ライフサイエンスコーパス: Western blot analyses

1 location, as shown by immunocytochemical and Western blot analyses.

2 ns were extracted for gelatin zymography and Western blot analyses.

3 the mTOR signaling networks was evaluated by Western blot analyses.

4 RC mRNA and protein expression determined by Western blot analyses.

5 SA), real-time PCR, immunoprecipitation, and Western blot analyses.

6 determined by subcellular fractionation and Western blot analyses.

7 COX-2 was confirmed by real-time RT-PCR and Western blot analyses.

8 c70) was measured by immunoprecipitation and Western blot analyses.

9 uring TAP, as shown by mass spectrometry and Western blot analyses.

10 ent assay, and a decrease of IkappaBalpha in Western blot analyses.

11 gy, real-time polymerase chain reaction, and Western blot analyses.

12 ted conditions for protein determination and Western blot analyses.

13 cells, as assessed by immunocytochemical and Western blot analyses.

14 n was confirmed by quantitative dot blot and Western blot analyses.

15 inity columns and by immunohistochemical and Western blot analyses.

16 gree of correlation with those obtained from Western blot analyses.

17 ls, which was confirmed by real-time PCR and Western blot analyses.

18 as assessed by immunofluorescence assays and Western blot analyses.

19 tyrosine nitration in the enzyme as shown by Western blot analyses.

20 rtrophic cells detected by real-time PCR and Western blot analyses.

21 d postmortem brain samples were subjected to Western blot analyses.

22 sed by enzyme-linked immunosorbent assay and Western blot analyses.

23 n the presence of the ribozyme, as judged by Western blot analyses.

24 levels of Hsc70-specific client proteins on Western blot analyses.

25 peptide of SARS-CoV S or the epitope tag in Western blot analyses.

26 keletal protein levels were determined using Western blot analyses.

27 diabetic rats was confirmed by Northern and Western blot analyses.

28 entified in normal retina and optic nerve by Western blot analyses.

29 -3 low invasive cells through cDNA array and Western blot analyses.

30 A, and tPA concentrations were determined by western blot analyses.

31 etermined by both receptor cross-linking and Western blot analyses.

32 tive real-time polymerase chain reaction and Western blot analyses.

33 LUT1 expression was measured by Northern and western blot analyses.

34 uent real-time polymerase chain reaction and Western blot analyses.

35 submandibular glands (mSMG), using qPCR and Western blot analyses.

36 hours after portal reperfusion, followed by Western blot analyses.

37 were examined by co-immunoprecipitation and Western blot analyses.

38 lectroretinographic (ERG), morphometric, and Western blot analyses.

39 owed by sacrifice and immunohistochemical or western blot analyses.

40 zed immunocytochemically and correlated with Western blot analyses.

41 zyme-linked immunosorbent assay, RT-PCR, and Western blot analyses.

42 analysis and confirmed by real-time PCR and Western blot analyses.

43 nts after stroke for immunohistochemical and Western blot analyses.

44 els, whereas protein levels were assessed by Western blot analyses.

45 tive real-time reverse transcription-PCR and Western blot analyses.

46 erified by quantitative PCR and Northern and Western blot analyses.

47 ollagen were assessed by Griess reaction and Western blotting analyses.

48 eratinocytes and in whole skin, by Q-PCR and Western blotting analyses.

49 lfate-polyacrylamide gel electrophoresis and Western blotting analyses.

50 ion as determined by immunohistochemical and Western blotting analyses.

51 s of big-IGF-II as demonstrated by ELISA and Western blotting analyses.

52 With Western blot analyses, 28 LQT2-Kv11.1 channels had a tra

53 Western blot analyses also showed decreased AKT and extr

54 Finally, analyses with Western blot analyses and antibodies against three surfa

55 activated on cardiomyocytes identified using Western blot analyses and chemical inhibitors.

56 st potent analogues was further evaluated by Western blot analyses and degradation of Hsp90-dependent

57 Western blot analyses and immunoaffinity studies confirm

58 Western blot analyses and immunocytochemistry studies we

59 Western blot analyses and immunofluorescence microscopy

60 essment, saliva flow rate, quantitative PCR, Western blot analyses and immunofluorescence.

61 Proteomic approaches including Western blot analyses and tandem mass spectrometry were

62 of 11E10 to recognize those hybrid toxins by Western blot analyses and to neutralize them in Vero cel

63 We used western blot analyses and trace-fear conditioning to det

64 identified proteins was further confirmed by Western blot analyses and/or immunohistochemical analysi

65 to interact with TLR4 by immunoprecipitation/Western blot analyses, and Ebola virus GP on VLPs was ab

66 Fos, c-Myc, and Bcl-2 using microarray, PCR, western blotting analyses, and a stromal cell culture sy

67 as confirmed by multiple tissue Northern and Western Blot analyses as well as quantitative reverse-tr

68 Using Northern and Western blot analyses, both mRNA and protein of EFA6A we

69 mRNA and protein isolated, and Northern and Western blot analyses conducted to detect changes in exp

70 Western blot analyses confirmed reduced cathepsin B/D co

71 Western blot analyses confirmed that 0.5 microg/ml doxyc

72 Western blot analyses confirmed that cMyBP-C was absent

73 Western blot analyses confirmed that LEF-12 was not synt

74 Western blot analyses confirmed that mitotic histones, e

75 Immunoprecipitation and Western blot analyses confirmed that the chimeric protei

76 Western blot analyses confirmed that threonine and serin

77 Western blot analyses confirmed the absence of Nox2 and

78 Western blot analyses confirmed the abundance of the nuc

79 Western blot analyses confirmed the formation of 4-HNE-d

80 Western blot analyses confirmed the involvement of Sirt2

81 DNA yielded lysoplasmalogenase activity, and Western blot analyses confirmed the synthesis of TMEM86b

82 Northern and Western blot analyses confirmed the upregulation of alph

83 Reverse transcription-PCR and Western blotting analyses confirmed the expression of An

84 Quantitative Western blot analyses demonstrate that the total level o

85 Both reverse transcriptase-PCR and Western blot analyses demonstrated endogenous expression

86 Western blot analyses demonstrated expression of a 250-k

87 Our beta2-toxin (CPB2) Western blot analyses demonstrated that all of the teste

88 globular C1q domain, immunoprecipitation and Western blot analyses demonstrated that EMILIN-3 forms d

89 itu binding assays, immunoprecipitation, and Western blot analyses demonstrated that mGPBP is a nucle

90 tase-polymerase chain reaction (RT-PCR), and Western blot analyses demonstrated that MMP-1 enhances m

91 RT-PCR and Western blot analyses demonstrated that Nrg-1 and its re

92 In addition, RT-PCR and Western blot analyses demonstrated the up-regulation of

93 Immunoprecipitation and Western blot analyses detected reduced levels of tyrosyl

94 In addition, Western blot analyses failed to detect differences in th

95 y quantitative reverse transcription-PCR and Western blot analyses for mRNA and protein expression of

96 ls were subjected to cell-cycle analysis and Western blot analyses for Notch-1 and p21(WAF1).

97 (CNV) by aCGH, exome sequencing, as well as western blot analyses for total and activated (pT68-Chk2

98 itoring, in vivo electrophysiologic studies, Western blot analyses for total and phosphorylated c-Src

99 AC activity and Western blot analyses further demonstrated high expressi

100 Western blot analyses further suggests that MSCs suppres

101 Transient transfection assays and Western blotting analyses further display that EGCG inte

102 Northern and Western blot analyses have revealed MLF1IP to be present

103 ioinformatic, luciferase reporter assay, and Western blot analyses identified RhoA as a target of miR

104 o-dimensional gel and mass spectrometry) and Western blot analyses identified significant changes in

105 Proteomic, enzymatic, and Western blot analyses identified the approximately 50-kD

106 Western blot analyses identified unique Rgp- and Kgp-imm

107 Mass spectrometric and Western blot analyses identify the tip-link antigen, a h

108 al fibroblasts were examined by Northern and Western blot analyses, immunocytochemistry, flow cytomet

109 ion of patch-clamp physiology, pharmacology, Western blot analyses, immunohistochemistry, and array t

110 Western blot analyses, immunohistochemistry, and immunoa

111 Microarray results were further confirmed by Western blot analyses, immunohistochemistry, fluorescent

112 concordance between immunohistochemical and Western blot analyses in a panel of 14 breast cell lines

113 ting results with flow cytometry, ELISA, and Western blot analyses in an additional 39 patients and 2

114 confirmed this finding by Northern blot and Western blot analyses in cultured vascular endothelial c

115 for 8-10 days) was analyzed by Northern and Western blot analyses in HTM, human umbilical vein endot

116 BIG1 was also identified by Western blot analyses in purified subnuclear fractions (

117 This was confirmed by western blot analyses in three of five patient biopsies

118 sion was studied by RT-PCR and Northern- and Western-blot analyses in cells stimulated with cPAF at d

119 Western blot analyses indicate that neither NHE2 nor NHE

120 Immunohistochemical and Western blot analyses indicate that they do not express

121 Quantitative RT-PCR and western blot analyses indicated that both Piezo1 and Pie

122 SDS-PAGE and Western blot analyses indicated that covalent interactio

123 Flow cytometric and Western blot analyses indicated that cytokine treatment

124 Western blot analyses indicated that mTOR (mammalian tar

125 Western blot analyses indicated that p38a, STAT1, STAT3,

126 Western blot analyses indicated that Sp1 was present in

127 Western blot analyses indicated that the regulatory alph

128 Isotope-coded protein labeling and western-blot analyses indicated that Cyclophilin18 is a

129 Western-blot analyses indicated that the CC has Rubisco

130 resis, multiple c-Fos bands were resolved by Western blot analyses, indicating post-translational mod

131 ies, H0120, agglutinated spirochetes, and in Western blot analyses, it bound to a 14-kDa protein of w

132 les were analyzed for MetMb formation and by Western blot analyses, LC-MS, LC-MS-MS, circular dichroi

133 structural studies as evidenced by SDS-PAGE, Western blot analyses, ligand binding assays, and a feas

134 ype and heterozygous animals by Northern and Western blot analyses, light and electron microscopy, an

135 transcription-polymerase chain reaction and Western blot analyses of ADAMTS-4, ADAMTS-5, and aggreca

136 cDNA microarray and Western blot analyses of adenocarcinomas for evidence of

137 We confirmed these findings with Western blot analyses of caspase-9 activation in time co

138 Furthermore, Western blot analyses of CEACAM16 under reducing and non

139 Based on Western blot analyses of cell lysates and virions, the e

140 These results, together with Western blot analyses of cell lysates, indicate that the

141 into pili in this foreign host, as shown by Western blot analyses of cell wall proteins and by immun

142 Immunofluorescence and Western blot analyses of colonic mucosa validated the sy

143 transcriptase-polymerase chain reaction, and Western blot analyses of colonic tissues from Smad3/Rag2

144 , decreases in beta-catenin were evident via Western blot analyses of cortical homogenates prepared f

145 Western blot analyses of cultures after 1 day of recover

146 Western blot analyses of epidermal extracts revealed red

147 tion induced by EGF or PDBu was monitored by Western blot analyses of four different subcellular frac

148 Furthermore, Western blot analyses of fractionated sf9 cell membranes

149 Western blot analyses of fractions from B. subtilis spor

150 sociated p.H331P variant was undetectable in Western blot analyses of HepG2 cells stably transduced w

151 Western blot analyses of HT-29 and NCI-H292 xenograft tu

152 Western blot analyses of irradiated HCT116 cells showed

153 Western blot analyses of lumbar spinal cord tissue from

154 Western blot analyses of lung homogenates confirmed appr

155 Western blot analyses of MP from NMBA11K3 demonstrated t

156 Western blot analyses of muscle extracts revealed FHL1 l

157 Confocal immunofluorescent images and Western blot analyses of nuclear and cytoplasmic fractio

158 Western blot analyses of nuclear and cytoplasmic fractio

159 Western blot analyses of p53-positive cancer cells treat

160 JNK activation was confirmed by Western blot analyses of phosphorylated JKN1/2 products.

161 Western blot analyses of platelet lysates for these two

162 Western blot analyses of proteins from cultured ocular t

163 Finally, Western blot analyses of rat liver mitochondria, using N

164 Western blot analyses of steady-state Mga levels suggest

165 azurophil granule protein of neutrophils by Western blot analyses of subcellular fractions as well a

166 Immunohistochemistry and Western blot analyses of TgHMW kidneys showed increased

167 on microscopy and by immunohistochemical and Western blot analyses of the autophagosome marker LC3-II

168 Immunohistochemistry and Western blot analyses of the brains were performed using

169 Western blot analyses of the same membrane preparations

170 Western blot analyses of these cells revealed altered ex

171 Western blot analyses of tumor tissues reveal up-regulat

172 the mRNA and protein levels by Northern and Western blot analyses of two independent hematopoietic c

173 assessed by immunohistochemical staining and Western blotting analyses of fractionated subcellullar e

174 g confocal immunofluorescence microscopy and Western blot analyses on purified phagosome extracts, we

175 and immunofluorescent stainings, as well as Western blot analyses, on cervical and lumbar sections o

176 By Western blot analyses, protein levels of alphaENaC, alph

177 Based on Western blot analyses, real-time PCR, and immunostaining

178 d proteins was verified by real-time PCR and Western blot analyses, respectively.

179 both mRNA and protein levels in qRT-PCR and Western blot analyses, respectively.

180 cDNA microarray and Western blot analyses reveal that the gap junctional int

181 Coimmunoprecipitation and Western blot analyses reveal the direct association of A

182 Western blotting analyses reveal a reduced iron-sulfur p

183 Western blotting analyses reveal that glucose-responsive

184 Western blot analyses revealed a transient increase of a

185 Western blot analyses revealed an induction of COX-2 pro

186 Western blot analyses revealed decreased renal protein a

187 Western blot analyses revealed decreases in p-phospholam

188 Reverse transcriptase-PCR and Western blot analyses revealed expression of the Mpzl3 g

189 Western blot analyses revealed Nix protein levels that w

190 -transcription polymerase chain reaction and Western blot analyses revealed quantitative increases in

191 Western blot analyses revealed specific bands that were

192 itionally, evidence from kinase activity and Western blot analyses revealed that activation of NO-PKG

193 Western blot analyses revealed that all three compounds

194 Microarray, quantitative PCR, and Western blot analyses revealed that both mRNA and protei

195 Microarray, qRT-PCR and Western blot analyses revealed that miR-31 negatively re

196 Western blot analyses revealed that OmcB was partially p

197 Western blot analyses revealed that SCF was required for

198 Northern and Western blot analyses revealed that TbPMC1 and TbPMC2 ar

199 Western blot analyses revealed that the cellular levels

200 Northern and Western blot analyses revealed that the expression of MC

201 Northern and Western blot analyses revealed that the genes/proteins e

202 Western blot analyses revealed that the processing of Ga

203 Surprisingly, Western blot analyses revealed that the specificities of

204 Western blot analyses revealed that the various caspases

205 Western blot analyses revealed that the virulence-associ

206 Northern and Western blot analyses revealed that these genes are up-r

207 Moreover, Western blot analyses revealed that whereas the 51-kDa p

208 transcription-polymerase chain reaction and Western blotting analyses, revealed that a serine protea

209 In addition, western blot analyses show obviously decreased expressio

210 of the soluble peptidoglycan precursors, and Western blot analyses show that increases in the precurs

211 Enzyme-linked immunosorbent assay and Western blot analyses show that LOX-PP inhibits FGF-2-in

212 The results of tandem mass spectrometry and Western blot analyses show that PduM is a component of t

213 Western blot analyses show that the soluble IIGlc exhibi

214 tent with the in situ hybridization pattern, Western blot analyses show that Trio levels in the hippo

215 Real-time polymerase chain reaction and Western blotting analyses show that de novo synthesis of

216 Northern blot, RT-PCR, and Western blot analyses showed Adh promoter-driven TaPCS1

217 Western blot analyses showed an increase in activities o

218 Gel shift assay and Western blot analyses showed dose-dependent increases in

219 Immunohistochemical staining and Western blot analyses showed increased EZH2 expression i

220 ft, real time reverse transcriptase-PCR, and Western blot analyses showed increased levels of c-Jun,

221 Western blot analyses showed increased phosphorylation o

222 Northern and Western blot analyses showed increases of approximately

223 tially low levels of acetone and butanol and Western blot analyses showed significantly low levels of

224 Western blot analyses showed that B728a secretes Hcp, a

225 Western blot analyses showed that both single and five c

226 Western blot analyses showed that exercise increased the

227 Results from immunofluorescence and Western blot analyses showed that inhibitory effects of

228 Proteome and Western blot analyses showed that integration of the pep

229 Non-reducing SDS-PAGE/Western blot analyses showed that macrophage apoE2 is mo

230 Northern and Western blot analyses showed that MTMR7 is expressed mai

231 se chain reaction, immunohistochemistry, and Western blot analyses showed that phenylmethimazole atte

232 Western blot analyses showed that serum antibodies to Po

233 Immunohistochemical and Western blot analyses showed that STAT3 is deleted from

234 transcription polymerase chain reaction and western blot analyses showed that TES was consistently a

235 Western blot analyses showed that the differential expre

236 Western blot analyses showed that the loss of LKB1 and p

237 Moreover, silver staining and Western blot analyses showed that the protein compositio

238 Coimmunoprecipitation and Western blotting analyses showed that VPS28, a component

239 lfate-polyacrylamide gel electrophoresis and western-blot analyses showed that the tla3 strain was de

240 r proteins in ocular tissues was examined by Western blot analyses, slot blot analyses, and immunocyt

241 By Western blot analyses, SRPK1 protein was found to be ove

242 odeling, surface plasmon resonance (SPR) and western blot analyses suggested a physical association b

243 Western blot analyses suggested that NCX isoforms were d

244 Results from Western blot analyses suggested that the above-mentioned

245 We observed by Western blot analyses that ablation of AgRP neurons resu

246 In Western blot analyses, the purified polyclonal antibody

247 amis) - were compared by electrophoretic and western blot analyses to identify biomarkers for BT.

248 tem was constructed and used in transfer and Western blot analyses to identify the differentially reg

249 based magnetic resonance imaging and ex vivo Western blot analyses to investigate putative structural

250 ent fusions to germination proteins and used Western blot analyses to measure germination protein lev

251 ated sodium channel (VGSC) currents, we used Western blot analyses to probe for these channels in con

252 everse transcription-PCR, Northern blot, and Western blot analyses, to characterize the gene expressi

253 ar Purkinje cells by immunocytochemistry and Western blot analyses using a phosphospecific PDE5 antib

254 Western blot analyses using anti-His tag monoclonal anti

255 In-gel kinase assays and Western blot analyses using fractionated extracts of LNC

256 ercaptoethanol-dependent artifact signals in western blot analyses using polyclonal antisera.

257 ption-polymerase chain reaction (RT-PCR) and Western blot analyses verified significant changes in ea

258 Western blot analyses verified that mitochondria were co

259 By Northern and Western blot analyses we demonstrate that the expression

260 th a panel of CD22 monoclonal antibodies and Western blot analyses, we could not detect surface or in

261 electrospray mass spectrometry (ESI-MS), and Western blot analyses, we examined the order of autophos

262 Using microarray, relative RT-PCR, and Western blot analyses, we have identified and confirmed

263 By using MS and Western blot analyses, we showed that Sfp1 is translated

264 , reverse transcriptase quantitative PCR and western blotting analyses, we confirm the direct regulat

265 Western blot analyses were carried out to confirm the pr

266 Western blot analyses were carried out using antibodies

267 Both Northern blot and Western blot analyses were conducted on samples isolated

268 Western blot analyses were conducted on selected protein

269 ileum, VE-cadherin, occludin, and claudin-3, Western blot analyses were conducted.

270 Western blot analyses were cross-reacted with MGP N-term

271 Western blot analyses were done using B0AT1 and SN2 spec

272 In some mice, gelatin zymography and Western blot analyses were performed on protein extracts

273 , histology, immunohistochemistry (IHC), and Western blot analyses were performed on the left ventric

274 brain barrier disruption were evaluated, and Western blot analyses were performed to determine the ef

275 Immunohistologic and Western blot analyses were performed to evaluate NIS pro

276 Immunolocalization and Western blot analyses were performed to evaluate the abu

277 Coimmunoprecipitation and Western blot analyses were performed to study interactio

278 Western blot analyses were performed with anti-SnoN and

279 Western blot analyses were used to assess signal transdu

280 RT-PCR and Northern and Western blot analyses were used to assess TauT mRNA and

281 and cell viability assays, TUNEL assays, and Western blot analyses were used to detect apoptotic and

282 RT-PCR, Northern blot, and Western blot analyses were used to detect the expression

283 Real time quantitative PCR and Western blot analyses were used to determine NCAM expres

284 Wholemount in situ hybridization and Western blot analyses were used to determine the express

285 to evaluate photoreceptor cell apoptosis and Western blot analyses were used to determine the levels

286 D and semiquantitative one dimensional (1-D) Western blot analyses were used to determine whether cha

287 ) and semiquantitative one-dimensional (1-D) Western blot analyses were used to determine whether cha

288 Immunohistochemical and Northern and Western blot analyses were used to examine the expressio

289 ochemical staining, RT-PCR, and northern and western blot analyses were used to identify putative ste

290 Northern and Western blot analyses were used to identify srds transcr

291 Immunofluorescence and Western blot analyses were used to localize and quantify

292 transcription-polymerase chain reaction and Western blot analyses were used to measure ANK expressio

293 transcription-polymerase chain reaction and Western blot analyses were used to measure CCN3 expressi

294 transcription-polymerase chain reaction and Western blot analyses were used to measure CTGF expressi

295 cretion of rfEPO protein was demonstrated by Western blot analyses, while rfEPO protein bioactivity w

296 t (KO) mice and littermates (LM) and used in Western blot analyses with Ab099 against the N terminus

297 Western blot analyses with anti-c-Myc and anti-HCV antib

298 89 kDa in rat and 105 kDa in mouse, although Western blot analyses with anti-SMGC antisera demonstrat

299 Western blot analyses with antigingipain antibodies show

300 Western blot analyses with immune IgM and IgG identified