ライフサイエンスコーパス: immunocytochemistry

1 calreticulin (immunoblot, mass spectrometry, immunocytochemistry).

2 ed the effects on cell differentiation using immunocytochemistry.

3 ylase in situ hybridization, and parvalbumin-immunocytochemistry.

4 protein was detected by Western blotting and immunocytochemistry.

5 r of co-localization with mitochondria using immunocytochemistry.

6 etected and identified by immunoblotting and immunocytochemistry.

7 stigated with in vitro electrophysiology and immunocytochemistry.

8 uals via flow cytometry, immunoblotting, and immunocytochemistry.

9 ssues from these animals were analyzed using immunocytochemistry.

10 immunoblot assay, immunohistochemistry, and immunocytochemistry.

11 Purity and phenotype was confirmed with immunocytochemistry.

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

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

14 mpared to that in untreated control cells by immunocytochemistry.

15 ystem and of its subcellular localization by immunocytochemistry.

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

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

18 ssing circadian clock proteins in the SCN by immunocytochemistry.

19 tein levels by Western blot and quantitative immunocytochemistry.

20 rf2 subcellular localization was assessed by immunocytochemistry.

21 re analyzed by Western blot and double label immunocytochemistry.

22 rat using electron microscopic dual-labeling immunocytochemistry.

23 gh-resolution light and electron microscopic immunocytochemistry.

24 lar localization of PKCdelta was examined by immunocytochemistry.

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

26 t shock on the localization of melanopsin by immunocytochemistry.

27 GDNF localization was examined by immunocytochemistry.

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

29 BSA by enzyme-linked immunosorbent assay and immunocytochemistry.

30 n was analyzed using quantitative RT-PCR and immunocytochemistry.

31 amping in isolated alpha-cells identified by immunocytochemistry.

32 ined using patch-clamp electrophysiology and immunocytochemistry.

33 orescence-activated cell sorter analysis and immunocytochemistry.

34 stern blot, and localization was examined by immunocytochemistry.

35 Fr) was determined in rabbit TCFs (RTCFs) by immunocytochemistry.

36 -treated mice were assessed by histology and immunocytochemistry.

37 itro is confirmed both by flow cytometry and immunocytochemistry.

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

39 RNA and plasmid constructs, and analyzed by immunocytochemistry.

40 e in flow cytometry, immunofluorescence, and immunocytochemistry.

41 philic marker MPO in human neutrophils using immunocytochemistry.

42 the intact rat brain by electron microscopy immunocytochemistry.

43 sue organization and biomarker expression by immunocytochemistry.

44 urity, as confirmed by electrophysiology and immunocytochemistry.

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

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

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

48 Using immunocytochemistry, Acvr2a, Acvr2b, and downstream Smad

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

50 Immunocytochemistry after S1P treatment was used to moni

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

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

53 hrough reciprocal coimmunoprecipitations and immunocytochemistry analyses the association between Gly

54 Western blot and immunocytochemistry analysis for alphaSMA were also perf

55 Accordingly, immunocytochemistry analysis showed that NKCC2 and OS9 c

56 Immunocytochemistry analysis shows that SR1848 induces r

57 Using immunocytochemistry and a blinded scoring system, we obs

58 Immunocytochemistry and biochemical fractionation studie

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

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

61 Neuronal survival was examined using immunocytochemistry and cell counting.

62 Using immunocytochemistry and cellular quantification analyses

63 Immunocytochemistry and confocal imaging of primary hipp

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

65 In addition, immunocytochemistry and electron microscopy revealed a s

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

67 Immunocytochemistry and electron microscopy were utilize

68 Importantly, functional analysis with immunocytochemistry and electrophysiological recordings

69 3 cells expressing the antigens were used in immunocytochemistry and enzyme-linked immunoabsorption a

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

71 Immunocytochemistry and hydroethidine-based detection of

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

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

74 By using immunocytochemistry and mass dye fills, we characterized

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

76 rgeting was assessed in clonal beta-cells by immunocytochemistry and proinsulin secretion, by radioim

77 Immunocytochemistry and proximity ligation assays reveal

78 Immunocytochemistry and qPCR analyses on freshly isolate

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

80 onizing radiation (IR) using flow cytometry, immunocytochemistry and quantitative real-time polymeras

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

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

83 Using immunocytochemistry and real-time quantitative PCR, we f

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 P expression in NPY cells was confirmed with immunocytochemistry and single-cell reverse transcriptio

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

88 Immunocytochemistry and Western blot analysis determinin

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

90 s p53 levels in mitochondria, as detected by immunocytochemistry and Western blot analysis.

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

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

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

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

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

96 hed electrophysiological recordings, RT-PCR, immunocytochemistry, and behavioral analysis.

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 vel interactors validated by bioinformatics, immunocytochemistry, and coimmunoprecipitation.

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

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

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

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

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

106 teins were detected by immunohistochemistry, immunocytochemistry, and immunoblot analysis.

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

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

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

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

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

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

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

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

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

122 By immunocytochemistry, antibody AF1-003 recognizes a small

123 Immunocytochemistry assays demonstrated that these chann

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

125 By using a series of ELISA and immunocytochemistry assays, we assessed the development

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

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

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

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

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

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

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

133 Immunocytochemistry by electron microscopy confirms both

134 By immunocytochemistry, CFTR was expressed in many hybrid c

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

136 Immunocytochemistry, co-immunoprecipitation and proximit

137 Immunocytochemistry colocalized many of these enzymes wi

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 Immunocytochemistry coupled with electron microscopy rev

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

146 Immunocytochemistry demonstrated a decrease of surface p

147 7a siRNA treatment followed by STREX protein immunocytochemistry demonstrated both reduced levels and

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

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

150 Immunocytochemistry demonstrates that Yy1 is expressed i

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

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

153 Using immunocytochemistry, electrophysiology and Ca(2+) imagin

154 elopment (neurospheres) to evaluate, through immunocytochemistry, electrophysiology, and molecular bi

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 By immunocytochemistry, Fat1 and Atrs colocalized at cell-c

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

167 Immunocytochemistry for the five molecules and their rel

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

169 Immunocytochemistry further revealed substantial Na(V)1.

170 Immunocytochemistry further revealed that a ventromedial

171 Immunocytochemistry further reveals that NL/MSO neurons

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

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

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

175 Immunoblot, microarray, and immunocytochemistry (ICC) assays were performed on undif

176 Immunocytochemistry (ICC) showed receptor-independent up

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

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

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

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

181 Immunocytochemistry, immunotransmission electron microsc

182 Indeed, Affymetrix microarray analysis and immunocytochemistry implicated MMP-12 (macrophage metall

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

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

185 Multiple-label immunocytochemistry in combination with neurobiotin back

186 Fluorescence immunocytochemistry in enhanced green fluorescent protei

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

188 y, we determined the distribution of WARP by immunocytochemistry in the human inner ear using auditor

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

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

191 ined by light-and electron-microscopic-level immunocytochemistry indicates that it could not serve to

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

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

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

195 Immunohistochemistry and immunocytochemistry located Sfp1 in granules stockpiled

196 On immunocytochemistry, MCPIP1 colocalized with HCV RNA.

197 By immunocytochemistry, mitochondrial fractionation, and We

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

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

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

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

202 Sequential immunocytochemistry of intact cells or isolated nucleopl

203 Confocal immunocytochemistry of juvenile animals localized EsGal1

204 Immunocytochemistry of Madin-Darby canine kidney cells s

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

206 Immunocytochemistry of phosphorylated SMAD1/5/8 (phospho

207 Electron microscopic immunocytochemistry of the rat brain shows that 1) Pcdh-

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

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

210 After indirect immunocytochemistry or the overexpression of EGFP-tagged

211 expression in the TMJ tissue was assayed by immunocytochemistry or Western blotting.

212 e number and distribution were evaluated via immunocytochemistry over 21 days in vitro (DIV).

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

214 Using immunocytochemistry, pharmacological treatments and beha

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

216 Immunocytochemistry probed for intracellular paxillin lo

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

218 and MAC formation were measured by FACS and immunocytochemistry, respectively.

219 , as determined by in situ hybridization and immunocytochemistry, respectively.

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

221 Immunocytochemistry revealed cytosolic and nuclear expre

222 stochastic optical reconstruction microscopy immunocytochemistry revealed foci of clustered mitofilin

223 Immunocytochemistry revealed greater numbers of aromatas

224 Immunocytochemistry revealed little interaction between

225 Immunocytochemistry revealed OPN4 expression at the base

226 Immunocytochemistry revealed symmetric distribution of P

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

228 Confocal immunocytochemistry revealed that MLF transection produc

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

230 Moreover, immunocytochemistry revealed that the mutation prevented

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

232 Immunocytochemistry revealed that these structures lack

233 Immunocytochemistry revealed wide distribution of MIP-re

234 Immunocytochemistry reveals that both PGRMC1 and SW120,

235 However, immunocytochemistry reveals that the same region exhibit

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

237 es of the two, and analyzed by Western blot, immunocytochemistry, semiquantitative reverse transcript

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

239 Immunocytochemistry showed that (phyto)ceramide was colo

240 Immunocytochemistry showed that apoER2 mediates Sepp1 up

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

242 Expression analysis and immunocytochemistry showed that Drgal1-L2 is induced de

243 Immunocytochemistry showed that the GAT2 protein was pre

244 Immunocytochemistry shows that >93% of the SCF(+) cells

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

246 Immunocytochemistry staining was used to determine filam

247 Cell fractionation and immunocytochemistry studies demonstrated that the propor

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

249 By using immunocytochemistry, subsets of TRCs within rat taste bu

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

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

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

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

259 We employed electron microscopic immunocytochemistry to evaluate alterations in the distr

260 was combined with in situ hybridization and immunocytochemistry to identify the induced cellular exp

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 ract tracing method with electron microscopy immunocytochemistry to study the ultrastructural relatio

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

265 Western blotting and immunocytochemistry under the electron microscope indica

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

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

268 the presence of GPER which was confirmed by immunocytochemistry using a specific GPER antibody.

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

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

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

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

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

274 Immunocytochemistry verified the dendritic localization

275 Immunocytochemistry was performed on nonconfluent or scr

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

277 Immunocytochemistry was performed under both non-permeab

278 rom rat middle cerebral arteries (RMCAs) and immunocytochemistry was performed using Kv7 subunit-spec

279 Cyclic GMP immunocytochemistry was used functionally to localize sG

280 Immunocytochemistry was used to correlate myelin status

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

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

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

284 With immunocytochemistry, we find that axonal dynorphin immun

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

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

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

288 Using immunocytochemistry, we show that ApGLNT1 is localized p

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

290 Histology and immunocytochemistry were used to confirm the findings.

291 Western Blot and immunocytochemistry were used to determine expression of

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

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

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

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

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

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

298 tions and connectivity, we used double-label immunocytochemistry with antisera to different isoforms

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