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 plex silver enhanced 'sandwich vertical flow
immunogold assay (SVIA)' based on disposable porous filt
5 Immunogold atomic force microscopy reveals, for the firs
6 Additionally, before photocleavage,
immunogold can be employed to label proteins that intera
7 echniques including immunohistochemistry and
immunogold can further evaluate the levels of the variou
8 in and the H(+)-ATPase were quantified using
immunogold cytochemistry and morphometric analysis.
9 Ultrastructural examination using
immunogold cytochemistry confirmed that activated caspas
10 isolation of synaptic vesicles confirmed the
immunogold data and showed vesicular colocalization of V
11 ent novel electron microscopic postembedding
immunogold data from mouse and rat brains showing that s
12 Electron microscopic
immunogold data further suggest that NMDA receptors are
13 The
immunogold data suggest that most MSBs would not generat
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 calized inside the in vivo pollen tube using
immunogold electron microscopy and found to be present i
28 ns of the suprastructures were determined by
immunogold electron microscopy and immunoblotting.
29 Immunogold electron microscopy and immunofluorescence te
30 Subsequent analyses of HSV-infected cells by
immunogold electron microscopy and live-cell confocal im
31 lanted and host neurons was identified using
immunogold electron microscopy and patch-clamp recording
32 c reticulum (ER) in cholangiocytes, but both
immunogold electron microscopy and super-resolution micr
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 g, immunofluorescence, confocal imaging, and
immunogold electron microscopy demonstrated that LRRC8A
40 Immunogold electron microscopy demonstrated that platele
41 ing rat brain slice, immunofluorescence, and
immunogold electron microscopy detection of VMAT2 (vesic
42 ts (MEFs) by indirect immunofluorescence and
immunogold electron microscopy in the presence or absenc
43 In addition, the results of
immunogold electron microscopy indicated a close associa
44 Here, pre-embedding
immunogold electron microscopy is applied to dissociated
45 Immunogold electron microscopy localized Ser(P)269-AQP2
46 Immunogold electron microscopy localized the allergen in
47 Transmission and
immunogold electron microscopy of extracted extracellula
48 Immunogold electron microscopy of hippocampal tissue sec
49 Immunogold electron microscopy of rat hippocampal neuron
50 raK-FLAG3 in otherwise wild-type cells using
immunogold electron microscopy of thin sections revealed
51 Immunofluorescence and
immunogold electron microscopy reveal a spectrin-rich do
52 In the present study,
immunogold electron microscopy revealed EC-SOD in membra
53 Immunogold electron microscopy revealed redistribution o
54 Consistently,
immunogold electron microscopy revealed that LTP stimula
55 Immunogold electron microscopy revealed that pU(L)31 cou
56 Immunogold electron microscopy revealed that these prote
57 Additionally, immunohistochemistry and
immunogold electron microscopy revealed that tibial marr
58 st exclusively in RPE Immunofluorescence and
immunogold electron microscopy showed that HFE protein w
59 Moreover,
immunogold electron microscopy showed that NR1 is expres
60 Immunogold electron microscopy showed that surface recep
61 Immunogold electron microscopy showed that the Uni2 prot
62 Additionally,
immunogold electron microscopy shows a greater accumulat
63 Direct
immunogold electron microscopy specifically localized de
64 High-resolution
immunogold electron microscopy supported the cellular lo
65 Confocal and
immunogold electron microscopy supported Trpv4 overexpre
66 Here, we used postembedding
immunogold electron microscopy techniques to examine the
67 ution structured illumination microscopy and
immunogold electron microscopy to localize major compone
68 ined immunocytochemistry and high-resolution
ImmunoGold electron microscopy to study cellular and sub
69 Immunogold electron microscopy using a TBC1D24-specific
70 Immunogold electron microscopy using antibodies raised a
71 In addition,
immunogold electron microscopy using antisera against Eb
72 Immunogold electron microscopy was used to determine whe
73 tative real-time PCR and in mouse kidneys by
immunogold electron microscopy, and its agonism 1) incre
74 ly at the pilus tip, a location supported by
immunogold electron microscopy, and suggests that, as fo
75 Using
immunogold electron microscopy, non-fibrillar forms of P
76 Using
Immunogold electron microscopy, PGRP-S was localized to
77 l approaches, including live immunolabeling,
immunogold electron microscopy, surface biotinylation an
78 Confocal immunofluorescent and
immunogold electron microscopy, together with subcellula
79 ted emission depletion (STED) microscopy and
immunogold electron microscopy, we determined the distri
80 bedding immunoperoxidase and silver-enhanced
immunogold electron microscopy, we localized T-channel s
81 lasma membrane microdomains, as localized by
immunogold electron microscopy.
82 calizes with NFL on single neurofilaments by
immunogold electron microscopy.
83 th cardiac amyloid deposits was confirmed by
immunogold electron microscopy.
84 he mitochondrial matrix of hepatocytes using
immunogold electron microscopy.
85 -exponential growth, which was reinforced by
immunogold electron microscopy.
86 calized the epitope on the capsid surface by
immunogold electron microscopy.
87 tophysin, syntaxin, and synaptotagmin and by
immunogold electron microscopy.
88 n blot analyses of cell wall proteins and by
immunogold electron microscopy.
89 These results were further validated via
immunogold electron microscopy.
90 coprotein (GPC) on the cell surface by using
immunogold electron microscopy.
91 ileptic DGCs was examined with postembedding
immunogold electron microscopy.
92 mouse retina was visualized by pre-embedding
immunogold electron microscopy.
93 situ hybridization, immunofluorescence, and
immunogold electron microscopy.
94 emonstrated by subcellular fractionation and
immunogold electron microscopy.
95 measured by mass spectrometry and located by
immunogold electron microscopy.
96 noblotting, immunofluorescence analysis, and
immunogold electron microscopy.
97 alizes with NF-M on single neurofilaments by
immunogold electron microscopy.
98 al compartments by confocal fluorescence and
immunogold electron microscopy.
99 bimolecular fluorescence complementation and
immunogold electron microscopy.
100 in IMCD cells of potassium-deprived rats by
immunogold electron microscopy.
101 -membrane-localized VLPs as visualized using
immunogold electron microscopy.
102 In addition,
immunogold-
electron microscopy revealed HCN2 as the domi
103 ed against these GIPCs were further used for
immunogold-
electron microscopy strategy, revealing the d
104 By confocal microscopy and
immunogold-
electron microscopy, these filaments are loca
105 Using
immunogold EM we detected LLO at several organelles with
106 -dimensional electrophoreses, nano-LC-MS/MS,
immunogold EM, and stimulated emission depletion microsc
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 Immunogold FIB-SEM offers the potential for broad applic
111 Here,
immunogold FIB-SEM, which combines antigen labeling with
112 that depends on special equipment, requires
immunogold for colabeling, and does not take advantage o
113 aments was strikingly similar to that of the
immunogold label for gephyrin.
114 Spatial analysis of the
immunogold label shows a nonrandom distribution for all
115 nd the third layer was refined with detector
immunogold labeled mAb.
116 on the inclusion surface, both of which were
immunogold-
labeled by a GFP-tagged 2xFYVE protein that b
117 electron microscopy revealed localization of
immunogold-
labeled CXCL10 to the bacterial cell surface
118 The presence of
immunogold-
labeled electron-dense bodies was correlated
119 et of criteria derived from the structure of
immunogold-
labeled GABAergic synapses.
120 on microscopy was used to localize alphaB in
immunogold-
labeled intact and permeabilized microvesicle
121 Electron microscopy of
immunogold-
labeled microsections revealed that the HCV e
122 Our in vivo EM images of
immunogold-
labeled rat IAPP and human IAPP show both for
123 eins and transmission electron microscopy of
immunogold-
labeled samples in the case of ABCB19.
124 n microscopy illustrates a unique pattern of
immunogold-
labeled SmNPP-5 within the tegument; some imm
125 Transmission electron microscopy of
immunogold-
labeled thawed cryosections of infected cells
126 Here, we use serial multiplex
immunogold labeling (siGOLD) and serial-section transmis
127 Immunogold labeling and electron microscopy analysis dem
128 Postembedding
immunogold labeling and electron microscopy provide evid
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 -mortem tissue using electron microscopy and
immunogold labeling and revealed dityrosine crosslinks i
134 Immunogold labeling and surface protein isolation identi
135 chemical observations were corroborated with
immunogold labeling and transmission electron microscopy
136 Using
immunogold labeling assays, we found PfN44 in both the n
137 Immunogold labeling combined with transmission electron
138 Ultrastructural analysis by
immunogold labeling confirmed colocalization and further
139 detection of collagen XII and tenascin-X by
immunogold labeling confirmed this finding.
140 Western blot, immunohistochemistry, and
immunogold labeling coupled to scanning and transmission
141 Electron microscopy with
immunogold labeling demonstrated labeled axon terminals
142 Immunogold labeling demonstrated localization of E1 prot
143 Immunogold labeling demonstrated that ABA is associated
144 Immunofluorescence and
immunogold labeling detected PHB2 at mitochondrial membr
145 Immunogold labeling for GABA confirmed that the transpla
146 While
Immunogold labeling for GluN2A at MF-CA3 synapses was co
147 globular aggregates that displayed positive
immunogold labeling for tau-P, as well as conformational
148 e GluN2A subunit antibody and the density of
immunogold labeling for this subunit was unchanged.
149 We found that in vivo
immunogold labeling improves epitope accessibility, ultr
150 tibody specific for toxic oligomers and cryo-
immunogold labeling in human IAPP transgenic mice, human
151 rsely, mGluR1a displayed the same pattern of
immunogold labeling in the two species.
152 Immunogold labeling indicates that WIP1 is associated wi
153 Here,
immunogold labeling is used to map the plasma membrane d
154 Immunogold labeling located PratA and pD1 to these disti
155 te this, we combined freeze-fracture replica
immunogold labeling of Cav2.1 channels, local [Ca(2+)] i
156 from the African clawed toad Xenopus laevis,
immunogold labeling of component proteins and subsequent
157 Immunogold labeling of CXCL10-treated spores demonstrate
158 maging analysis of DAT was combined with the
immunogold labeling of DAT and quantitative electron mic
159 Moreover,
immunogold labeling of DMSO reductase subunits reveals t
160 s of OBAP1 to yellow fluorescent protein and
immunogold labeling of embryo transmission electron micr
161 Immunogold labeling of endogenous Toc75 POTRA domains in
162 in sections were collected on slot grids for
immunogold labeling of GnRH immunoreactivity.
163 Cryo-
immunogold labeling of gp91(phox) and CeCl(3) cytochemis
164 preautonomic PVN neurons were identified by
immunogold labeling of pseudorabies virus (PRV) transpor
165 Immunogold labeling of the auxiliary replication protein
166 y, and transmission electron microscopy with
immunogold labeling of the bacteria.
167 es in proximal dendrites using postembedding
immunogold labeling of tissues from rats withdrawn for 2
168 osition was investigated using postembedding
immunogold labeling of tropomyosin, spectrin, beta-actin
169 Furthermore, we show through
immunogold labeling of ultrathin sections that P64 is a
170 Immunogold labeling on plasma membrane sheets coupled wi
171 We performed electron microscopy (EM) with
immunogold labeling on skin biopsy specimens from 7 pati
172 munofluorescence and freeze-fracture replica
immunogold labeling revealed a large variability in gap
173 Immunogold labeling revealed abundant alphaS intimately
174 Immunogold labeling revealed differences in synaptic str
175 Immunogold labeling revealed glutamate receptors in nasc
176 Subcellular analysis of
immunogold labeling revealed strongest polycystin-2 expr
177 Pre-embedding
immunogold labeling revealed that the receptors and chan
178 Freeze-fracture replica
immunogold labeling revealed the presence of the alpha1
179 Immunogold labeling showed RANK was enriched in 1 in eve
180 Native
immunogold labeling showed tetherin molecules located on
181 Immunogold labeling showed that FL1 resides in the endop
182 Electron microscopy-
immunogold labeling shows that in MSNs, plasma membrane
183 inated by vertically oriented filaments, and
ImmunoGold labeling shows that PSD-95 is a component of
184 Immunogold labeling studies demonstrate the redistributi
185 GFP localization and
immunogold labeling studies show that this biochemical s
186 ver the glomerular filtration barrier, in an
immunogold labeling study of internalization of oncolyti
187 tudy, we used electron tomography as well as
immunogold labeling to analyze the morphology and distri
188 We used postembedding
immunogold labeling to determine whether the subcellular
189 Here we use light microscopy and in vivo
immunogold labeling to directly visualize the interphase
190 e specificity of glycoprotein recruitment by
immunogold labeling viral glycoproteins and imaging thei
191 M2R
immunogold labeling was predominately seen in somatodend
192 The alpha4
immunogold labeling was present more commonly within the
193 Postsynaptic GluK2/3
Immunogold labeling was substantially reduced in Neto-nu
194 Immunogold labeling with a monoclonal antibody that reco
195 microscopy of purified NiV particles showed
immunogold labeling with anti-factor I antibodies.
196 Immunogold labeling with antibody against HCV envelope p
197 c membrane and in the heterocyst neck, using
immunogold labeling with antibody raised to the N-termin
198 Immunogold labeling with two sizes of gold beads reveale
199 opy, and grid-mapped freeze-fracture replica
immunogold labeling, 10 close appositions revealing axoa
200 Here, immunofluorescence,
immunogold labeling, and cell fractionation demonstrated
201 , correlative light and electron microscopy,
immunogold labeling, and thioflavin-S binding establishe
202 Using replica
immunogold labeling, here we show that all CA1 PC somati
203 EM replica
immunogold labeling, however, demonstrated only 1.15 tim
204 lica electron microscopy in combination with
immunogold labeling, we demonstrate that individual acti
205 scence and electron microscopy combined with
immunogold labeling, we examined the surfaces of transfe
206 Using electron microscopy imaging with
immunogold labeling, we found in mouse plasma that cBIN1
207 combining electron microscopy with glutamate
immunogold labeling, we identified decreased intracellul
208 Using
immunogold labeling, we specifically examined the associ
209 expressed a lower density of synaptic GluA2
immunogold labeling, which correlated with lower recogni
210 dult mouse hippocampus using high-resolution
immunogold labeling, with a particular emphasis on synap
211 s) in single membranes by negative stain and
immunogold labeling.
212 l microscopy, subcellular fractionation, and
immunogold labeling.
213 llow fluorescent protein) were identified by
immunogold labeling.
214 L17 and UL25 on B capsids was examined using
immunogold labeling.
215 ization within the podocyte was confirmed by
immunogold labeling.
216 enin in dense core granules was confirmed by
immunogold labeling.
217 otin-peroxidase and GABA with post-embedding
immunogold labeling.
218 mutant together with rhizobia, and by using
immunogold labeling.
219 tomography and a compositional analysis via
immunogold labeling.
220 ring the movement of Oxtr-EGFP as well as by
immunogold labeling.
221 aptic vesicle protein synapsin and glutamate
immunogold labeling.
222 Immunogold-
labeling electron microscopy showed that LPF
223 of curli was confirmed by Congo red binding,
immunogold-
labeling electron microscopy, immunoblotting,
224 -scanning electron microscopy with Annexin V
immunogold-
labeling revealed a complex organization of t
225 aAN101D- relative to WTalphaA protein during
immunogold-
labeling- and western blot analyses, includin
226 mice was determined by immunohistochemical-,
immunogold-
labeling-, and western blot analyses.
227 Electron microscopic analysis of
immunogold-
labelled freeze-fracture replicas confirms th
228 acked mutants, biochemical activity studies,
immunogold labelling and in vivo biosensing.
229 Finally,
immunogold labelling confirmed that inter-MT bridges in
230 were examined by atomic force microscopy and
immunogold labelling electron microscopy.
231 Immunogold labelling for TEM confirmed that labelling wa
232 Immunogold labelling in electron micrographs revealed th
233 us and annexin A2-GFP transfected cells, and
immunogold labelling.
234 ce localization of the LDLR-Y807C using LDLR-
immunogold,
LDL-gold and beta-VLDL-gold probes revealed
235 Postembedding
immunogold localization of GABA combined with peroxidase
236 oroplast import and fractionation assays and
immunogold localization of SCY2-green fluorescent protei
237 Immunogold localization, dual-axis electron tomography,
238 ulus (SC) and identified using postembedding
immunogold methods.
239 y both z-stack confocal and pre-embedding EM
immunogold microscopy, with stereociliary tip-link and s
240 uman strains, as shown by flow-cytometry and
immunogold microscopy.
241 ocampal pyramidal cells and EM postembedding
immunogold of the intact hippocampus we show that, in ad
242 erium leprae-specific antibodies: the visual
immunogold OnSite Leprosy Ab Rapid test [Gold-LFA] and t
243 ld-labeled SmNPP-5 within the tegument; some
immunogold particles are scattered throughout the tissue
244 The spatial localization of
immunogold particles associated with each NMDAR subunit
245 ion produced a significant increase in GluR1
immunogold particles at the plasma membrane and postsyna
246 Immunogold particles for AMPARs were distributed over th
247 gnificantly lower density of cytoplasmic D2R-
immunogold particles in medium parvalbumin-labeled dendr
248 nsmission immunoelectron microscopy, showing
immunogold particles in OVS, and fusion stalks on sperm
249 Kv1.3
immunogold particles in the terminals were arrayed along
250 ood pressure and an increased density of NR1
immunogold particles located in the cytoplasm of nNOS-co
251 ImmunoGold particles representing all subunits were conc
252 Plasmalemmal
immunogold particles representing alpha(1)1.2-IR were mo
253 Electron tomography revealed that
immunogold particles specific to pU(L)31 protein bind to
254 ant was heterogeneous among BETCs, and INCW2
immunogold particles were approximately four times more
255 mber of insulin granules and insulin-labeled
immunogold particles were counted.
256 INCW2-specific
immunogold particles were detected in WIGs, the endoplas
257 trans-Golgi network in the Mn1 BETCs, while
immunogold particles were extremely rare in the mutant B
258 In somata, M2R
immunogold particles were often associated with Golgi la
259 In cortex, approximately 73% of
immunogold particles were present in close proximity to
260 tive status, but a high density of pS214-tau
immunogold particles within presynaptic cytoplasmic and
261 the majority of synapses contained pS214-tau
immunogold particles, which were predominantly localized
262 Super-resolution and
immunogold platinum replica electron microscopy revealed
263 Immunogold PREM revealed that the coat contains a networ
264 FZP withdrawal was examined by postembedding
immunogold quantitative electron microscopy.
265 The
immunogold receptor labeling also identified differences
266 ysis of material processed for postembedding
immunogold revealed AIDA-1 label within postsynaptic den
267 Using serial
immunogold scanning electron microscopy, we show that PK
268 electron microscopy, NR1-silver-intensified
immunogold (
SIG) was mainly in ERbeta-EGFP dendrites.
269 ions between GPR177 and MOR using a combined
immunogold-
silver and peroxidase detection approach in c
270 bined immunoperoxidase labeling for Orx with
immunogold-
silver labeling for GABA or for tyrosine hydr
271 fused and tissue sections were processed for
immunogold-
silver localization of DOR.
272 en-specific IgE and IgG, antibodies using an
immunogold-
silver signal amplification method.
273 We utilized immunoperoxidase and
immunogold-
silver staining to examine the morphological
274 d by electron microscopy of thin sections of
immunogold-
stained cells.
275 Immunogold staining and electron microscopy demonstrate
276 f IVa2 in the virion has been analyzed using
immunogold staining and electron microscopy, and the cop
277 In addition,
Immunogold staining and secretion studies demonstrate th
278 synapse in vivo, we performed postembedding
immunogold staining for CaMKII in quick-fixed tissue, an
279 hat contained amorphic material with reduced
immunogold staining for mature insulin.
280 Immunogold staining indicates that TpMnSOD is localized
281 Immunogold staining revealed synaptic and perisynaptic G
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 ents (Fab) conjugated to gold nanoparticles (
immunogold)
to map the available epitopes on a transferr
291 Immunogold transmission electron microscopy of membrane
292 th the plasma membrane was also confirmed by
immunogold transmission electron microscopy.
293 determined by biochemical fractionation and
immunogold transmission electron microscopy.
294 Applying
immunogold transmission EM, and force-volume atomic forc
295 Using superresolution and
immunogold transmission EM, we observed that, upon trans
296 nzidine and orexinergic neurons labeled with
immunogold was confirmed by electron microscopy.
297 In axonal profiles M2R
immunogold was localized to plasmalemmal and cytoplasmic
298 on of CaMKIIalpha (assessed by pre-embedding
immunogold)
was significantly higher in dendritic shafts
299 ansmission electron microscopy revealed FLAG
immunogold within mitochondria.
300 The density of pS214-tau
immunogold within the active zone, cytoplasmic, and plas