ライフサイエンスコーパス: firefly

1 st predators as well as specialist predatory fireflies.

2 f biological oscillators such as neurons and fireflies.

3 to explain the efficient bioluminescence of 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 en as experimental support for mechanisms of firefly bioluminescence color that require only a single

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

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

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

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

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

16 The FireFly camera system can easily detect tilmanocept labe

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

63 72 glutamines fused to the N-terminal end of firefly luciferase (httQ72-Luc).

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

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

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

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

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

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

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

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

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

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

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

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

76 Firefly luciferase activity was maximally rescued by tre

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

78 Firefly luciferase adenylates and oxidizes d-luciferin t

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

95 Model substrates firefly luciferase and malate dehydrogenase form strong

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

111 Firefly luciferase can be mutated to accept and utilize

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

113 Firefly luciferase catalyzes two sequential partial reac

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

130 0.9% found from a previous qHTS against the firefly luciferase from Photinus pyralis (lucPpy).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

153 into functionally important residues in the firefly luciferase gene.

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

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

156 Firefly luciferase gives a stable luminescent signal tha

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

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

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

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

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

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

163 Firefly luciferase is homologous to fatty acyl-CoA synth

164 Firefly luciferase is roughly 100 times more efficient a

165 Firefly luciferase is the most widely used optical repor

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

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

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

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

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

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

172 Firefly luciferase produces light by converting substrat

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

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

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

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

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

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

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

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

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

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

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

184 A firefly luciferase reporter gene under control of the Ad

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

205 Firefly luciferase utilizes the chemical energy of ATP a

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

246 lding efficiency of the model client protein firefly luciferase.

247 ally induced aggregation of non-glycosylated firefly luciferase.

248 for subsequent bioluminescent reaction with 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 erase gene based on the crystal structure of firefly luciferase.

258 tation of pancreatic cancer cells expressing firefly luciferase.

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

260 ted to adenosine triphosphate and coupled to firefly luciferase.

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

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

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

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

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

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

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

268 we reported that the synthetic adenylate of firefly luciferin analogue D-5,5-dimethylluciferin was t

269 Five novel firefly luciferin analogues in which the benzothiazole r

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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