ライフサイエンスコーパス: firefly luciferase

1 ally induced aggregation of non-glycosylated firefly luciferase.

2 transgene that expresses both HPV-16 E7 and firefly luciferase.

3 for subsequent bioluminescent reaction with firefly luciferase.

4 ) convert adenine to ATP for quantitation by firefly luciferase.

5 T cells and tumor cells modified to express firefly luciferase.

6 terminal and COOH terminal fragments of the firefly luciferase.

7 el substrates malate dehydrogenase (MDH) and firefly luciferase.

8 echanism of the anesthetic inhibition of the firefly luciferase.

9 rescence of a Ca(2+) dye and luminescence of firefly luciferase.

10 erase gene based on the crystal structure of firefly luciferase.

11 pGRE.Luc drives the expression of firefly luciferase.

12 signed to alter the substrate specificity of firefly luciferase.

13 translation of PTEN and a heterologous gene firefly luciferase.

14 M175/18f virus genome with sequence encoding firefly luciferase.

15 ld be detected by bioluminescence imaging of firefly luciferase.

16 tation of pancreatic cancer cells expressing firefly luciferase.

17 ments containing an E-box and E'-box driving firefly luciferase.

18 ted to adenosine triphosphate and coupled to firefly luciferase.

19 ed to express a green fluorescent protein or firefly luciferase.

20 lding efficiency of the model client protein firefly luciferase.

21 a bioluminescent response in the presence of firefly luciferase.

22 ne myeloma cells stably transfected with the firefly luciferase (5TGM1/luc) were inoculated from tail

23 Within the highest expressor clone, the firefly luciferase activity decreased progressively from

24 elongation errors by monitoring the level of firefly luciferase activity from a mutant allele inactiv

25 cation, produced dose-dependent decreases in firefly luciferase activity that correlated with changes

26 Firefly luciferase activity was maximally rescued by tre

27 uminescence imaging of CD1 promoter-directed firefly luciferase activity), and progression to cell di

28 tions and ranged from 0.01 to 4% of the full firefly luciferase activity.

29 us carrying cytomegalovirus promoter-driving firefly luciferase (Ad-CMV-Fluc).

30 left thoracotomy with adenovirus-expressing firefly luciferase (Ad-CMV-Fluc; n=30).

31 Firefly luciferase adenylates and oxidizes d-luciferin t

32 en complementary non-functional fragments of firefly luciferase allows direct detection of IP(3) in p

33 In conclusion, the split firefly luciferase-alphaSYN complementation assay will i

34 struct containing a gamma promoter linked to firefly luciferase and a beta promoter linked to renilla

35 izing two different split-protein reporters, firefly luciferase and beta-lactamase, while also testin

36 Two independent screens, firefly luciferase and CFTR-mediated transepithelial chl

37 inhibitor of metalloproteinases 3 (TIMP3) or firefly luciferase and designated them rQT3 and rQLuc, r

38 a double-fusion reporter gene consisting of firefly luciferase and enhanced GFP.

39 background) that constitutively express both firefly luciferase and enhanced green fluorescence prote

40 ng double-fusion reporter gene consisting of firefly luciferase and enhanced green fluorescent protei

41 asts were lentivirally transduced to express firefly luciferase and green fluorescent protein (GFP).

42 ts were genetically modified to express both firefly luciferase and green fluorescent protein (mH9c2)

43 FVB mice with a beta-actin promoter driving firefly luciferase and green fluorescent protein double

44 by sectioning mouse hearts (n=40) expressing firefly luciferase and green fluorescent protein into sl

45 ell line transduced with a vector expressing firefly luciferase and green fluorescent protein were tr

46 ransgenic mice, which constitutively express firefly luciferase and green fluorescent protein.

47 sion (TF; monomeric red fluorescent protein, firefly luciferase and herpes simplex virus thymidine ki

48 lar bioenergetics and the signal obtained by firefly luciferase and human sodium-iodide symporter lab

49 he hydrophobic substrate binding site within firefly luciferase and inhibit its activity.

50 ltures in 96-well plates were incubated with firefly luciferase and luciferin for the ATP assay or lo

51 Model substrates firefly luciferase and malate dehydrogenase form strong

52 ransduced with an ubiquitin promoter driving firefly luciferase and monomeric red fluorescence protei

53 ally brighter signals from deep tissues than firefly luciferase and other bioluminescent proteins.

54 conformational changes in two model systems: firefly luciferase and the bovine TRiC complex.

55 attached to the C-terminal fragment of split-firefly luciferase and the coiled-coil Fos, which is spe

56 i.v. administration of Ad vectors expressing firefly luciferase and to retarget virus to hepatic colo

57 We characterized this system with firefly luciferase and went on to apply it to members of

58 ntiviral vectors encoding the reporter genes firefly-luciferase and murine interleukin-10 were admini

59 ontaining monomeric red fluorescent protein, firefly luciferase, and herpes simplex virus thymidine k

60 mes that also includes acyl-CoA synthetases, firefly luciferase, and nonribosomal peptide synthetases

61 nterfering RNA (siRNA) against a model gene, firefly luciferase, and PEI25 or PEI87 afforded a 77% an

62 cludes other acyl- and aryl-CoA synthetases, firefly luciferase, and the adenylation domains of the m

63 of Sindbis virus were engineered to express firefly luciferase, and the Xenogen IVIS system was used

64 knockin mouse were genetically modified with firefly luciferase (APL(luc)) to allow tracking by biolu

65 f the C-terminal domain and conserved in all firefly luciferases, are each essential for only one of

66 ect effect on the FLuc reporter, implicating firefly luciferase as a molecular target of PTC124.

67 We developed a destabilized firefly luciferase as a reporter for rhythmic promoter a

68 introduction of green fluorescent protein or firefly luciferase as fusions with replicase proteins.

69 Using firefly luciferase as reporter gene, additional experime

70 has Renilla luciferase as the 5' cistron and firefly luciferase as the 3' cistron, has been found to

71 ach of chemiluminescence (CL) detection with firefly luciferase as the probe.

72 l promoter partial deletion constructs using firefly luciferase as the reporter gene.

73 The traditional firefly luciferase assays measure the ATP release as a s

74 ord chemiluminescence (CL) from an optimized firefly luciferase-ATP bioluminescence reaction system,

75 The reporter system uses a firefly luciferase-based protein fragment complementatio

76 the bioluminescent fusion reporters beta-cat firefly luciferase (beta-cat-FLuc) and beta-cat click be

77 l BRET-FRET energy transfer process based on firefly luciferase bioluminescence can be employed to as

78 ransducer also controls bioluminescence from firefly luciferase by affecting solution pH.

79 aK, but was unable to stimulate refolding of firefly luciferase by DnaK, and inhibited refolding by D

80 e molecules are hydrolyzed to substrates for firefly luciferase by the enzyme fatty acid amide hydrol

81 Firefly luciferase can be mutated to accept and utilize

82 Herein, we show that mutants of firefly luciferase can discriminate between natural and

83 Firefly luciferase catalyzes the highly efficient emissi

84 Firefly luciferase catalyzes two sequential partial reac

85 We demonstrate that firefly luciferase cDNA can be efficiently delivered dow

86 sHSPs with three different model substrates, firefly luciferase, citrate synthase, and malate dehydro

87 Lesions were positioned within the firefly luciferase coding region, transformed into bacte

88 new crystal structures of the product-bound firefly luciferase combined with the previously determin

89 Therefore, we optimized a firefly luciferase complementation assay to screen again

90 We developed a split firefly luciferase complementation system to visualize o

91 K3beta and CK1alpha reporter (BGCR) based on firefly luciferase complementation.

92 Analogues of dihydrofolate reductase and firefly luciferase containing glycosylated amino acids a

93 luciferase indicator vector together with a firefly luciferase control vector.

94 rine CT26 colorectal cancer cells expressing firefly luciferase (CT26-Luc), and the ACE-CD vector was

95 different from the results obtained by free firefly luciferase detection.

96 Surprisingly, heat-denaturing firefly luciferase did not interact significantly with T

97 elii YM strain (PyLuc) that stably expresses firefly luciferase driven by a constitutive promoter.

98 gment complementation associated recovery of firefly luciferase enzyme activity with intact firefly l

99 based on the expression of a variant of the firefly luciferase enzyme in vivo and measurement of lum

100 lementation, splicing, and activation of the firefly luciferase enzyme.

101 nd shown to be a competent substrate for the firefly luciferase enzyme.

102 nt protein, as well as bioluminescence using Firefly luciferase enzyme/protein (FL).

103 Using a firefly luciferase-expressing adenovirus and in vivo bio

104 Tumors generated by implantation of firefly luciferase-expressing B16-F10 melanoma cells exh

105 ion of the biophotonic signal of established firefly luciferase-expressing Burkitt lymphoma xenograft

106 on henipavirus pathogenesis, we generated a firefly luciferase-expressing NiV and monitored virus re

107 selective accumulation of i.v. administered firefly luciferase-expressing T cells in intracerebral x

108 ransfecting mutant HIV clones expressing the firefly luciferase expression gene with a WT clone expre

109 o the GRE was demonstrated by an increase in firefly luciferase expression in transfected cells treat

110 odification was used to engineer an enhanced firefly luciferase (ffLuc) vector.

111 yc activity in living subjects using a split Firefly luciferase (FL) complementation strategy to dete

112 etween the three luciferases [mtfl, tfl, and firefly luciferase (fl)] both in cell culture and in liv

113 simplex virus type I thymidine kinase [tk], firefly luciferase [fl], and Renilla luciferase [rl]) pl

114 s (SkMb), and fibroblasts (Fibro) expressing firefly luciferase (Fluc) and green fluorescence protein

115 ally implanted NPC-FL-sTRAIL expressing both firefly luciferase (Fluc) and S-TRAIL was shown to migra

116 very frequently use reporter enzymes such as firefly luciferase (FLuc) as indicators of target activi

117 g of mice infected with parasites expressing firefly luciferase (FLUC) driven by the SAG2D promoter,

118 noninvasively, we developed a chimeric EGFR-firefly luciferase (FLuc) fusion reporter to directly mo

119 The model uses a firefly luciferase (fLUC) gene inserted by homologous re

120 VLA-4-negative MDA-MB-231/firefly luciferase (fluc) human breast tumor cells were

121 Here, we report new firefly luciferase (FLuc) inhibitors based on 5-benzyl-3

122 m cells (gADSCs) were transduced with either Firefly luciferase (Fluc) or Gaussia luciferase (Gluc) r

123 la luciferase (RLuc), beta-galactosidase and firefly luciferase (FLuc) ORFs linked in frame and separ

124 Because reaction of d-luciferin with firefly luciferase (fLuc) produces photons of sufficient

125 We also present a firefly luciferase (FLuc) reporter gene based molecular

126 LK1 confers MAPK specificity by activating a firefly luciferase (FLuc) reporter gene when the Ets-lik

127 diomyoblasts (3x10(6) to 5x10(5)) expressing firefly luciferase (Fluc) reporter gene.

128 its activity to an off-target effect on the Firefly luciferase (FLuc) reporter used in the developme

129 mouse model that constitutively expresses a firefly luciferase (FLuc) split reporter complementation

130 ed by beta-gal before it can be catalyzed by firefly luciferase (FLuc) to generate light.

131 or VEEV (subtype IC strain 3908) expressing firefly luciferase (fLUC) to simulate mosquito infection

132 nsgenic reporter mouse strain that expresses firefly luciferase (Fluc) under the regulatory control o

133 imaging reporter mice in which expression of firefly luciferase (FLuc) was placed under the control o

134 to synthesize d-luciferin, the substrate for firefly luciferase (Fluc), along with a novel set of ele

135 Firefly luciferase (FLuc), an ATP-dependent bioluminesce

136 r finding that d-luciferin, the substrate of firefly luciferase (fLuc), is a specific substrate of AB

137 tation biosensor based on optical imaging of Firefly luciferase (FLuc), to quantitatively image p53 s

138 Using EGFR-GFP-Rluc/firefly luciferase (Fluc)-DsRed2 glioma model, we show t

139 that elicit red-shifted bioluminescence with firefly luciferase (Fluc).

140 ic promoter virus expressing either a large, firefly luciferase (fLuc; 1,650 nucleotides), or small,

141 harge-coupled device camera, the analysis of firefly luciferase fragment complementation in transient

142 mbinations of nonoverlapping and overlapping firefly luciferase fragments that can be used for studyi

143 AdPSE-BC-luc, which expresses firefly luciferase from an enhanced prostate-specific an

144 ic islets (200 per recipient) expressing the firefly luciferase from FVB/NJ strain (H-2q) mice were t

145 binant CII proteins more efficiently protect firefly luciferase from insolubilization during heating

146 0.9% found from a previous qHTS against the firefly luciferase from Photinus pyralis (lucPpy).

147 sses a bioluminescent reporter consisting of firefly luciferase fused to a region of HIF that is suff

148 xpressing enhanced green fluorescent protein-firefly luciferase fusion protein (Ad-EGFPLuc).

149 novel transcriptionally coupled IkappaBalpha-firefly luciferase fusion reporter and characterized the

150 c mouse by fusing the GADD45beta promoter to firefly luciferase (Gadd45beta-luc).

151 uired for chlorophyll formation; and (2) the firefly luciferase gene (luc).

152 anking region was inserted upstream from the firefly luciferase gene and the chimeric construct was t

153 kinases using an HCV replicon expressing the firefly luciferase gene as a genetic reporter.

154 We identified different fragments of the firefly luciferase gene based on the crystal structure o

155 abidopsis thaliana (Col-0) line containing a firefly luciferase gene controlled by a promoter region

156 herpesvirus 68) was constructed to express a firefly luciferase gene driven by the viral M3 promoter

157 veloped a transgenic mouse model wherein the firefly luciferase gene expression was dependent on the

158 -based methodology for rapidly integrating a firefly luciferase gene in somatic cells under the contr

159 this end, the APP1 promoter was fused to the firefly luciferase gene in the C. neofor-mans GAL7:IPC1

160 transfected with a reporter comprised of the firefly luciferase gene interrupted by an abnormally spl

161 explants from transgenic mice containing the firefly luciferase gene luc controlled by the mPer1 prom

162 ed Dhc 16S rRNA gene fragment (Dhc*) and the firefly luciferase gene luc.

163 g the IFN-stimulated gene 56 promoter-driven firefly luciferase gene stably integrated in a TLR3-expr

164 we constructed reporter lines expressing the firefly luciferase gene under the control of the SAR-ind

165 nstructed a di-cistronic reporter in which a firefly luciferase gene was linked to a chloramphenicol

166 ation of an adenovirus vector containing the firefly luciferase gene was measured serially and noninv

167 ression of the coding region of the enhanced firefly luciferase gene were employed to identify region

168 Using a model siRNA targeting the firefly luciferase gene with subnanomolar IC50, we found

169 inoma cells were genetically modified with a firefly luciferase gene, and light emission was used for

170 c and Cfluc are the N and C fragments of the firefly luciferase gene, respectively): Nfluc (1-475)/Cf

171 uman genes and for 201 shRNAs derived from a firefly luciferase gene.

172 into functionally important residues in the firefly luciferase gene.

173 iral capsid sequences were replaced with the firefly luciferase gene.

174 N- and C-terminal fragments of firefly luciferase genes were fused with H2AX and MDC1 g

175 ic region was cloned between the Renilla and firefly luciferase genes, which acted as reporters of OR

176 stably express green fluorescent protein and firefly luciferase (GFP(+)/Luc(+)) were used for the tra

177 Firefly luciferase gives a stable luminescent signal tha

178 talysts (cysteamine) was used to encapsulate firefly luciferase, green and blue fluorescent proteins

179 using the human clusterin promoter fused to firefly luciferase (hCLUp-Luc).

180 72 glutamines fused to the N-terminal end of firefly luciferase (httQ72-Luc).

181 ct organisms, we engineered an IkappaB alpha-firefly luciferase (IkappaB alpha-FLuc) fusion reporter.

182 -invasive, repetitive Renilla luciferase and Firefly luciferase imaging, respectively.

183 translation of a downstream cistron encoding Firefly luciferase in a dicistronic expression vector.

184 the Sse1p mutants maintained heat-denatured firefly luciferase in a folding-competent state in vitro

185 scence imaging in transgenic mice expressing firefly luciferase in the brain.

186 to achieve specific and robust expression of firefly luciferase in the prostate glands of transgenic

187 , and Malpighian tubules compared with dsRNA firefly luciferase-injected control mosquitoes.

188 e-containing mRNA comprising codon-optimized firefly luciferase into stable LNPs.

189 Destabilized firefly luciferase is a good reporter of cell cycle posi

190 Firefly luciferase is homologous to fatty acyl-CoA synth

191 Firefly luciferase is roughly 100 times more efficient a

192 Firefly luciferase is the most widely used optical repor

193 by using dual-luciferase reporters, in which firefly luciferase is used as the retrotransposition ind

194 hat D-luciferin, the endogenous substrate of firefly luciferase, is a specific substrate for ABCG2.

195 ismate synthase (ICS1) promoter was fused to firefly luciferase (luc) and a homozygous transgenic lin

196 of human NoV, and rVSV-Luc-VP1, coexpressing firefly luciferase (Luc) and VP1 genes.

197 consensus sequence was sufficient to target firefly luciferase (LUC) for low protein accumulation eq

198 second construct was generated in which the firefly luciferase (Luc) gene was inserted in place of H

199 the red fluorescent protein (mCherry) or the firefly luciferase (Luc) genes are inserted into the RSV

200 d in transgenic mice containing an inducible firefly luciferase (luc) reporter gene under transcripti

201 melanogaster were individually fused to the firefly luciferase (luc) reporter gene.

202 ter mouse model that predominantly expresses firefly luciferase (luc2p) in the paw epidermis--the reg

203 rate/reporter bioluminescence imaging (Fluc: firefly luciferase-luciferin and Rluc: Renilla luciferas

204 The magnitude of bioluminescence from firefly luciferase measured in vivo correlated directly

205 e-fusion (TF) reporter gene that consists of firefly luciferase, monomeric red fluorescence protein,

206 ple-fusion reporter, fluc-mrfp-ttk (encoding firefly luciferase, monomeric red fluorescent protein, a

207 zacytidine treatment led to higher levels of firefly luciferase mRNA (RT-PCR) and protein (Western bl

208 represses the translation of non-adenylated firefly luciferase mRNAs and that mutations in two core

209 siRNA in skin was tested by co-delivering a firefly luciferase/mutant K6a bicistronic reporter const

210 ate-forming enzyme superfamily that includes firefly luciferase, nonribosomal peptide synthetases, an

211 and resolubilization of thermally denatured firefly luciferase occurred independently of NEF activit

212 n-replicating mammalian construct within the firefly luciferase open reading frame, or at the 5' or 3

213 Delivery studies with pDNA containing the firefly luciferase or beta-galactosidase reporter genes

214 t inhibited activation of MMTV attached to a firefly luciferase or beta-galactosidase reporter.

215 e (5' NTS) positioned upstream of either the firefly luciferase or green fluorescent protein coding s

216 (DF; enhanced green fluorescent protein and firefly luciferase) or triple fusion (TF; monomeric red

217 on-ribosomal peptide synthetases (NRPS), and firefly luciferase, perform two half-reactions in a ping

218 n HIV-1-derived lentiviral vector expressing firefly luciferase permitting the use of bioluminescence

219 Firefly luciferase produces light by converting substrat

220 ns in cells and living animals, we optimized firefly luciferase protein fragment complementation by s

221 erization state of each mutant using a split firefly luciferase protein fragment-assisted complementa

222 ansfected with nonoxidized mRNA encoding the firefly luciferase protein were cultured in the presence

223 Plasmodium falciparum strain expressing the firefly luciferase protein, we present a luminescence-ba

224 are monitored in cells stably expressing the firefly luciferase protein.

225 and intein-mediated reconstitution of split firefly luciferase proteins driven by the interaction of

226 Hence, we constructed biotinylated fused firefly luciferase proteins, immobilized the proteins on

227 A highly sensitive RAP2.6 promoter-firefly luciferase (RAP2.6-LUC) reporter line was develo

228 on proteins that could lead to split Renilla/firefly luciferase reporter complementation in the prese

229 ds carrying cytomegalovirus promoter driving firefly luciferase reporter gene (CMV-Fluc) and passaged

230 ation cassette, which amplifies AR-dependent firefly luciferase reporter gene activity, was injected

231 oying parasites with an integrated copy of a firefly luciferase reporter gene and a secondary flow cy

232 gnificantly reduce the expressions of both a firefly luciferase reporter gene and an ectopic MLH1 gen

233 inescent Arabidopsis plants that express the firefly luciferase reporter gene driven by the stress-re

234 Firefly luciferase reporter gene expression is driven by

235 ovirus enhancer (CMVe) strategy, to maximize firefly luciferase reporter gene expression.

236 th genome or a replicon (P/L) containing the firefly luciferase reporter gene in place of the capsid

237 Experiments using plasmid DNA containing the firefly luciferase reporter gene show that these complex

238 Remarkably, firefly luciferase reporter gene studies in the highly c

239 ow in transgenic mouse experiments using the firefly luciferase reporter gene that, despite relativel

240 ULTR1;2 promoter (2.2 kb) was fused with the firefly luciferase reporter gene to quantitatively repor

241 A firefly luciferase reporter gene under control of the Ad

242 screen using Arabidopsis plants carrying the firefly luciferase reporter gene under the control of th

243 iana mutants for deregulated expression of a firefly luciferase reporter gene under the control of th

244 onse element-incorporated promoter driving a firefly luciferase reporter gene.

245 iven by an inducible promoter, TREalb, for a firefly luciferase reporter gene.

246 mplified by PCR and linked to a promoterless firefly luciferase reporter gene.

247 iving expression of either the yeast Gal4 or firefly luciferase reporter genes.

248 lated region and regulated the expression of firefly luciferase reporter in a dose-dependent manner.

249 erformed with a bicistronic Renilla-HCV IRES-firefly luciferase reporter in Huh7 cells.

250 We used a codon-optimized firefly luciferase reporter initiated with AUG or each o

251 ng furans situated 2, 5 or 12 bps apart in a firefly luciferase reporter plasmid caused a decrease in

252 The rabbit Aldh1a1 promoter-firefly luciferase reporter transgene (-3519 to +43) was

253 e strain harboring a chromogranin A promoter/firefly luciferase reporter transgene.

254 Expression of a firefly luciferase reporter under control of the proxima

255 because this factor inhibits expression of a firefly luciferase reporter under the control of the BAG

256 bioluminescence imaging using a constitutive firefly luciferase reporter, while TGFbeta signaling in

257 ter and fragments of the promoter fused to a firefly luciferase reporter.

258 he human ubiquitin C promoter coupled to the firefly luciferase reporter.

259 the 5'-flanking region cloned upstream of a firefly-luciferase reporter were generated.

260 Using separate Renilla or Firefly luciferase reporters, we found that an estrogen

261 used with other split reporters (e.g., split firefly luciferase) should help to monitor different com

262 We hypothesized that the firefly luciferase substrate d-luciferin and its analogs

263 e (WIN1), a protein phosphatase (WIN2) and a firefly luciferase superfamily protein (WIN3).

264 1 might belong to the acyl adenylate-forming firefly luciferase superfamily.

265 st created a mutant (mtfl) of a thermostable firefly luciferase (tfl) bearing the peroxisome localiza

266 For the modified firefly luciferases, the effect of these substitutions o

267 We delivered mRNA encoding firefly luciferase to colons of healthy C57BL/6 mice.

268 estern Reserve vaccinia virus that expresses firefly luciferase to infect wild-type C57BL/6 and TLR3-

269 tein fragment complementation assay based on firefly luciferase to investigate dimerization of chemok

270 ATP as substrate, pyruvate kinase (PK), and firefly luciferase) to generate ATP, with measurement of

271 cules from the murine Hmox1 locus, including firefly luciferase, to allow long-term, non-invasive ima

272 trate that both the engineered and wild-type firefly luciferases tolerate much greater steric bulk at

273 nal siRNAs targeting a different site on the firefly luciferase transcript or endogenously expressed

274 A piggyBac donor plasmid modified to encode firefly luciferase under control of schistosome gene pro

275 to contain like green fluorescent protein or firefly luciferase under control of the cytomegalovirus

276 ering them with reporter plasmids expressing firefly luciferase under the translational control of th

277 amino acids were targeted to position 14 in firefly luciferase using an amber mutation or introducin

278 Firefly luciferase utilizes the chemical energy of ATP a

279 We have demonstrated that a firefly luciferase variant containing cysteine residues

280 fusion proteins consisting of a thermostable firefly luciferase variant that catalyze yellow-green (5

281 When the firefly luciferase variants were codon-optimized and ret

282 As a proof-of-principle, photoregulation of firefly luciferase was achieved in live cells by caging

283 ured fibroblasts, in which the expression of firefly luciferase was driven by the promoter of the cir

284 refly luciferase enzyme activity with intact firefly luciferase was estimated for different fragment

285 ns on the wavelength of the light emitted by firefly luciferase was investigated.

286 In this assay, denatured firefly luciferase was treated with a mixture of DnaK an

287 etection of PP(i), using ATP sulfurylase and firefly luciferase, was adapted to monitor poliovirus 3D

288 nto the cytoplasm, measured by expression of firefly luciferase, was increased more than 10-fold by e

289 encapsulation of horseradish peroxidase and firefly luciferase, we demonstrate that this new protoco

290 transgenic T. cruzi Y luc strain expressing firefly luciferase, we prioritized the biaryl and N-aryl

291 AAV vectors encoding firefly luciferase were administered to the LG and lucif

292 nd carboxy-fragment (395-550 amino acids) of firefly luciferase were fused to amino-terminal of Apaf-

293 y-four hours later, 2 x 10(5) MSC-expressing firefly luciferase were injected i.v.

294 n (FVB/NJ-luc) that constitutively expressed firefly luciferase were transplanted to various implanta

295 They share 19 to 21% sequence identity with firefly luciferases, which produce light using ATP and t

296 the fusion of green fluorescent protein and firefly luciferase with either nonstructural protein 2 o

297 strategy to identify a novel split site for firefly luciferase with improved characteristics over pr

298 rter mouse line that pairs the expression of firefly luciferase with quantifiable expression of a hum

299 vity in HeLa cells of siRNA duplexes against firefly luciferase with substitutions in the guide stran

300 colons of mice administered an mRNA encoding firefly luciferase with ultrasound and the D-luciferin s