ライフサイエンスコーパス: immunogold labeling

1 enin in dense core granules was confirmed by immunogold labeling.

2 otin-peroxidase and GABA with post-embedding immunogold labeling.

3 oscopic observations of immunoperoxidase and immunogold labeling.

4 tural techniques together with postembedding immunogold labeling.

5 by immunoblotting, immunocytochemistry, and immunogold labeling.

6 tomography and a compositional analysis via immunogold labeling.

7 was studied by biochemical fractionation and immunogold labeling.

8 with dendrites, some of which contained MOR immunogold labeling.

9 sing confocal microscopy and ultrastructural immunogold labeling.

10 these fractions and was detected on CCVs by immunogold labeling.

11 orescent microscopy and electron microscopic immunogold labeling.

12 luorescence and by electron microscopy using immunogold labeling.

13 ring the movement of Oxtr-EGFP as well as by immunogold labeling.

14 aptic vesicle protein synapsin and glutamate immunogold labeling.

15 mutant together with rhizobia, and by using immunogold labeling.

16 s) in single membranes by negative stain and immunogold labeling.

17 l microscopy, subcellular fractionation, and immunogold labeling.

18 llow fluorescent protein) were identified by immunogold labeling.

19 L17 and UL25 on B capsids was examined using immunogold labeling.

20 ization within the podocyte was confirmed by immunogold labeling.

21 opy, and grid-mapped freeze-fracture replica immunogold labeling, 10 close appositions revealing axoa

22 Using Western analysis and immunogold labeling, A-RAF was selectively localized in

23 Immunoblot and electron microscopic immunogold labeling analyses confirmed the absence of th

24 based on biochemical and electron microscopy immunogold labeling analyses, AtPEP12 is likely to be lo

25 g of the complexes by immunofluorescence and immunogold labeling and by their distribution on Percoll

26 Immunogold labeling and electron microscopy analysis dem

27 was more dramatic than that of CD4INTRA; 6) immunogold labeling and electron microscopy demonstrated

28 Immunogold labeling and electron microscopy of the adipo

29 Postembedding immunogold labeling and electron microscopy provide evid

30 Immunogold labeling and electron microscopy shows there

31 embedding immunoperoxidase and postembedding immunogold labeling and electron microscopy to determine

32 Immunogold labeling and electron microscopy were used to

33 Using immunogold labeling and electron microscopy, L2 was dete

34 Immunogold labeling and EM demonstrated that the HA and

35 ytoplasmic face of these native membranes by immunogold labeling and high-resolution TEM analysis.

36 Immunogold labeling and histochemical procedures offer w

37 also reacted with P. gingivalis fimbriae in immunogold labeling and immunoblot analysis, thereby ind

38 Immunogold labeling and immunoblots show a significant d

39 By using immunogold labeling and immunohistochemical assays, here

40 Toward that end, we also demonstrated by immunogold labeling and mass spectrometry that PilA is i

41 By immunogold labeling and negative staining we have detect

42 was visualized by electron microscopy using immunogold labeling and probed by fluorescence resonance

43 -mortem tissue using electron microscopy and immunogold labeling and revealed dityrosine crosslinks i

44 Immunogold labeling and surface protein isolation identi

45 associated tyrosine kinases, Lyn and Syk, by immunogold labeling and transmission electron microscopi

46 chemical observations were corroborated with immunogold labeling and transmission electron microscopy

47 y immunoperoxidase staining and confirmed by immunogold labeling and was found to be in the cytosol a

48 nscription-PCR, immunoblotting, double-sided immunogold labeling, and attachment inhibition assays de

49 Here, immunofluorescence, immunogold labeling, and cell fractionation demonstrated

50 mutations using immunofluorescence staining, immunogold labeling, and PrP-green fluorescent protein c

51 , correlative light and electron microscopy, immunogold labeling, and thioflavin-S binding establishe

52 me c was found by immunoperoxidase staining, immunogold labeling, and Western blot.

53 Using immunogold labeling assays, we found PfN44 in both the n

54 Triple immunogold labeling at the electron-microscopic level re

55 Immunogold labeling combined with transmission electron

56 Ultrastructural analysis by immunogold labeling confirmed colocalization and further

57 Ultrastructural immunohistochemistry with immunogold labeling confirmed that the MCT1 immunoreacti

58 tions along individual membrane tubules, and immunogold labeling confirmed the association of DLP1 wi

59 detection of collagen XII and tenascin-X by immunogold labeling confirmed this finding.

60 n based on immunoblot (Western) analysis and immunogold labeling correlated positively with nitrogena

61 Western blot, immunohistochemistry, and immunogold labeling coupled to scanning and transmission

62 sed on green fluorescent protein fusions and immunogold labeling data, the proteins are associated wi

63 s, the expression density of alpha 1 subunit immunogold labeling decreased by 37%, whereas that of al

64 not seen in a sla2/end4-1 mutant, and double-immunogold labeling demonstrated colocalization of Rsp5p

65 Electron microscopy with immunogold labeling demonstrated labeled axon terminals

66 Immunogold labeling demonstrated localization of E1 prot

67 Double immunogold labeling demonstrated that a sizeable proport

68 Immunogold labeling demonstrated that ABA is associated

69 Immunogold labeling demonstrated that, although the dens

70 Immunogold labeling demonstrates that the central region

71 In contrast, the immunogold labeling density of the alpha 1, alpha 5, gam

72 Immunofluorescence and immunogold labeling detected PHB2 at mitochondrial membr

73 Immunogold-labeling electron microscopy showed that LPF

74 Immunogold-labeling electron microscopy was used to anal

75 of curli was confirmed by Congo red binding, immunogold-labeling electron microscopy, immunoblotting,

76 protein cytoplasmic domain were analyzed by immunogold-labeling electron microscopy.

77 Using immunogold labeling/electron microscopy, cell fractionat

78 of ultrastructural morphometry together with immunogold labeling enables the identification and quant

79 Immunofluorescence and immunogold labeling experiments also revealed that the n

80 abeling in the presence of 0.3 M MgCl(2) and immunogold labeling for collagen types II and IX were an

81 We examined immunogold labeling for DAT and immunoperoxidase localiz

82 In the SN, immunogold labeling for DAT was localized to cytoplasmic

83 Immunogold labeling for GABA confirmed that the transpla

84 During the entire process of dispersal, immunogold labeling for GalNAc-T2-VSV and GalT showed th

85 Immunogold labeling for GLAST was greater overall in the

86 While Immunogold labeling for GluN2A at MF-CA3 synapses was co

87 Immunogold labeling for GluR4 was confined to synaptic s

88 Electron microscopy and immunogold labeling for glutamate terminals within the s

89 vagal afferent axon terminals, 33% contained immunogold labeling for MOR within the axon terminal.

90 Electron microscopy showed that immunogold labeling for NBAT was distributed along plasm

91 asymmetric synapses on dendrites containing immunogold labeling for NMDAR1, but NMDAR1 was more ofte

92 Immunogold labeling for PROT was detected in close conta

93 examined at the electron microscopic level, immunogold labeling for PRV was localized to neuronal so

94 <48 hr, extensive dendritic distribution of immunogold labeling for PRV was observed in cortico-accu

95 globular aggregates that displayed positive immunogold labeling for tau-P, as well as conformational

96 e GluN2A subunit antibody and the density of immunogold labeling for this subunit was unchanged.

97 In dopaminergic perikarya, immunogold labeling for VMAT2 was localized to the Golgi

98 Immunogold-labeling for MOR1 was found in all RVL bulbos

99 (for CAM II kinase-alpha) and postembedding immunogold labeling [for glutamate or gamma-aminobutyric

100 s question directly, freeze-fracture replica immunogold labeling (FRIL) and immunofluorescence (IF) w

101 focal microscopy and freeze-fracture replica immunogold labeling (FRIL), we demonstrate that gap junc

102 lized along the length of the flagella while immunogold labeling further localizes the PF16 protein t

103 and NHP2L1 colocalize to the nucleolus, and immunogold labeling further resolved the location of NHP

104 By immunofluorescence and immunogold labeling, G beta subunits were detected on PM

105 with intracellular membranes, not the PM; by immunogold labeling GAIP was found on clathrin-coated bu

106 Using replica immunogold labeling, here we show that all CA1 PC somati

107 EM replica immunogold labeling, however, demonstrated only 1.15 tim

108 We found that in vivo immunogold labeling improves epitope accessibility, ultr

109 cytometry and by both immunofluorescent and immunogold labeling in a subpopulation of IFN-gamma + LP

110 tibody specific for toxic oligomers and cryo-immunogold labeling in human IAPP transgenic mice, human

111 n, immunohistochemistry, and ultrastructural immunogold labeling in human white adipose tissue and in

112 Preembedding immunogold labeling in STN dendrites revealed that 60-70

113 rsely, mGluR1a displayed the same pattern of immunogold labeling in the two species.

114 Electron microscopy immunogold labeling indicated that recombinant eNOS prot

115 Subcellular immunogold labeling indicates that the biotin carboxyl-c

116 Immunogold labeling indicates that WIP1 is associated wi

117 We show that in both the shell and core, DAT immunogold labeling is present in tyrosine hydroxylase-i

118 Here, immunogold labeling is used to map the plasma membrane d

119 By immunogold labeling it was detected on clathrin-coated p

120 Immunogold labeling localized Vfl1p inside the lumen of

121 Immunogold labeling localizes it specifically to trans-G

122 Immunogold labeling located PratA and pD1 to these disti

123 utamate receptor subunit 1 (GluR1) and GluR4 immunogold labeling measurements, at both the soma and m

124 ion of DOR was examined using a preembedding immunogold-labeling method and ultrastructural analysis

125 For electron microscopic analysis using immunogold labeling, MV were divided into five zones fro

126 Second, at the ultrastructure level, immunogold labeling of 'unroofed' cells showed that Hip1

127 unocytochemistry and freeze-fracture replica immunogold labeling of adult rat CNS, we investigated wh

128 Immunogold labeling of bovine retina revealed that the e

129 te this, we combined freeze-fracture replica immunogold labeling of Cav2.1 channels, local [Ca(2+)] i

130 Immunogold labeling of chronically rejected visceral epi

131 from the African clawed toad Xenopus laevis, immunogold labeling of component proteins and subsequent

132 Immunogold labeling of CXCL10-treated spores demonstrate

133 erminals in the striatum contained extensive immunogold labeling of cytoplasmic surfaces of plasma me

134 maging analysis of DAT was combined with the immunogold labeling of DAT and quantitative electron mic

135 Moreover, immunogold labeling of DMSO reductase subunits reveals t

136 ral immunoperoxidase localization of KOR and immunogold labeling of Dyn to determine the major cellul

137 s of OBAP1 to yellow fluorescent protein and immunogold labeling of embryo transmission electron micr

138 Immunogold labeling of endogenous Toc75 POTRA domains in

139 Immunogold labeling of fibulin-2 on microfibrils in skin

140 Immunogold labeling of geranyl diphosphate synthase occu

141 in sections were collected on slot grids for immunogold labeling of GnRH immunoreactivity.

142 Cryo-immunogold labeling of gp91(phox) and CeCl(3) cytochemis

143 Using immunogold labeling of isolated nuclear envelopes, we fo

144 Immunogold labeling of L-selectin, which is normally clu

145 Previous immunogold labeling of membrane sheets showed that resti

146 Double immunogold labeling of mouse cardiac muscle reveals that

147 of granular translocation, and that surface immunogold labeling of myeloperoxidase occurs only in th

148 face of the outer membrane was confirmed by immunogold labeling of non-permeabilized mitochondria.

149 Immunogold labeling of OGFr was detected on the outer nu

150 By double-immunogold labeling of PML and LYSP100, some LANDs were

151 preautonomic PVN neurons were identified by immunogold labeling of pseudorabies virus (PRV) transpor

152 Immunogold labeling of receptors containing alpha7 subun

153 Here, we use immunogold labeling of SCs in Drosophila ovaries to loca

154 cyte square arrays contain AQP4, we employed immunogold labeling of SDS-washed freeze-fracture replic

155 Immunogold labeling of the auxiliary replication protein

156 y, and transmission electron microscopy with immunogold labeling of the bacteria.

157 In addition, postembedding immunogold labeling of the glycine receptor alpha1 subun

158 Consistent with its role in yolk uptake, immunogold labeling of the receptor reveals Yl in endocy

159 es in proximal dendrites using postembedding immunogold labeling of tissues from rats withdrawn for 2

160 osition was investigated using postembedding immunogold labeling of tropomyosin, spectrin, beta-actin

161 Furthermore, we show through immunogold labeling of ultrathin sections that P64 is a

162 Immunogold labeling of wild-type axonemes indicates that

163 owever, a marked increase in ultrastructural immunogold-labeling of L-selectin was observed in respon

164 Immunogold labeling on plasma membrane sheets coupled wi

165 We performed electron microscopy (EM) with immunogold labeling on skin biopsy specimens from 7 pati

166 We used an in situ immunogold labeling procedure to visualize the extrusion

167 An improved immunogold labeling procedure was used to examine the su

168 stributed in the vesicles, as revealed by an immunogold labeling procedure.

169 n be localized in the X-ray microscope using immunogold labeling protocols, tomography enables 3-D mo

170 ultivesicular bodies of perikarya containing immunogold labeling representing NT-LI.

171 munofluorescence and freeze-fracture replica immunogold labeling revealed a large variability in gap

172 Immunogold labeling revealed abundant alphaS intimately

173 Immunogold labeling revealed differences in synaptic str

174 Immunogold labeling revealed glutamate receptors in nasc

175 Immunogold labeling revealed peri- and extrasynaptic loc

176 Subcellular analysis of immunogold labeling revealed strongest polycystin-2 expr

177 on microscopic level, pre- and postembedding immunogold labeling revealed that 70-76% of connexin-36-

178 Electron microscopic studies using immunogold labeling revealed that gamma-tubulin is mainl

179 Immunogold labeling revealed that the induced G4L protei

180 Pre-embedding immunogold labeling revealed that the receptors and chan

181 Freeze-fracture replica immunogold labeling revealed the presence of the alpha1

182 -scanning electron microscopy with Annexin V immunogold-labeling revealed a complex organization of t

183 dimensional structure of isolated PSDs using immunogold labeling, rotary shadowing, and electron micr

184 py on plasmid and genomic DNAs, and shown by immunogold labeling, SDS/PAGE, and immunoblotting to con

185 Cell fractionation and immunogold labeling show that in quiescent fibroblasts b

186 Immunogold labeling showed RANK was enriched in 1 in eve

187 Native immunogold labeling showed tetherin molecules located on

188 Dual immunoperoxidase and immunogold labeling showed that 35% of DOR-labeled axons

189 Immunogold labeling showed that CCRC-M1 labeling within

190 Immunogold labeling showed that FL1 resides in the endop

191 Quantification of glutamate immunogold labeling showed that the UBC axon terminals h

192 Electron microscopy-immunogold labeling shows that in MSNs, plasma membrane

193 inated by vertically oriented filaments, and ImmunoGold labeling shows that PSD-95 is a component of

194 Here, we use serial multiplex immunogold labeling (siGOLD) and serial-section transmis

195 Immunogold labeling studies demonstrate the redistributi

196 Electron microscopy (EM) immunogold labeling studies indicated that intersectin a

197 Immunogold labeling studies reveal that BAMT is a cytoso

198 GFP localization and immunogold labeling studies show that this biochemical s

199 ver the glomerular filtration barrier, in an immunogold labeling study of internalization of oncolyti

200 s, the putative axon, had a greater level of immunogold labeling than that of the shorter processes,

201 ermore, we also show evidence by FRIL double-immunogold labeling that the NR1 subunit of the NMDA glu

202 Using immunogold labeling, the chimeric proteins were polarize

203 On the basis of immunogold labeling, the protein is in the outer spore c

204 tudy, we used electron tomography as well as immunogold labeling to analyze the morphology and distri

205 We used postembedding immunogold labeling to determine whether the subcellular

206 Here we use light microscopy and in vivo immunogold labeling to directly visualize the interphase

207 In the present study, we used immunogold labeling to elucidate the subsynaptic localiz

208 rons (i.e., from V1 to LM) and postembedding immunogold labeling to identify GABAergic interneurons.

209 which sperm enter the egg, was confirmed by immunogold labeling under electron microscopy.

210 Immunogold labeling using AufA antiserum revealed the pr

211 Immunogold labeling verified the expression of E-selecti

212 e specificity of glycoprotein recruitment by immunogold labeling viral glycoproteins and imaging thei

213 not, however, exclusively found at the PSD; immunogold labeling was also associated with filaments a

214 Interestingly, strong caveolin-1 immunogold labeling was observed in podocytes, where som

215 M2R immunogold labeling was predominately seen in somatodend

216 The alpha4 immunogold labeling was present more commonly within the

217 No immunogold labeling was seen in normal enamel.

218 Axonal SERT immunogold labeling was seen mainly at nonsynaptic sites

219 Postsynaptic GluK2/3 Immunogold labeling was substantially reduced in Neto-nu

220 tion of retrograde tracing and postembedding immunogold labeling was used to quantify intracellular r

221 By immunogold labeling, we demonstrate that "millipede-like

222 lica electron microscopy in combination with immunogold labeling, we demonstrate that individual acti

223 ce and transmission electron microscopy with immunogold labeling, we demonstrate that undegraded CFTR

224 scence and electron microscopy combined with immunogold labeling, we examined the surfaces of transfe

225 Using electron microscopy imaging with immunogold labeling, we found in mouse plasma that cBIN1

226 Using immunogold labeling, we found that Xgrip210 is localized

227 Using immunofluorescence and postembedding immunogold labeling, we investigated the distributions o

228 Electron microscopy and immunogold labeling were performed for osteopontin.

229 expressed a lower density of synaptic GluA2 immunogold labeling, which correlated with lower recogni

230 e-impermeable biotinylation reagent, and its immunogold labeling with an antibody to a peptide compri

231 Immunogold labeling with anti-amelogenin antibodies loca

232 ession of an active enzyme that was shown by immunogold labeling with anti-CPB antibodies to be targe

233 microscopy of purified NiV particles showed immunogold labeling with anti-factor I antibodies.

234 ype eyes, except Descemet's membrane, showed immunogold labeling with antibodies against collagen XVI

235 Immunogold labeling with antibody against HCV envelope p

236 c membrane and in the heterocyst neck, using immunogold labeling with antibody raised to the N-termin

237 Immunogold labeling with domain-specific anti-Zip1 antib

238 Immunogold labeling with GR-specific antibodies showed t

239 Immunofluorescent-antibody staining and immunogold labeling with these MAbs showed that these an

240 Immunogold labeling with two sizes of gold beads reveale

241 dult mouse hippocampus using high-resolution immunogold labeling, with a particular emphasis on synap

242 Immunogold labeling, with the use of the monoclonal MAb5