co-immunoprecipitation and proximit

136 Immunocytochemistry colocalized many of these enzymes wi

137 i67, p-histone H3, and Aurora B confirmed by immunocytochemistry compared with control cells.

138 Immunocytochemistry confirmed a decrease in hSlo1 plasma

139 Immunocytochemistry confirmed AKT activation in cultured

140 ellular tight junction protein complexes and immunocytochemistry confirmed expression of the tight ju

141 Immunocytochemistry confirmed presence of glial- and neu

142 Western blot and immunocytochemistry confirmed the lack of caspase-6 prot

143 Ultrastructural immunocytochemistry confirmed the presence of GABA(A)R b

144 e, and the experimental readout of foci when immunocytochemistry coupled to 2D fluorescence microscop

145 Immunocytochemistry coupled with electron microscopy rev

146 and HEK293 cells, Western blot analysis and immunocytochemistry data demonstrate that RNF207 and the

147 Immunocytochemistry demonstrated a decrease of surface p

148 7a siRNA treatment followed by STREX protein immunocytochemistry demonstrated both reduced levels and

149 omal uptake studies and electron microscopic immunocytochemistry demonstrated knockdown of GLT-1 in t

150 RT-PCR and immunocytochemistry demonstrated that in knockout mice a

151 ults from RT-PCR, Western blot analysis, and immunocytochemistry demonstrated that whirlin expressed

152 Immunocytochemistry demonstrates that Yy1 is expressed i

153 Western immunoblotting and immunocytochemistry determined FST and Act A protein lev

154 Here we show by immunocytochemistry, electron microscopy, and postsynapt

155 tion at pubertal onset, electron microscopic-immunocytochemistry (EM-ICC) was employed.

156 fetal organs were examined by histology and immunocytochemistry employing anti-Toxoplasma stage-spec

157 Our immunocytochemistry experiments reveal that Brdt colocal

158 Finally, immunoprecipitation and immunocytochemistry experiments revealed an association

159 h-throughput automated electrophysiology and immunocytochemistry-flow cytometry.

160 translocation of NF-kappaB was evaluated by immunocytochemistry followed by confocal laser scanning

161 gregate formation by Triton-X extraction and immunocytochemistry followed by fluorescence microscopy.

162 [3H]PiB autoradiography and immunocytochemistry for beta-amyloid (Abeta) and beta-am

163 ts in type A-C synapses were identified with immunocytochemistry for CAMKIIalpha, a marker of glutama

164 Using immunocytochemistry for either total or phosphorylated e

165 fying soluble factors, receptor mapping, and immunocytochemistry for extracellular matrix molecules.

166 First, immunocytochemistry for glutamatergic (VGlut1 and VGlut2

167 , and 15 control subjects were processed for immunocytochemistry for SST and neuropeptide Y, a neurop

168 ermined using GLP-1 receptor binding assays, immunocytochemistry for the receptor and injection of fl

169 tin (alpha-SMA)+ myofibroblasts (verified by immunocytochemistry for vimentin, alpha-SMA, desmin, and

170 Immunocytochemistry further revealed substantial Na(V)1.

171 Immunocytochemistry further revealed that a ventromedial

172 Immunocytochemistry further reveals that NL/MSO neurons

173 DIM) and then analyzed with a combination of immunocytochemistry, gene expression, and high-content i

174 ctions were processed for Nissl stain, Prox1-immunocytochemistry, GluR2-immunocytochemistry, Timm sta

175 Timm stain, glial fibrillary acidic protein-immunocytochemistry, glutamic acid decarboxylase in situ

176 confidence and 22 of these antibodies are of immunocytochemistry grade.

177 In addition to classical neurotransmitters, immunocytochemistry has provided evidence for a major co

178 Employing multiple-label immunocytochemistry, histochemistry, and backfills, we s

179 Immunocytochemistry (ICC) showed receptor-independent up

180 Immunoblotting, immunocytochemistry (ICC), and functional assays using I

181 MMP-9 expression was evaluated by immunocytochemistry (ICC), WB, zymography, and RT-PCR.

182 on was assessed by Western blotting (WB) and immunocytochemistry (ICC).

183 s were tested for mitochondrial integrity by immunocytochemistry, immunoblotting, flow cytometry, and

184 Flow cytometry, immunocytochemistry, immunofluorescence, Western blot, a

185 TRPP Ca(2+) channels were investigated using immunocytochemistry, immunohistochemistry, and electron

186 Immunocytochemistry, immunotransmission electron microsc

187 and Abeta and beta-amyloid precursor protein immunocytochemistry in autopsy-acquired brain tissue.

188 the Western blot technique, a real-time PCR, immunocytochemistry in combination with confocal microsc

189 Multiple-label immunocytochemistry in combination with neurobiotin back

190 Fluorescence immunocytochemistry in enhanced green fluorescent protei

191 n using confocal microscopy and quantitative immunocytochemistry in primary cultures of rat neocortic

192 Immunocytochemistry, in situ hybridization and RT-qPCR w

193 Co-immunoprecipitation and immunocytochemistry indicated that Na(v)1.7 formed stabl

194 Analyses with western blotting and immunocytochemistry indicated that the expression of alp

195 eroids are formed, Matrigel is dissolved and immunocytochemistry is performed in the chamber slides.

196 e measured dendritic formation and growth by immunocytochemistry, kallikrein 8 (KLK8) mRNA by reverse

197 ntigens were performed in those samples with immunocytochemistry labeling but negative for NMDA recep

198 was confirmed by subcellular fractionation, immunocytochemistry, lipophilic dye fluorescence microsc

199 Immunohistochemistry and immunocytochemistry located Sfp1 in granules stockpiled

200 On immunocytochemistry, MCPIP1 colocalized with HCV RNA.

201 organization over time by light microscopy, immunocytochemistry, metabolic imaging and electron micr

202 ssays, immunomicroarrays, flow cytometry and immunocytochemistry methods, and it shortens overall ass

203 Using fluorescence microscopy combined with immunocytochemistry, monoclonal antibodies were used to

204 ary neuroscience referral center and ex vivo immunocytochemistry of autopsy-acquired brain tissue fro

205 Both the neurite length assay and the immunocytochemistry of enlargeosomes exocytosis revealed

206 antigen-specific antibodies were detected by immunocytochemistry of HBV-transfected BHK-21 cells.

207 Sequential immunocytochemistry of intact cells or isolated nucleopl

208 Confocal immunocytochemistry of juvenile animals localized EsGal1

209 Immunocytochemistry of Madin-Darby canine kidney cells s

210 rite outgrowth and branching as evaluated by immunocytochemistry of neuronal markers.

211 MMP9 expression was confirmed by qPCR and immunocytochemistry of odontoclasts located in TR lesion

212 Quantification and subsequent immunocytochemistry of phosphatidylinositol-3,4,5-trisph

213 Immunocytochemistry of phosphorylated SMAD1/5/8 (phospho

214 Immunocytochemistry of the subcellular localization of P

215 However, neither immunocytochemistry on a trans-differentiation model of

216 r in the coronal plane, were stained for CTb immunocytochemistry or for CytOx histochemistry or for N

217 After indirect immunocytochemistry or the overexpression of EGFP-tagged

218 neuron-specific manipulations combined with immunocytochemistry, paired recordings, and two-photon C

219 Using immunocytochemistry, pharmacological treatments and beha

220 ls, as evidenced through single-cell RT-PCR, immunocytochemistry, pharmacology, and single-channel re

221 rentiation was performed using pigmentation, immunocytochemistry, protein/mRNA expression, transepith

222 Intravital blood vessel labeling and immunocytochemistry revealed a vascular plasticity in wh

223 Immunocytochemistry revealed cytosolic and nuclear expre

224 stochastic optical reconstruction microscopy immunocytochemistry revealed foci of clustered mitofilin

225 Immunocytochemistry revealed greater numbers of aromatas

226 Immunocytochemistry revealed little interaction between

227 Immunocytochemistry revealed OPN4 expression at the base

228 ble staining using in situ hybridization and immunocytochemistry revealed that BDNF mRNA was restrict

229 Confocal immunocytochemistry revealed that MLF transection produc

230 Analyses by flow cytometry and immunocytochemistry revealed that monocytes home to the

231 Immunocytochemistry revealed that nuclei of both BMD and

232 Moreover, immunocytochemistry revealed that the mutation prevented

233 dings combined with axonal Na(+) imaging and immunocytochemistry revealed that these compensatory alt

234 Immunocytochemistry revealed that these structures lack

235 Immunocytochemistry revealed that while DDR1b clusters c

236 Immunocytochemistry revealed wide distribution of MIP-re

237 Immunocytochemistry reveals that both PGRMC1 and SW120,

238 d substitutions) was studied in vitro, using immunocytochemistry, selective western blot and mass spe

239 Western blots, ELISAs, and confocal immunocytochemistry showed EsMIF was at highest abundanc

240 lue-native gels, whereas denaturing gels and immunocytochemistry showed reduced core subunit MTCO1.

241 Immunocytochemistry showed that (phyto)ceramide was colo

242 Immunocytochemistry showed that apoER2 mediates Sepp1 up

243 gy studies using intramolecular epitopes and immunocytochemistry showed that CNNM2 has an extracellul

244 Immunocytochemistry showed that OsPIP1;3 majorly accumul

245 Immunocytochemistry showed that the GAT2 protein was pre

246 TSP-1 on neurons with mature synapses using immunocytochemistry, single-particle tracking, surface b

247 Cell fractionation and immunocytochemistry studies demonstrated that the propor

248 Western blot analyses and immunocytochemistry studies were used to elucidate the i

249 en compared with conventional time consuming immunocytochemistry technique which prompted us to exten

250 The clearing method is compatible with immunocytochemistry techniques and can be used in concer

251 ting neurospheres were evaluated in vitro by immunocytochemistry techniques.

252 We present data from development and immunocytochemistry that identify a role for hornwort st

253 imaging, patch-clamp electrophysiology, and immunocytochemistry, the present study reveals that thes

254 ion by using in situ hybridization, PCR, and immunocytochemistry throughout the early development of

255 issl stain, Prox1-immunocytochemistry, GluR2-immunocytochemistry, Timm stain, glial fibrillary acidic

256 e used fluorescent in situ hybridization and immunocytochemistry to analyze the localization of AMPAR

257 esent a protocol that combines MALDI-MS with immunocytochemistry to assay over a thousand individual

258 Here, we used electron microscopic immunocytochemistry to assess directly integration of GF

259 evaluate retinal function and postembedding immunocytochemistry to determine the changes in cellular

260 l densities (the inverse of cell size) using immunocytochemistry to Iba1 in samples of free cell nucl

261 We applied single- and double-label immunocytochemistry to normative frontal or parietal (as

262 We used whole-mount immunocytochemistry to study the neurochemistry and anat

263 Ceramides were labeled by immunocytochemistry to visualize their distribution on t

264 Western blotting and immunocytochemistry under the electron microscope indica

265 th other endogenous IFs, as demonstrated via immunocytochemistry using a chicken-specific antibody.

266 aphy (OCT) was compared with high-resolution immunocytochemistry using a range of cellular markers to

267 e expression induced by BDNF, as assessed by immunocytochemistry using an extracellular N-terminal Gl

268 h-affinity fluorescent phalloidin as well as immunocytochemistry using anti-actin antibodies demonstr

269 howing any staining were further examined by immunocytochemistry using live hippocampal neurons and c

270 Presence of DTCs in BM was determined by immunocytochemistry using pan-cytokeratin monoclonal ant

271 o determined their phenotype by double-label immunocytochemistry using type-specific markers.

272 Immunocytochemistry verified the dendritic localization

273 Immunocytochemistry was performed to detect the neuronal

274 Then, electron microscopic immunocytochemistry was performed to determine the subce

275 Immunocytochemistry was performed under both non-permeab

276 Serial section electron microscopic immunocytochemistry was then performed to quantitatively

277 Cyclic GMP immunocytochemistry was used functionally to localize sG

278 Immunocytochemistry was used to correlate myelin status

279 were isolated from all 4 groups of mice, and immunocytochemistry was used to quantify total enteric n

280 By immunocytochemistry we show that endogenous Kir2.1 and K

281 By RT-PCR, Western blot, and immunocytochemistry we showed the FXYD2b splice variant

282 otal Notch intracellular domain levels using immunocytochemistry, we also demonstrated that Notch int

283 Using synaptosomal proteomics and immunocytochemistry, we demonstrate the presence of Bbs

284 With immunocytochemistry, we find that axonal dynorphin immun

285 bimolecular fluorescence complementation and immunocytochemistry, we found that Liat1 is targeted to

286 ording, real-time PCR, Western blotting, and immunocytochemistry, we identified a previously unrecogn

287 esponses, and light and electron microscopic immunocytochemistry, we show in the rabbit retina that b

288 Using electron microscopy and immunocytochemistry, we show that AOE elongates the AN n

289 Using immunocytochemistry, we show that ApGLNT1 is localized p

290 ctivated CaMKII molecules detected via STORM immunocytochemistry were concentrated in spines both at

291 Histology and immunocytochemistry were used to confirm the findings.

292 Western Blot and immunocytochemistry were used to determine expression of

293 ntitative RT-PCR, Western blot analysis, and immunocytochemistry were used to determine the different

294 (far) Western blot, immunoprecipitation, and immunocytochemistry were used to study the expression, i

295 functional readouts were evaluated by using immunocytochemistry, Western blotting, DNA binding assay

296 DDAH1 deletion was confirmed through immunocytochemistry, whereas Western blotting showed tha

297 where amyloid deposition was demonstrated by immunocytochemistry; white matter showed Abeta and beta-

298 via fluorescent imaging and high-resolution immunocytochemistry with an anti-EMD antibody.

299 protein of 25 kDa), a key SNARE protein, by immunocytochemistry with cell type-specific markers in t

300 density of GABAergic synapses as detected by immunocytochemistry within 30 min, much more rapidly tha