ライフサイエンスコーパス: immunolabel

1 s from young and aged donor normal eyes were immunolabeled.

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

3 t only live cells can define surface epitope immunolabeling.

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

5 The mCherry distribution was evaluated by immunolabeling.

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

7 ntrol rats showed cytoplasmic but no nuclear immunolabeling.

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

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

10 ntrast, was strikingly similar to octopamine immunolabeling.

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

12 were visualized by thioflavin S and insulin immunolabeling.

13 Protein localization was ascertained by immunolabeling.

14 brain vascular elements revealed by laminin immunolabeling.

15 y or following intensification of EGFP using immunolabeling.

16 ence; and is robustly compatible with direct immunolabeling.

17 ctionator technique in combination with SOX9 immunolabeling.

18 d is robustly compatible with antibody-based immunolabeling.

19 he ON-BC dendritic tips, albeit with reduced immunolabelling.

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

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

22 rally transfected fluorescent labeling or by immunolabeling after fixation.

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

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

25 Triple immunolabeling allowed distinguishing between cells type

26 Immunolabeling also revealed a clustered organization of

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

28 Immunolabelling analysis and ultrastructural observation

29 After recording, slices were immunolabeled and OPCs were defined by strong expression

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

31 4 weeks and monitored albumin passage using immunolabeling and correlative light-electron microscopy

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

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

34 Reduced RANKL immunolabeling and fewer TRAP-positive multinucleated ce

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

36 Immunolabeling and Fourier transform infrared analyses s

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

38 Immunolabeling and immunoblotting studies confirmed the

39 Using specific immunolabeling and knockin mice in which green fluoresce

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

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

42 Immunolabeling and proximity ligation assay identified t

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

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

45 We used immunolabeling and tissue clearing to image the vascular

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

47 Stronger OPG immunolabeling and weaker RANKL immunolabeling were obse

48 opment we combined fate-mapping of ENCC with immunolabelling and intravascular dye injection to visua

49 s able to selectively isolate, fluorescently immunolabel, and count breast cancer cells that are posi

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

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

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

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

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

55 y ending markers revealed an increase in the immunolabeled area, supporting abnormally elevated excit

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

57 SUMO1 knock-out mice showed that anti-SUMO1 immunolabelling at synapses is non-specific.

58 ns described here demonstrate that CE-LIF of immunolabeled autophagy organelles is a powerful techniq

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

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

61 Using immunolabeling, biochemical analysis, genetic approaches

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

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

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

65 PRIMMUS (PRoteomic analysis of Intracellular iMMUnolabelled cell Subsets) approach, we now compare pr

66 At D7, CD31+ / Ki67+ double-immunolabeled cells and VEGFa and Ang2 expression were s

67 Single time point images of PCNA-immunolabeled cells are acquired using confocal and wide

68 ically classifying cell cycle phases in PCNA-immunolabeled cells from single time point images, indep

69 surface and number of IL-6, MMP-1, and MMP-9-immunolabeled cells in the gingival mucosa were quantifi

70 fied air and the spatial distribution of Fos-immunolabeled cells was quantified.

71 itive osteoclasts and IL-6, MMP-1, and MMP-9-immunolabeled cells was significantly lower than in PDSG

72 Immunolabeled cells were quantified.

73 otential cation channel subfamily M member 8 immunolabeled (cold receptor) axons ended almost exclusi

74 Immunolabeling combined with confocal microscopy of the

75 Immunolabeling, combined with chemical analyses and tran

76 and confocal microscopy of cryosectioned and immunolabeled contralateral eyes.

77 Immunolabeling data demonstrate that EphA7+ striatofugal

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

79 Moreover, immunolabeling demonstrated close apposition of ryanodin

80 Immunolabeling demonstrated that BI were composed of mes

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

82 Immunolabeling demonstrated that Clrn1 localized to the

83 Immunolabelling demonstrated a high density of PDGFRalph

84 Immunolabelling demonstrated TMC1 throughout the stereoc

85 Myelin basic protein and neurofilament immunolabelling demonstrates that axons in these adjacen

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

87 Dn-unsupplemented mice displayed region- and immunolabel-dependent increased BFCN number, larger area

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

89 Immunolabeling detected synaptic proteins, cone and rod

90 By analyzing the movements of immunolabeled ECM components (fibronectin, fibrillin-2)

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 Purkinje cell bodies were the most strongly immunolabeled elements.

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

95 Immunolabeling experiments and transmission electron mic

96 Furthermore, immunolabeling experiments attested that GDSL1 is essent

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

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

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

100 ells were identified in electron microscopic immunolabeling experiments.

101 ing of brain tissue containing transgenic or immunolabeled fluorescent proteins.

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

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

104 These cells immunolabeled for an RGC marker, not amacrine cell marke

105 (NCI), mild cognitive impairment, or AD were immunolabeled for both p75(NTR) and Rac1b.

106 Whole retinas were immunolabeled for both populations, and every labeled so

107 were dissected out and coronal sections were immunolabeled for calbindin, calretinin, NeuN, and reeli

108 Here, mouse distal colon was immunolabeled for CGRP, a marker of putative IPANs.

109 aformaldehyde, and brains were sectioned and immunolabeled for choline acetyltransferase (ChAT) or p7

110 ure II-methylene blue and on frozen sections immunolabeled for cone, rod, or glial proteins.

111 astatic cases after a 5-year follow-up, were immunolabeled for DAXX/ATRX and analyzed for alternative

112 had the same numerical density of synapses, immunolabeled for either the postsynaptic density (PSD)

113 ojection neurons (mean diameter 11.6 microm) immunolabeled for GluR1, and about one third of these we

114 ain sections (100-300 microm) were multiplex immunolabeled for IBA1 and Hoechst, and imaged by step-a

115 f schizophrenia and comparison subjects were immunolabeled for the vesicular GABA transporter (vGAT)

116 Surprisingly, these cells immunolabeled for tyrosine hydroxylase, a key component

117 enia and unaffected comparison subjects were immunolabeled for vGAT, GAD67, and CB.

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

119 Immunolabeling for carboxymethyllysine, biglycan, and li

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

121 Immunolabeling for cone opsins showed the presence of bo

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

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

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

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

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

127 We then measured immunolabeling for phosphorylated tyrosine hydroxylase (

128 Triple immunolabeling for PKCalpha, nitric oxide synthetase (NO

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

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

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

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

133 es of mdx mice was associated with increased immunolabelling for utrophin and beta-dystroglycan in th

134 Increases in sarcolemmal immunolabelling for utrophin and beta-dystroglycan sugge

135 ellular sites within cells, and as nanoscale immunolabels for enhanced tissue penetration and improve

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

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

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

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

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

141 Immunolabeled hair cells were used to visualize the spir

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

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

144 Quantitative analysis of multiple immunolabeled images revealed small within-cell, but lar

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

160 logical evidence on decreased neuronal LMTK2 immunolabelling in AD, with implications for pathogenesi

161 ffective and specific use as intrabodies and immunolabels in mammalian cells including brain neurons.

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

163 Immunolabeling indicates that GABA neurons in the rostro

164 However, PSD95 immunolabeling intensities were substantially lower in c

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

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

167 Immunolabelling localised DRP2A/B to the tips of root ha

168 smFP immunolabeling localized weakly expressed proteins not w

169 Fourier analysis of immunolabelled lysosomes suggests a sarcomeric pattern (

170 n intermediates that are readily detected by immunolabeling methods.

171 muscle regeneration at the protein level by immunolabelling muscle biopsies for developmental myosin

172 density of microtubule-associated protein 2-immunolabeled neurons in the ventricular/subventricular

173 immunoreactivity within tyrosine hydroxylase-immunolabeled neurons of VTA, but did attenuate cocaine-

174 cked NF triplet proteins, such as calretinin-immunolabeled nonpyramidal cells, showed no alterations

175 Here, we developed FIN-Seq (Frozen Immunolabeled Nuclei Sequencing), a method that accompli

176 OT immunolabeling occurred in axonal boutons identified by

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

178 Immunolabeling of cryostat-sectioned eyes harvested from

179 Dual immunolabeling of dendritic spines revealed that NHE6 pa

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

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

182 Concomitantly, immunolabeling of excitatory ending markers revealed an

183 rix metalloproteinase activity and decreased immunolabeling of fibronectin.

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

185 Immunolabeling of ganglia associated with the vagina ind

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

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

198 Immunolabeling of the connexins showed differential chan

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

200 Immunolabeling of transforming growth factor-beta signal

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

202 Immunolabeling of tumors in KPC mice of different ages a

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

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

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

206 Immunolabelling of 12 weeks old skin specimens showed st

207 ction in hexaploid wheat (2n = 42) by triple immunolabelling of CENH3 protein marking functional cent

208 We optimize immunolabelling of tail epidermal wholemounts to allow s

209 Immunolabelling of the recellularised scaffolds demonstr

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

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

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

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

214 Cochlear structure was characterized in immunolabeled organ of Corti whole mounts using confocal

215 Immunolabeling patterns for the receptor activator of nu

216 These immunolabeling patterns were similar for both homozygous

217 Calcitonin gene-related peptide immunolabeled (peptidergic) axons ended mostly in simple

218 These puncta were juxtaposed to immunolabeled presynaptic efferent terminals.

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

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

221 we show that by using specific intracellular immunolabelling protocols, FACS separation of interphase

222 ver, a significant increase in synaptophysin immunolabeled puncta in the hippocampal subregion, CA1,

223 5, which was further supported for mGluR5 by immunolabeling results.

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

225 Immunolabeling revealed expression in lamina glia, in la

226 Immunolabeling revealed glial cells and hyalocytes in ma

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

228 Immunolabeling revealed that Arr2 in the cell body coloc

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

230 Immunolabeling revealed that Nav1.6 is already present a

231 Such immunolabelling revealed one or more regenerating myofib

232 Immunolabelling revealed reduced density of sensory (CGR

233 However, double immunolabelling revealed that TFAM was reduced in neuron

234 Here we provide evidence from immunolabel, RNA expression and mass spectrometry analys

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 Immunolabeling shows that PKCiota and Rab14 colocalize i

240 Critically, immunolabelling shows the dynamics of these presynaptic

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

242 t mouse lymphoid organs from a collection of immunolabeled slices.

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

244 The HMB45-immunolabeled specimens were additionally developed with

245 d are verified by quantitative stereology of immunolabelled spinal cord sections at selected time poi

246 iDISCO enables facile volume imaging of immunolabeled structures in complex tissues.

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

248 Immunolabeling studies showed that the IL-6 receptor was

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

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

251 hair cell lateral membrane was confirmed by immunolabeling studies.

252 Tyrosine hydroxylase-immunolabeled (sympathetic) nerve terminals originating

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

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

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

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

257 odendritic terminals, we examined the VGLUT2-immunolabeled thalamic input to striatal cholinergic int

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

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

260 sed tissue hybrids supports the diffusion of immunolabels throughout intact tissue, whereas RIMS (ref

261 Brains were immunolabeled to evaluate in vivo gene expression, choli

262 ssue from D(1) and D(2) mice that was double immunolabeled to reveal the EGFP and VGluT1 or VGluT2.

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

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

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

266 lds were further assessed histologically and immunolabelled using makers for odontoblastic differenti

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

268 Data were obtained from immunolabeled vertical sections of six postmortem male a

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

270 Positive antineurofibromin immunolabeling was detected in normal control corneal en

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

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

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

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

275 AKH immunolabeling was significantly higher in animals with

276 GluA2 immunolabelling was stronger in MCs than in BCs.

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

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

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

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

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

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

283 Intercalated disk morphology and connexin 43 immunolabelling were not different in hypertrophy.

284 the optical microscope revealed that the NP immunolabels were not homogeneously distributed.

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

286 Synapsin-immunolabeled whole-mount brains reveal that during the

287 tions were stained for H&E and trichrome and immunolabeled with antibodies against protein gene produ

288 eny of genetically labeled RG cells could be immunolabeled with antibodies to CalR and GABA or ventra

289 -fixed paraffin-embedded tumor sections were immunolabeled with antibodies to serotonin.

290 The specimens were immunolabeled with human melanoma black 45 (HMB45), mela

291 rn blots, and cells in the PFCTX were double immunolabeled with MPO, indicating they were neutrophils

292 axon tips and adjacent shafts were intensely immunolabeled with synapse markers.

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

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

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

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

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

298 isoforms at the PSD, with a high density of immunolabel within the PSD core under basal conditions.

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