ライフサイエンスコーパス: immunolabeling

1 ntrast, was strikingly similar to octopamine immunolabeling.

2 ctionator technique in combination with SOX9 immunolabeling.

3 d is robustly compatible with antibody-based immunolabeling.

4 ation were quantified by keratin-19 and CD45 immunolabeling.

5 were visualized by thioflavin S and insulin immunolabeling.

6 Protein localization was ascertained by immunolabeling.

7 brain vascular elements revealed by laminin immunolabeling.

8 y or following intensification of EGFP using immunolabeling.

9 by its endogenous fluorescence or following immunolabeling.

10 Similar results were observed with GluR2/3 immunolabeling.

11 CCK and PV synapses was supported by dual EM immunolabeling.

12 s and hRSCs displayed photoreceptor-specific immunolabeling.

13 ressed in the CG based on immunoblotting and immunolabeling.

14 Cx30 in the saccule, utricle, and ampulla by immunolabeling.

15 he progressive loss of cone alpha-transducin immunolabeling.

16 other lobster neuropeptides had no effect on immunolabeling.

17 sponded to U50,488 by increasing phospho-p38 immunolabeling.

18 pared with no-choice, as measured with c-Fos immunolabeling.

19 in cavernosal endothelial cells using double immunolabeling.

20 t only live cells can define surface epitope immunolabeling.

21 centrally, including Ki-67 index and hormone immunolabeling.

22 The mCherry distribution was evaluated by immunolabeling.

23 situ), a method for whole-body clearing and immunolabeling.

24 ntrol rats showed cytoplasmic but no nuclear immunolabeling.

25 n induced by vmPFC DBS was mapped with c-Fos immunolabeling.

26 ed by calretinin, PKCalpha, and CtBP2 triple immunolabeling.

27 roxylase (TH), and serotonin (5HT) by double immunolabelings.

28 reparatory steps and without any chemical or immunolabeling, a parasitemia level of fewer than ten pa

29 rally transfected fluorescent labeling or by immunolabeling after fixation.

30 Triple immunolabeling allowed distinguishing between cells type

31 t one-third of axon terminals containing CB1 immunolabeling also exhibited DbetaH labeling.

32 y and microheterogeneity in NUP62 and NUP214 immunolabeling among in NPC populations.

33 Using immunolabeling and confocal microscopy, we have analyzed

34 Using immunolabeling and confocal microscopy, we identified bl

35 4 weeks and monitored albumin passage using immunolabeling and correlative light-electron microscopy

36 in polymerization step (16 h), the protocol (immunolabeling and EM procedures) can be completed in 8

37 Bromodeoxyuridine (BrdUrd) immunolabeling and enzyme-linked immunosorbent assay ind

38 progenitor cells based on phospho-histone H3 immunolabeling and experiments showing that Musashi-immu

39 Reduced RANKL immunolabeling and fewer TRAP-positive multinucleated ce

40 Analysis of cellular location by immunolabeling and fluorescence microscopy suggests that

41 Immunolabeling and Fourier transform infrared analyses s

42 -the-shelf antibodies for multiple rounds of immunolabeling and imaging of a tissue's magnified prote

43 Immunolabeling and immunoblotting studies confirmed the

44 Using specific immunolabeling and knockin mice in which green fluoresce

45 Brains were processed to reveal Fos immunolabeling and lesion extent.

46 r, and its identity as Ara h 1 was proven by immunolabeling and mass spectrometry.

47 Recent advances in multiple immunolabeling and multispectral imaging have enabled si

48 The examination of Tbr1 and Lmx1a immunolabeling and Nissl staining confirmed the loss of

49 isted processing of whole seedlings prior to immunolabeling and observation in the transmission elect

50 Hence, we performed immunolabeling and quantitative analysis of the subcellu

51 in endothelial cells, as revealed by double immunolabeling and quantitative flow cytometric analysis

52 hip with the quantification of RGCs by Rbpms immunolabeling and retrograde labeling with FG.

53 found little overlap between group-III mGluR immunolabeling and that for the vesicular glutamate tran

54 ons of the core yeast complex, combined with immunolabeling and two-dimensional (2D) EM analysis of t

55 Immunolabeling and ultrastructural analyses of Caspr kno

56 The immunolabeling and ultrastructure of NS cells were inves

57 Stronger OPG immunolabeling and weaker RANKL immunolabeling were obse

58 TRPV4 protein expression was measured by immunolabeling and Western blotting.

59 ral analysis using 3-dimensional tomography, immunolabeling, and a proximity ligation assay next reve

60 on, in vivo and in vitro pollen germination, immunolabeling, and biochemical analyses was used on wil

61 Live fluorescence measurements, immunolabeling, and quantitative gene expression analysi

62 root ganglion, and spinal cord preparation, immunolabeling, and reverse transcriptase-PCR assays.

63 iosis, as demonstrated by a decrease in GFAP immunolabeling, and suppressed the activation of matrix

64 degenerate canine and human retinas, strong immunolabeling appeared in rod and cone photoreceptors,

65 line treated rats showed very little laminin immunolabeling around capillaries, arteries and in the m

66 Electron microscopy did not reveal any Cx50-immunolabeling at the membrane of horizontal cell tips i

67 Immunolabeling autoradiography was used to map and quant

68 The method uses a pre-embedding approach (immunolabeling before standard processing for transmissi

69 By two-dimensional (2D) and 3D imaging after immunolabeling, both proteins also colocalized with VZV

70 Immunolabeling, combined with chemical analyses and tran

71 ve analyses of primary and transsynaptic PRV immunolabeling confirmed an age-dependent assembly of hy

72 TDP-43 antibodies was assessed using double-immunolabeling confocal microscopy, immunoelectron micro

73 Immunolabeling data demonstrate that EphA7+ striatofugal

74 From EM immunolabeling data, we calculate that the PSD/cytoplasm

75 Moreover, immunolabeling demonstrated close apposition of ryanodin

76 Immunolabeling demonstrated that BI were composed of mes

77 mation of a macromolecular complex, and live immunolabeling demonstrated that both proteins co-locali

78 Immunolabeling demonstrated that Clrn1 localized to the

79 EBA-laminin double immunolabeling demonstrated that the expressions of lami

80 Confocal immunolabeling demonstrated that, whereas this cell trac

81 so had significantly higher enkephalin (ENK) immunolabeling densities in the POM than high singers.

82 Immunolabeling detected synaptic proteins, cone and rod

83 In that study, active caspase-3 immunolabeling did not markedly colocalize with Ki67, a

84 tiple-fluorescence confocal microscopy, dual-immunolabeling electron-microscopy, and optogenetic meth

85 T mutants using a combination of behavioral, immunolabeling, electrophysiological, and pharmacologica

86 GFP, DsRed, or beta-gal using the method of immunolabeling-enabled three-dimensional imaging of solv

87 ) and the podocyte marker anti-GLEPP1 showed immunolabeling exclusively within podocytes.

88 Discrete, punctate immunolabeling, exclusively in the inner plexiform layer

89 Immunolabeling experiments and transmission electron mic

90 Furthermore, immunolabeling experiments attested that GDSL1 is essent

91 glion cells was studied by double and triple immunolabeling experiments by using various cell markers

92 In mammalian brain, immunolabeling experiments have shown staining for Slo1

93 Immunolabeling experiments show reduced colocalization o

94 Their bipolar cell input was studied by immunolabeling experiments using various bipolar cell ma

95 Immunolabeling experiments were performed using antibodi

96 ells were identified in electron microscopic immunolabeling experiments.

97 Areas which showed intense laminin immunolabeling following KA or 3-NPA exposure correlated

98 employed a dual-labeling approach, combining immunolabeling for a retrograde tract tracer, Fluoro-Gol

99 The extent and cellular localization of immunolabeling for AGEs and their receptor, RAGE, were d

100 ells (RGCs) and glia exhibited intracellular immunolabeling for AGEs, increased AGE immunolabeling in

101 Immunolabeling for androgen (AR) and estrogen (ER alpha)

102 d by relative cell size and characterized by immunolabeling for beta1 integrin, nuclear transcription

103 ent survival times were combined with double immunolabeling for BrdU and DCX.

104 ac progenitor cell population as assessed by immunolabeling for c-kit in combination with myocyte-spe

105 Immunolabeling for carboxymethyllysine, biglycan, and li

106 In this study, we used an immunolabeling for choline acetyltransferase to demonstr

107 e islet-exocrine interface was identified by immunolabeling for collagen I, IV, V or VI and islets id

108 Immunolabeling for cone opsins showed the presence of bo

109 ombined with filipin labeling of sterols and immunolabeling for connexin43 (Cx43), we demonstrated th

110 No immunolabeling for ERalpha was observed.

111 ts for phase-contrast microscopy followed by immunolabeling for fluorescence microscopy and embedding

112 Lithium decreased immunolabeling for Gsk-3beta and increased expression fo

113 We also observed strong immunolabeling for HCN3, with no labeling for HCN1 and H

114 lets identified either morphologically or by immunolabeling for insulin.

115 lar K19 epithelial loss; however, multicolor immunolabeling for K19, vimentin, E-Cadherin, SNAIL, and

116 otubes of KO mice displayed already moderate immunolabeling for markers of oxidative stress (peroxire

117 We then measured immunolabeling for phosphorylated tyrosine hydroxylase (

118 Triple immunolabeling for PKCalpha, nitric oxide synthetase (NO

119 g cell-specific reporter gene expression and immunolabeling for postsynaptic glutamate receptors, sig

120 Immunolabeling for prodynorphin and enkephalin revealed

121 Immunolabeling for proopiomelanocortin (POMC), the precu

122 H-proline and 35S-sulfate incorporation, and immunolabeling for specific extracellular matrix compone

123 DSP-4 treatment reduced immunolabeling for the immediate early gene ZENK within

124 Immunolabeling for the inhibitory neurotransmitter gamma

125 ophagosomes that are easily detectable after immunolabeling for the LC3 protein.

126 Similarly, immunolabeling for the paranodal marker caspr reveals ir

127 Cell counts and immunolabeling for the proliferation marker Ki-67 and th

128 In aged monkey and rat optic nerves, immunolabeling for voltage-dependent potassium channels

129 (P30) to postnatal month 9.5 (PNM9.5) using immunolabeling for well-known cell- and synapse-specific

130 d TaGT47_2 RNAi transgenics showed decreased immunolabeling for xylan and arabinoxylan epitopes and a

131 erirhinal terminals containing PHAL and GABA immunolabeling formed symmetric synapses onto GABA-negat

132 Immunolabeling identified Cx29 exclusively in the Schwan

133 rated apoptotic cells in all samples; double immunolabeling identified these as trophoblasts, leukocy

134 Immunolabeling identifies AVs in the brain as a major re

135 rent experimental approaches, including live immunolabeling, immunogold electron microscopy, surface

136 In addition, beta2/3 immunolabeling in aged monkeys was characterized by mark

137 alpha1 immunolabeling in aged monkeys was significantly reduced

138 d vesicular glutamate transporter 2 (VGlut2) immunolabeling in animals with retrograde tracer injecti

139 Subsequent triple immunolabeling in anterior VTA showed that Fos-ir in tyr

140 press more estrogen receptor alpha (ERalpha) immunolabeling in CA1sr spine synapse complexes than age

141 rate here that noble metal nanoparticle (NP) immunolabeling in combination with plasmon coupling micr

142 detectable on RGCs; however, increased RAGE immunolabeling in glaucomatous eyes was predominant on g

143 lular immunolabeling for AGEs, increased AGE immunolabeling in glaucomatous eyes was predominantly ex

144 rom laminae II-V, although the occurrence of immunolabeling in individual varicosities varied widely

145 D1 result in marked variability in kindlin-1 immunolabeling in KS skin, which is mirrored by similar

146 l analysis of the PVN demonstrated p47(phox) immunolabeling in many glial and neuronal profiles, most

147 This was reflected by the extent of HLA-DR immunolabeling in MS GM which was significantly elevated

148 Molecules that were identified by immunolabeling in NS cells included nestin, Chx-10, vime

149 on microscopy of the neocortex revealed NOX2 immunolabeling in postsynaptic somata and dendrites that

150 epcidin injected eyes had increased ferritin immunolabeling in retinal vascular endothelial cells.

151 ed sickle mouse models, with increased PAI-1 immunolabeling in sickle mouse lung, bronchial epithelia

152 tidine in PD may be due to reduction of IL-6 immunolabeling in the inflamed gingival mucosa.

153 GBR-12909 also increased cFOS immunolabeling in the ventromedial nucleus of the hypoth

154 hologies of SIFamide-immunoreactive neurons: immunolabeling in various insect species revealed four i

155 erein an optimizedapplication of multiplexed immunolabeling in vivo for optical imaging of AML cellxe

156 Patch-clamp recordings and synaptic CaV1.3 immunolabeling indicated a larger number of Ca(2+) chann

157 Accordingly, double immunolabeling indicated that Cx35 and CaMKII were coloc

158 Immunolabeling indicates that GABA neurons in the rostro

159 However, PSD95 immunolabeling intensities were substantially lower in c

160 (comparable numerical densities but reduced immunolabeling intensity for PSD95) were found in the so

161 ilitated OLM and decreased synaptic p-ERK1/2 immunolabeling intensity without affecting numbers of p-

162 Together, these results show that immunolabeling is applicable to reliable, quantitative i

163 smFP immunolabeling localized weakly expressed proteins not w

164 n intermediates that are readily detected by immunolabeling methods.

165 OT immunolabeling occurred in axonal boutons identified by

166 rified antibodies reproduced the hippocampal immunolabeling of all patients' antibodies and colocaliz

167 Our patients' serum or CSF showed immunolabeling of antigens that were expressed at the cy

168 region, we examined the electron microscopic immunolabeling of antisera recognizing CRF or CRFr.

169 Immunolabeling of beta2 and alpha4 subunits was quantita

170 the hindbrain vasculature allows whole-mount immunolabeling of blood vessels and high-resolution imag

171 Immunolabeling of cell fractions, isolated by sucrose gr

172 Functional analysis and immunolabeling of CENH3, the centromere-specific histone

173 collagenous structure) by observing specific immunolabeling of COS cells transfected with human MARCO

174 Immunolabeling of cryostat-sectioned eyes harvested from

175 prominent features of staining were evident: immunolabeling of degenerating astrocytes in proximity t

176 Dual immunolabeling of dendritic spines revealed that NHE6 pa

177 Concomitantly, immunolabeling of excitatory ending markers revealed an

178 rix metalloproteinase activity and decreased immunolabeling of fibronectin.

179 rse co-immunoprecipitation, and (iii) double immunolabeling of freshly isolated myocytes revealing ca

180 can target their respective epitope showing immunolabeling of gamma-tubulin, actin, Golgi protein, a

181 Immunolabeling of ganglia associated with the vagina ind

182 In situ hybridization and immunolabeling of GFFD/GdFFD-positive neurons and fibers

183 Therefore, we examined electron microscopic immunolabeling of GluR1 and tyrosine hydroxylase (TH) in

184 a but not hippocampus, as shown by decreased immunolabeling of glutamic acid decarboxylase-65 (GAD65)

185 Immunolabeling of human mammary carcinoma showed that WN

186 Notably, immunolabeling of kidney proteins revealed that claudin-

187 eurons by examining the electron microscopic immunolabeling of M2R and the dopamine transporter (DAT)

188 We examined the electron microscopic dual immunolabeling of M2Rs and the vesicular acetylcholine t

189 Immunolabeling of MHS-related peptides was retrospective

190 developed a novel protocol for fixation and immunolabeling of microglia processes.

191 a3-tubulin+/Nissl], accompanied by increased immunolabeling of microglial/monocyte (Mac 3+) cells sur

192 g a flow cytometry live cell-based assay and immunolabeling of murine primary neurons.

193 mRNA expression by in situ hybridization and immunolabeling of neurons indicates that the primary sit

194 Immunolabeling of resin-embedded tissue confirmed the ph

195 peptide sequences of scleritin, we obtained immunolabeling of scleroblasts and OM of the sclerites w

196 Immunolabeling of sections with a panel of antibodies di

197 Immunolabeling of skeletal myofibers with antibodies to

198 The results demonstrate IAA-RP immunolabeling of subpopulations of vestibular neurons i

199 of cancer cells to different doses, and the immunolabeling of the apoptotic cells using quantum dot

200 Immunolabeling of the connexins showed differential chan

201 Immunolabeling of transforming growth factor-beta signal

202 Additionally, we checked for immunolabeling of tryptophan hydroxylase, an enzyme asso

203 Immunolabeling of tumors in KPC mice of different ages a

204 nexpected given previous findings that Cabp5 immunolabeling of type 3 bipolar cell axon terminals is

205 cf7a-Citrine fusion protein in zebrafish and immunolabeling of vestibular and cochlear mouse hair cel

206 entry into cells by electron microscopy and immunolabeling of virus proteins with antibodies conjuga

207 (ZIKV)-associated microcephaly, we performed immunolabeling on brain tissue from a 20-week fetus with

208 mice had a significant increase in p47(phox) immunolabeling on endomembranes just beneath the plasmal

209 m these patterns of staining, we carried out immunolabeling on sections from Kv1.3(-/-) mice.

210 contrast, AngII infusion decreased p47(phox) immunolabeling on the plasma membrane (-35.5 +/- 16.5%;

211 (i.e., nucleus accumbens) differences in the immunolabeling pattern between rostral, medial and cauda

212 Abnormal immunolabeling patterns are not restricted to photorecep

213 Immunolabeling patterns for the receptor activator of nu

214 Notably, the most intense 5-HT(3A) immunolabeling patterns were observed in the cerebral co

215 Using immunolabeling procedures in conjunction with confocal a

216 Next, we investigated via immunolabeling procedures whether proteins involved in E

217 These immunolabeling profiles suggest that there are four immu

218 d analyzed their behavior at the membrane by immunolabeling protocols, fluorescence recovery after ph

219 tifiable by both fluorescence microscopy and immunolabeling, resulting in a permanent marker identify

220 ing neuronal-specific nuclear protein (NeuN) immunolabeling, retrograde labeling, and optic nerve axo

221 atomic force microscopy studies, and fluoro-immunolabeling revealed a "supercomplex" structure withi

222 Anti-5-bromodeoxyuridine immunolabeling revealed a significant increase in myocyt

223 Protein kinase Calpha (PKCalpha) immunolabeling revealed abundant rod bipolar cells (RBCs

224 Double immunolabeling revealed beclin-1 expression predominantl

225 Immunolabeling revealed expression in lamina glia, in la

226 Immunolabeling revealed glial cells and hyalocytes in ma

227 Double immunolabeling revealed LILRA2 expression on CD14+, CD68

228 s glycinergic postsynaptic currents and GlyR immunolabeling revealed that A8 cells express GlyRs cont

229 Immunolabeling revealed that approximately 85% of the Hu

230 Immunolabeling revealed that Arr2 in the cell body coloc

231 Immunolabeling revealed that cholesterol trafficking pro

232 CRALBP and cytochrome C (Cyt C) immunolabeling revealed that hyperreflective bands 1 and

233 Immunolabeling revealed that Nav1.6 is already present a

234 s spectrometry, Western blotting, and tissue immunolabeling revealed the presence of different 14-3-3

235 sing the lysosomal marker protein 2 (LAMP-2) immunolabeling showed higher neuronal lysosomal counts i

236 terograde tract tracing combined with VGluT2 immunolabeling showed that 1) ventromedial nucleus-deriv

237 Bidirectional PALM and single-molecule immunolabeling showed that dense nanodomains of PSD-95 w

238 Dual immunolabeling shows that MFG-E8 colocalizes with both a

239 Immunolabeling shows that PKCiota and Rab14 colocalize i

240 , allowed us to identify distinct neurons by immunolabeling small subsets of sections within larger s

241 paraformaldehyde fixation severely affected immunolabeling, so this study used unfixed sections.

242 However, Dpc4 immunolabeling status of carcinoma tissues harvested at

243 Cell fractionation and electron-microscopic immunolabeling studies demonstrated that prohibitin is l

244 However, immunolabeling studies revealed that electrocytes do not

245 Immunolabeling studies showed that the IL-6 receptor was

246 In contrast, ultrastructural and immunolabeling studies verified the presence of myogenic

247 Consistent with the immunolabeling studies, TprK was also found to lack amph

248 hair cell lateral membrane was confirmed by immunolabeling studies.

249 receptor (A(2A)R) mRNA was combined with the immunolabeling technique for parvalbumin and transneuron

250 ould have skills in yeast molecular biology, immunolabeling techniques and access to a microscope equ

251 sed a combination of electron tomography and immunolabeling techniques to examine Golgi stacks and as

252 ng/freeze substitution, electron tomography, immunolabeling techniques, and subcellular fractionation

253 g three-dimensional tomography combined with immunolabeling techniques, we show that the plastoglobul

254 isolated for biochemical assays or used for immunolabeling techniques.

255 h when cells were subdivided by intensity of immunolabeling, the most heavily labeled ERalpha cells i

256 For UBCs, using Tbr2 immunolabeling, these cells are significantly reduced in

257 In addition, we performed CD11b immunolabeling to evaluate the effect of 3-NPA and KA on

258 age, using choline acetyltransferase (ChAT) immunolabeling to identify cholinergic interneurons.

259 We have used electron tomography and immunolabeling to investigate the consequences of PG kno

260 We have employed single immunolabeling to localize laminin in the brains.

261 We provide examples of double and triple immunolabeling using light, electron and correlated micr

262 ive Western blot analysis and retinal tissue immunolabeling using specific antibodies to selected pro

263 ha4-null mutation effects on [(125)I]mAb 270 immunolabeling varied widely among brain regions.

264 e cellular distribution of CRF in the VTA by immunolabeling VTA sections with anti-CRF antibodies and

265 BB), endothelial brain barrier antigen (EBA) immunolabeling was also performed.

266 p-CREB1/ATF1 immunolabeling was assessed in normal and rcd1 dogs trea

267 Some RAGE immunolabeling was detectable on RGCs; however, increase

268 Positive antineurofibromin immunolabeling was detected in normal control corneal en

269 TRPA1 or PLAP immunolabeling was detected not only on many thin-calibe

270 Enkephalin immunolabeling was detected within a single morphologica

271 Iba1-immunolabeling was found within the thin shell of perika

272 The extent of AGE and RAGE immunolabeling was greater in older than in younger dono

273 D1 and D2 immunolabeling was localized to cochlear nerve fibers, n

274 formance, the intensity of synaptic p-ERK1/2 immunolabeling was negatively correlated with OLM scores

275 r somas, NeuN and neurofilament-heavy (NF-H) immunolabeling was performed along with quantitative rev

276 Topographic analysis of Rbpms immunolabeling was performed on retinal wholemounts.

277 In male CRF-OE mice, CRF(1) immunolabeling was prominent in the cytoplasm of LC neur

278 At the light microscopic level, immunolabeling was prominent in the neuropil, in multipl

279 AKH immunolabeling was significantly higher in animals with

280 ining genetics, atomic force microscopy, and immunolabeling, we demonstrate that contiguous cell wall

281 Based on SOX9 immunolabeling, we document that astrocytes constitute a

282 Using RT-PCR and immunolabeling, we show that these genes are expressed w

283 Cells exhibiting intense GABA immunolabeling were also found in the same LSO locations

284 Stronger OPG immunolabeling and weaker RANKL immunolabeling were observed in the SRP/SA group at 15 a

285 CHIKV isolation and immunolabeling were performed on eye tissue specimens.

286 In situ hybridization and cell-type-specific immunolabeling were performed on ONH sections from DBA/2

287 ocesses exhibiting GPR177, 32% contained MOR immunolabeling while for profiles exhibiting MOR, 37% al

288 Sections of rat medulla were examined by immunolabeling with a polyclonal antibody directed again

289 Immunolabeling with an antibody specific for Cx43 phosph

290 of VTA glutamatergic neurons, we did triple immunolabeling with antibodies against VGluT2, tyrosine

291 Routine and electron microscopy (EM), immunolabeling with fluorescein-labeled Vicia villosa le

292 We have also combined laminin immunolabeling with Fluoro-Jade C labeling to evaluate t

293 analyzed in retinal sections by using double immunolabeling with primary antibodies against Muller an

294 Here, we used immunolabeling with specific antibodies against Kv4.2 an

295 ere further characterized at 37 degrees C by immunolabeling with specific antibodies recognizing orde

296 Whole-mount immunolabeling with this antibody showed that this pepti

297 mice by using either neuromelanin pigment or immunolabeling with tyrosine hydroxylase (TH) or calbind

298 ive method, iDISCO, that permits whole-mount immunolabeling with volume imaging of large cleared samp

299 sed and includes the study of antibodies and immunolabeling within the cell.

300 the relative lateral distribution of GluN2B-immunolabeling within the postsynaptic density did not c