ライフサイエンスコーパス: Western immunoblot

1 strains of these serotypes was confirmed by Western immunoblot.

2 mma vesicle protein (PLVAP) were detected by Western immunoblot.

3 were tested by IFA assay and by recombinant Western immunoblot.

4 tography and analyzed by electrophoresis and Western immunoblot.

5 TIMP levels were evaluated by zymography and Western immunoblot.

6 rable levels of 85-kDa PLA(2) as assessed by Western immunoblot.

7 junction protein expression was measured by Western immunoblot.

8 levels in the media were then determined by Western immunoblot.

9 ng of tissue complementary DNAs (cDNAs), and Western immunoblots.

10 avage site, failed to label purified mZP3 on Western immunoblots.

11 ine time points after exposure to CTGF using Western immunoblots.

12 orm and recognized a 23-kDa sporozoite Ag in Western immunoblots.

13 collagen fibril assay, by zymography, and in Western immunoblots.

14 mals showed a diverse array of antibodies on Western immunoblots.

15 primary antibodies was further confirmed by Western immunoblots.

16 zae HifD and HifE proteins, respectively, on Western immunoblots.

17 xes were identified by mass spectrometry and western immunoblots.

18 n were assessed using immunocytochemistry or Western immunoblots.

19 TGF-beta1, and caspase-3 were determined by Western immunoblotting.

20 zyme from the cytosol to membrane as seen by Western immunoblotting.

21 tically activated forms of these caspases by Western immunoblotting.

22 GAD(65) protein levels were quantified using western immunoblotting.

23 PDH for standardizing protein samples during western immunoblotting.

24 d detection of virus in cell supernatants by Western immunoblotting.

25 resenting gag, pol, and env gene products by Western immunoblotting.

26 we analyzed histone H3 and H4 acetylation by Western immunoblotting.

27 keletal muscle, Kell protein was detected by Western immunoblotting.

28 ile specific collagenases were identified by Western immunoblotting.

29 ase-polymerase chain reactions (RT-PCR), and Western immunoblotting.

30 ed cardioprotective proteins was analyzed by Western immunoblotting.

31 anced serology consisting of two-dimensional Western-immunoblotting.

32 37 as detected by the anti-protC antibody in Western immunoblots, accumulated unenveloped capsids in

33 Myocilin expression was also analyzed by Western immunoblots after addition of dexamethasone (10(

34 e analysis, confocal immunolocalization, and Western immunoblotting after 24 and 48 hours.

35 By Western immunoblotting all defined terminal organelle pr

36 wing proteins were confirmed by conventional western immunoblotting: all-trans-retinoic acid increase

37 ific monoclonal antibodies Pp-PS-W and 3D11, Western immunoblot analyses demonstrated that the LPS an

38 Western immunoblot analyses demonstrated that this alter

39 ycosaminoglycan) and lactate quantification, Western immunoblot analyses of aggrecan degradation prod

40 Western immunoblot analyses of cerebellar extracts also

41 Western immunoblot analyses of crude cytosolic and post-

42 mitochondria to the cytosol as determined by Western immunoblot analyses of mitochondrial- and cytoso

43 Western immunoblot analyses revealed that the RscS(+) st

44 crylamide gel electrophoresis (SDS-PAGE) and western immunoblot analyses showed selective interaction

45 P-ribose) polymerase (PARP) as determined by Western immunoblot analyses using antibodies capable of

46 Western immunoblot analyses were performed on trigeminal

47 ese factors in the epidermis is confirmed by western immunoblot analyses.

48 transcription-polymerase chain reaction and western-immunoblot analyses showed that SGF14c mRNA and

49 h purified whole organisms, rP28, or rP30 by Western immunoblot analysis (100% relative diagnostic sp

50 for each of these samples was determined by Western immunoblot analysis (MarDx Marblot Test System)

51 Western immunoblot analysis also detected hBD-1 peptide

52 the affinity-purified rP44 was evaluated by Western immunoblot analysis and dot blot immunoassay.

53 on of both FHL2 and IGFBP-5 was evident from Western immunoblot analysis and immunofluorescence.

54 Within this framework, western immunoblot analysis and immunohistochemistry rev

55 Western immunoblot analysis and real-time PCR analysis o

56 Western immunoblot analysis confirmed that activated mon

57 Western immunoblot analysis confirmed that protein level

58 and could be eluted with a high salt buffer; Western immunoblot analysis confirmed that the 100-kD pr

59 Western immunoblot analysis demonstrated that anti-GALV

60 In the current study, Western immunoblot analysis demonstrated that CPE bound

61 Western immunoblot analysis demonstrated that the OM had

62 luorescence emission spectroscopy as well as western immunoblot analysis demonstrated that the purifi

63 eins rhodopsin and arrestin was evaluated by Western immunoblot analysis in the macular and periphera

64 Western immunoblot analysis indicated a higher level of

65 been maintained in contemporary strains, and Western immunoblot analysis indicated that multiple SET

66 However, Western immunoblot analysis indicated that SpdR is prese

67 Western immunoblot analysis indicates that PBLs possess

68 ctrophoretic mobility shift assay (EMSA) and Western immunoblot analysis of affinity purified protein

69 First, Western immunoblot analysis of AtT-20 cells treated with

70 Western immunoblot analysis of cell lysates was used to

71 Western immunoblot analysis of immunoprecipitated Hib pi

72 Perfusion medium was collected for Western immunoblot analysis of myocilin (MYOC).

73 erived human TM cell lines was quantified by Western immunoblot analysis of protein levels and quanti

74 Western immunoblot analysis of sera obtained from 80 pat

75 Western immunoblot analysis of serum samples obtained fr

76 Western immunoblot analysis of subcellular fractions of

77 stry of the laser-treated organ cultures and western immunoblot analysis of the conditioned medium we

78 of stunned myocardium, we performed PAGE and Western immunoblot analysis of the contractile proteins.

79 Further Western immunoblot analysis of the same strains using po

80 Western immunoblot analysis of three strains of H. muris

81 role of the TS protein-p53 mRNA interaction, Western immunoblot analysis revealed nearly undetectable

82 Western immunoblot analysis revealed that 52- and 54-kDa

83 Western immunoblot analysis revealed that antibodies dir

84 Western immunoblot analysis revealed that p-DARPP-32 exp

85 Data from Western immunoblot analysis revealed that the EGF-stimul

86 Here, Western immunoblot analysis reveals that this pre-pro-B

87 Tissue arrays and Western immunoblot analysis show that NEK6 is overexpres

88 Western immunoblot analysis showed that contact with epi

89 Western immunoblot analysis showed that mouse anti-rP44

90 Western immunoblot analysis using anti-myocilin peptide

91 crylamide gel electrophoresis (SDS-PAGE) and Western immunoblot analysis using anti-phosphotyrosine a

92 ive only with the HGE agent were examined by Western immunoblot analysis using purified whole organis

93 Therefore, Western immunoblot analysis using rP44 and rP30 may be u

94 Western immunoblot analysis was used to detect secreted

95 he immune rabbit serum (IRS) was assessed by Western immunoblot analysis with protein lysates derived

96 y molecular population genetic analysis, and Western immunoblot analysis with sera from infected pati

97 Immunofluorescence, Western immunoblot analysis, and Akt kinase assays were

98 ELISA, Western immunoblot analysis, and immunohistochemistry we

99 nd have characterized it by epitope mapping, Western immunoblot analysis, and immunohistochemistry.

100 recognized the recombinant 44-kDa protein by Western immunoblot analysis, but MAb 3E65 did not.

101 y SDS-polyacrylamide electrophoresis (PAGE), Western immunoblot analysis, Edman degradation, circular

102 lymerase chain reaction, flow cytometry, and Western immunoblot analysis, we have demonstrated that h

103 sphorylation of PLCgamma1 were determined by Western immunoblot analysis, with the appropriate antibo

104 ls were determined by gelatin zymography and Western immunoblot analysis.

105 approximately 47-kDa N protein of APV/US by Western immunoblot analysis.

106 ochemical cellular fractionation followed by western immunoblot analysis.

107 two-dimensional electrophoresis followed by Western immunoblot analysis.

108 MP-PDEs as well as the denatured proteins on Western immunoblot analysis.

109 protein production by Northern analysis and Western immunoblot analysis.

110 crylamide gel electrophoresis (SDS-PAGE) and Western immunoblot analysis.

111 ed human TM cells by quantitative RT-PCR and Western immunoblot analysis.

112 ls by using RT-PCR, quantitative RT-PCR, and Western immunoblot analysis.

113 in were analyzed by quantitative (Q)-PCR and Western immunoblot analysis.

114 y and analyzed by SDS-PAGE, native PAGE, and Western immunoblot analysis.

115 regulation of HSP70 protein as determined by Western immunoblot analysis.

116 desorption ionization-mass spectrometry and Western immunoblotting analysis identified this co-purif

117 Western immunoblotting analysis verified that the altere

118 Western (immunoblot) analysis with monoclonal antibodies

119 Western immunoblot and autoradiographic assays showed en

120 Western immunoblot and enzyme-linked immunosorbent assay

121 GTP-bound Rho G-proteins were quantified by Western immunoblot and GTP-binding ELISA, respectively.

122 as detected on the membrane of N. fowleri by Western immunoblot and immunofluorescence analyses with

123 Western immunoblot and immunohistochemical analyses conf

124 ction in BMPR-IA expression was confirmed by Western immunoblot and immunohistochemistry in the flox/

125 Based on the western immunoblot and immunostaining analysis, the 1 kD

126 er complex in keratinocytes as determined by Western immunoblot and mass spectrometry analyses, a fin

127 Western immunoblot and microaffinity DNA pull-down assay

128 Western immunoblots and confocal immunohistochemistry we

129 forms were identified and localized by using Western immunoblots and confocal immunohistochemistry.

130 Western immunoblots and immunoflourescence show that Sp-

131 Western immunoblots and immunohistochemical preparations

132 Western immunoblots and in vitro phosphorylation experim

133 roteins in A. tumefaciens was measured using Western immunoblots and OOHL sequestration, while the ha

134 Western immunoblots and pulse-chase experiments demonstr

135 ssion of the dspp gene in bone, we performed Western immunoblots and reverse-transcription polymerase

136 the recombinant NucA protein was reactive on Western immunoblots and whole-cell ELISA with all H. inf

137 Quantitative RT-PCR, Western immunoblotting and an HA ELISA assay were used t

138 frontal cortex, amygdala and pituitary using Western immunoblotting and ELISA, respectively.

139 HUVECs were also analyzed by Western immunoblotting and enzyme activity assays for NA

140 Western immunoblotting and enzyme-linked immunosorbent a

141 Western immunoblotting and flow cytometry revealed highe

142 ing an enzyme-linked immunosorbent assay and Western immunoblotting and found that PAO almost complet

143 Western immunoblotting and immunocytochemistry determine

144 Western immunoblotting and immunofluorescence imaging al

145 Western immunoblotting and immunohistochemistry were use

146 tron), 2 additional techniques consisting of Western immunoblotting and infrared spectroscopy, and 4

147 uction, flow cytometry, quantitative RT-PCR, Western immunoblotting and intracellular recordings.

148 Oxtr localization was conclusively shown by Western immunoblotting and MS of nuclear lysate proteins

149 Using Western immunoblotting and quantitative polymerase chain

150 , laser scanning confocal microscopy (LSCM), Western immunoblotting and RT-PCR to investigate the exp

151 nd beta1 integrin expression was detected by Western immunoblotting and the ability of alpha-melanocy

152 when the two EIA strategies were followed by Western immunoblotting and when used in an MTTT, respect

153 otein was detected at approximately 60kDa by Western immunoblotting and, in the isolated extracts, we

154 Western immunoblotting and/or immunofluorescent microsco

155 by a marked increase in p65 content (+164%; Western immunoblotting) and NF-kappaB DNA binding activi

156 were aligned with the phosphoproteins on the Western immunoblot, and identified by matrix-assisted la

157 ied brain tubulin was confirmed in ELISA and Western immunoblot, and significant levels of anti-tubul

158 ific primers for IGFBP-5, Northern analysis, Western immunoblots, and immunohistochemical analysis, c

159 cription-polymerase chain reaction (RT-PCR), Western immunoblotting, and ELISA to evaluate NGF expres

160 ed by electrophoretic mobility shift assays, Western immunoblotting, and enzyme-linked immunoassays,

161 using electrophoretic mobility shift assay, Western immunoblotting, and immunofluorescence imaging.

162 ice was studies by core and envelope ELISAs, Western immunoblotting, and immunofluorescence.

163 Enzyme-linked immunosorbent assay, Western immunoblotting, and immunohistochemistry were us

164 arated, and assessed by Stains-All staining, Western immunoblotting, and mass spectrometry.

165 Binding assays, Western immunoblotting, and reverse transcription-PCR an

166 etermined by indirect immunofluorescence and Western immunoblotting, and the distribution and quantit

167 that if positive or equivocal is reflexed to Western immunoblotting as the second tier.

168 Western immunoblot assay and colorimetry revealed signif

169 evelopment and validation of a PERV-specific Western immunoblot assay for the diagnostic testing of p

170 tissue blot technique and a semiquantitative Western immunoblot assay.

171 increased in ocular hypertensive retinas by Western immunoblot assay.

172 s and TIMPs were evaluated by zymography and Western immunoblot assay.

173 ption-polymerase chain reaction (RT-PCR) and Western immunoblot assay.

174 BPalpha expression that could be detected by Western immunoblot assays even in KSHV-negative DG75 cel

175 rongly decreased the accumulation of TraR in Western immunoblot assays, and also strongly influenced

176 Data from Western immunoblot assays, pulse-chase assays, and immun

177 on GluR1 phosphorylation using quantitative Western immunoblotting assays.

178 human alpha-crystallin and was recognized on Western immunoblots by antiserum raised against human al

179 ged caspase-specific substrate peptides, and Western immunoblotting confirmed the involvement of prim

180 Western immunoblotting confirmed the presence of ER beta

181 Western immunoblotting confirmed the production of: LFN-

182 rther analysis by RNase protection assay and Western immunoblot demonstrated the presence of higher l

183 Western immunoblots demonstrated decreased free ubiquiti

184 Reverse transcription-PCR and Western immunoblots demonstrated that FA2H is expressed

185 Western immunoblotting demonstrated ABGA reactivity to t

186 In VSMC treated with aldosterone, Western immunoblotting detected evidence of GC beta(1)-s

187 ed by protein N-glycosidase F digestions and Western immunoblotting, did not enable it to function as

188 Using a two-step microaffinity isolation/Western immunoblot DNA binding assay, we observe that th

189 Western immunoblots elucidated the intracellular signali

190 Moreover, results of Western immunoblot experiments showed mice developed ser

191 rtin (POMC) was analyzed by means of RT-PCR, Western immunoblotting, fluorescence-activated cell sort

192 Western immunoblots for actin, tropomyosin, troponin C,

193 extracellular portion of the ComD receptor, Western immunoblots for ComD did not reveal changes in p

194 examined both by enzyme immunoassays and by Western immunoblotting for autoantibodies to MAP-2.

195 ng phospholipase A(2) (PLA(2)) activity, and Western immunoblotting for protein expression.

196 infected, drug-treated cells and examined by Western immunoblotting for the presence of two packaging

197 Western immunoblots from E2-treated cortical neuronal cu

198 of an initial EIA followed by a confirmatory Western immunoblot, has been advised by the Centers for

199 Western immunoblots identified shifts in ubiquitin pools

200 qPCR, Western immunoblotting, immunocytochemistry, and ELISA i

201 Western immunoblotting, immunoprecipitation, and immunod

202 hBH was also detected by Western immunoblotting in a high-speed particulate fract

203 C/EBPdelta was detected by Western immunoblotting in osteoblast nuclear extracts af

204 nhanced IL-13-dependent eotaxin release, and Western immunoblot indicated that fibronectin expression

205 The detection of 14-3-3 protein by Western immunoblot is a sensitive and specific cerebrosp

206 Using Western immunoblotting, it was demonstrated that the acu

207 Western immunoblotting, liquid chromatography, and mass

208 -d fetus, newborn lambs, and adult sheep, by Western immunoblot (n= 5 for each age) we quantified the

209 Neither the level (as revealed by Western immunoblotting) nor the cellular distribution (a

210 Oryza sativa L. leaves was characterized by Western immunoblotting, Northern blotting, and electron

211 hern blot analyses of ARPKD whole kidney and Western immunoblot of ARPKD cells showed approximately t

212 Western immunoblot of membranes from mucus-grown bacteri

213 ed more than one protein band as detected by Western immunoblot of P. gallinaceum ookinete supernatan

214 Probing of Western immunoblots of affinity-precipitated proteins sh

215 Western immunoblots of BALB/c3T3 cells using rabbit anti

216 In Western immunoblots of culture media containing RetA, pr

217 5) was specifically recognized by 3E2 in 2-D Western immunoblots of IEF-isolated CSL.

218 In Western immunoblots of retinal homogenates, MAb 6A2 reco

219 Western immunoblots of several proteins demonstrated pro

220 These findings were corroborated by Western immunoblotting of mitochondrial membrane isolate

221 Western immunoblotting of patient sera demonstrated an e

222 Western immunoblotting of polysome fractions showed that

223 ron fusion were corroborated by quantitative Western immunoblotting of SerC (PdxF), which was present

224 performed a comprehensive evaluation (using Western immunoblotting) of the expression and subcellula

225 r gene expression by Northern hybridization, Western immunoblot, or immunohistochemistry.

226 ites, time course of antigen expression, and Western immunoblot patterns.

227 Induction of HO-1 was also evaluated by Western immunoblots, performed at 24 h after the insult.

228 In Western immunoblots, procollagenase and active interstit

229 C) cells using reverse transcription-PCR and Western immunoblots, respectively.

230 e quantitative polymerase chain reaction and Western immunoblotting, respectively.

231 Western immunoblots revealed detectable B2 receptor prot

232 Western immunoblotting revealed a 56 +/- 6% decrease in

233 nd vir-phoA translational fusions as well as Western immunoblotting revealed that the expression of V

234 Western immunoblotting revealed that these catalytic pro

235 c analysis of IL-1R2 RNA message levels with Western immunoblotting revealed tight coupling of de nov

236 Finally, results of western immunoblotting show that yohimbine does not sign

237 Nuclear run-off assays and Western immunoblot showed low levels of transcription an

238 Northern blots and Western immunoblots showed that the sea urchin integrin,

239 In genipin-treated TM cells, Western immunoblotting showed a reduction of active MMP2

240 Quantitative RT-PCR and Western immunoblotting showed a reduction of each HAS in

241 ere purified using streptavidin-agarose, and Western immunoblotting showed HSP27 was present.

242 Western immunoblotting showed increases of the iron stor

243 Furthermore, western immunoblotting showed that 95% of EL patients ha

244 Quantitative Western immunoblotting showed that MiaA is an abundant p

245 Western immunoblotting showed that platelet ERbeta migra

246 Results of Western immunoblotting showed that the HMW gelatinase wa

247 Western immunoblotting showed that the UL25 protein was

248 Western immunoblotting showed that transformants produce

249 Western immunoblotting shows enrichment of both isoforms

250 tent of dopamine (DA) terminal changes using Western immunoblotting [striatal dopamine transporter (D

251 Western immunoblots suggested that this adsorbed IMS was

252 obulin G reactivity with recombinant PomA in Western immunoblots, suggesting the presence of antibodi

253 , reverse transcription-PCR, sequencing, and Western immunoblot techniques to characterize decorin ex

254 spreading, growth, and differentiation using Western immunoblotting techniques, image analysis, flow

255 f molecular weights, isoelectric points, and Western immunoblots, the methyl-14C-labeled proteins wer

256 Similar to Western immunoblots, the results of RT-PCR indicated tha

257 owed an E. ewingii infection-like profile by Western immunoblotting, the results of Western and dot b

258 ls as demonstrated by DNA flow cytometry and Western immunoblot to detect cleavage of poly(ADP-ribose

259 We used DNA binding (gel shift) assays and Western immunoblots to demonstrate that cellular levels

260 e TIMP-1 gene into INS-1 cells and performed Western immunoblotting to demonstrate expression of TIMP

261 Using Western immunoblotting to examine the cytosolic and memb

262 ectron microscopy, immunohistochemistry, and Western immunoblotting to examine the morphology and mic

263 ificantly elevated antibody were examined by Western immunoblotting to outer membrane antigens from A

264 xpression in renal cortex were determined by Western immunoblotting; urine sFlt-1, urine free VEGF-A,

265 from SEC-enriched fractions were examined by Western immunoblotting, urokinase plasminogen activator

266 n normal and inflamed smooth muscle cells by Western immunoblots using an antibody directed against t

267 Western immunoblots using the anti-NUC70 antibody and DN

268 Western immunoblotting using an antibody directed agains

269 The antigen was clearly identified by Western immunoblotting using antihistidine antibody and

270 The antigen was clearly identified by Western immunoblotting using antihistidine antibody.

271 Western immunoblotting using purified E. chaffeensis and

272 d chromatin modifications were determined by Western immunoblotting using specific antibodies.

273 Western immunoblot was performed to determine expression

274 Western immunoblot was used to measure connexin-32 and c

275 Western immunoblot was used to measure the protein expre

276 period, MAP kinase content as determined by Western immunoblotting was constant.

277 Western immunoblotting was performed to analyze the anti

278 Western immunoblotting was performed to identify various

279 Western immunoblotting was used to detect Fas, FasL, sFa

280 Western immunoblotting was used to detect FN fragments i

281 Western immunoblotting was used to evaluate alphaA cryst

282 and subjected to quantitative PCR (qPCR) and Western immunoblotting (WB) for BMP1.

283 e disease (LD), with EIA testing followed by Western immunoblotting (WB) of EIA-equivocal and -positi

284 e assay (IFA), enzyme immunoassay (EIA), and Western immunoblotting (WB) using HL-60 cell culture-der

285 nd herein, using RT-PCR, flow cytometry, and western immunoblot we demonstrate for the first time tha

286 With Western immunoblots, we detected DSP in the Gdm/EDTA ext

287 aging, fluorescent immunohistochemistry, and Western immunoblotting, we investigated (1) the expressi

288 Western immunoblots were performed with specific antibod

289 Western immunoblots were used to determine the effects o

290 Western immunoblots were used to determine whether some

291 Western immunoblots were used to evaluate MMP-3, MMP-9,

292 Quantitative real-time PCR and Western immunoblotting were used to examine the mRNA and

293 Quantitative RT-PCR and Western immunoblotting were used to study the effect of

294 oximately 90,000-120,000), were confirmed by Western immunoblotting, when compared with Caco-2 cell c

295 ncogene-transformed mouse fibroblasts, using Western immunoblot with an IRF-1-specific antiserum, to

296 Using Western immunoblots with the anti-prion protein (PrP) 3F

297 ) for 24 h before 2D gel electrophoresis and Western immunoblotting with antiphosphotyrosine monoclon

298 ransgenic mice, and samples were analyzed by Western immunoblotting with antisera specific for the CO

299 ntities of all three bands were confirmed by Western immunoblotting with specific antibodies.

300 ells and was detected in nuclear extracts by Western immunoblotting with TRP120-specific antibody.