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 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 ctionator technique in combination with SOX9 immunolabeling.

11 brain vascular elements revealed by laminin immunolabeling.

12 y or following intensification of EGFP using immunolabeling.

13 by its endogenous fluorescence or following immunolabeling.

14 Similar results were observed with GluR2/3 immunolabeling.

15 d is robustly compatible with antibody-based immunolabeling.

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

17 s and hRSCs displayed photoreceptor-specific immunolabeling.

18 ressed in the CG based on immunoblotting and immunolabeling.

19 pared with no-choice, as measured with c-Fos 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 ltaneously to characterize these vesicles by immunolabelling.

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

25 rally transfected fluorescent labeling or by immunolabeling after fixation.

26 Triple immunolabeling allowed distinguishing between cells type

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

28 Immunolabelling analysis and ultrastructural observation

29 nd guanosine triphosphate (GTP) (RacGTP) was immunolabeled and analyzed using confocal microscopy.

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

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

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

35 Reduced RANKL immunolabeling and fewer TRAP-positive multinucleated ce

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

37 Immunolabeling and Fourier transform infrared analyses s

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

39 Immunolabeling and immunoblotting studies confirmed the

40 Using specific immunolabeling and knockin mice in which green fluoresce

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

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

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

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

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

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

47 Immunolabeling and ultrastructural analyses of Caspr kno

48 Stronger OPG immunolabeling and weaker RANKL immunolabeling were obse

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

50 peptidase in Escherichia coli, was mapped by immunolabelling and by visualization of GFP fusion prote

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

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

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

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

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

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

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

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

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

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

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

62 Previously we found 5-HT-immunolabeled axons that spanned the transection site on

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

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

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 chemical analyses and tran

75 and confocal microscopy of cryosectioned and immunolabeled contralateral eyes.

76 Immunolabeling data demonstrate that EphA7+ striatofugal

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

78 Moreover, immunolabeling demonstrated close apposition of ryanodin

79 Immunolabeling demonstrated that BI were composed of mes

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

81 Immunolabeling demonstrated that Clrn1 localized to the

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

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 Immunolabeling detected synaptic proteins, cone and rod

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

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

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

92 Purkinje cell bodies were the most strongly immunolabeled elements.

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 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 Immunolabeling experiments show reduced colocalization o

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

100 Immunolabeling experiments were performed using antibodi

101 ells were identified in electron microscopic immunolabeling experiments.

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

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 Tibial sections were immunolabeled for cathepsin B and septoclasts were count

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

109 Frozen sections were immunolabeled for collagenase, insulin, CK19, collagen V

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

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

112 sumed inhibitory synapses), similar synapses immunolabeled for GABA (F-GABA), primary afferent synaps

113 In striatum, about 65% of striatal neurons immunolabeled for GluR1, 75%-79% immunolabeled for GluR2

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

115 , and the remainder of the neurons that were immunolabeled for GluR2 coincided with projection neuron

116 tal neurons immunolabeled for GluR1, 75%-79% immunolabeled for GluR2 or GluR2/3, and only 2.5% posses

117 ns the size of cholinergic interneurons were immunolabeled for GluR2, and the remainder of the neuron

118 neurons the size of cholinergic interneurons immunolabeled for GluR4 and seemingly all neurons in the

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

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

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

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

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

124 Immunolabeling for carboxymethyllysine, biglycan, and li

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

126 Immunolabeling for cone opsins showed the presence of bo

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

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

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

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

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

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

133 We then measured immunolabeling for phosphorylated tyrosine hydroxylase (

134 Triple immunolabeling for PKCalpha, nitric oxide synthetase (NO

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

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

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

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

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

140 the second set, sections of the medulla were immunolabelled for V(1A) receptors, and the V(1A) recept

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

159 Immunolabeling indicates that GABA neurons in the rostro

160 However, PSD95 immunolabeling intensities were substantially lower in c

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

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

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

164 smFP immunolabeling localized weakly expressed proteins not w

165 Fourier analysis of immunolabelled lysosomes suggests a sarcomeric pattern (

166 n intermediates that are readily detected by immunolabeling methods.

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

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

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

170 OT immunolabeling occurred in axonal boutons identified by

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

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

173 Immunolabeling of cell fractions, isolated by sucrose gr

174 Immunolabeling of cryostat-sectioned eyes harvested from

175 Dual immunolabeling of dendritic spines revealed that NHE6 pa

176 Concomitantly, immunolabeling of excitatory ending markers revealed an

177 rix metalloproteinase activity and decreased immunolabeling of fibronectin.

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

179 Immunolabeling of ganglia associated with the vagina ind

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

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

182 Immunolabeling of human mammary carcinoma showed that WN

183 Notably, immunolabeling of kidney proteins revealed that claudin-

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

185 Immunolabeling of MHS-related peptides was retrospective

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

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

188 Immunolabeling of resin-embedded tissue confirmed the ph

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

190 Immunolabeling of sections with a panel of antibodies di

191 Immunolabeling of skeletal myofibers with antibodies to

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

193 Immunolabeling of the connexins showed differential chan

194 Immunolabeling of transforming growth factor-beta signal

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

196 Immunolabeling of tumors in KPC mice of different ages a

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

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

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

200 Immunolabelling of 12 weeks old skin specimens showed st

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

202 We optimize immunolabelling of tail epidermal wholemounts to allow s

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

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

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

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

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

208 Immunolabeling patterns for the receptor activator of nu

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

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

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

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

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

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

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

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

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

218 Double immunolabeling revealed beclin-1 expression predominantl

219 Immunolabeling revealed expression in lamina glia, in la

220 Immunolabeling revealed glial cells and hyalocytes in ma

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

222 Immunolabeling revealed that Arr2 in the cell body coloc

223 Immunolabeling revealed that cholesterol trafficking pro

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

225 Immunolabeling revealed that Nav1.6 is already present a

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

227 Immunolabelling revealed reduced density of sensory (CGR

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

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

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

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

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

233 Immunolabeling shows that PKCiota and Rab14 colocalize i

234 Critically, immunolabelling shows the dynamics of these presynaptic

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

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

237 The HMB45-immunolabeled specimens were additionally developed with

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

239 ouse cortex increased the proportion of NR2A-immunolabeled spines within 30 minutes relative to basal

240 ch colabels isolated CD8(+) CD205(+) DCs, to immunolabel spleen sections.

241 However, Dpc4 immunolabeling status of carcinoma tissues harvested at

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

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

244 Immunolabeling studies showed that the IL-6 receptor was

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

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

247 hair cell lateral membrane was confirmed by immunolabeling studies.

248 Tyrosine hydroxylase-immunolabeled (sympathetic) nerve terminals originating

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

250 isolated for biochemical assays or used for immunolabeling techniques.

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

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

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

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

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

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

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

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

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

264 Positive antineurofibromin immunolabeling was detected in normal control corneal en

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

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

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

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

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

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

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

272 AKH immunolabeling was significantly higher in animals with

273 GluA2 immunolabelling was stronger in MCs than in BCs.

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

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

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

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

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

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

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

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

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

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

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

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

286 Sections were also immunolabeled with antibodies to vesicular glutamate tra

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

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

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

290 ections of postmortem fixed monkey eyes were immunolabeled with well-characterized and specific monoc

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

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

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

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

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

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

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