ライフサイエンスコーパス: reporter gene

1 hat is placed between the synthetic gene and reporter gene.

2 s along with the increased expression of the reporter gene.

3 heterodimers-mediated transactivation of GUS reporter gene.

4 atural introns previously tested in the same reporter gene.

5 e promoter, TREalb, for a firefly luciferase reporter gene.

6 HYDROGENASE1 promoter::luciferase (ADH1-LUC) reporter gene.

7 cells carrying the beta-glucuronidase intron reporter gene.

8 ite of an identical constitutively expressed reporter gene.

9 ally infected woman and a NanoLuc luciferase reporter gene.

10 imizing the intron insertion site within the reporter gene.

11 e family of fluorogenic probes with a single reporter gene.

12 3 to induce expression of a STAT3-responsive reporter gene.

13 nt basal translation level of the luciferase reporter gene.

14 ced expression of an Asc promoter-luciferase reporter gene.

15 or, which stimulates the expression of a GFP reporter gene.

16 racts the gene-silencing effect of H-NS on a reporter gene.

17 NIH-3T3 cells transfected with a beta-klotho reporter gene.

18 elements (AREs), were cloned downstream of a reporter gene.

19 e the NSs open reading frame replaced with a reporter gene.

20 g at the promoter, and the reactivation of a reporter gene.

21 tion, and activity of the NF-kappaB-specific reporter gene.

22 implex virus type 1 thymidine kinase (hsvTK) reporter genes.

23 reactivation of transposable element-driven reporter genes.

24 rotransposon in P3 reduced expression of the reporter genes.

25 hmark' vector titres are achieved with inert reporter genes.

26 either the yeast Gal4 or firefly luciferase reporter genes.

27 ence, bioluminescence imaging, and human PET reporter genes.

28 uses expressing each of six commonly used RV reporter genes.

29 express the green fluorescent protein (GFP) reporter gene (abbreviated as G in virus designations) a

30 conditional hair cell-specific gene deletion/reporter gene activation in the inner ear.

31 through Cre recombinase-mediated fluorescent reporter gene activation only in Stra8-expressing cells,

32 e Gfi1(Cre) mice, both for gene deletion and reporter gene activation, these data are significant and

33 l MRTF/SRF inhibitor, markedly decreased SRF reporter gene activity and showed a greater inhibitory e

34 , this can be effectively distinguished from reporter gene activity by the combination of the WM and

35 In the absence of Msi1 and miR130a and -206, reporter gene activity decreased, indicating that Msi1 e

36 viral latency locus showed high, persistent reporter gene activity in non-neuronal cells while an in

37 o, gga-miR-429 directly repressed luciferase reporter gene activity via binding to 3' untranslated re

38 2 inhibitors on TGF-beta1-induced migration, reporter gene activity, and Smad activation.

39 o suppress TGF-beta1-induced cell migration, reporter gene activity, and Smad3 activation.

40 approximately 2-fold increase in luciferase reporter gene activity.

41 In addition, the use of reporter genes allows FACS-purification and tracking of

42 in situ hybridization experiments, promoter-reporter gene analyses, and ZmSUT1 localization studies

43 in glucose-depleted conditions, and in vivo reporter gene analysis indicated reduced expression of t

44 es of CRM function undetected by traditional reporter gene analysis.

45 of a secreted placental alkaline phosphatase reporter gene and accumulation of (3)H-cAMP, we examined

46 vity from the NtPDR1 promoter in situ with a reporter gene and found that, although NtPDR1 expression

47 1848 reduced LRH-1-dependent expression of a reporter gene and in cells that endogenously express LRH

48 Reporter gene and in silico transcription factor binding

49 onally synergize with FKBP51, as revealed by reporter gene and protein association analyses.

50 cting specific hybridoma cells with aequorin reporter gene and the bioluminescence activities of stab

51 The promoter was fused with gusA reporter gene and was expressed in Arabidopsis and rice

52 required for transcription of both chimeric reporter genes and authentic chromosomal Rap1 enhancer-c

53 ciferase (Fluc) or Gaussia luciferase (Gluc) reporter genes and injected in isolated goat interverteb

54 atory effect of HBx both on extrachromosomal reporter genes and on hepatitis B virus transcription.

55 of-concept studies using overexpression with reporter genes and SOCS1-deficient mice.

56 causes DNA hypermethylation and silencing of reporter genes and some endogenous genes.

57 ad3, Smad-dependent activity of a luciferase reporter gene, and cell migration.

58 evels when fused to a transfected luciferase reporter gene, and Elavl1a binds the gata1 3'-UTR sequen

59 tations; expression of foreign, modified, or reporter genes; and even targeted gene disruptions.

60 We show that mRNA half-lives for a reporter gene are increased in both fast and slow Pol II

61 n, target bacteria become identifiable since reporter genes are expressed from the engineered phage g

62 We found that reporter genes are expressed to higher levels from the N

63 decreased the activity of two p53-dependent reporter genes as well as the expression of p53 target g

64 antioxidant response element beta lactamase reporter gene assay (ARE-bla), which identifies chemical

65 w up on this study, a commercially available reporter gene assay (GeneBLAzer PPARgamma1 non-DA Assay,

66 nstream gene Hes1 promoter-driven luciferase reporter gene assay and Western blotting showed that rec

67 A dioxin-responsive luciferase reporter gene assay confirmed that the CYP1A4 inductions

68 rGHI) was examined using a narG-lip (lipase) reporter gene assay in vivo.

69 ve stress using antioxidant response element reporter gene assay models and big data.

70 By employing a pregnane X receptor (PXR) reporter gene assay to prioritize compounds for further

71 is a highly potent partial FXR agonist in a reporter gene assay with an EC50 value of 8 +/- 3 nM and

72 A fragment-based screening, reporter gene assay, and pharmacophore search were utili

73 d potent transcriptional activities in a VDR reporter gene assay, and significantly ameliorated cardi

74 llular localization of RIP1 was monitored by reporter gene assay, immunofluorescent staining, and Wes

75 the hit compound, identified in a NF-kappaB reporter gene assay, led to compound 9b, exhibiting a ce

76 Using a reporter gene assay, we identified novel mutations, PB2

77 human GR were investigated using luciferase reporter gene assay.

78 monstrated regulating enhancer activity in a reporter gene assay.

79 luciferase activity measured by a luciferase reporter gene assay.

80 ter sensitivity as compared to a traditional reporter gene assay.

81 Mechanistic data from luciferase reporter-gene assay revealed that the anti-inflammatory

82 plements investigated by biological in vitro reporter gene assays (RGAs).

83 iated, and verified, using H3K27ac ChIP-seq, reporter gene assays and CRISPR-mediated activation, tha

84 ithin transcription factor binding sites and reporter gene assays confirmed that they affect gene exp

85 tions in clock genes, RNA-seq, ChIP-seq, and reporter gene assays coupled with measurements of DNA-pr

86 Likewise, reporter gene assays demonstrated significantly lower GU

87 Promoter-driven reporter gene assays demonstrated that IFI35 overexpress

88 ChIP and reporter gene assays demonstrated that the -82 kb HRE re

89 ative regulators identified were analysed in reporter gene assays in cells and in chick embryos.

90 ied on selected TGF-beta target genes and by reporter gene assays in multiple cell lines.

91 lar analyses by gene expression analysis and reporter gene assays indicated an effect of rs385076 on

92 Transcriptome sequencing (RNA-seq) and reporter gene assays may be useful for testing engineere

93 Reporter gene assays revealed cyclin-dependent kinase 3

94 Notably, reporter gene assays revealed that both naturally occurr

95 ) to DLCs in vitro via the use of luciferase reporter gene assays using COS-7 cells transfected with

96 MTHFR promoter region by means of luciferase reporter gene assays using human umbilical vein endothel

97 ndocrine disruption effects (transcriptional-reporter gene assays) were checked in bottled water extr

98 ms underlying the induction of IL-31, EMSAs, reporter gene assays, and small interfering RNA-based si

99 As shown in cell-based dual-luciferase reporter gene assays, functional interaction occurred be

100 Using multiple luciferase reporter gene assays, we could demonstrate that editing

101 supershift EMSA, ChIP, re-ChIP, and promoter-reporter gene assays, we demonstrate that the STAT1 and

102 ied proteins, surface plasmon resonance, and reporter gene assays, we discovered that human Cerberus

103 Using reporter gene assays, we show that the response of hASH1

104 oinformatic target prediction and luciferase reporter gene assays.

105 47 like ETS transcription factor 5 (ELF5) in reporter gene assays.

106 ing 5-LO and confirmed direct interaction by reporter gene assays.

107 ts from these regions directed expression in reporter gene assays.

108 anscript, which was further confirmed in NMD reporter gene assays.

109 lead risk variant region were analyzed with reporter gene assays.

110 However, reporter-gene assays, impedance-based assays with a sele

111 ta set, which traced the expression level of reporter genes at single-cell resolution on a nearly con

112 We also present a firefly luciferase (FLuc) reporter gene based molecular biosensor (ARE-FLuc) to me

113 However, existing MRI reporter genes based on metalloproteins or chemical exch

114 C4 protein by 2.2-fold and the activity of a reporter gene bearing the 3'-untranslated region (UTR) o

115 eported that an H5N1 virus bearing the Venus reporter gene became more pathogenic to mice and that it

116 relate with the level of derepression of the reporter genes between the two had6 alleles.

117 duced atrophy and activated a STAT-dependent reporter gene but not reporter genes dependent on SMAD,

118 for DNA double-strand breaks on the GFP-Pem1 reporter gene by homologous recombination, the persisten

119 The activation of reporter genes by artificial fusion of Mediator subunits

120 R-loop formation by synonymous changes in a reporter gene can lower mutation rate by >80%.

121 pha (the alpha complementing region of lacZ) reporter gene carried by an HIV-1 vector that replicates

122 Nevertheless, a reporter gene cassette inserted into the vector flanked

123 An independent reporter gene cassette located in an intergenic region r

124 no ability to activate transcription of the reporter gene CDKN1A, and in situ subcellular fractionat

125 ctionation approach, a downscaled luciferase reporter gene cell-based anti-AR-CALUX assay and LC-HRMS

126 es the translational ability of a luciferase reporter gene coding sequence when it is preceded by mul

127 Transient expression of a carboxyl-terminal reporter gene construct directed SaB4H to the endoplasmi

128 While employing reporter genes constructed with inducible promoters and

129 s has applications in vaccine production and reporter gene construction.

130 vation assays using full-length RXRalpha and reporter gene constructs (RXRE-Luc) transfected into COS

131 Analysis of reporter gene constructs revealed a functional cAMP resp

132 the CREB-binding site was demonstrated with reporter gene constructs that were induced by CREB activ

133 regulation, was investigated using promoter-reporter gene constructs with and without retrotransposo

134 Furthermore, the expression of a luciferase reporter gene containing the 3'-UTR of CYP2C9 and the en

135 e performed chromatin immunoprecipitation on reporter genes containing these elements in different em

136 opoiesis and by doing so validate the use of reporter gene-coupled enhancers as probes to gain insigh

137 show that human EC cells efficiently express reporter genes delivered by vectors based on human immun

138 long-term knockdown of a corneal epithelial reporter gene, demonstrating gene disruption via NHEJ in

139 nd the proteins Mre11 and Esc2 can silence a reporter gene dependent on the Sir, as well as on other

140 vated a STAT-dependent reporter gene but not reporter genes dependent on SMAD, FOXO, C/EBP, NF-kappaB

141 A previous study in D. melanogaster used a reporter gene driven by a testis-specific promoter to sh

142 AGL1 harboring the beta-glucuronidase (GUS) reporter gene driven by the cauliflower mosaic virus 35S

143 ing for altered expression of the luciferase reporter gene driven by the promoter from the heat-induc

144 iscosoma sp. red fluorescent protein (DsRed) reporter genes driven by either CaMV35S or intron-interr

145 Previous work shows that expression of reporter genes driven by testis-specific promoters is co

146 Induction of reporter genes, driven by truncated Ifit1 promoters, ide

147 of silencing of a dominant selectable kanMX reporter gene embedded within fission yeast centromeric

148 ransformation markers, fluorescent proteins, reporter genes, epitope tagged proteins, and even therap

149 H2.35 cells expressing an estrogen receptor reporter gene, estrogen receptor 1, and/or PGC1A/B.

150 We also show that linked reporter genes exhibit coordinated bursting profiles whe

151 eport comprehensive ChIP-Seq, transgenic and reporter gene experimental data that have allowed us to

152 ioned vectors, thereby reducing the level of reporter gene expression after transduction into target

153 This CpG island region was found to repress reporter gene expression and bind the Polycomb group pro

154 ha- and IL-1beta-induced NF-kappaB-dependent reporter gene expression and the transcription and produ

155 targeted DNA capture with a high-throughput reporter gene expression assay.

156 n exhibited unaltered levels of enhanced GFP reporter gene expression at early times after delivery t

157 aluate the activation of p21 promoter-driven reporter gene expression by in vitro confocal fluorescen

158 l heterologous RNA tethering assays in which reporter gene expression depended on interactions betwee

159 wild-type AAV2 (wtAAV2) replication but also reporter gene expression from both single-stranded and d

160 o-2 cells and the ability of zinc to repress reporter gene expression from corresponding promoter-rep

161 hat the ICP4 locus cassette permitted robust reporter gene expression in a diversity of neurons follo

162 , we used quantitative PCR and also analyzed reporter gene expression in a mouse line carrying a cons

163 Moreover, gar enhancers drive reporter gene expression in both the wrist and digits of

164 urther, we show that the Vcan enhancer drove reporter gene expression in endocardial lineages in a TB

165 Both elements direct reporter gene expression in Schwann cells and are respon

166 15 DHSs from pha-4, icl-1, and ceh-13 drove reporter gene expression in transgenic C. elegans Overal

167 ere non-coding DNA from invertebrates drives reporter gene expression in transgenic vertebrates in pa

168 The reporter gene expression level was confirmed via immunob

169 Differences in reporter gene expression levels from the NP and GPC loci

170 A dramatic drop of reporter gene expression of the oxytocin exon 1-intron-e

171 Further reporter gene expression suggested that variant -842C-66

172 , and rs164390 are associated with increased reporter gene expression through binding of transcriptio

173 WT1 regulates reporter gene expression through interaction with 3' UTR

174 rupt the ability of these enhancers to drive reporter gene expression to hypothalamic POMC neurons in

175 We have used imaging of reporter gene expression to track transcription in livin

176 when comparing single modified mRNAs) higher reporter gene expression upon transfection into cell lin

177 The cell lineage specificity of reporter gene expression was confirmed by demonstration

178 ith human PBMCs or hematopoietic stem cells, reporter gene expression was predominantly detected in l

179 Enhanced green fluorescent protein (EGFP) reporter gene expression was quantified and Cx32 express

180 We uncover a H1 enhancer sufficient to drive reporter gene expression within the crNCCs of the distal

181 d assays, including SMAD-mediated luciferase reporter gene expression, and differentiation of a multi

182 to efficiently suppress NF-kappaB-dependent reporter gene expression, in contrast with the vaccine s

183 n, determined by promoter-beta-glucuronidase reporter gene expression, is associated with vascular ti

184 inhibited endogenous Sost transcription and reporter gene expression, respectively.

185 otides, using their inferred contribution to reporter gene expression.

186 ctivating hypoxia response element-dependent reporter gene expression.

187 easy monitoring of the tumor growth based on reporter gene expression.

188 onse element (GRE) and exclusively increased reporter-gene expression.

189 ate mapping with a thymidine kinase (sr39tk) reporter gene for cell detection by positron emission to

190 We then develop reporter genes for each of these responses that will ena

191 Plasmids were generated carrying reporter genes for fluorescence, bioluminescence imaging

192 n alternative class of sensitive, metal-free reporter genes for non-invasive imaging.

193 erization of nine antibiotic cassettes, four reporter genes, four promoters, and a ribozyme-based ins

194 approaches to evaluate expression levels of reporter genes from the nucleoprotein (NP) and glycoprot

195 ells, trigger changes in the expression of a reporter gene fused to representative ZTP riboswitches i

196 ding the transcription start site (TSS) of a reporter gene fusion in Arabidopsis thaliana The intron

197 Using reporter gene fusions and transcriptomics, here we repor

198 ransgenic plants expressing either ProCgNIN::reporter gene fusions or CgNIN RNAi constructs.

199 rapeseed lines expressing Bn-FAE1.1 promoter:reporter gene fusions revealed a strong expression in th

200 Using reporter gene fusions to QS target genes, we found that

201 e expression of CsLOB1 and CsSWEET1 promoter reporter gene fusions when coexpressed in citrus or Nico

202 Expression of the reporter genes (GFP and YFP) was also confirmed using re

203 technological advances in microfluidics and reporter genes have improved this scenario.

204 Serial in vivo bioluminescence reporter gene imaging in mice with tMCAO revealed that b

205 l manganese-enhanced MRI and bioluminescence reporter gene imaging were applied to follow myocardial

206 enetic lineage tracing, specific-fluorescent reporter genes, immunofluorescence, high-resolution conf

207 an enhanced green fluorescent protein (EGFP) reporter gene in a panel of 12 organs after IP injection

208 vate the expression of a pathogen-responsive reporter gene in Arabidopsis (Arabidopsis thaliana).

209 of the pathogen-responsive CaBP22(-333)::GUS reporter gene in Arabidopsis thaliana (Arabidopsis), 33

210 SPFMV gene products coagroinfiltrated with a reporter gene in Nicotiana benthamiana revealed that P1N

211 ogy based on the conditional activation of a reporter gene in response to sequence errors occurring a

212 b promoter supports enhanced expression of a reporter gene in sphk2(MZ) embryos compared to wildtype

213 This strategy prevents expression of the reporter gene in the transfected cells but permits its e

214 chromatin structure and loss of silencing of reporter genes in constitutive heterochromatin regions.

215 erences in expression levels of gus and egfp reporter genes in forward orientation and rfp in reverse

216 logical staining confirmed the expression of reporter genes in glial cells as well as astrocytes.

217 ng for targeted integration of human imaging reporter genes in human embryonic stem cells for long-te

218 The ability to express exogenous reporter genes in intact, externally developing embryos,

219 s (ULG8), which we have leveraged to express reporter genes in mature male and female gametocytes.

220 By targeting the c-kit locus with multiple reporter genes in mice, we find that c-kit expression ra

221 Expression of these reporter genes in transient assays as well as in T1 stab

222 lements and it was able to transactivate the reporter genes in yeast.

223 sues, and analyzed the expression of several reporter genes, including ProHY5:HY5-GFP and Pro35S:CFP-

224 arted by the 5 UTR can be transferred onto a reporter gene, indicative that the 5 UTR can solely driv

225 locus 4) and Skt(Gt) (Sickle tail) are lacZ reporter gene integrations into the same locus on mouse

226 s contain an antisense-oriented promoter and reporter gene interrupted by a sense-oriented intron fro

227 We succeeded in transferring a GFP reporter gene into adult hematopoietic stem cells in viv

228 We show that insertion of a luciferase reporter gene into the endogenous tyrosine hydroxylase (

229 to induce stable expression of human imaging reporter genes into the safe-harbor locus adeno-associat

230 tandem duplication of an unrelated synthetic reporter gene is overactive (2.3- to 5.1-fold) at all si

231 pression of the bacterial beta-galactosidase reporter gene (lacZ) in the vector used for the Knockout

232 Surprisingly, using a reporter gene linked to activation of the MAPK substrate

233 g within the Shh second intron activates the reporter gene located at distances of hundreds of kiloba

234 We utilized a reporter gene (mURA3) integrated adjacent to the leftmos

235 that a small ( approximately 500-nucleotide) reporter gene (NanoLuc; Promega) is very stable and caus

236 main responsive to the chemical to control a reporter gene necessary for survival under selective con

237 n neuroscience, it is now routine to express reporter genes, neuronal activity indicators, and opsins

238 the lacZ gene showed that activation of the reporter gene occurs in response to low copper condition

239 Silencing of flanking reporter genes occurs at all sites, but the spread of si

240 We created a library of circuits with two reporter genes, one constitutive and the other inducible

241 llators using a mouse model expressing three reporter genes: one labeling alpha cells, one specific f

242 ent on the cell type or species, the type of reporter gene, or the method of transfection.

243 ng that promoter and derivatives between two reporter genes oriented head to head, we show that the T

244 , supported ligand-dependent activation of a reporter gene over a broad spectrum of lengths from 3 to

245 mechanism of action of each of four factors (reporter gene, p160 coactivator TIF2, and two pharmaceut

246 with three plasmids carrying a fluorescence reporter gene (pEF-GFP with the EF1 alpha promoter, pUB-

247 The reporter genes permit detailed and dynamic visualisation

248 ail target enhancers were attached to an MS2 reporter gene, permitting detection of nascent transcrip

249 ges were monitored using a novel fluorescent reporter gene, pMitoTimer, that allows assessment of mit

250 revealed to strongly express a fluorescence reporter gene primarily in integuments, anther tapetum,

251 enhancers positioned downstream of synthetic reporter genes produce transcriptional bursts with simil

252 istinct opposite methylation profiles on two reporter gene promoters.

253 hieve a 110-fold increase in expression of a reporter gene relative to non-replicating controls.

254 A comparison of different reporter gene-reporter probe systems for imaging of T ce

255 venous injection of rAAV2/9 carrying an eGFP-reporter gene results in binaural transduction of inner

256 eplicons with CpGs and UpAs removed from the reporter gene showed 100-fold greater luminescence.

257 The KAK promoter fused with a reporter gene showed activity in the vascular cambium, p

258 ibited serum response factor (SRF)-dependent reporter gene (SRE-LUC) activity and mRNA expression of

259 A collection of cat reporter-gene strains containing mutant derivatives of i

260 diated by the cAMP response element (CRE) in reporter gene studies (10-fold vs. control; n = 4 transf

261 In contrast, reporter gene studies have identified >60 Bcd-dependent

262 In reporter gene studies, we observe that FCRL4 expression

263 At the cellular level, pCkx3::YFP reporter-gene studies revealed that the Ckx3 promoter is

264 xpression were identified using a transgenic reporter gene system subdividing the B cell progenitors

265 Using a reporter gene system, we showed that Msi1 competes with

266 Therefore, we focused on human reporter gene systems that have the potential for transl

267 on, angiogenesis, and even the assessment of reporter gene technologies.

268 ielded >10-fold higher expression of the GFP reporter gene than the mutant U79 promoter with abrogate

269 R) and promotes expression of a heterologous reporter gene that carries PPM1D 3'-UTR in a dose-depend

270 Tagging donor sequences with reporter genes that can be subsequently excised improves

271 M22alpha locus combined with Cre-activatable reporter genes that were integrated into the ROSA26 locu

272 Here, using a single endogenous reporter gene, the X-chromosomal disease gene encoding h

273 moted T lymphocyte-specific transcription of reporter genes throughout T cell development; however, i

274 Here the authors use a mitochondrial reporter gene to demonstrate the occurrence of mitophagy

275 omoter directed strong expression of the GUS reporter gene to fruits and developing floral organs in

276 t mouse strain expressing the bacterial LacZ reporter gene to monitor the physiological expression pa

277 s the transcription status of the downstream reporter gene to provide a rapid and facile readout of t

278 We used destabilized reporter genes to determine spatial expression patterns.

279 with RNAi, we employed the stably expressed reporter genes to develop efficient siRNA delivery proto

280 rry plasmid DNA (pDNA, containing luciferase reporter gene) to form a liposomal-plasmid DNA (LpDNA) c

281 -retinoid X receptor (RXR) complex and drove reporter gene transcription in response to 1,25-dihydrox

282 the Smc5/6 complex enhances extrachromosomal reporter gene transcription in the absence of HBx, resto

283 at the mutant-type 439 A-SNP-pGL3 in driving reporter gene transcription is significantly higher than

284 nd herbicide (aad1) resistance, and a phiyfp reporter gene using a single ZMUbi1 bidirectional promot

285 We also discuss employing NIS as a reporter gene using viral vectors and stem cells in imag

286 Gene expression was not blocked when the reporter gene was delivered by microbombardment.

287 Fluorescence signal from the reporter gene was detected a few hours after transfectio

288 of the Sleeping Beauty transposon, the lacZ reporter gene was dispersed throughout the Shh region to

289 en a leaf of this mutant was wounded, the JA reporter gene was expressed in distal leaves.

290 became more pathogenic to mice and that its reporter gene was more highly expressed and more stably

291 virus), became more lethal to mice, and the reporter gene was stably maintained after mouse adaptati

292 s relying on green fluorescent protein (GFP) reporter genes, we found that targeted mutagenesis by CR

293 carrying the green fluorescent protein (GFP) reporter gene were intravenously administered to fetal a

294 resulted in higher expression levels of the reporter genes, whereas the presence of LINE in P2 or gy

295 ported that an H5N1 virus carrying the Venus reporter gene, which was inserted into the NS gene segme

296 nalized virus remained capable of expressing reporter genes while viral replication was blocked.

297 ly 14,000 E. coli strains, each expressing a reporter gene with a unique 5' architecture.

298 on of specific cell types by combining a PET reporter gene with Cre-dependent activation that can be

299 expression of the activity-dependent fosGFP reporter gene, would be preferentially activated by whis

300 s of real-time PCR for the neuronal activity reporter gene zif268.