1 Quantitative
immunogold analyses reveal that the density of VGLUT3 go
2 Quantitative immunoperoxidase and
immunogold analysis showed that both subunits display a
3 ing to bacterial surfaces can be detected by
immunogold analysis.
4 Immunogold atomic force microscopy reveals, for the firs
5 Additionally, before photocleavage,
immunogold can be employed to label proteins that intera
6 echniques including immunohistochemistry and
immunogold can further evaluate the levels of the variou
7 in and the H(+)-ATPase were quantified using
immunogold cytochemistry and morphometric analysis.
8 Ultrastructural examination using
immunogold cytochemistry confirmed that activated caspas
9 isolation of synaptic vesicles confirmed the
immunogold data and showed vesicular colocalization of V
10 ent novel electron microscopic postembedding
immunogold data from mouse and rat brains showing that s
11 Electron microscopic
immunogold data further suggest that NMDA receptors are
12 The
immunogold data suggest that most MSBs would not generat
13 Confocal microscopy and electron microscopy-
immunogold demonstrated that fetuin-A was internalized b
14 GluN1-
immunogold density and the percentage of immunopositive
15 In contrast, GluR2
immunogold density was not significantly different betwe
16 In addition, GluR1
immunogold density was significantly increased by 30% in
17 Immunogold detection of gp65 in vivo complemented virion
18 By using silver-enhanced
immunogold detection, we compared the morphological char
19 Immunogold electron microscopic analysis indicated that,
20 To address these questions, we undertook an
immunogold electron microscopic study of Tg(PG14) mice.
21 current assumptions, pre- and postembedding
immunogold electron microscopy (EM) revealed that MHCI p
22 ng immunoprecipitation of COPII vesicles and
immunogold electron microscopy (EM), we characterize the
23 With double-labeling
immunogold electron microscopy (EM), we confirmed that I
24 Immunogold electron microscopy and analysis were used to
25 Based on
immunogold electron microscopy and co-immunoprecipitatio
26 Previous examination by
immunogold electron microscopy and electron tomography s
27 Immunogold electron microscopy and flow cytometric analy
28 calized inside the in vivo pollen tube using
immunogold electron microscopy and found to be present i
29 ocalizes in lamellar bodies as determined by
immunogold electron microscopy and immunoblot of lamella
30 ns of the suprastructures were determined by
immunogold electron microscopy and immunoblotting.
31 Immunogold electron microscopy and immunofluorescence te
32 Subsequent analyses of HSV-infected cells by
immunogold electron microscopy and live-cell confocal im
33 Immunogold electron microscopy confirmed the association
34 facilitate nutrient uptake from host blood,
immunogold electron microscopy confirms that the protein
35 We now show by quantitative
immunogold electron microscopy coupled with analysis of
36 Immunogold electron microscopy data support the conclusi
37 Immunogold electron microscopy demonstrated increased ni
38 Immunogold electron microscopy demonstrated that E4 34K
39 Immunogold electron microscopy demonstrated that platele
40 ing rat brain slice, immunofluorescence, and
immunogold electron microscopy detection of VMAT2 (vesic
41 ts (MEFs) by indirect immunofluorescence and
immunogold electron microscopy in the presence or absenc
42 In addition, the results of
immunogold electron microscopy indicated a close associa
43 Here, pre-embedding
immunogold electron microscopy is applied to dissociated
44 Immunogold electron microscopy localized Ser(P)269-AQP2
45 Immunogold electron microscopy localized the allergen in
46 Transmission and
immunogold electron microscopy of extracted extracellula
47 Immunogold electron microscopy of hippocampal tissue sec
48 Immunogold electron microscopy of rat hippocampal neuron
49 raK-FLAG3 in otherwise wild-type cells using
immunogold electron microscopy of thin sections revealed
50 Immunofluorescence and
immunogold electron microscopy reveal a spectrin-rich do
51 In the present study,
immunogold electron microscopy revealed EC-SOD in membra
52 Immunogold electron microscopy revealed redistribution o
53 Immunogold electron microscopy revealed that pU(L)31 cou
54 pared with non-MTLE hippocampi, quantitative
ImmunoGold electron microscopy revealed that the density
55 Immunogold electron microscopy revealed that these prote
56 Additionally, immunohistochemistry and
immunogold electron microscopy revealed that tibial marr
57 st exclusively in RPE Immunofluorescence and
immunogold electron microscopy showed that HFE protein w
58 Moreover,
immunogold electron microscopy showed that NR1 is expres
59 Immunogold electron microscopy showed that surface recep
60 Immunogold electron microscopy showed that the Uni2 prot
61 Direct
immunogold electron microscopy specifically localized de
62 High-resolution
immunogold electron microscopy supported the cellular lo
63 Confocal and
immunogold electron microscopy supported Trpv4 overexpre
64 Here, we used postembedding
immunogold electron microscopy techniques to examine the
65 In this study, we used
immunogold electron microscopy to demonstrate that BxpB
66 ution structured illumination microscopy and
immunogold electron microscopy to localize major compone
67 In this study, we used
immunogold electron microscopy to show that the CTD of B
68 ined immunocytochemistry and high-resolution
ImmunoGold electron microscopy to study cellular and sub
69 Immunogold electron microscopy using antibodies raised a
70 In addition,
immunogold electron microscopy using antisera against Eb
71 Immunogold electron microscopy was used to determine whe
72 tative real-time PCR and in mouse kidneys by
immunogold electron microscopy, and its agonism 1) incre
73 ly at the pilus tip, a location supported by
immunogold electron microscopy, and suggests that, as fo
74 Using
immunogold electron microscopy, non-fibrillar forms of P
75 Using
Immunogold electron microscopy, PGRP-S was localized to
76 l approaches, including live immunolabeling,
immunogold electron microscopy, surface biotinylation an
77 Confocal immunofluorescent and
immunogold electron microscopy, together with subcellula
78 ted emission depletion (STED) microscopy and
immunogold electron microscopy, we determined the distri
79 Using
immunogold electron microscopy, we examine and compare t
80 By cell fractionation and
immunogold electron microscopy, we have identified an en
81 bedding immunoperoxidase and silver-enhanced
immunogold electron microscopy, we localized T-channel s
82 calizes with NFL on single neurofilaments by
immunogold electron microscopy.
83 th cardiac amyloid deposits was confirmed by
immunogold electron microscopy.
84 -exponential growth, which was reinforced by
immunogold electron microscopy.
85 calized the epitope on the capsid surface by
immunogold electron microscopy.
86 tophysin, syntaxin, and synaptotagmin and by
immunogold electron microscopy.
87 n blot analyses of cell wall proteins and by
immunogold electron microscopy.
88 These results were further validated via
immunogold electron microscopy.
89 coprotein (GPC) on the cell surface by using
immunogold electron microscopy.
90 ileptic DGCs was examined with postembedding
immunogold electron microscopy.
91 mouse retina was visualized by pre-embedding
immunogold electron microscopy.
92 situ hybridization, immunofluorescence, and
immunogold electron microscopy.
93 emonstrated by subcellular fractionation and
immunogold electron microscopy.
94 measured by mass spectrometry and located by
immunogold electron microscopy.
95 noblotting, immunofluorescence analysis, and
immunogold electron microscopy.
96 alizes with NF-M on single neurofilaments by
immunogold electron microscopy.
97 interact, we employed immunofluorescence and
immunogold electron microscopy.
98 d in lung tissue by immunohistochemistry and
immunogold electron microscopy.
99 al compartments by confocal fluorescence and
immunogold electron microscopy.
100 bimolecular fluorescence complementation and
immunogold electron microscopy.
101 in IMCD cells of potassium-deprived rats by
immunogold electron microscopy.
102 -membrane-localized VLPs as visualized using
immunogold electron microscopy.
103 lasma membrane microdomains, as localized by
immunogold electron microscopy.
104 , immunofluorescent confocal microscopy, and
immunogold-
electron microscopy reveal that the 15b-IDE p
105 ed against these GIPCs were further used for
immunogold-
electron microscopy strategy, revealing the d
106 By confocal microscopy and
immunogold-
electron microscopy, these filaments are loca
107 onfirmed in cerebral malaria by quantitative
immunogold EM; however, polarized distribution of AQP4 a
108 Radioligand binding assays allied to in situ
immunogold-
EM analysis and furosemide-sensitive tonic cu
109 .3(-/-) mice either at the light level or in
immunogold experiments.
110 that depends on special equipment, requires
immunogold for colabeling, and does not take advantage o
111 ase in single labeling and with preembedding
immunogold for double labeling, was localized in cell bo
112 aments was strikingly similar to that of the
immunogold label for gephyrin.
113 n electron microscopy with a glycan-specific
immunogold label showed that this saccharide was distrib
114 Spatial analysis of the
immunogold label shows a nonrandom distribution for all
115 electron microscopy revealed localization of
immunogold-
labeled CXCL10 to the bacterial cell surface
116 The presence of
immunogold-
labeled electron-dense bodies was correlated
117 et of criteria derived from the structure of
immunogold-
labeled GABAergic synapses.
118 on microscopy was used to localize alphaB in
immunogold-
labeled intact and permeabilized microvesicle
119 Electron microscopy of
immunogold-
labeled microsections revealed that the HCV e
120 Our in vivo EM images of
immunogold-
labeled rat IAPP and human IAPP show both for
121 eins and transmission electron microscopy of
immunogold-
labeled samples in the case of ABCB19.
122 n microscopy illustrates a unique pattern of
immunogold-
labeled SmNPP-5 within the tegument; some imm
123 Transmission electron microscopy of
immunogold-
labeled thawed cryosections of infected cells
124 Here, we use serial multiplex
immunogold labeling (siGOLD) and serial-section transmis
125 Immunogold labeling and electron microscopy analysis dem
126 Postembedding
immunogold labeling and electron microscopy provide evid
127 Immunogold labeling and electron microscopy shows there
128 Immunogold labeling and electron microscopy were used to
129 Using
immunogold labeling and electron microscopy, L2 was dete
130 Immunogold labeling and histochemical procedures offer w
131 By using
immunogold labeling and immunohistochemical assays, here
132 Toward that end, we also demonstrated by
immunogold labeling and mass spectrometry that PilA is i
133 was visualized by electron microscopy using
immunogold labeling and probed by fluorescence resonance
134 -mortem tissue using electron microscopy and
immunogold labeling and revealed dityrosine crosslinks i
135 Immunogold labeling and surface protein isolation identi
136 chemical observations were corroborated with
immunogold labeling and transmission electron microscopy
137 Using
immunogold labeling assays, we found PfN44 in both the n
138 Immunogold labeling combined with transmission electron
139 Ultrastructural analysis by
immunogold labeling confirmed colocalization and further
140 detection of collagen XII and tenascin-X by
immunogold labeling confirmed this finding.
141 Western blot, immunohistochemistry, and
immunogold labeling coupled to scanning and transmission
142 Electron microscopy with
immunogold labeling demonstrated labeled axon terminals
143 Immunogold labeling demonstrated localization of E1 prot
144 Double
immunogold labeling demonstrated that a sizeable proport
145 Immunogold labeling demonstrated that ABA is associated
146 Immunofluorescence and
immunogold labeling detected PHB2 at mitochondrial membr
147 of ultrastructural morphometry together with
immunogold labeling enables the identification and quant
148 abeling in the presence of 0.3 M MgCl(2) and
immunogold labeling for collagen types II and IX were an
149 Immunogold labeling for GABA confirmed that the transpla
150 While
Immunogold labeling for GluN2A at MF-CA3 synapses was co
151 globular aggregates that displayed positive
immunogold labeling for tau-P, as well as conformational
152 e GluN2A subunit antibody and the density of
immunogold labeling for this subunit was unchanged.
153 We found that in vivo
immunogold labeling improves epitope accessibility, ultr
154 tibody specific for toxic oligomers and cryo-
immunogold labeling in human IAPP transgenic mice, human
155 Preembedding
immunogold labeling in STN dendrites revealed that 60-70
156 rsely, mGluR1a displayed the same pattern of
immunogold labeling in the two species.
157 Immunogold labeling indicates that WIP1 is associated wi
158 Here,
immunogold labeling is used to map the plasma membrane d
159 Immunogold labeling located PratA and pD1 to these disti
160 utamate receptor subunit 1 (GluR1) and GluR4
immunogold labeling measurements, at both the soma and m
161 te this, we combined freeze-fracture replica
immunogold labeling of Cav2.1 channels, local [Ca(2+)] i
162 from the African clawed toad Xenopus laevis,
immunogold labeling of component proteins and subsequent
163 Immunogold labeling of CXCL10-treated spores demonstrate
164 maging analysis of DAT was combined with the
immunogold labeling of DAT and quantitative electron mic
165 Moreover,
immunogold labeling of DMSO reductase subunits reveals t
166 s of OBAP1 to yellow fluorescent protein and
immunogold labeling of embryo transmission electron micr
167 Immunogold labeling of endogenous Toc75 POTRA domains in
168 Immunogold labeling of geranyl diphosphate synthase occu
169 in sections were collected on slot grids for
immunogold labeling of GnRH immunoreactivity.
170 Cryo-
immunogold labeling of gp91(phox) and CeCl(3) cytochemis
171 preautonomic PVN neurons were identified by
immunogold labeling of pseudorabies virus (PRV) transpor
172 Here, we use
immunogold labeling of SCs in Drosophila ovaries to loca
173 Immunogold labeling of the auxiliary replication protein
174 y, and transmission electron microscopy with
immunogold labeling of the bacteria.
175 es in proximal dendrites using postembedding
immunogold labeling of tissues from rats withdrawn for 2
176 osition was investigated using postembedding
immunogold labeling of tropomyosin, spectrin, beta-actin
177 Furthermore, we show through
immunogold labeling of ultrathin sections that P64 is a
178 Immunogold labeling on plasma membrane sheets coupled wi
179 We performed electron microscopy (EM) with
immunogold labeling on skin biopsy specimens from 7 pati
180 munofluorescence and freeze-fracture replica
immunogold labeling revealed a large variability in gap
181 Immunogold labeling revealed abundant alphaS intimately
182 Immunogold labeling revealed differences in synaptic str
183 Immunogold labeling revealed glutamate receptors in nasc
184 Immunogold labeling revealed peri- and extrasynaptic loc
185 Subcellular analysis of
immunogold labeling revealed strongest polycystin-2 expr
186 Pre-embedding
immunogold labeling revealed that the receptors and chan
187 Freeze-fracture replica
immunogold labeling revealed the presence of the alpha1
188 Immunogold labeling showed RANK was enriched in 1 in eve
189 Native
immunogold labeling showed tetherin molecules located on
190 Immunogold labeling showed that FL1 resides in the endop
191 Electron microscopy-
immunogold labeling shows that in MSNs, plasma membrane
192 inated by vertically oriented filaments, and
ImmunoGold labeling shows that PSD-95 is a component of
193 Immunogold labeling studies demonstrate the redistributi
194 GFP localization and
immunogold labeling studies show that this biochemical s
195 ver the glomerular filtration barrier, in an
immunogold labeling study of internalization of oncolyti
196 tudy, we used electron tomography as well as
immunogold labeling to analyze the morphology and distri
197 We used postembedding
immunogold labeling to determine whether the subcellular
198 Here we use light microscopy and in vivo
immunogold labeling to directly visualize the interphase
199 e specificity of glycoprotein recruitment by
immunogold labeling viral glycoproteins and imaging thei
200 M2R
immunogold labeling was predominately seen in somatodend
201 The alpha4
immunogold labeling was present more commonly within the
202 Postsynaptic GluK2/3
Immunogold labeling was substantially reduced in Neto-nu
203 microscopy of purified NiV particles showed
immunogold labeling with anti-factor I antibodies.
204 Immunogold labeling with antibody against HCV envelope p
205 c membrane and in the heterocyst neck, using
immunogold labeling with antibody raised to the N-termin
206 Immunogold labeling with two sizes of gold beads reveale
207 opy, and grid-mapped freeze-fracture replica
immunogold labeling, 10 close appositions revealing axoa
208 Here, immunofluorescence,
immunogold labeling, and cell fractionation demonstrated
209 , correlative light and electron microscopy,
immunogold labeling, and thioflavin-S binding establishe
210 Using replica
immunogold labeling, here we show that all CA1 PC somati
211 EM replica
immunogold labeling, however, demonstrated only 1.15 tim
212 For electron microscopic analysis using
immunogold labeling, MV were divided into five zones fro
213 lica electron microscopy in combination with
immunogold labeling, we demonstrate that individual acti
214 scence and electron microscopy combined with
immunogold labeling, we examined the surfaces of transfe
215 Using electron microscopy imaging with
immunogold labeling, we found in mouse plasma that cBIN1
216 expressed a lower density of synaptic GluA2
immunogold labeling, which correlated with lower recogni
217 dult mouse hippocampus using high-resolution
immunogold labeling, with a particular emphasis on synap
218 enin in dense core granules was confirmed by
immunogold labeling.
219 mutant together with rhizobia, and by using
immunogold labeling.
220 s) in single membranes by negative stain and
immunogold labeling.
221 l microscopy, subcellular fractionation, and
immunogold labeling.
222 llow fluorescent protein) were identified by
immunogold labeling.
223 L17 and UL25 on B capsids was examined using
immunogold labeling.
224 ization within the podocyte was confirmed by
immunogold labeling.
225 tomography and a compositional analysis via
immunogold labeling.
226 oscopic observations of immunoperoxidase and
immunogold labeling.
227 ring the movement of Oxtr-EGFP as well as by
immunogold labeling.
228 otin-peroxidase and GABA with post-embedding
immunogold labeling.
229 aptic vesicle protein synapsin and glutamate
immunogold labeling.
230 Immunogold-
labeling electron microscopy showed that LPF
231 of curli was confirmed by Congo red binding,
immunogold-
labeling electron microscopy, immunoblotting,
232 -scanning electron microscopy with Annexin V
immunogold-
labeling revealed a complex organization of t
233 Finally,
immunogold labelling confirmed that inter-MT bridges in
234 were examined by atomic force microscopy and
immunogold labelling electron microscopy.
235 us and annexin A2-GFP transfected cells, and
immunogold labelling.
236 ce localization of the LDLR-Y807C using LDLR-
immunogold,
LDL-gold and beta-VLDL-gold probes revealed
237 patch-clamp recordings, electron microscopic
immunogold localization of AMPARs, partial three-dimensi
238 Postembedding
immunogold localization of GABA combined with peroxidase
239 oroplast import and fractionation assays and
immunogold localization of SCY2-green fluorescent protei
240 Immunogold localization, dual-axis electron tomography,
241 ulus (SC) and identified using postembedding
immunogold methods.
242 y both z-stack confocal and pre-embedding EM
immunogold microscopy, with stereociliary tip-link and s
243 uman strains, as shown by flow-cytometry and
immunogold microscopy.
244 ocampal pyramidal cells and EM postembedding
immunogold of the intact hippocampus we show that, in ad
245 erium leprae-specific antibodies: the visual
immunogold OnSite Leprosy Ab Rapid test [Gold-LFA] and t
246 ld-labeled SmNPP-5 within the tegument; some
immunogold particles are scattered throughout the tissue
247 The spatial localization of
immunogold particles associated with each NMDAR subunit
248 ion produced a significant increase in GluR1
immunogold particles at the plasma membrane and postsyna
249 Immunogold particles for AMPARs were distributed over th
250 e distribution of pairwise distances between
immunogold particles in immunoelectron micrographs.
251 gnificantly lower density of cytoplasmic D2R-
immunogold particles in medium parvalbumin-labeled dendr
252 nsmission immunoelectron microscopy, showing
immunogold particles in OVS, and fusion stalks on sperm
253 Kv1.3
immunogold particles in the terminals were arrayed along
254 ood pressure and an increased density of NR1
immunogold particles located in the cytoplasm of nNOS-co
255 ImmunoGold particles representing all subunits were conc
256 Plasmalemmal
immunogold particles representing alpha(1)1.2-IR were mo
257 Electron tomography revealed that
immunogold particles specific to pU(L)31 protein bind to
258 ant was heterogeneous among BETCs, and INCW2
immunogold particles were approximately four times more
259 mber of insulin granules and insulin-labeled
immunogold particles were counted.
260 INCW2-specific
immunogold particles were detected in WIGs, the endoplas
261 trans-Golgi network in the Mn1 BETCs, while
immunogold particles were extremely rare in the mutant B
262 In somata, M2R
immunogold particles were often associated with Golgi la
263 In cortex, approximately 73% of
immunogold particles were present in close proximity to
264 Immunogold PREM revealed that the coat contains a networ
265 d (GABA) or glycine by using a postembedding
immunogold procedure.
266 FZP withdrawal was examined by postembedding
immunogold quantitative electron microscopy.
267 The
immunogold receptor labeling also identified differences
268 To ensure that our
immunogold results were not a consequence of coexpressio
269 ysis of material processed for postembedding
immunogold revealed AIDA-1 label within postsynaptic den
270 electron microscopy, NR1-silver-intensified
immunogold (
SIG) was mainly in ERbeta-EGFP dendrites.
271 ions between GPR177 and MOR using a combined
immunogold-
silver and peroxidase detection approach in c
272 bined immunoperoxidase labeling for Orx with
immunogold-
silver labeling for GABA or for tyrosine hydr
273 fused and tissue sections were processed for
immunogold-
silver localization of DOR.
274 We utilized immunoperoxidase and
immunogold-
silver staining to examine the morphological
275 labeled by tract-tracing in combination with
immunogold-
silver to identify different calcium-binding
276 d by electron microscopy of thin sections of
immunogold-
stained cells.
277 Immunogold staining and electron microscopy demonstrate
278 f IVa2 in the virion has been analyzed using
immunogold staining and electron microscopy, and the cop
279 In addition,
Immunogold staining and secretion studies demonstrate th
280 synapse in vivo, we performed postembedding
immunogold staining for CaMKII in quick-fixed tissue, an
281 Immunogold staining indicates that TpMnSOD is localized
282 Annexin V-
immunogold staining revealed that the calcium-binding li
283 icroscopic analysis in conjunction with GABA-
immunogold staining showed that (1) GAD-positive termina
284 tion of viral components, yet our dual-label
immunogold staining studies failed to reveal a spatial a
285 st Kv4.2 and Kv4.3, in combination with GABA
immunogold staining, to determine the cellular, subcellu
286 ns in planar sheets of plasma membrane using
immunogold staining.
287 Fluorescent protein tagging and
immunogold studies revealed that the localization patter
288 Immunogold studies showed that both Munc18-2 and STX3 ar
289 VEGFR1 and VEGFR2 cellular localization with
Immunogold techniques.
290 We confirmed this interpretation with
immunogold TEM, where expression at postsynaptic membran
291 ents (Fab) conjugated to gold nanoparticles (
immunogold)
to map the available epitopes on a transferr
292 Immunogold transmission electron microscopy of membrane
293 ted fluorescently labelled SipB and parallel
immunogold transmission electron microscopy revealed tha
294 determined by biochemical fractionation and
immunogold transmission electron microscopy.
295 th the plasma membrane was also confirmed by
immunogold transmission electron microscopy.
296 Applying
immunogold transmission EM, and force-volume atomic forc
297 nzidine and orexinergic neurons labeled with
immunogold was confirmed by electron microscopy.
298 In axonal profiles M2R
immunogold was localized to plasmalemmal and cytoplasmic
299 on of CaMKIIalpha (assessed by pre-embedding
immunogold)
was significantly higher in dendritic shafts
300 ansmission electron microscopy revealed FLAG
immunogold within mitochondria.