ライフサイエンスコーパス: Northern blotting

1 pletion, confirmed experimentally using tRNA Northern blotting.

2 d as demonstrated by quantitative RT-PCR and Northern blotting.

3 on using immunolabeling, immunoblotting, and northern blotting.

4 NA) from bovine chondrocytes was analyzed by Northern blotting.

5 uine differential expression was achieved by Northern blotting.

6 the mt-ERK-transfected cells by Western and Northern blotting.

7 ependent decrease in NK3r-mRNA abundance via Northern blotting.

8 al difference analysis, DNA microarrays, and Northern blotting.

9 and decreasing the amounts of mRNA found on northern blotting.

10 or 7 days as evidenced by flow cytometry and Northern blotting.

11 n by Western blotting and for TFPI-2 mRNA by Northern blotting.

12 t the protein and mRNA levels by Western and Northern blotting.

13 transcription-polymerase chain reaction and Northern blotting.

14 s highly expressed in placenta and spleen by Northern blotting.

15 anscription-polymerase chain reaction and by Northern blotting.

16 transcription polymerase chain reaction, and Northern blotting.

17 s was confirmed by both array technology and Northern blotting.

18 eq data and nine microRNAs were confirmed by northern blotting.

19 many tissues and cell lines as determined by Northern blotting.

20 RNA sequencing, quantitative PCR (qPCR), and Northern blotting.

21 and enhanced transcription was confirmed by Northern blotting.

22 from left ventricular tissues by Western and Northern blotting.

23 pression for specific cDNAs was confirmed by Northern blotting.

24 d inner medulla AQP-2 mRNA was determined by Northern blotting.

25 evels of MDR-1 and MRP mRNA as determined by Northern blotting.

26 ozygous (-/-) mice lacked detectable mRNA on Northern blotting.

27 ted cell scanning and class I and II mRNA by Northern blotting.

28 er, kidney, lung and adult nervous system by Northern blotting.

29 messenger RNA (mRNA) levels were assessed by Northern blotting.

30 me size as that of the liver, as measured by Northern blotting.

31 after treatment with NaBT, as determined by Northern blotting.

32 rget BCR-ABL mRNA expression was analyzed by Northern blotting.

33 Arabidopsis by in situ hybridization and by northern blotting.

34 sceral leishmaniasis (VL), was determined by Northern blotting.

35 e transcriptase-polymerase chain reaction or Northern blotting.

36 transcriptase-polymerase chain reaction and Northern blotting.

37 RNA samples and their subsequent analysis by Northern blotting.

38 s evaluated by reverse transcription-PCR and Northern blotting.

39 enic tiling microarray and were confirmed by northern blotting.

40 press Slc34a1 sense/antisense transcripts by northern blotting.

41 eal-time polymerase chain reaction (PCR) and northern blotting.

42 was used to detect mRNA for the Lcn2 gene in Northern blotting.

43 nal for BPAG1 in the brain of dt-Alb mice by Northern blotting.

44 ing real-time quantitative PCR (RT-qPCR) and Northern blotting.

45 ated by microarray analysis and confirmed by Northern blotting.

46 pel-like factor 4 (Klf4), was verified using Northern blotting.

47 p in GCB-DLBCL cells were verified using RIP-Northern blotting.

48 ature miRNA expression profile determined by northern blotting.

49 ld increase in fabA transcripts as judged by Northern blotting, Affymetrix array analysis, and real-t

50 By Northern blotting, AGS3 shows 2.3-kb and 3.5-kb mRNAs in

51 Northern blotting analyses demonstrated that neuropeptid

52 Northern blotting analyses demonstrated that the steady-

53 Northern blotting analyses indicate that long and short

54 Northern blotting analyses revealed that PZR is widely e

55 is study, we used proteomics and Western and Northern blotting analyses to demonstrate that alcohol d

56 roarray, reverse transcription (RT)-PCR, and Northern blotting analyses, we identified 11 virally enc

57 characterized the expression of this gene by Northern blotting analysis and in situ hybridization to

58 Northern blotting analysis demonstrated that the express

59 Northern blotting analysis has shown that the ACEH mRNA

60 Northern blotting analysis indicates that SRG is highly

61 Northern blotting analysis revealed increased LO express

62 Northern blotting analysis revealed that 49 of the 72 At

63 Northern blotting analysis revealed that loxN1 correspon

64 Northern blotting analysis showed that cultured HVSMCs e

65 Northern blotting analysis showed that the major transcr

66 Northern blotting analysis using an Mta1 cDNA probe reve

67 xpressed sequence tag data base analysis and Northern blotting analysis.

68 in vivo primer extension experiments and by Northern blotting analysis.

69 rimer extension experiments, consistent with Northern blotting analysis.

70 K-i was detected in embryonic fibroblasts by Northern blotting analysis.

71 transgene mRNA and protein were confirmed by Northern blotting and 2-dimensional gel electrophoresis

72 ine leukemia virus (MLV) using nondenaturing Northern blotting and a novel RNA dimer capture assay.

73 the peripheral liver using a combination of Northern blotting and a unique biliary tree isolation te

74 The splice sites were confirmed by Northern blotting and autoradiography.

75 S messenger RNA expression was determined by Northern blotting and cNOS protein expression by Western

76 by Livny et al., we tested 40 candidates by Northern blotting and confirmed the expression of nine n

77 Using Northern blotting and cyclin D1 promoter/luciferase assa

78 Northern blotting and flow cytometric analysis were used

79 Northern blotting and fluorescence microscopy indicate t

80 Northern blotting and gene expression profiling results

81 dom cDNA isolation and evaluation by reverse Northern blotting and high throughput microarray analysi

82 , and antioxidant enzymes were determined by Northern blotting and hybridization with gene-specific o

83 Array results were validated with Northern blotting and immunoblotting.

84 the PDGF-A gene and protein as evidenced by Northern blotting and immunocytochemistry was noted.

85 acid, and UCP-2 expression was evaluated by Northern blotting and immunocytochemistry.

86 Northern blotting and immunohistochemistry were used to

87 Candidates were validated by Northern blotting and immunohistochemistry.

88 Expression analysis by northern blotting and in situ hybridization showed highe

89 Northern blotting and in situ hybridization studies with

90 Northern blotting and in situ hybridization were employe

91 Using Northern blotting and in situ hybridization, we have exa

92 Intrahepatic VEGF expression was analyzed by Northern blotting and in situ hybridization.

93 oid and erythroid tissues as demonstrated by Northern blotting and mRNA in situ hybridization.

94 Northern blotting and nuclear run-on analyses demonstrat

95 Northern blotting and nuclear run-on transcription analy

96 DeltaoxyR and overexpressing oxyR strains by Northern blotting and oxyR'::xylB fusions revealed that

97 Northern blotting and primer extension analyses revealed

98 Northern blotting and primer extension analyses showed t

99 Northern blotting and primer extension analysis defined

100 Although the new binding site was near dsbG, Northern blotting and primer extension assays showed tha

101 ll length hsp 70 (dnaK) mRNA was detected by northern blotting and quantitated after heat shock by sl

102 Using Northern blotting and quantitative reverse transcriptase

103 Analyses by Northern blotting and rapid amplification of cDNA ends r

104 Both Northern blotting and real-time reverse transcription-PC

105 Northern blotting and reporter assay demonstrated that t

106 Northern blotting and reverse transcriptase PCR demonstr

107 Northern blotting and reverse transcriptase-polymerase c

108 Northern blotting and reverse transcriptase-polymerase c

109 -FasL-transduced allografts was confirmed by Northern blotting and reverse transcriptase-polymerase c

110 Northern blotting and reverse transcription-PCR indicate

111 Northern blotting and reverse transcription-polymerase c

112 Northern blotting and reverse-transcriptase polymerase c

113 both in vivo immunoprecipitation followed by Northern blotting and RNA degradation assays, we confirm

114 Northern blotting and RT-PCR experiments demonstrated ex

115 As shown by Northern blotting and RT-PCR, Xenopus TIMP3 mRNA is mate

116 human chondrocytes (T/C28a4) was analyzed by Northern blotting and specific enzyme-linked immunosorbe

117 Northern blotting and studies with a series of chromosom

118 nfirmed the expression of four new miRNAs by Northern blotting and used a more sensitive PCR approach

119 , (ii) extracted for total RNA isolation for Northern blotting and, (iii) analysed immunohistochemica

120 Using Northern-blotting and Western-blotting analyses, we obse

121 ected predominantly in spleen and thymus (by Northern blotting) and in skin-resident DC, i.e. Langerh

122 ive and 8 nonresponsive ORFs by conventional Northern blotting, and 48 of these 50 ORFs responded as

123 and subgenomic RNA strands were detected by Northern blotting, and crystalline lattices of viral par

124 ECV-304 cells by reverse transcription-PCR, Northern blotting, and DNA microarray analysis.

125 was characterized by Western immunoblotting, Northern blotting, and electron microscopy of thin secti

126 criptase-polymerase chain reaction (RT-PCR), Northern blotting, and immunoblotting analyses that the

127 r demonstrated by nuclease protection assay, Northern blotting, and immunoblotting in CHRF cells.

128 detected as a 2.2 kb mRNA in Hep 3B cells by Northern blotting, and it encodes a putative 168 amino a

129 Receptor binding assays, Northern blotting, and nuclear run-on analyses demonstra

130 Pulse-chase, Northern blotting, and primer extension analyses in the

131 ghput deep RNA sequencing, quantitative PCR, Northern blotting, and rapid amplification of cDNA ends

132 firmed by multiprobe RNase protection assay, Northern blotting, and reverse transcription-PCR.

133 library and analyzed by reverse Northern and Northern blotting approaches.

134 ctron microscopy, in situ hybridization, and Northern blotting are used to analyze osteopontin protei

135 roteasome component lmp7 was investigated by Northern blotting at all stages of development.

136 his shortcoming by demonstrating multiplexed northern blotting based on the mechanism of hybridizatio

137 xes with MS-based protein identification and Northern blotting-based rRNA detection approaches identi

138 Northern blotting can be done in 2 d, but detection of a

139 As shown by Northern blotting, CMMP mRNA of 1.8 kilobase pairs was c

140 Northern blotting confirmed increased expression of skel

141 Northern blotting confirmed increased transcript amounts

142 Northern blotting confirmed that these changes in gene e

143 in membranes prepared from these cells, and Northern blotting confirmed the absence of message for o

144 Northern blotting confirmed the overexpression of wnt5a

145 Northern blotting confirmed these results and showed tha

146 Polymerase chain reaction and Northern blotting demonstrated a 3.4-kilobase message, w

147 Analysis by Northern blotting demonstrated mRNAs encoding TRAIL as w

148 Northern blotting demonstrated only a 1.7- to 2.5-fold i

149 Northern blotting demonstrated that CML28 is highly expr

150 Northern blotting demonstrated that message for calcycli

151 Northern blotting demonstrated that TC3aR was expressed

152 ent quantitative real-time PCR (qRT-PCR) and Northern blotting demonstrated that the ebpABC mRNA tran

153 transcription polymerase chain reaction and Northern blotting demonstrated the presence of FS mRNA i

154 The NOH-1S transcript was not observed by Northern blotting, despite claims of its abundance based

155 Northern blotting detects a 2.2-kb Atp6v1b1 transcript i

156 Expression of ncRNAs was studied by northern blotting during (i) the normal developmental cy

157 When using northern blotting during these studies, we discovered th

158 Ribonuclease protection assays, Northern blotting, enzyme-linked immunosorbent assay, an

159 Northern blotting established that HCV dsRNA contained g

160 Furthermore, Northern blotting experiments demonstrate that the Xenop

161 Northern blotting experiments indicate that CIRL-2 is ex

162 Northern blotting experiments revealed a major 2.0-kb AS

163 Northern blotting experiments revealed that the expressi

164 Northern blotting experiments with rifampicin disclosed

165 usions to soxR, combined with the results of Northern blotting experiments, verified this regulation

166 d the detection of miRNA by hybridization in northern blotting experiments.

167 Northern blotting for five of these genes (alpha-Catenin

168 Northern blotting for individual miRNAs showed that the

169 blood was analyzed by flow cytometry and by Northern blotting for LPL.

170 CR paralleled the mature miRNA expression by northern blotting for most of the conditions studied.

171 ression of SIRPs on five cell lines, whereas Northern blotting for SIRPalpha transcripts showed mRNA

172 his is present at a low level as detected by Northern blotting for the Fas mRNA and flow cytometric a

173 Northern blotting found TCR mRNA expression predominantl

174 tronic p28 mRNA transcripts were detected by Northern blotting from E. canis infected DH82 cells, ind

175 By Northern blotting, full-length VWFCP mRNA was detected o

176 Northern blotting, gene-specific RT-PCR, RNA pull-down a

177 ons near c-myc by Southern blotting, whereas Northern blotting has shown that most tumors have two- t

178 Northern blotting identified IL-16 mRNA predominantly in

179 glycoprotein and document its expression by Northern blotting, immunoblotting, and immunofluorescenc

180 rotein mass, and function were determined by Northern blotting, immunoblotting, and taurocholate (TC)

181 Northern blotting, immunoblotting, and transfection stud

182 , only liver X receptor-beta was observed on northern blotting in adult mouse epidermis.

183 2 and -5 are below the level of detection by Northern blotting in both normal and cancer samples.

184 e transcriptase-polymerase chain reaction or Northern blotting in human chondrocytes, synovial fibrob

185 at the mRNA level using quantitative PCR or Northern blotting in lymphocytes from aged and young sub

186 Several viral transcripts were found by Northern blotting in the adult thymus.

187 ated plaice CYP1A, only being detectable, by Northern blotting, in gill tissue.

188 Northern blotting, in situ hybridization, and blocking t

189 d, and expression of PepT1 was determined by Northern blotting, in situ hybridization, and immunohist

190 Northern blotting, in situ hybridization, and reporter g

191 mud cDNAs and a survey of mud transcripts by Northern blotting indicate that the gene is subject to d

192 g the P-element insertion, which Western and Northern blotting indicated is a severely hypomorphic al

193 ains, and transcript analysis (by RT-PCR and northern blotting) indicated the effect was mainly trans

194 Northern blotting indicates that the mRNA of PDE7B is 5.

195 RNase H digestion coupled with Northern blotting indicates that the two early crosslink

196 This improved northern blotting is particularly useful to analyze prod

197 We established, using Northern blotting, nuclear run-on assays, and RT-PCR, th

198 small interfering RNAs (siRNAs) followed by Northern blotting of GAPDH, expression of N(pro) had no

199 cE7 is detectable by both inverse RT-PCR and northern blotting of HPV16-transformed cells.

200 alyzed by reverse transcription (RT)-PCR and Northern blotting of lens total RNA, immunoblotting of l

201 Northern blotting of mouse and human tissues is in agree

202 Northern blotting of RNA extracted from BCBL-1 cells wit

203 levated ocular transcripts were confirmed by Northern blotting of RNA from Bbs4(-/-) and three additi

204 Northern blotting of RNA from NHL revealed a 1.8-kb NTCP

205 RNA of approximately 3.9 kilobases, found by Northern blotting of RNA from rat lung and kidney.

206 aches that complement RNA-seq, discover that northern blotting of small RNAs is biased against short

207 FimA protein as assessed by both Western and Northern blotting or fimbriae visible by electron micros

208 presumed expression pattern was confirmed by Northern blotting or reverse transcription-polymerase ch

209 er to perform and more sensitive than either northern blotting or ribonuclease protection assays.

210 any of the dCSTs was further demonstrated by northern blotting or RT-PCR.

211 mtv-vSAg-encoding mRNA, as characterized by Northern blotting, PCR, and RNase protection.

212 We identified four novel transcripts using Northern blotting, phage library screening, and 5' rapid

213 lear and cytoplasmic reporter RNA species by Northern blotting, primer extension, and reverse transcr

214 Cells were analyzed by Western blotting, Northern blotting, pulse-chase analysis, and immunofluor

215 ethods used in detection of miRNAs including northern blotting, quantitative real time PCR (qRT-PCR)

216 y used to monitor gene expression, including Northern blotting, real-time polymerase chain reaction,

217 (mRNA) were detected by Western blotting and Northern blotting, respectively.

218 ression were evaluated by immunoblotting and Northern blotting, respectively.

219 Northern blotting revealed a complex transcription patte

220 Northern blotting revealed a coordinated time-of-day-dep

221 Northern blotting revealed no effects of the cytokine on

222 Northern blotting revealed no expression of TDAG51 in TD

223 While northern blotting revealed only these two mRNAs, both PC

224 Northern blotting revealed that ntcp messenger RNA (mRNA

225 Northern blotting revealed that RAD9B transcripts are hi

226 Northern blotting revealed variable expression of the hu

227 the 73 genes was analysed by microarray and Northern blotting, revealing 24 genes/operons (including

228 Northern blotting reveals ubiquitous distribution of Nrd

229 Analyses of GFP fusions, Northern blotting, reverse transcription polymerase chai

230 Northern blotting, reverse transcription-PCR, and SMART-

231 Using Northern blotting, RNase H cleavage, primer extension, a

232 Northern blotting, RNase protection analysis, and Wester

233 Messenger RNA (mRNA) was measured by Northern blotting, RNase protection assay, and real-time

234 urified RNA can be used for analyses such as northern blotting, RT-PCR and microarrays.

235 Northern blotting, RT-PCR, and in situ hybridization ana

236 examined TLR mRNA and protein expression by Northern blotting, RT-PCR, real-time RT-PCR, Western blo

237 erse transcription-PCR, Western blotting and Northern blotting showed alternative splicing in nervous

238 Northern blotting showed that a significantly decreased

239 Northern blotting showed that all three of the mlp genes

240 Reverse transcription-PCR analysis and Northern blotting showed that Np-opcA was transcribable.

241 Northern blotting showed that overexpression of c-Jun en

242 Northern blotting showed that the gene was expressed in

243 Northern blotting showed that the level of MUC16 mRNA co

244 Analysis of p35 mRNA by Northern blotting showed that the message from monocytes

245 Northern blotting showed that transcription of 2.4/2.1-k

246 Northern blotting showed that WdCHS3 was highly expresse

247 iae and other class IV chitin synthases, and Northern blotting showed that WdCHS4 was expressed at co

248 uencing, and extended by a 5'-RACE assay and Northern blotting, showing that meiotic cells induce the

249 Northern blotting shows broad expression of MT-SP1 in a

250 Tissue Northern blotting studies demonstrated robust expression

251 Northern blotting studies of multiple vascular and non-v

252 Quantitative RT-PCR and Northern blotting studies showed reduced or loss of expr

253 Northern blotting studies showed that the levels of the

254 Northern blotting studies showed that tTG is rapidly and

255 Northern blotting suggests that these anti-CRISPRs manip

256 otransferases were examined by employing the Northern blotting technique.

257 ne macrophages, by using gel retardation and Northern blotting techniques.

258 show by rapid amplification of cDNA ends and Northern blotting that Drosophila CCDC56 protein and mtT

259 We showed by using microarray analysis and Northern blotting that several genes are negatively regu

260 phospholipid biosynthesis were determined by Northern blotting to be differentially expressed in all

261 ifferentially expressed clones and performed Northern blotting to detect increased expression levels.

262 ority of published studies to date have used northern blotting to detect the expression of miRNAs.

263 amined by immunofluorescence and Western and Northern blotting to determine the effect of tsk-Fbn1 on

264 o inhibit the TGF-beta signaling pathway, by Northern blotting to elevate inhibitory Smad7 expression

265 Toure et al, 2004 used Northern blotting to show that the Y-linked genes Ssty1

266 Studies of the pilT-pilU locus by using Northern blotting, transcriptional fusions, and reverse

267 By northern blotting, TRX mRNA levels were increased in PDA

268 By northern blotting, two distinct mRNA transcripts of 5.9

269 f Akt in H(+)/K(+)-ATPase gene expression by Northern blotting using a canine H(+)/K(+)-ATPase alpha-

270 ntron 6 sequence, together with Southern and Northern blotting using an intron 6-specific probe, conf

271 y 3'-RACE followed by DNA sequencing, and by Northern blotting using probes derived from different re

272 Northern blotting using probes specific to hrcA, igr66 o

273 ript of approximately 4.5 kb was detected by Northern blotting using total RNA from QT35 cells.

274 Northern blotting was used to quantify the message for M

275 toxin gene, whose transcript was detected by Northern blotting, was found next to the SCCcap1 locus.

276 By Northern blotting, we also demonstrated the constitutive

277 By Northern blotting, we confirm these results and find tha

278 Finally, by Northern blotting, we established that the truncated tra

279 in situ hybridization (ISH), and Western and Northern blotting, we found that both c-neu and c-met ar

280 By reporter gene fusion and Northern blotting, we found that sbcDC regulated capsule

281 By Northern blotting, we found the highest concentrations o

282 Using RT-PCR and Northern blotting, we have examined the expression of a

283 Moreover, by Northern blotting, we have shown that several miRs locat

284 By Northern blotting, we identified two types of vinexin mR

285 Using in situ hybridization and Northern blotting, we observed the presence of endogenou

286 Immunoblotting and Northern blotting were used to assess the effects of bil

287 screening of a complementary DNA library and Northern blotting were used to clone the target antigen

288 RT-PCR and Northern blotting were used to examine rNKp30 RNA expres

289 ression of alpha-hemolysin, as determined by Northern blotting, Western blotting, and a rabbit erythr

290 lls was confirmed by fluorescent microscopy, Northern blotting, Western blotting, and an enzymatic ol

291 ds, including S1 nuclease protection assays, Northern blotting, Western blotting, and bioconversion a

292 ith vector, sense, and antisense constructs, Northern blotting, Western blotting, and gelatin zymogra

293 enomedullary chromaffin cells as detected by Northern blotting, Western blotting, and specific PAI-1

294 Northern blotting with a CTV derived probe for assessmen

295 Northern blotting with a P2X1-specific probe revealed a

296 Northern blotting with comX probes revealed two distinct

297 ansins, as well as an expression analysis by northern blotting with materials from young and mature m

298 d with expression of viral Env glycoprotein; Northern blotting with specific hybridization probes ide

299 Northern blotting with the bovine BBB LAT1 cDNA showed t

300 By northern blotting, Zfr is expressed at highest levels wi