ライフサイエンスコーパス: immunolabeling

1 The mCherry distribution was evaluated by immunolabeling.

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

3 ntrol rats showed cytoplasmic but no nuclear immunolabeling.

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

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

6 ntrast, was strikingly similar to octopamine immunolabeling.

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

8 were visualized by thioflavin S and insulin immunolabeling.

9 Protein localization was ascertained by immunolabeling.

10 brain vascular elements revealed by laminin immunolabeling.

11 y or following intensification of EGFP using immunolabeling.

12 by its endogenous fluorescence or following immunolabeling.

13 Similar results were observed with GluR2/3 immunolabeling.

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

15 s and hRSCs displayed photoreceptor-specific immunolabeling.

16 ressed in the CG based on immunoblotting and immunolabeling.

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

18 he progressive loss of cone alpha-transducin immunolabeling.

19 other lobster neuropeptides had no effect on immunolabeling.

20 ence; and is robustly compatible with direct immunolabeling.

21 ctionator technique in combination with SOX9 immunolabeling.

22 d is robustly compatible with antibody-based immunolabeling.

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

24 t only live cells can define surface epitope immunolabeling.

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

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

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

28 Immunolabeling after 4-5 days in organ culture caused lo

29 rally transfected fluorescent labeling or by immunolabeling after fixation.

30 L) subregions of the mPFC had elevated c-Fos immunolabeling after TMT and vanilla compared to H(2)O.

31 The use of the modified proteins as immunolabeling agents was also demonstrated.

32 Triple immunolabeling allowed distinguishing between cells type

33 Immunolabeling also revealed a clustered organization of

34 The laminin and beta-dystroglycan immunolabelings altered along the vessels such as in the

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

36 ated from canine and human cell cultures for immunolabeling and characterized using NTA, transmission

37 Using immunolabeling and confocal microscopy, we have analyzed

38 4 weeks and monitored albumin passage using immunolabeling and correlative light-electron microscopy

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

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

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

42 Reduced RANKL immunolabeling and fewer TRAP-positive multinucleated ce

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

44 Immunolabeling and Fourier transform infrared analyses s

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

46 Immunolabeling and immunoblotting studies confirmed the

47 Using specific immunolabeling and knockin mice in which green fluoresce

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

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

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

51 Immunolabeling and proximity ligation assay identified t

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

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

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

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

56 We used immunolabeling and tissue clearing to image the vascular

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

58 Immunolabeling and ultrastructural analyses of Caspr kno

59 The immunolabeling and ultrastructure of NS cells were inves

60 Stronger OPG immunolabeling and weaker RANKL immunolabeling were obse

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

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

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

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

65 ation, small interfering RNA knockdown, PCR, immunolabeling, and recordings of Ca(2+)-activated Cl(-)

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

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

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

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

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

71 ods were proposed to evaluate the success of immunolabeling based on paired particle detection in NTA

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

73 Using immunolabeling, biochemical analysis, genetic approaches

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

75 Here, genetic manipulations, coupled with immunolabeling, Ca(2+) imaging, electrophysiology, and b

76 florescence-based connectomics, advances in immunolabeling capabilities, and resources for recording

77 Immunolabeling combined with confocal microscopy of the

78 Immunolabeling, combined with chemical analyses and tran

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

80 Immunolabeling data demonstrate that EphA7+ striatofugal

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

82 Moreover, immunolabeling demonstrated close apposition of ryanodin

83 Immunolabeling demonstrated that BI were composed of mes

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

85 Immunolabeling demonstrated that Clrn1 localized to the

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

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

88 channel at the transduction site assessed by immunolabeling, despite the persistence of tip links.

89 Immunolabeling detected synaptic proteins, cone and rod

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

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

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

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

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

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

96 Immunolabeling experiments and transmission electron mic

97 Furthermore, immunolabeling experiments attested that GDSL1 is essent

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

99 Immunolabeling experiments show reduced colocalization o

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

101 Immunolabeling experiments were performed using antibodi

102 ichotomy was revealed by pharmacological and immunolabeling experiments, which found GluN2B-containin

103 ells were identified in electron microscopic immunolabeling experiments.

104 rategies for improving antibody-based tissue immunolabeling, fluorophore multiplexing, large-volume m

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

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

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

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

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

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

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

112 Immunolabeling for carboxymethyllysine, biglycan, and li

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

114 Immunolabeling for cone opsins showed the presence of bo

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

116 No immunolabeling for ERalpha was observed.

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

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

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

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

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

122 We then measured immunolabeling for phosphorylated tyrosine hydroxylase (

123 Triple immunolabeling for PKCalpha, nitric oxide synthetase (NO

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

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

126 Immunolabeling for the inhibitory neurotransmitter gamma

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

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

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 loma increases from stage I to stage IV, the immunolabeling fraction of CD3(+) cells decreases, while

132 owed that in culture-positive cows, the mean immunolabeling fraction of CD3(+) T cells decreased as t

133 age, IFN-gamma(+), TNF-alpha(+), and iNOS(+) immunolabeling fractions increased from stage I to stage

134 age, IFN-gamma(+), TNF-alpha(+), and iNOS(+) immunolabeling fractions increases.

135 acrophage (P = 0.03) and iNOS(+) (P = 0.007) immunolabeling fractions than culture-positive cows.

136 Immunolabeling identified Cx29 exclusively in the Schwan

137 In wild-type samples, double immunolabeling identified overlapping distribution of PM

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

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

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

141 alpha1 immunolabeling in aged monkeys was significantly reduced

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

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

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

145 Adipo-Clear and immunolabeling in combination with light-sheet microscop

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

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

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

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

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

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

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

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

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

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

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

157 An increased number of cells showed SMN immunolabeling in spinal cord of treated patients, but w

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

159 Electron microscopic immunolabeling in the PL-PFC of adult mice that had rece

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

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

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

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

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

165 Immunolabeling indicates that GABA neurons in the rostro

166 However, PSD95 immunolabeling intensities were substantially lower in c

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

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

169 smFP immunolabeling localized weakly expressed proteins not w

170 n intermediates that are readily detected by immunolabeling methods.

171 OT immunolabeling occurred in axonal boutons identified by

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

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

174 Immunolabeling of cell fractions, isolated by sucrose gr

175 Immunolabeling of cryostat-sectioned eyes harvested from

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

177 Dual immunolabeling of dendritic spines revealed that NHE6 pa

178 Retrieval and immunolabeling of epithelial markers, an obstacle for pr

179 The described method for indirect immunolabeling of EV and single vesicle detection using

180 Concomitantly, immunolabeling of excitatory ending markers revealed an

181 rix metalloproteinase activity and decreased immunolabeling of fibronectin.

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

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

184 Immunolabeling of ganglia associated with the vagina ind

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

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

187 Immunolabeling of human mammary carcinoma showed that WN

188 Notably, immunolabeling of kidney proteins revealed that claudin-

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

190 Immunolabeling of MHS-related peptides was retrospective

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

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

193 Immunolabeling of resin-embedded tissue confirmed the ph

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

195 Immunolabeling of sections with a panel of antibodies di

196 st a rigorous method of indirect fluorescent immunolabeling of single EV with subsequent evaluation u

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 (BLA), we examined electron microscopic dual immunolabeling of these receptors in the prelimbic PFC (

202 Immunolabeling of transforming growth factor-beta signal

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

204 Immunolabeling of tumors in KPC mice of different ages a

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

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

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

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

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

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

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

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

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 These immunolabeling patterns were similar for both homozygous

216 Using immunolabeling procedures in conjunction with confocal a

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

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

219 5, which was further supported for mGluR5 by immunolabeling results.

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 Immunolabeling showed that cortical terminals target bot

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

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

240 Immunolabeling shows that PKCiota and Rab14 colocalize i

241 Immunolabeling signals of endogenous Kv2.1, Nir2, and VA

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

243 However, Dpc4 immunolabeling status of carcinoma tissues harvested at

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

245 However, immunolabeling studies revealed that electrocytes do not

246 Immunolabeling studies showed that the IL-6 receptor was

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

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

249 hair cell lateral membrane was confirmed by immunolabeling studies.

250 Clearing and immunolabeling take ~1-2 weeks, depending on the size of

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

252 trophysiological mapping, tract tracing, and immunolabeling techniques were combined to delineate spe

253 isolated for biochemical assays or used for immunolabeling techniques.

254 a pressure-driven, nanobody-based whole-body immunolabeling technology to enhance the signal of fluor

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

256 (ON mBCs) in 57 goldfish of various sizes by immunolabeling their retinas with an antibody against PK

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

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

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

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

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

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

263 Indirect fluorescent immunolabeling utilizing quantum dots (Qd) resulted in r

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

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

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

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

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

269 Positive antineurofibromin immunolabeling was detected in normal control corneal en

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

271 Enkephalin immunolabeling was detected within a single morphologica

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

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

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

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

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

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

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

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 BMP2/4 and OCN immunolabeling were higher in DBG/HV when compared with

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 Immunolabeling with an antibody specific for Cx43 phosph

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

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

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

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

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

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

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

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

297 in situ hybridization as well as whole-mount immunolabeling with volume imaging (iDISCO+) in 3 dimens

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