ライフサイエンスコーパス: reporter plasmid

1 riven activating protein-1 (AP-1)-luciferase reporter plasmid.

2 ntaining nuclear extract also encapsidated a reporter plasmid.

3 ation of an estrogen response element-driven reporter plasmid.

4 ed with an interleukin-8 promoter-luciferase reporter plasmid.

5 rease the mutation frequency measured in the reporter plasmid.

6 the activity of a p73-driven Bax-luciferase reporter plasmid.

7 luciferase expression from a PXR-responsive reporter plasmid.

8 ansiently transfected with an IL-13 promoter-reporter plasmid.

9 ansfected into cells expressing an NF-kappaB reporter plasmid.

10 two variant loxP sites that are located on a reporter plasmid.

11 sion from a squalestatin 1-responsive CYP2B1 reporter plasmid.

12 -cell activation signals by using a promoter reporter plasmid.

13 nducing the activation of an IL-6-responsive reporter plasmid.

14 ells with a nuclear factor-kappaB luciferase reporter plasmid.

15 a heat shock protein 70 promoter-luciferase reporter plasmid.

16 co-localised with expression of the pCMVbeta reporter plasmid.

17 e insulin-increased expression of a LexA-CAT reporter plasmid.

18 ferase from a matrilysin promoter-luciferase reporter plasmid.

19 activate p53-dependent transactivation of a reporter plasmid.

20 activates transcription of the same chimeric reporter plasmid.

21 ty in ASM cells transfected with a NF-kappaB reporter plasmid.

22 by using a chloramphenicol acetyltransferase reporter plasmid.

23 beta-galactosidase activity produced from a reporter plasmid.

24 the HPV18 promoter present in a transfected reporter plasmid.

25 Fbeta induction of luciferase by the 3TP-Lux reporter plasmid.

26 nthesis and activity of an aggrecan enhancer reporter plasmid.

27 le pole body is reminiscent of that of a CEN reporter plasmid.

28 n Estrogen Response Element (ERE)-Luciferase reporter plasmid.

29 control cells transfected with the pTOPFLASH reporter plasmid.

30 maviral-based gene transfer vectors carrying reporter plasmids.

31 y and sufficient to enhance transcription in reporter plasmids.

32 -induced transcriptional activation of these reporter plasmids.

33 fluorescent protein or luciferase genes from reporter plasmids.

34 upregulated expression from ED-L1 and L1-TR reporter plasmids.

35 ional inhibition of both ERE- and NRE-driven reporter plasmids.

36 s E(2)-induced transcriptional activation to reporter plasmids.

37 ed with estrogen response element-luciferase reporter plasmids.

38 t DNA sequences and repressed PAX3-dependent reporter plasmids.

39 entional transient transfection of analogous reporter plasmids.

40 ells transfected with such chimeric promoter-reporter plasmids.

41 AR-induced transactivation of ARE-containing reporter plasmids.

42 inhibition of Renilla luciferase (RLuc) HCV reporter plasmids.

43 3 in cells transfected with recombinant ORF3 reporter plasmids.

44 e and constructed a series of dp5-luciferase reporter plasmids.

45 ties of pG13-luc, PUMA-luc, and p21/WAF1-luc reporter plasmids.

46 rase assay after transient transfection with reporter plasmids.

47 iant with transfected CHGA 3'-UTR/luciferase reporter plasmids.

48 Using luciferase reporter plasmids, ABT-737 was shown to stimulate NF-kap

49 accessibility of a triplex target site on a reporter plasmid after injection into nuclei.

50 transfection with the IL-1beta promoter-CAT reporter plasmid alone.

51 to -676 bp and -786 to -728 bp) ligated into reporter plasmids also showed increases in reporter acti

52 ed expression of transiently transfected LTR reporter plasmids, an analysis of factors required for e

53 eased readout of an NFkappaB promoter-driven reporter plasmid and decreased NFkappaB binding to DNA.

54 ional decline of a differentiation-sensitive reporter plasmid and enhances survival of NT2/D1 cells f

55 th hormone reporter gene in a growth hormone reporter plasmid and examined the effects of 1 alpha,25(

56 nsfection experiments using a p53-responsive reporter plasmid and gamma-irradiation studies demonstra

57 in transient-transfection assays using a p53 reporter plasmid and in induction of p53-responsive gene

58 line stably transfected with AP-1-luciferase reporter plasmid and in vivo using AP-1-luciferase repor

59 were transiently transfected with the P1CAT reporter plasmid and levels of CAT activity in response

60 co-transfection of the OGA-3'UTR containing reporter plasmid and miR-539 overexpression plasmid sign

61 splice reporter, binds RNA derived from the reporter plasmid and punctually co-localises with nascen

62 ional decline of a differentiation-sensitive reporter plasmid and represses induction of immunophenot

63 anslation start was cloned into a luciferase reporter plasmid and shown to contain promoter activity

64 were cloned onto the 5'-end of a luciferase reporter plasmid and transient transfection experiments

65 native RNAi tracking methods (co-delivery of reporter plasmids and end-labeling the siRNA), QDs exhib

66 ence on CBP/p300 was often different between reporter plasmids and endogenous genes.

67 enhancer and the epsilon-globin promoter in reporter plasmids and integrated the plasmids into eryth

68 al p21(waf1/cip1) promoter-driven luciferase reporter plasmids and observed that UCN-01 activated the

69 Luciferase assays using the p53 and p21 reporter plasmids and probing of immunoblots with antibo

70 Analyses of fluorescence-tagged single-copy reporter plasmids and/or the plasmid partitioning protei

71 ivation by P4 delta in vivo, by using a lacZ reporter plasmid, and a subset of mutants was assayed in

72 cells were transfected with the EpRE/TK-GFP reporter plasmid, and clones with low GFP background exp

73 internal ribosome entry site in bicistronic reporter plasmids, and it requires the 5'-proximal posit

74 finding by generating bicistronic luciferase reporter plasmids, and we were able to map a potential i

75 erase I (pol I) was assessed in vivo using a reporter plasmid bearing a ColE1-type origin and an ochr

76 By assaying the expression levels of a reporter plasmid bearing a umuC :lacZ fusion, we show th

77 ck sternal chondrocytes and fibroblasts with reporter plasmids bearing progressively deleted portions

78 o large scale degradation or mutation of the reporter plasmid, but dramatically lowered mRNA levels.

79 site activity using a bicistronic luciferase reporter plasmid, but none was detected.

80 decreased constitutive expression of a COX-2 reporter plasmid by >50%.

81 contrast, EKLF increased the activity of the reporter plasmid by 3-fold.

82 ation of an HNF-4 alpha-dependent luciferase reporter plasmid by 3.2- and 1.6-fold, respectively.

83 oter expression required modification of the reporter plasmid by bracketing the GFP reporter gene wit

84 terized the segregation of a single-copy STB reporter plasmid by manipulating mitosis to force sister

85 ited expression from an EBNA1-dependent oriP reporter plasmid by more than 90% in these cells but did

86 and vascular endothelial growth factor-based reporter plasmids by both estrogen-deficient FBS (ED-FBS

87 We constructed a reporter plasmid carrying the genomic regulatory region

88 2, 5 or 12 bps apart in a firefly luciferase reporter plasmid caused a decrease in luciferase activit

89 d protein response element (UPRE) luciferase reporter plasmid confirmed that the UPRE was activated o

90 ZnT5b was co-expressed with an MT2a promoter-reporter plasmid construct in human intestinal Caco-2 ce

91 t transfection of an OPN promoter-luciferase reporter plasmid construct showed that promoter activity

92 NFKB1 promoter/exon 1 luciferase reporter plasmid constructs containing the -94delATTG al

93 SOX9 synergistically activated a luciferase reporter plasmid containing a Col2a1 enhancer and increa

94 T2AA significantly delayed reactivation of a reporter plasmid containing an ICL.

95 NHBE cells transfected with a luciferase reporter plasmid containing an NF-kappaB-inducible promo

96 and transcription-competent dual-luciferase reporter plasmid containing both the OriS and the interg

97 irway smooth muscle cells transfected with a reporter plasmid containing kappa B enhancer elements.

98 stably transfecting HMEC-1 cells with a cis-reporter plasmid containing luciferase reporter gene lin

99 omoter and can activate transcription from a reporter plasmid containing multiple copies of the IRS.

100 In contrast, transfection of a linear GFP-reporter plasmid containing site-specific, cisplatin les

101 activation were quantified with a luciferase reporter plasmid containing SOX9 binding sites from the

102 atments induced luciferase expression from a reporter plasmid containing the 2.8-kb but not the 1.9-k

103 ual luciferase assay after transfection of a reporter plasmid containing the antioxidant response ele

104 plasmid overexpressing CTCF constructs and a reporter plasmid containing the APP promoter.

105 y Northern blots, it stimulated a luciferase reporter plasmid containing the EGF-responsive sequence

106 demonstrated that ATF-1 and CREB activated a reporter plasmid containing the H-2 BF1 motif.

107 SAKA-T cells transfected with the luciferase reporter plasmid containing the hRANKL HSE region (-2 kb

108 nsformed an NTHI otitis media isolate with a reporter plasmid containing the lux gene cluster driven

109 In cells transfected with a reporter plasmid containing this region, expression of l

110 A reporter plasmid containing this site was markedly activ

111 report, we describe the use of a luciferase reporter plasmid containing two TBEs that can be used as

112 tional activities in normal human T cells of reporter plasmids containing 1.1 kb of all three of the

113 with chloramphenicol acetyltransferase (CAT) reporter plasmids containing a mouse IRBP promoter and A

114 base pair, ERbeta activates transcription of reporter plasmids containing A2, pS2, B1, and OT EREs to

115 To this end, we developed a panel of reporter plasmids containing all 83 putative viral promo

116 were transiently transfected with luciferase reporter plasmids containing an 8.3-kilobase human iNOS

117 , PGC-1alpha enhanced the transactivation of reporter plasmids containing an estrogen response elemen

118 Transcription of reporter plasmids containing CD13/APN proximal promoter

119 Reporter plasmids containing directly repeated mwr, or t

120 ent transfection assays were performed using reporter plasmids containing E2F-binding sites.

121 ransient transfection of a series of sgk-CAT reporter plasmids containing either 5' deletions or cont

122 onstructed chloramphenicol acetyltransferase reporter plasmids containing either a wild-type or mutan

123 sfected with miR 21a-3p mimic and luciferase reporter plasmids containing either intact nox-4 3'-UTR

124 Transient transfections of luciferase reporter plasmids containing either the full-length huma

125 e validated using 3'-untranslated region-Luc reporter plasmids containing either wild-type sequences

126 for PPAR-mediated upregulation, we prepared reporter plasmids containing fragments of the SULT1C3 5'

127 romoter, as shown by transfecting cells with reporter plasmids containing mutations in this element.

128 alpha-mediated transcriptional activation of reporter plasmids containing PPARalpha target elements.

129 Transfection of osteoblasts with reporter plasmids containing TGF-beta 2 promoter DNA fro

130 Transcriptional reporter plasmids containing the 255-bp lsrACDBFG-lsrRK

131 Results from luciferase assays with reporter plasmids containing the 3' untranslated region

132 cantly suppressed the luciferase activity of reporter plasmids containing the 3'-UTR (untranslated re

133 cantly suppressed the luciferase activity of reporter plasmids containing the 3'-UTR sequences comple

134 ly enhanced ERbeta-mediated transcription of reporter plasmids containing the A2, pS2, B1, and OT ERE

135 ferase assay after transient transfection of reporter plasmids containing the antioxidant response el

136 dual luciferase assay after transfection of reporter plasmids containing the antioxidant response el

137 YF5 and MYOD can activate gene expression of reporter plasmids containing the E-box element.

138 In NIH3T3 cells, luciferase reporter plasmids containing the identified binding site

139 occurred with either integrated or episomal reporter plasmids containing the native mouse metallothi

140 In transfection experiments, reporter plasmids containing the reiterated dhfr Sp1 sit

141 Luciferase reporter plasmids, containing mutations in AP-1 and NF-k

142 cells are deficient in repair of luciferase reporter plasmids damaged by UV irradiation.

143 ranscription start site) promoter-luciferase reporter plasmid demonstrated a significant (4 fold) inc

144 ssays in CV-1 cells using an AP-1 responsive reporter plasmid demonstrated that t-RA (1), 6, and 16 e

145 ssays involving a RANTES promoter-luciferase reporter plasmid demonstrated that the heat shock respon

146 tion of EPRO-Gr cells with a RARE-containing reporter plasmid demonstrates increased activity in the

147 agents of cell wall stress of a set of lacZ reporter plasmids derived from several Rlm1-responsive g

148 the loss of expression of a c-Myc-dependent reporter plasmid despite the fact that c-Myc-Max heterod

149 It was also possible to encapsidate reporter plasmids devoid of BPV1 DNA sequences.

150 acilitate transfection of luciferase and GFP reporter plasmid DNA in vitro and in vivo under various

151 bles coupled to a luciferase bioluminescence reporter plasmid DNA were shown to transfect tumors impl

152 e we show that merely forming a triplex in a reporter plasmid does not disrupt transcription, but whe

153 MYF5 or MYOD to activate transcription of a reporter plasmid driven by a portion of the Hom3a enhanc

154 and DNA binding and stimulated activity of a reporter plasmid driven by multiple Oct-1 elements.

155 ion assays of 23 different cell lines with a reporter plasmid driven by the JSRV long terminal repeat

156 constructed an NTHI strain containing a Lux reporter plasmid driven by the sapA promoter and demonst

157 Transfection assays using reporter plasmids driven by different segments of the co

158 d that S. gordonii containing the PamyB-'gfp reporter plasmid exhibited mean fluorescence levels 20-f

159 raFGH genes and harbored the transporter and reporter plasmids, exhibited all-or-none behavior.

160 promoter and green fluorescent protein (GFP) reporter plasmids exposed to a 1 Hz, 2 Hz, and 4 Hz osci

161 measured with 3TP-lux, a TGF-beta-sensitive reporter plasmid expressing luciferase.

162 on HCV translation by codelivering them with reporter plasmids expressing firefly luciferase under th

163 4 cDNA and an NF-kappaB-dependent luciferase reporter plasmid followed by stimulation with lipopolysa

164 with naked or liposome-complexed luciferase reporter plasmid for 3 hours.

165 cells, each containing a green fluorescence reporter plasmid for a gene of interest.

166 en 1 (EBNA-1) were stably transfected with a reporter plasmid for GAL4-dependent expression of the gr

167 A promoter reporter plasmid for S. pneumoniae was devised to charac

168 says with a RegA-disrupted strain containing reporter plasmids for Mg-protoporphyrin IX monomethyl es

169 ons, we have engineered specific fluorescent reporter plasmids for quantitative measurements of 8-oxo

170 teins in rkr1Delta [PSI+] strains but, using reporter plasmids, found that rtf1Delta decreases nonsto

171 sfected with CDK6 promoter-linked luciferase reporter plasmids, I3C inhibited CDK6 promoter activity

172 ession of a TNF-alpha 3' untranslated region reporter plasmid in an orientation-dependent manner.

173 s minireplicon was sufficient to replicate a reporter plasmid in B. thuringiensis subsp. israelensis

174 activated the hPR (-711 to +822)-luciferase reporter plasmid in breast cancer cells.

175 (HEK) 293 cells transfected with a NF-kappaB reporter plasmid in combination with NOD1 or NOD2 expres

176 as studied using a green fluorescent protein reporter plasmid in cultured arterial smooth muscle cell

177 SF-2 with the RANKL gene promoter-luciferase reporter plasmid in human osteoblastic cells (NOBC) demo

178 were cotransfected with a beta-galactosidase reporter plasmid in transient-transfection assays in rat

179 fested as increased transactivation of a p53-reporter plasmid in undamaged hepatocytes, and accelerat

180 ylenediamine can inhibit the expression of a reporter plasmid in Xenopus oocytes if the triplex is pr

181 ription of simple and complex ERE-containing reporter plasmids in a dose-dependent manner.

182 ort that transfections with hMMP1 luciferase reporter plasmids in fibroblast-like synoviocytes reveal

183 Using luciferase reporter plasmids in glioma cells, we found that hypoxia

184 CNAIP expression constructs with luciferase reporter plasmids in HMC-1 cells resulted in activation

185 vitro studies using transfection of promoter/reporter plasmids in human tissue culture cell lines, DN

186 Using transfection of promoter/reporter plasmids in human tissue culture cell lines, in

187 pression of transcription from E2-responsive reporter plasmids in mammalian cell culture.

188 lted in up to 93% gene silencing of RLuc-HCV reporter plasmids in mouse liver.

189 ndogenous genes and exogenous p53-luciferase reporter plasmids in RKO and HCT 116 colon cancer cells.

190 inhibited the c-Myc-dependent expression of reporter plasmids in transient assays; moreover, overexp

191 ll lines (LCLs), to stimulate LMP-1 promoter reporter plasmids in transient-cotransfection assays, an

192 single injection of CP-mag-micelles carrying reporter plasmids in vivo expressed genes for at least o

193 Using lacZ transcription reporter plasmids in wild-type strain 2.4.1 and PrrA- mu

194 e protection assays of heterologous promoter/reporter plasmids indicate that basal instability of RAN

195 Transfection assays using a c-myc reporter plasmid indicated that the TBLV long terminal r

196 IH 3T3 cells, using an SRE-driven luciferase reporter plasmid, indicated that PKC-alpha and PKC-epsil

197 strong Sp1 binding site rendered the HTLV-1 reporter plasmid insensitive to Sp1 activation, and dram

198 Borde and colleagues reported that a reporter plasmid inserted at different genomic locations

199 kappa B binding motif in the wild-type MCP-1 reporter plasmid into a motif with affinity to p65p65.

200 -kappa B-binding motif in the wild-type IL-8 reporter plasmid into a motif with exclusive affinity to

201 BP was cotransfected with a ChoRE-containing reporter plasmid into human embryonic kidney 293 cells,

202 d, methylated, and partially single-stranded reporter plasmid into the nuclei of Xenopus oocytes and

203 Transient transfection of reporter plasmids into control or Ski producing mouse L

204 gene by transient transfection of luciferase reporter plasmids into cultured cell lines.

205 s target mRNAs by transfection of Luciferase reporter plasmids into Huh7, BNL-1ME, and HEK293 culture

206 on of L1/L2 particles capable of transducing reporter plasmids into mammalian cells are technically d

207 Transfection of ankyrin promoter/reporter plasmids into tissue culture cell lines yielded

208 transiently transfected, estrogen-responsive reporter plasmid is decreased.

209 irus structural proteins around heterologous reporter plasmids is surprisingly promiscuous and may be

210 pecific expression using GFP transcriptional reporter plasmids lead to the identification of three no

211 Mutating all three sites in the reporter plasmid led to a complete loss of induction by

212 rs, cells were transfected with a luciferase reporter plasmid linked to a glucocorticoid response ele

213 Transfection with luciferase reporter plasmids linked to glucocorticoid response elem

214 as assessed with the TOPFLASH (T cell factor reporter plasmid) luciferase assay.

215 ted ICR repressed expression from a CpG-free reporter plasmid more than 1000-fold compared with its u

216 As isolated from cells transfected only with reporter plasmid or co-transfected with an active mutant

217 tional activation of an NF-kappaB luciferase reporter plasmid; or on the cytokine-stimulated upregula

218 had no effect on the expression of a UGT1A7 reporter plasmid, p(-965/+56)1A7-Luc, in primary rat hep

219 ronJet hereafter) device was used to deliver reporter plasmids (pCMVbeta and pEGFP-N1) into viable ex

220 tivation of the p53/p73-dependent luciferase reporter plasmid (pG13-luc).

221 (T) cells were transfected with the promoter reporter plasmid pGL3p containing either allelic variant

222 n MMP3 promoter was cloned into a luciferase reporter plasmid, pMMP3, and its activity was examined f

223 factor kappaB (NF-kappaB) in vivo activation reporter plasmid pNF-kappaB-Luc.

224 s, and transient cotransfection studies with reporter plasmids (pNF-kappaB-Luc and pTK-PPREx3-Luc) an

225 sfected with an NF-kappaB in vivo activation reporter plasmid, pNF-kappaB-Luc.

226 K promoter/chloramphenicol acetyltransferase reporter plasmid (pPL32) with a consensus C/EBP-binding

227 ted chloramphenicol acetyl transferase (CAT) reporter plasmid (pRGC.FOS.CAT), containing a minimal FO

228 mulates SF1-dependent transcription of CYP17 reporter plasmids, promotes coactivator recruitment, and

229 Incorporation of a reporter plasmid "pseudogenome" was dependent on the pre

230 ozyme involved, we used a sod2 gene response reporter plasmid, pSODLUC-3340-I2E-C, capable of sensing

231 duced recovery of a transfected, replicating reporter plasmid (pSP189) in 293 cells but did not incre

232 Using a green fluorescent protein gene reporter plasmid regulated by an MEF-responsive promoter

233 (Q63L) along with the IL-1beta promoter-CAT reporter plasmid resulted in a marked increase in NF-kap

234 y acting as a Survivin antisense with a lacZ reporter plasmid resulted in loss of viability of HeLa c

235 c THP1 cells with lbc with a kappaB promoter reporter plasmid results in a marked increase in NF-kapp

236 active form of RhoA (Q63L) with the promoter reporter plasmid results in a marked increase in NF-kapp

237 prior to transfection of a linear, undamaged reporter plasmid revealed no reduction in NHEJ compared

238 Transient transfection assays of reporter plasmids revealed repressor sequences located b

239 noviocytes with p53 expression and hMMP13CAT reporter plasmids revealed that (i) hMMP13, another memb

240 transfection with promoter-linked luciferase reporter plasmids revealed that artemisinin strongly inh

241 vidual sites, in the context of a luciferase reporter plasmid, revealed that the NF1, Oct1, AP1, E4BP

242 nsfection assays of IL-6 promoter/luciferase reporter plasmids, Sar1 Ang II treatment induced IL-6 tr

243 Cotransfection of AKR1B10 with a luciferase reporter plasmid showed reduced retinoic acid response e

244 aining the NtcA binding sites in P(sigE)-gfp reporter plasmids showed that the sites contribute to no

245 the Mu SGS individually cloned into a pUC19 reporter plasmid, showed that the Mu SGS and the E. coli

246 nnot activate transcription of a kappaB site reporter plasmid, suggesting that it is a transcription

247 6 promoter in liver in vivo, and activated a reporter plasmid that contains five nuclear receptor 1 (

248 trate a novel application of a TBE-dependent reporter plasmid that could be used for the high-through

249 oquinone caused reactivation of a methylated reporter plasmid that was prevented by the addition of N

250 ructure affects ICL repair in nonreplicating reporter plasmids that contain a mispaired N(4)C-ethyl-N

251 Experiments with HIV gag reporter plasmids that contain inactivated INS-1 indicat

252 ffin cell-transfected CHGA 3'-UTR/luciferase reporter plasmid, the +87T allele associated with lower

253 ased on transient expression of a luciferase reporter plasmid, the DNA fragment encompassing the 3-bp

254 can inhibit the activity of a Wnt responsive reporter plasmid through its COOH-terminal domain.

255 in-STAT3 and induction of a c-fos luciferase reporter plasmid through OBRl, OBRs was without effect i

256 of lytic replication, orilyt, must be on the reporter plasmid to support activation of the late gene

257 Transfection with a reporter plasmid (TOPflash) was performed to assess whet

258 Reporter plasmid transfection and genomic run-on sequenc

259 To investigate the mechanism, luciferase reporter plasmids under the control of P1 [p(-1078/+27)1

260 nts were introduced into a CYP2C9/luciferase reporter plasmid using site-directed mutagenesis, and th

261 Conformational studies of reporter plasmids using confocal Raman spectra, S1 nucle

262 Transient transfection assays using reporter plasmids verified that mutations within the HRE

263 sponded similarly to transiently transfected reporter plasmids, verifying that this assay accurately

264 thermore, the ability of B-Myb to activate a reporter plasmid was enhanced by the cotransfection of c

265 docytes, expression of a Fas ligand promoter reporter plasmid was higher in HIVAN podocytes, indicati

266 When the reporter plasmid was inverted within the chromosome, swi

267 se construct or a hypoxia-inducible factor 1 reporter plasmid was not affected by addition of flavopi

268 ssayed by transient transfection assays with reporter plasmids was high in AGS cells but low in HeLa

269 n acid ceramidase promoter driven luciferase reporter plasmid, we demonstrated that CerS1 has no effe

270 Using a TCF-4 reporter plasmid, we directly demonstrate that Wnt signa

271 Using a Rev-dependent p24 reporter plasmid, we found that RBM14 depletion decrease

272 By using a luciferase reporter plasmid, we identified a 433-bp region spanning

273 Using a specially constructed reporter plasmid, we show here that this promoter (tadp)

274 By using luciferase reporter plasmids, we examined whether oncogenes that ac

275 al p21(waf1/cip1) promoter-driven luciferase reporter plasmids, we observed that perifosine activates

276 e promoter elements cloned into a luciferase reporter plasmid were analyzed to determine the ability

277 a retinoic acid response element (RARE)-luc reporter plasmid were treated with different concentrati

278 In all, 40 different SERCA1 reporter plasmids were constructed and tested.

279 Click beetle luciferase (CBLuc) reporter plasmids were mixed with cationic or neutral MB

280 Human TH promoter haplotype/reporter plasmids were transfected into chromaffin cells

281 The transporter and reporter plasmids were transformed into E. coli strains

282 mutant strains harboring the transporter and reporter plasmids were uniformly induced across the popu

283 or glutamate prevented the translation of a reporter plasmid where bim-3'UTR mRNA sequence was clone

284 methylated and unmethylated pHrD-IRES-Luc, a reporter plasmid where the rDNA promoter drives lucifera

285 yeast cells carrying the beta-galactosidase reporter plasmid, which contains an ERR alpha-1-binding

286 induced transcriptional activation of a CRE reporter plasmid, which was inhibited by dominant negati

287 , and transcriptional activation of the AP-1 reporter plasmid, which was inhibited by dominant negati

288 Cells were transfected with luciferase reporter plasmids, which contained up to 1363 bp of the

289 inhibit expression from a beta-galactosidase reporter plasmid, while HSV type 1 vhs abolished reporte

290 to suppress the intracellular activity of a reporter plasmid with a preformed triple helix, likely d

291 over, cotransfection of the human involucrin reporter plasmid with C/EBPalpha increases promoter acti

292 Colocalization of a 2 micron reporter plasmid with Kip1p in close proximity to the sp

293 For that purpose, we constructed a reporter plasmid with the lux operon under control of th

294 denylation signal sequence in the luciferase reporter plasmid with the mda-7-ARE-3'-UTR renders the L

295 ection of a c-myc promoter-driven luciferase reporter plasmid with triplex-forming oligonucleotides t

296 of the pG13-luc, PUMA-luc, and p21/WAF1-luc reporter plasmids with reduction in the protein levels o

297 f pDNA to shuttle proteins by re-engineering reporter plasmids with shuttle binding sequences enhance

298 fection of chloramphenicol acetyltransferase reporter plasmids with various sizes of truncated 5' ups

299 -S mutations on transcription of ybt genes, reporter plasmids with ybtP or psn promoters controlling

300 ly stimulated expression of an E2-responsive reporter plasmid yet was completely defective for growth