ライフサイエンスコーパス: Northern blot analyses

1 tive reverse transcription-PCR (qRT-PCR) and Northern blot analyses.

2 Several of these changes were confirmed by Northern blot analyses.

3 CK are detected only in skin by Southern and Northern blot analyses.

4 ne brain, by using in situ hybridization and northern blot analyses.

5 of phospholamban transcripts was examined by Northern blot analyses.

6 artilage but not normal cartilage by PCR and Northern blot analyses.

7 uct was used as a probe in Southern blot and Northern blot analyses.

8 ytometry and at the level of mRNA by PCR and Northern blot analyses.

9 ion, Western blot, immunohistochemistry, and Northern blot analyses.

10 pairs identified in dsRNAs were confirmed by Northern blot analyses.

11 n as confirmed by transcriptional fusion and Northern blot analyses.

12 utant by either reverse transcriptase PCR or Northern blot analyses.

13 Results were confirmed by microarray and Northern blot analyses.

14 achieved, as confirmed by PCR, Southern, and Northern blot analyses.

15 eting was demonstrated by flow cytometry and Northern blot analyses.

16 regulation of these operons were examined by Northern blot analyses.

17 ses at that time, as shown by microarray and Northern blot analyses.

18 el by Western blot, immunoprecipitation, and Northern blot analyses.

19 cistronic transcripts were not detectable on Northern blot analyses.

20 tinct tissue-specific expression patterns by Northern blot analyses.

21 tive AP-2B gene was confirmed by RT--PCR and Northern blot analyses.

22 describe expression in L. pennellii through northern-blot analyses.

23 house-grown banana plants were determined by northern-blot analyses.

24 ression using quantitative real-time PCR and Northern blots analyses.

25 Northern blot analyses after the addition of the transcr

26 Northern blot analyses also demonstrated a positive role

27 veolin-1alpha, an identification verified by Northern blot analyses and by the cloning of a cDNA usin

28 Northern blot analyses and complementation experiments i

29 We next performed Northern blot analyses and determined that the 1.4-kb Ni

30 Northern blot analyses and in situ hybridization studies

31 ld restore GADD45beta expression in HepG2 in Northern blot analyses and quantitative real-time polyme

32 normal CD5+ B cells; data were confirmed by Northern blot analyses and real-time RT-PCR.

33 We show by Northern blot analyses and reverse transcription-polymer

34 Northern blot analyses and RT-PCR from 10 different adul

35 We applied Southern and Northern blot analyses and slot blotting of nuclear runo

36 ed by genomic Southern blot, immunoblot, and Northern blot analyses, and two-dimensional gel electrop

37 evels of endogenous D3 mRNA, as indicated by Northern blot analyses, and was significantly reduced wh

38 TTase activity assay, Western blot, and Northern blot analyses confirmed that hTTase gene was su

39 Oligonucleotide microarray and Northern blot analyses confirmed that the transcription

40 Northern blot analyses confirmed the associated molecula

41 Northern blot analyses confirmed the differential displa

42 Northern blot analyses confirmed the in vivo expression

43 Northern blot analyses demonstrate a wide distribution o

44 Northern blot analyses demonstrate that CvMT-IV is down-

45 transcriptase polymerase chain reaction and Northern blot analyses demonstrate that neither CIITA no

46 Southern and Northern blot analyses demonstrate that the gene for p62

47 Northern blot analyses demonstrated a complex pattern of

48 Northern blot analyses demonstrated both the induction o

49 Northern blot analyses demonstrated distinct tissue-spec

50 Southern blot and Northern blot analyses demonstrated hybridization of a r

51 Northern blot analyses demonstrated reduced or absent FH

52 Immunohistochemical, Western, and Northern blot analyses demonstrated that AR expression i

53 Western and Northern blot analyses demonstrated that Cox-2 protein a

54 Northern blot analyses demonstrated that HUVEC express t

55 isolated from endotoxin-exposed rat livers, Northern blot analyses demonstrated that Kupffer cells b

56 Northern blot analyses demonstrated that liver expressed

57 Northern blot analyses demonstrated that the gene has di

58 Northern blot analyses demonstrated that the major SULT1

59 Northern blot analyses demonstrated that the TSA gene is

60 Northern blotting analyses demonstrated that neuropeptid

61 Northern blotting analyses demonstrated that the steady-

62 Northern-blot analyses demonstrated that the AtPP2CA tra

63 duction of IL-2R components was derived from northern blot analyses demonstrating TIF-induced decreas

64 Northern blot analyses detect a single message of 8.9 an

65 Northern blot analyses detected full-length replicon RNA

66 and WEHV2 were also similar to that of WDSV; Northern blot analyses detected only low levels of the o

67 Northern blot analyses for mRNA steady state levels for

68 xpression profiling using DNA microarray and northern-blot analyses identified 82 transcript types fr

69 ession of an AM receptor was not detected by Northern blot analyses in either embryo or trophoblast g

70 rapid amplification of cDNA ends (RACE) and Northern blot analyses in several EBV-positive (EBV(+))

71 On the basis of time course studies, Northern blot analyses, in situ hybridization results, a

72 Northern blot analyses indicate brain exclusive and brai

73 Northern blot analyses indicate that Mt4 transcripts are

74 Both immunoblot and Northern blot analyses indicate that myr 8b is the predo

75 Transcriptional fusions and Northern blot analyses indicate that NanR represses the

76 Northern blot analyses indicate that OSBP1 is broadly ex

77 Northern blot analyses indicate that PEK mRNA is express

78 Northern blot analyses indicate that SA suppresses GA-in

79 and polyamine transport and metabolism, and Northern blot analyses indicate that the AbcR sRNAs acce

80 Northern blot analyses indicate that the fer mRNA is exp

81 Northern blot analyses indicate that the GMD transcript

82 Northern blot analyses indicate that the predominant iso

83 Southern and Northern blot analyses indicate that the protein is enco

84 Northern blot analyses indicate that the psaA transcript

85 Northern blot analyses indicate that this gene is expres

86 Northern blotting analyses indicate that long and short

87 Northern blot analyses indicated a highly restricted mRN

88 Results of Northern blot analyses indicated a transient increase in

89 In agreement, strand-specific RT-PCR and Northern blot analyses indicated that antisense transcri

90 Northern blot analyses indicated that frxA mRNA, and per

91 Northern blot analyses indicated that KAS III transcript

92 Northern blot analyses indicated that the CDO gene displ

93 Northern blot analyses indicated that the gene is select

94 In addition, Northern blot analyses indicated the CYP1A1 was not expr

95 Northern-blot analyses indicated that both genes display

96 Northern-blot analyses indicated that these transcripts

97 By Northern blot analyses, it was found widely distributed

98 By Northern blot analyses, Lp(a), but not Lp(a-), caused up

99 oarray and/or quantitative real-time PCR and northern blot analyses, microRNA-218 (miR-218) was speci

100 out using a conventional dicistronic vector, Northern blot analyses might not be sensitive enough to

101 oliferation and colony reduction assays, and Northern blot analyses, neither blocking of the binding

102 By Western and Northern blot analyses, NK1-FL and NK1-Tr were coexpress

103 Cell proliferation assays and Northern blot analyses of a number of ES cell markers (e

104 Northern blot analyses of a subset of the neuronal genes

105 Northern blot analyses of ARPKD whole kidney and Western

106 Northern blot analyses of bovine tissues showed a single

107 he N-terminal amino acid residues of ACC2 in Northern blot analyses of different human and mouse tiss

108 Northern blot analyses of infected-cell RNA showed that

109 Northern blot analyses of liver RNA during a period prec

110 Northern blot analyses of mitochondrial transcripts indi

111 Northern blot analyses of mouse tissues showed moderate

112 At both stages of hypertrophy, Northern blot analyses of mRNA from LV myocytes showed u

113 Northern blot analyses of rat lacrimal glands, with a pr

114 Northern blot analyses of RNA isolated from different ti

115 nd 15.5 days of gestation, respectively, and Northern blot analyses of RNAs from dissected embryos re

116 Northern blot analyses of the two mouse genes show disti

117 Northern blot analyses of total RNAs from mouse tissues

118 Northern blot analyses of whole brain homogenates reveal

119 RNase protection, in situ hybridization, and Northern blot analyses of wild-type and germ-cell-defici

120 mRNA species are detectable in the brain by Northern blot analyses or in neuroblastoma cell lines.

121 In Western and Northern blot analyses, palladin expression is ubiquitou

122 In Northern blot analyses, PBF mRNA was ubiquitously expres

123 Northern blot analyses performed on 3 transfected and 3

124 Northern blot analyses performed on total RNA from root,

125 Northern-blot analyses performed on chloroplast transgen

126 Northern blot analyses provided evidence that three mRNA

127 sense construct was verified by Southern and Northern blot analyses, respectively, and resulted in de

128 p primary cell culture system by Western and Northern blot analyses, respectively.

129 otein and mRNA was determined by Western and Northern blot analyses, respectively.

130 miquantitative reverse transcription-PCR and Northern blot analyses, resulting in confirmation of six

131 Northern blot analyses reveal that ARA267-alpha is expre

132 Northern blot analyses reveal that induction of DHAPAT c

133 Northern blot analyses reveal that KCNQ2 and KCNQ3 exhib

134 Molecular cloning and Northern blot analyses reveal that the HDAC10 transcript

135 Northern blotting analyses reveal that prk expression is

136 Northern blot analyses revealed a 2-kilobase pair mRNA s

137 Northern blot analyses revealed four FLAP messages of ap

138 Northern blot analyses revealed low expression levels of

139 Northern blot analyses revealed multiple bands of Uncx-4

140 cDNA cloning and Northern blot analyses revealed multiple Rc transcripts,

141 Southern and Northern blot analyses revealed stable integration and l

142 Northern blot analyses revealed that BRAG-1 is expressed

143 Northern blot analyses revealed that C2-ceramide and sph

144 Northern blot analyses revealed that Candida biofilms ex

145 Surprisingly, Northern blot analyses revealed that cidABC and lrgAB tr

146 Northern blot analyses revealed that HDAC8 expression pa

147 Flow cytometric and Northern blot analyses revealed that KM12-L4 cells did n

148 Further Northern blot analyses revealed that some mutants accumu

149 Northern blot analyses revealed that the cidR gene produ

150 Northern blot analyses revealed that the cidR mutation c

151 Northern blot analyses revealed that the zebrafish IGFBP

152 Northern blot analyses revealed that YH439 rapidly incre

153 Northern blotting analyses revealed that PZR is widely e

154 Northern-blot analyses revealed mRNA of two different si

155 Northern-blot analyses revealed stable transcripts that

156 Northern blot analyses show that human MKRN2 and RAF1 ar

157 Northern blot analyses show that Stx1 causes increased T

158 Northern blot analyses show that these IL-1s are highly

159 Northern blot analyses show that while the DcAGP1 transc

160 Western and Northern blot analyses showed a higher density of the im

161 tions, enzyme-linked immunosorbent assay and Northern blot analyses showed downregulation of VEGF in

162 Northern blot analyses showed expression of EDIII antige

163 s transduced with retroviral constructs, and Northern blot analyses showed high steady-state antisens

164 Ribonuclease protection and Northern blot analyses showed that a significant percent

165 ptase-polymerase chain reaction (RT-PCR) and Northern blot analyses showed that C(6)-ceramide signifi

166 Northern blot analyses showed that CF-TRX is expressed i

167 Northern blot analyses showed that chitinase mRNA is ind

168 Furthermore, reverse transcriptase PCR and Northern blot analyses showed that cpb2 genes in all of

169 Northern blot analyses showed that Gal beta 1-4GlcNAc al

170 Macroarrays and Western and Northern blot analyses showed that hypoxia activated the

171 ults of OLE1 promoter-lacZ reporter gene and Northern blot analyses showed that hypoxia- and cobalt-i

172 Northern blot analyses showed that Klf6 was already expr

173 DNA microarray and Northern blot analyses showed that Rfm1 is required for

174 Microarray and Northern blot analyses showed that RR06 is specifically

175 Northern blot analyses showed that the levels of express

176 Northern blot analyses showed that the mRNA levels of ai

177 Subsequent Northern blot analyses showed that the up-regulated tran

178 ure rodent microRNAs and quantitative RT-PCR/Northern blot analyses showed that Trx1 upregulates memb

179 Northern blot analyses showed the six genes to be develo

180 onal analyses by transient transfections and Northern blot analyses suggest APBP-1 has the capacity t

181 Northern blot analyses suggest that Hog1p regulates Ptp2

182 Using a full-length caveolin-1 probe, Northern blot analyses suggest that the expression of ca

183 Northern blot analyses suggest the presence of multiple

184 Northern blots analyses suggest that Myo J may function

185 Sequence and Northern blot analyses suggested that natB forms an oper

186 Microarray and Northern blot analyses suggested that the expression of

187 ith the use of polymerase chain reaction and Northern blot analyses, the NPC in HSMCs was identified

188 , we have used reverse transcription-PCR and Northern blot analyses to ascertain the spectrum of SPC

189 GHRH-R mRNA has been demonstrated by Northern blot analyses to be present specifically in the

190 In this study, we used microarray and Northern blot analyses to determine the S. pyogenes mRNA

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

192 ssed for immunocytochemistry and Western and Northern blot analyses, to determine stromal cell densit

193 interaction in BCBL-1 cells by ORF57 RIP and Northern blot analyses using a (32)P-labeled oligonucleo

194 Northern blot analyses using a CYP9E2 or CYP4C21 probe s

195 Northern blot analyses using a radiolabeled cDNA probe f

196 d proteins and RNA collected for western and northern blot analyses using antibodies specific for alp

197 Northern blot analyses using cDNA probes designed from L

198 Northern blot analyses using different probes demonstrat

199 a late transcript of 1.8 kb are detected in Northern blot analyses using probes containing the EICP0

200 Southern and northern blot analyses using the 137 bp sequence as a pr

201 of the cDNA partial TIP-B1 clone, as well as Northern blot analyses using the cDNA insert as a probe,

202 In Northern blot analyses, VEGF induced Egr-1 mRNA levels i

203 By using Northern blot analyses we show that transcription of bot

204 Using in situ hybridization and Northern blot analyses, we found that most of the olfact

205 Using reverse transcription-PCR and Northern blot analyses, we found that Nox4, a homolog of

206 Based on northern blot analyses, we found that the expression in

207 re, through in vivo cross-linking assays and Northern blot analyses, we have demonstrated that Ets-1

208 Using 3'-rapid amplification cDNA end and Northern blot analyses, we identified the complete 3'-un

209 By using Northern blot analyses, we quantitated duodenal expressi

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

211 ic techniques, and in situ hybridization and Northern blot analyses were conducted to characterize, l

212 erence, bfpA-cat transcriptional fusions and northern blot analyses were employed to monitor bfpA exp

213 nzyme-linked immunosorbent assay (ELISA) and Northern blot analyses were performed to determine secre

214 Northern blot analyses were performed with probes to TIM

215 Western and Northern blot analyses were used to assess the specifici

216 d in chronic diarrheas, cDNA microarrays and Northern blot analyses were used to compare global mRNA

217 Northern blot analyses were used to identify sialomucin

218 n was glycoxidized in vitro, and Western and Northern blot analyses were used to investigate NOSIII e

219 Northern blot analyses were used to verify gene expressi

220 ifferential display technique and subsequent Northern blot analyses were used.

221 o these two regulatory regions, we performed Northern blot analyses, which showed the presence of ets

222 Northern blot analyses with erythroid cell lines express

223 Southern and Northern blot analyses with probes from different segmen

224 ls during gizzard development by Western and Northern blot analyses, with a large increase just prece

225 From Northern blot analyses, XAP2 is ubiquitously expressed i