ライフサイエンスコーパス: bioluminescent

1 ita surprisingly reveals that the species is bioluminescent.

2 l biosensor, we developed a smartphone-based bioluminescent 3D cell biosensor platform for effect-bas

3 n be used to describe the synchronization of bioluminescent activity of abyssopelagic organisms with

4 ted in oral tumor development with increased bioluminescent activity within 6 days that reached a max

5 ction in size that still retains significant bioluminescent activity, in conjunction with a more repr

6 rception by rhizosphere bacteria, containing bioluminescent and fluorescent biosensors.

7 Reporter expression serves as detectable bioluminescent and fluorescent markers of VEEV and WEEV

8 CONCLUSIONS/SIGNIFICANCE: Bioluminescent and fluorescent optical imaging was combi

9 uction algorithm was used to co-register the bioluminescent and fluorescent signals with muCT images.

10 imodality imaging platform to firstly detect bioluminescent and fluorescent signals, and secondly, re

11 . chabaudi parasites expressing fluorescent, bioluminescent and model antigens that can be used in vi

12 Moreover, the proportion of bioluminescent and non-bioluminescent animals within tax

13 More than 97% of Cnidarians were bioluminescent, and 9 of the 13 taxonomic categories wer

14 The percentage of bioluminescent animals is remarkably uniform over depth.

15 er, the proportion of bioluminescent and non-bioluminescent animals within taxonomic groups changes w

16 Here we present a bioluminescent assay for the identification and characte

17 tive as compared to a commercially available bioluminescent assay in detecting mycoplasma contaminati

18 hermal nucleic acid amplification (LAMP) and bioluminescent assay in real time (BART), with droplet m

19 Using a bioluminescent assay, the efficacy and potency of kappa

20 ened for endocrine disrupting activity using bioluminescent assays.

21 decorin binding protein (dbpBA) by utilizing bioluminescent B. burgdorferi reporter strains and in vi

22 eneral toxicity determination rely on either bioluminescent bacteria and specific medium solution (i.

23 These results demonstrate the usefulness of bioluminescent bacteria for quantifying feeding and gene

24 The majority of bioluminescent bacteria localized in the cecum by 3 h po

25 We show that photons from bioluminescent bacteria radiate over mesoscopic distance

26 se progression of C57BL/6 mice infected with bioluminescent bacteria, imaged using optical tomography

27 Vibrio fischeri is a bioluminescent bacterium that colonizes and proliferates

28 Vibrio fischeri is a bioluminescent bacterium that enters into a symbiosis wi

29 ted in the light-organ symbiosis between the bioluminescent bacterium Vibrio fischeri and the Hawaiia

30 The bioluminescent bacterium Vibrio fischeri initiates a spe

31 between the squid Euprymna scolopes and the bioluminescent bacterium Vibrio fischeri.

32 The proposed hardware and software, called bioluminescent-based analyte quantitation by smartphone

33 6700) is a genetically engineered lux-based bioluminescent bioreporter.

34 Genetically encodable fluorescent and bioluminescent biosensors enable the direct visualizatio

35 ion of genetically encodable fluorescent and bioluminescent biosensors that have led to scientific or

36 As such, in vivo imaging of bioluminescent Borrelia provides a sensitive means to de

37 A similar gene was recently predicted from a bioluminescent brittle star, indicating that RLuc-like l

38 grazers, allowing for a brighter flash when bioluminescent capacity is stimulated.

39 reated with copepodamides to induce a higher bioluminescent capacity.

40 Here we develop bioluminescent circadian reporter mice that are Cre depe

41 ructure of a generally low species diversity bioluminescent community at shallower epipelagic depths

42 Collectively, we show a winter bioluminescent community in the high Arctic with vertica

43 Additionally, the bioluminescent construct allowed for increased speed and

44 The bioluminescent constructs passed/exceeded pharmacopoeia-

45 ocument an association between the origin of bioluminescent courtship and increased accumulation of s

46 ishes, we find more species in lineages with bioluminescent courtship compared to their sister groups

47 e find under a Yule model that lineages with bioluminescent courtship displays have significantly hig

48 Here we show that lineages with bioluminescent courtship, almost certainly a sexually se

49 hat malignant cells expressing CXCR7 reduced bioluminescent CXCL12 secreted in the primary tumor micr

50 Capitalizing on sensitive detection of bioluminescent CXCL12, we also demonstrated that CXCR7+

51 However, correct interpretation of bioluminescent data is limited: the bioluminescence is d

52 n of E. coli K1 strain A192PP and a virulent bioluminescent derivative, E. coli A192PP-lux2.

53 The combination of sensitive ratiometric bioluminescent detection and the intrinsic modularity of

54 Isothermal DNA amplification with bioluminescent detection is a fast, low-cost, highly spe

55 ecules enable highly sensitive and selective bioluminescent detection of FAAH activity in vitro, in l

56 , we describe a mouse model that enables the bioluminescent detection of GPCR activation in real time

57 assay for PI 4-kinase activity based on the bioluminescent detection of the ADP produced by kinase r

58 Bioluminescent dinoflagellates grow at one third the rat

59 of voltage-gated proton channels in 1972 in bioluminescent dinoflagellates, where they were thought

60 the 13 taxonomic categories were found to be bioluminescent dominant.

61 To expedite this method, we used bioluminescent E. coli in a simplified checkerboard assa

62 was also assessed in liquid cultures using a bioluminescent E. coli-O157:H7 strain.

63 Red-shifted bioluminescent emitters allow improved in vivo tissue pe

64 Furthermore, bioluminescent energy transfer assays indicated that whi

65 Using aqueous in situ polymerization on a bioluminescent enzyme anchored with polymerizable vinyl

66 y we examine the influence that locating the bioluminescent enzyme luciferase in different microcapsu

67 tissue, and the limited set of near-infrared bioluminescent enzymes, BLI is largely restricted to mon

68 s in complex environmental samples, based on bioluminescent Escherichia coli genotoxicity bioreporter

69 Here, we used a bioluminescent Escherichia coli strain to quantify C. el

70 terial kill curves constructed by exposing a bioluminescent Escherichia coli target, as a surrogate c

71 By multiplexing fluorescent and bioluminescent EV membrane reporters, we reveal the rapi

72 hese 'dark' V. fischeri strains remained non-bioluminescent even after treatment with both autoinduce

73 ET processes or use of initial chemical and bioluminescent excitation are treated similarly.

74 variants of Gluc, which maintain attractive bioluminescent features, and have characterized their sp

75 firefly species (Coleoptera: Lampyridae) use bioluminescent flashes for signaling.

76 ing glutamate stimulation, discrete Arc-Gluc bioluminescent flashes representing sites of de novo tra

77 lls from this donor mouse and image them for bioluminescent (fluc2), fluorescent (tdTomato), and posi

78 ne holocrine glands capable of discharging a bioluminescent fluid, potentially upon a given movement

79 In vivo bioluminescent, fluorescent, X-ray and muCT imaging were

80 question, we developed a genetically encoded bioluminescent Forster resonance energy transfer (BRET)

81 a diverse lineage comprising the majority of bioluminescent fungi.

82 emission-tomography tracers and validate the bioluminescent glucose-uptake probe as a tool for the id

83 Here, we report the development of a bioluminescent glucose-uptake probe for real-time, non-i

84 Some bioluminescent groups may be cultured, including some cn

85 Here we report development of the bioluminescent GSK3beta and CK1alpha reporter (BGCR) bas

86 Bioluminescent images of living mice, of excised whole i

87 Two days later, bioluminescent images were acquired in each mouse every

88 to study Plasmodium liver stages by means of bioluminescent imaging (BLI) of the rodent malaria paras

89 Bioluminescent imaging (BLI) of transplanted ASCs reveal

90 responses after injection with the oHSV and bioluminescent imaging (BLI) to determine oHSV replicati

91 The other group was first screened by bioluminescent imaging (BLI) to select only mice with vi

92 tor tumor angiogenesis and growth by in vivo bioluminescent imaging (BLI).

93 Bioluminescent imaging and direct counts were used to fo

94 Bioluminescent imaging and histopathological and PCR-bas

95 umor growth and metastasis were monitored by bioluminescent imaging and immunohistochemistry.

96 we evaluated the therapeutic efficacy using bioluminescent imaging and showed that the lung tumor gr

97 rates and localizations were confirmed using bioluminescent imaging and SPECT/CT after the (188)Re-BM

98 In this study, we report that bioluminescent imaging can be reproducibly achieved with

99 . yoelii infection with sporozoites and that bioluminescent imaging can be used to monitor protective

100 Noninvasive bioluminescent imaging confirmed that DNase I treatment

101 Furthermore, bioluminescent imaging in live mice to monitor macrophag

102 The GFAP signal, revealed by bioluminescent imaging in the living animal, was signifi

103 Bioluminescent imaging of encapsulated murine neonatal i

104 With a transgenic mouse line permitting the bioluminescent imaging of FAP(+) cells, we find that the

105 Bioluminescent imaging of ferrets infected with A/Califo

106 Thus, bioluminescent imaging of influenza infections rapidly d

107 Bioluminescent imaging of the reporter virus permits ser

108 In vivo bioluminescent imaging of these parasites allows for qua

109 Bioluminescent imaging of tumor metastases to the liver,

110 In vivo bioluminescent imaging permits the visualization of bact

111 In vivo bioluminescent imaging showed that a GRA15-deficient typ

112 ics, estimated dosimetry, nano-SPECT/CT, and bioluminescent imaging suggest that the PEGylated liposo

113 ibronectin adhesin BBK32, were quantified by bioluminescent imaging to further evaluate their pathoge

114 Furthermore, using bioluminescent imaging to maximize data acquisition, we

115 ally quantified the infections using in vivo bioluminescent imaging within individual mice.

116 asures included tumor growth, as measured by bioluminescent imaging, and median survival time.

117 ng virus in living mice can be visualized by bioluminescent imaging, bioluminescence being detected i

118 ence of phototoxicity, and photobleaching in bioluminescent imaging, combined with the ratiometric as

119 A combination of bioluminescent imaging, cultivation of infected tissues,

120 In the current studies, we used in vivo bioluminescent imaging, in vivo BrdU labeling, and three

121 Bioluminescent imaging, magnetic resonance imaging and i

122 Using bioluminescent imaging, we now demonstrate that H9 line

123 f patient-derived multiple myeloma cells and bioluminescent imaging, we were able to follow pMM cells

124 ESC engraftment was analyzed by bioluminescent imaging.

125 eralized loss of MCMV in brain, confirmed by bioluminescent imaging.

126 ed at 3, 5, 7, and 10 days post-treatment by bioluminescent imaging.

127 d protein inhibition measured by noninvasive bioluminescent imaging.

128 Since it is bioluminescent, imaging LOTUS-V does not require externa

129 o generate an optical signal (fluorescent or bioluminescent) in the presence of the target compound(s

130 development of the first genetically encoded bioluminescent indicator for membrane voltage called LOT

131 t fluorescent influenza B reporter virus and bioluminescent influenza B reporter virus.

132 ith transducing and transmitting traditional bioluminescent information.

133 the environment, such as a heat source or a bioluminescent life form, but we know little about how t

134 orescent proteins with the bright, glow-type bioluminescent light generated by an enhanced small luci

135 Here, we investigate photosensitivity in the bioluminescent light organs (photophores) of deep-sea sh

136 This approach relies on the generation of bioluminescent light when two distinct cell populations

137 Analysis of bioluminescent live-cell imaging shows a significantly g

138 mel2, that displays similarity to bacterial bioluminescent loci and plays an important role during p

139 n, luminopsin 3 (LMO3), which consisted of a bioluminescent luciferase, Gaussia luciferase, and an op

140 herry, mScarlet-I), colorimetric (lacZ), and bioluminescent (luxCDABE from Aliivibrio fischeri and Ph

141 To identify the bioluminescent machinery, we sequenced P. atlanticum tra

142 Vibrio fischeri, a bioluminescent marine bacterium, exists in an exclusive

143 The importance of bioluminescent marine taxa is highlighted in the water c

144 th different combinations of fluorescent and bioluminescent marker proteins and employing multi-modal

145 ion of FcgammaRs to this therapy model using bioluminescent measurement of lung metastases loads, nov

146 more, two-way ANOVA analysis showed that the bioluminescent method and traditional plate counting met

147 the traditional plate counting and the novel bioluminescent method for all bioluminescent strains.

148 The proteinase activity was analysed with a bioluminescent method using the light intensity decay co

149 all bioluminescent strains and therefore the bioluminescent method was accurate according to the crit

150 These strains demonstrated that the bioluminescent method was accurate, precise and equivale

151 Percentage recoveries using the bioluminescent method were between 70% and 130% for all

152 traditional plate counting method or the ATP bioluminescent method.

153 for the first time and applied as a label in bioluminescent microplate assay to detect target antibod

154 roup of Motyxia, the only genus of New World bioluminescent millipedes.

155 erase chain reaction and recently introduced bioluminescent miRNA detection, require systematic study

156 Although bioluminescent molecular beacons designed around resonan

157 Using a new bioluminescent mouse model, we monitored p27 translation

158 Infection of BALB/c mice with a bioluminescent mouse-adapted EV71 construct (mEV71-NLuc)

159 Stimulation of adoptively transferred bioluminescent MPhis and B-1a cells by amyloid fibrils r

160 ength, which extends the application of such bioluminescent nanocapsules, especially in deep tissue.

161 riety of luminescent--such as fluorescent or bioluminescent--objects.

162 Bioluminescent optical imaging and transcutaneous ultras

163 injected VEEV or WEEV, engineered to express bioluminescent or fluorescent reporters (fLUC and DsRed,

164 ression of imaging reporter genes for either bioluminescent or positron emission tomography (PET) ima

165 s of various habitats and the variability of bioluminescent organism distributions.

166 Bioluminescent organisms are likely to have an evolution

167 Among the least studied bioluminescent organisms are phylogenetically rare fungi

168 Laboratory culture of bioluminescent organisms from diverse taxonomic groups i

169 t overall variability in the distribution of bioluminescent organisms is related to the major differe

170 200 m, there is little ambient sunlight, but bioluminescent organisms provide another light source th

171 ning and isolating luminescent proteins from bioluminescent organisms, bioluminescence has been widel

172 on of the entire transcriptomes in symbiotic bioluminescent organs (bacterial photophores) from two d

173 Here we show that bioluminescent organs of the squid Euprymna scolopes pos

174 erous small subcutaneous (s.c.) photophores (bioluminescent organs) embedded throughout the muscle ti

175 e of these droplets are controllable and the bioluminescent output during DNA amplification can be im

176 nonhybrid natural fimbrolides as revealed by bioluminescent P. aeruginosa QS reporter assays and biof

177 In vivo imaging of bioluminescent parasites has previously been shown to be

178 The reporter phage conferred a bioluminescent phenotype to Y. pestis within 12 min of i

179 all, this study demonstrates that the use of bioluminescent primary ALL allows the detection and quan

180 as a highly sensitive, specific, and simple bioluminescent probe for in vitro detection of superoxid

181 Caged Luciferin-1 (PCL-1), a chemoselective bioluminescent probe for the real-time detection of H(2)

182 ization of iron-caged luciferin-1 (ICL-1), a bioluminescent probe that enables longitudinal monitorin

183 Traditional bioluminescent probes are limited in scope, though, as t

184 Bioluminescent probes with emission in near-infrared (NI

185 Model simulations show that predicted bioluminescent profiles can be very different from chang

186 of fluorescent ligands in combination with a bioluminescent protein (NanoLuc) that can be readily exp

187 put (564-nm peak wavelength) of any reported bioluminescent protein that utilizes its natural substra

188 Since the light is generated internally by a bioluminescent protein, BRET does not rely on an externa

189 molecular aptamer beacon (MAB) attached to a bioluminescent protein, Gaussia luciferase (GLuc), and a

190 s article reviews the most pertinent current bioluminescent-protein-based technologies and suggests t

191 Bioluminescent proteins are used in a plethora of analyt

192 rent reporter systems, using fluorescent and bioluminescent proteins as well as radionuclide-based re

193 While the use of bioluminescent proteins for molecular imaging is a power

194 perates with biochemical energy generated by bioluminescent proteins to excite fluorophores and offer

195 ep tissues than firefly luciferase and other bioluminescent proteins.

196 dyes, luminescent lanthanide complexes, and bioluminescent proteins.

197 e we demonstrate that the light emitted by a bioluminescent reaction can be used to directly monitor

198 with protein microcrystals that catalyse the bioluminescent reaction using ATP and the substrate coel

199 action to release d-luciferin for subsequent bioluminescent reaction with firefly luciferase.

200 uded microfluidics, ATP measurements using a bioluminescent reaction, and rheology.

201 Bioluminescent recording of circadian clock protein (PER

202 Herein, we describe a multiplexed bioluminescent repair reporter (BLRR) for non-invasive m

203 broblasts longitudinally over 5 days using a bioluminescent reporter (Per2-luc).

204 Furthermore, cryogels impregnated with bioluminescent reporter cells provided enhanced survival

205 Firefly luciferase (FLuc), an ATP-dependent bioluminescent reporter enzyme, is broadly used in chemi

206 tions of Copper-Caged Luciferin-1 (CCL-1), a bioluminescent reporter for tissue-specific copper visua

207 Bioluminescent reporter genes are sensitive in situ tool

208 ificity of the promoter, which regulates the bioluminescent reporter genes, limits the metal detectio

209 chnologies rely on the use of fluorescent or bioluminescent reporter genes, which need to be stably e

210 led Antares, functions as a highly sensitive bioluminescent reporter in vivo, producing substantially

211 lcium-dependent photoprotein, as a potential bioluminescent reporter protein of superoxide anion.

212 cally modify cells to express fluorescent or bioluminescent reporter proteins to enable tracking or q

213 were used to evaluate luminescence from the bioluminescent reporter Pseudomonas fluorescens M3A.

214 Thus, a robust bioluminescent reporter strategy enabled rigorous quanti

215 scent protein CyOFP, has emerged as a bright bioluminescent reporter with orthogonal substrate specif

216 Using a kappaB(5)-->IkappaBalpha-FLuc bioluminescent reporter, we rigorously evaluated the dyn

217 we monitored the replication and spread of a bioluminescent reporter-expressing NiV in susceptible mi

218 Secreted luciferases are highly useful bioluminescent reporters for cell-based assays and drug

219 Bioluminescent reporters were employed to detect active

220 s thus pave the way to an extended family of bioluminescent reporters.

221 -time monitoring of LAMP reactions either by bioluminescent reporting (BART) or by fluorescent dye bi

222 By using radioligand binding and bioluminescent resonance energy transfer (BRET) assays i

223 previously shown that a genetically encoded bioluminescent resonance energy transfer (BRET) biosenso

224 these assays benefit from the specificity of bioluminescent resonance energy transfer and the high si

225 In addition, bioluminescent resonance energy transfer is used to quan

226 teraction of P2Y12 with PAR4 but not PAR1 by bioluminescent resonance energy transfer when the recept

227 etent 293T transfectants when assessed using bioluminescent resonance energy transfer.

228 release firefly luciferin, which triggers a bioluminescent response in the presence of firefly lucif

229 ts on the backs of mice were infected with a bioluminescent S. aureus (methicillin sensitive) or USA3

230 possess EGFP-fluorescent neutrophils, and a bioluminescent S. aureus strain (Xen29; 1x10(3) CFUs) wa

231 A novel bioluminescent S. flexneri strain (S. flexneri lux1) was

232 likely to cause reflections), and under the bioluminescent searchlights of potential predators, anim

233 Here, a bioluminescent sensor is developed for non-invasively an

234 A new study finds that the evolution of bioluminescent sexual displays drives high species richn

235 Here, we found evidence that bioluminescent sharks instead emit a constant light outp

236 A novel luciferin from a bioluminescent Siberian earthworm Fridericia heliota was

237 firefly luciferin in situ, giving rise to a bioluminescent signal if and only if both chemical trigg

238 Tomographic reconstruction of the bioluminescent signal in mice expressing luciferase only

239 adjacent organs and observing a predominant bioluminescent signal in the pancreas compared with live

240 he fused fluorophore generates the brightest bioluminescent signal known to date, including improved

241 The bioluminescent signal measured for these mice on Day 4 p

242 tis by rapidly and specifically conferring a bioluminescent signal response to these cells.

243 ure culture and human serum by transducing a bioluminescent signal response.

244 ion of Ca(2+) solution and discriminated via bioluminescent signal spectral and time resolution.

245 nally verified by the ability to transduce a bioluminescent signal to recipient cells.

246 ter phage, E. coli O157:H7 produces a strong bioluminescent signal upon addition of commercial lucife

247 nal design providing a 1000-fold increase in bioluminescent signal upon addition of the TEV protease.

248 Peak background subtracted bioluminescent signal was fourfold higher when cells wer

249 ration of the substrate D-luciferin, the luc bioluminescent signal was substantially greater than the

250 extGLuc+ cells emitted significantly higher bioluminescent signal when compared to cells expressing

251 or did it significantly quench the resulting bioluminescent signal.

252 ting photophores were partially co-opted for bioluminescent signalling, leading to complex patterns.

253 extrapancreatic tissues, we did not observe bioluminescent signals from extrapancreatic tissues of d

254 perior to LH(2) for the spectral unmixing of bioluminescent signals in vivo; which led to this novel

255 The bacterial bioluminescent signals of the S. aureus-infected mice pe

256 rin in most neurons generated large and fast bioluminescent signals that were related to neural activ

257 d a progressive increase in their pancreatic bioluminescent signals, which were positively correlated

258 and the possibilities of detecting low-level bioluminescent signals.

259 ruggle to perceive dim downwelling light and bioluminescent sources and the need to remain unseen gen

260 are conspicuous when illuminated by directed bioluminescent sources due to reflection from the body s

261 phy, and PET), tomographic reconstruction of bioluminescent sources, and two unique, complementary mo

262 entation allows animals to absorb light from bioluminescent sources, rendering them visually undetect

263 Analyses of synteny across genomes of bioluminescent species resolved how the luciferase clust

264 were infected by intranasal instillation of bioluminescent strain 536 and received 536_P1 intranasal

265 veloped an in vitro agar based model using a bioluminescent strain of Pseudomonas aeruginosa to measu

266 ent method were between 70% and 130% for all bioluminescent strains and therefore the bioluminescent

267 he hypothesis that these newly described non-bioluminescent strains exhibit monophyly within the V. f

268 omonas aeruginosa ATCC9027 and its validated bioluminescent strains for preservative efficacy tests u

269 ation was evaluated against lawn biofilms of bioluminescent strains of Staphylococcus aureus and Pseu

270 characterization of naturally occurring, non-bioluminescent strains of Vibrio fischeri.

271 plicability of five constitutively-expressed bioluminescent strains was evaluated for preservative ef

272 Validation of the bioluminescent strains was performed in accordance with

273 ed a competitive disadvantage against native bioluminescent strains when colonizing the light organ o

274 Pseudomonas aeruginosa and Escherichia coli bioluminescent strains, we studied the combination of L-

275 and the novel bioluminescent method for all bioluminescent strains.

276 O activity in human plasma samples using the bioluminescent substrate L-012.

277 for determining the biosynthetic pathways of bioluminescent substrates, which may lead to new tools f

278 n of the ponyfish supports the growth of the bioluminescent symbiont Photobacterium leiognathi.

279 he squid Euprymna scolopes and its specific, bioluminescent symbiont, Vibrio fischeri.

280 A few enigmatic bioluminescent symbionts have not been successfully cult

281 The majority of bacteria engaged in bioluminescent symbiosis are environmentally acquired an

282 a morphologically and biochemically distinct bioluminescent system which evolved independently, requi

283 rin and genomic manipulation of an autogenic bioluminescent system.

284 Finally, four other rarely studied bioluminescent systems (those of limpet Latia, earthworm

285 The origins and functions of some bioluminescent systems, however, remain obscure.

286 We developed a new approach to bioluminescent T cell imaging using a membrane-anchored

287 eventh the volume), slower growing, and less bioluminescent than P-form cells; they are also avirulen

288 goes from being the preferred prey when non-bioluminescent to near complete rejection when pre-treat

289 mple of Rosetta-guided design in engineering bioluminescent tools and expands the scope of orthogonal

290 e pair is red-shifted compared to well-known bioluminescent tools.

291 , is an important simple model for efficient bioluminescent transformations.

292 d the variability of the circadian period of bioluminescent TTFL rhythms in SCN slices recorded ex vi

293 y permuted luciferase construct that becomes bioluminescent upon protease cleavage.

294 inducer of apoptosis (TWEAK), we developed a bioluminescent variant of soluble TWEAK (GpL-FLAG-TNC-TW

295 oreover, intravenous administrated PSES-TSTA bioluminescent vector correctly identified tibial bone m

296 experimentally evolved ecologically distinct bioluminescent Vibrio fischeri by colonization and growt

297 e subsequently challenged on day 24 with the bioluminescent WT CO92 strain (20 to 28 LD50s), 40 to 70

298 trans-tibial implant that was precoated with bioluminescent Xen36 S. aureus.

299 5I-Bcr-Abl without appreciable toxicity in a bioluminescent xenograft mouse model using a transformed

300 report the development and optimization of a bioluminescent yeast assay for the detection of organoti