ライフサイエンスコーパス: firefly

1 to explain the efficient bioluminescence of fireflies.

2 st predators as well as specialist predatory fireflies.

3 f biological oscillators such as neurons and fireflies.

4 H(+) channels activating bioluminescence in firefly and jellyfish.

5 lication of both viruses, generated suitable firefly and Renilla luciferase reporter constructs, resp

6 Firefly and Renilla luciferases were used to monitor tra

7 t-regulated shRNA transgenic lines targeting Firefly and Renilla luciferases, Oct4 and tumor suppress

8 PDAC cells genetically engineered to express firefly- and Gaussia luciferase, simplifying the ability

9 Many key advances in our understanding of firefly biology and signaling have been made over the pa

10 re compared with the broadband time-resolved firefly bioluminescence recorded in vivo.

11 the physics underlying the varied colors of firefly bioluminescence remains elusive because it is di

12 l-1,2-dioxetanone, a more adequate model for firefly bioluminescence, and found a singlet quantum yie

13 ial for only one of the partial reactions of firefly bioluminescence, supporting the proposal that th

14 rum related to the color-tuning mechanism of firefly bioluminescence.

15 The FireFly camera system can easily detect tilmanocept labe

16 animal model to determine the ability of the FireFly camera system to detect fluorescent SLNs after a

17 s, were dissected with the assistance of the FireFly camera system, a fluorescence-capable endoscopic

18 iteal lymph nodes was easily detected by the FireFly camera system.

19 Finally, we review recent findings on firefly chemical defenses, and discuss their implication

20 bservation of selective DYRK1A inhibition by firefly d-luciferin, we have explored static and dynamic

21 hotinus nuptial gifts contain lucibufagin, a firefly defensive toxin.

22 Other groups, including terrestrial fireflies, do synthesize their own luciferin, but cultur

23 ond time-resolved spectroscopic study of the firefly emitter oxyluciferin and two of its chemically m

24 hin the family Lampyridae, new insights into firefly flash control, and the discovery of firefly nupt

25 This review provides new insight into how firefly flash signals have been shaped by the dual evolu

26 excited-state keto-enol tautomerization of a firefly fluorophore, and it could be important in resolv

27 A recent study on fireflies has found that signal production is energetica

28 biological oscillators, such as observed in fireflies, heartbeats, and circadian rhythms.

29 Kornicker & Baker, 1977, the California Sea Firefly) in the laboratory.

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

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

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

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

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

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

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

37 ter with orthogonal substrate specificity to firefly luciferase (FLuc) and its derivatives such as Ak

38 for in vivo delivery using saRNA coding for firefly luciferase (fLuc) as a reporter protein in vivo.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

56 at by combining stabilised colour mutants of firefly luciferase (FLuc) with the luciferin (LH(2)) ana

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

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

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

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

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

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

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

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

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

66 72 glutamines fused to the N-terminal end of firefly luciferase (httQ72-Luc).

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

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

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

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

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

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

73 2 strain D39, we transcriptionally fused the firefly luciferase (luc) to competence-specific genes an

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

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

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

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

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

79 Firefly luciferase adenylates and oxidizes d-luciferin t

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

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

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

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

84 An intravenous injection of AAV8 containing firefly luciferase and eGFP under transcriptional contro

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

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

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

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

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

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

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

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

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

94 Epstein-Barr virus (EBV), encoding enhanced firefly luciferase and green fluorescent protein.

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

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

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

98 Model substrates firefly luciferase and malate dehydrogenase form strong

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

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

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

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

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

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

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

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

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

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

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

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

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

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

113 Firefly luciferase can be mutated to accept and utilize

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

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

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

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

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

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

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

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

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

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

124 the constitutive hsp70 promoter, as well as firefly luciferase driven by the schizont-specific lisp2

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

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

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

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

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

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

131 0.9% found from a previous qHTS against the firefly luciferase from Photinus pyralis (lucPpy).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

151 Firefly luciferase gives a stable luminescent signal tha

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

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

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

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

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

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

158 Firefly luciferase is homologous to fatty acyl-CoA synth

159 Firefly luciferase is roughly 100 times more efficient a

160 Firefly luciferase is the most widely used optical repor

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

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

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

164 Firefly luciferase produces light by converting substrat

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

166 vity, as well as the bio distribution of the firefly luciferase protein in a series of three heart tr

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

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

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

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

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

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

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

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

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

176 A firefly luciferase reporter gene under control of the Ad

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

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

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

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

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

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

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

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

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

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

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

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

189 We developed firefly luciferase reporters for the long-term monitorin

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

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

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

193 luciferin, which is subsequently oxidized by firefly luciferase to generate a light signal.

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

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

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

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

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

199 Firefly luciferase utilizes the chemical energy of ATP a

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

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

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

203 0(13) total viral particles of an Adenoviral firefly luciferase vector with a cytomegalovirus (CMV) p

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

205 EBV-firefly luciferase was detectable 1 week after infection

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

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

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

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

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

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

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

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

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

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

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

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

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

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

220 Firefly luciferase, a 550 residue three-domain protein,

221 hermoprotection against heat inactivation of firefly luciferase, and (iv) sequence homology analysis

222 es including polyglutamine (PolyQ) proteins, firefly luciferase, and Abeta40.

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

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

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

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

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

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

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

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

231 h luminescence levels that are comparable to firefly luciferase, thus enabling autonomous bioluminesc

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

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

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

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

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

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

238 nthesis time in translation reactions with a firefly luciferase-encoding mRNA.

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

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

241 th the growth dynamics in our experiments of firefly luciferase-expressing Hep3B tumor xenografts and

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

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

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

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

246 ted to adenosine triphosphate and coupled to firefly luciferase.

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

248 lding efficiency of the model client protein firefly luciferase.

249 a bioluminescent response in the presence of firefly luciferase.

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

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

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

253 terminal and COOH terminal fragments of the firefly luciferase.

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

255 echanism of the anesthetic inhibition of the firefly luciferase.

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

257 ally induced aggregation of non-glycosylated firefly luciferase.

258 for subsequent bioluminescent reaction with firefly luciferase.

259 tation of pancreatic cancer cells expressing firefly luciferase.

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

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

262 on kinetics is reported using functionalized firefly-luciferase nanocapsules as the probe.

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

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

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

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

267 Five novel firefly luciferin analogues in which the benzothiazole r

268 ng animals that employs in situ formation of firefly luciferin from two complementary caged precursor

269 Once released, HCBT and D-cysteine form firefly luciferin in situ, giving rise to a bioluminesce

270 PCL-1 is a boronic acid-caged firefly luciferin molecule that selectively reacts with

271 s difficult and the biosynthetic pathway for firefly luciferin remains unclear.

272 ch produce light using ATP and the unrelated firefly luciferin substrate.

273 selectively reacts with H(2)O(2) to release firefly luciferin, which triggers a bioluminescent respo

274 assay that uses a substrate derivatized with firefly luciferin.

275 complexed with luciferase from the Japanese firefly (Luciola cruciata).

276 ascades, design of peroxide-based medicines, firefly luminescence, and reductive repair of DNA photod

277 Simulated data derived from the Firefly model provided a close match with empirical data

278 Based on these findings, the Firefly model was developed, which proposes that both ev

279 The Firefly Model, therefore, provides not only a unifying a

280 g for expression of both renilla (tumor) and firefly (MSC) luciferase.

281 firefly flash control, and the discovery of firefly nuptial gifts.

282 he steady-state and time-resolved spectra of firefly oxyluciferin complexed with luciferase from the

283 pectroscopy to compare the absorption by the firefly oxyluciferin lumophore isolated in vacuo and com

284 North American firefly Photinus pyralis luciferase, which emits yellow-

285 Light emission from the North American firefly Photinus pyralis, which emits yellow-green (557

286 Light emission from the North American firefly Photinus pyralis, which emits yellow-green (557-

287 Firefly (Photinus pyralis) luciferase (Luciferase, 550 r

288 ell line that was transfected to express the firefly (Photinus pyralis) luciferase gene.

289 rony's behavioral role in the North American firefly, Photinus carolinus.

290 e of the spermatophore in the common Eastern firefly, Photinus pyralis.

291 he ATP-dependent luciferase derived from the firefly Photuris pennsylvanica that was optimized using

292 system to examine the expression profiles of firefly reporter mRNAs bearing alternative combinations

293 we developed a dual-luciferase (Renilla and Firefly) reporter system for high-throughput screening (

294 luciferases obtained from beetle, including fireflies, result in novel properties and offer opportun

295 The reproductive tracts of female fireflies showed increased gene expression for several p

296 Most firefly species (Coleoptera: Lampyridae) use bioluminesc

297 tion between S1P1 and beta-arrestin2 via the firefly split luciferase fragment complementation system

298 The Japanese firefly squid Hotaru-ika (Watasenia scintillans) produce

299 lampyrids, including evidence from Photinus fireflies that females choose their mates on the basis o

300 During mating, male Photinus fireflies transfer to females a spermatophore gift manuf