ライフサイエンスコーパス: far-red

1 ifferent light colors: blue, green, red, and far-red.

2 els with excitation ranging from blue to the far-red.

3 usly unidentified role for long hypocotyl in far red 1, a negative regulator of the PIFs.

4 spectral range from the near UV through the far red (330 to 760 nm).

5 compounds can be switched with light in the far-red (650 nm).

6 sting of blue 455 nm, red 627 and 660 nm and far red 735 nm LEDs, was supplemented with UV-A 380 nm,

7 The recent discovery of far-red absorbing CBCRs (frCBCRs) has garnered considera

8 Far-red absorbing chlorophylls are constitutively presen

9 Here, we present a far-red absorbing fluoromodule-based reporter/probe syst

10 es act as photoswitches between the red- and far-red absorbing parent states of phytochromes (Pr and

11 orphogenesis are phytochrome B (phyB), a red/far-red absorbing photoreceptor, and cryptochrome 1 (CRY

12 JSC1_58120g3 can also yield a far-red-absorbing adduct with the more widespread linear

13 mediates the formation of the FHY1/FHL/PHYA far-red-absorbing form complex, whereby it plays a role

14 Phytochromes (phy) are red/far-red-absorbing photoreceptors that regulate the adapt

15 tructurally heterogeneous chromophore in the far-red-absorbing photostate.

16 a few eukaryotic phototrophs, JSC1_58120g3's far-red absorption arises from incorporation of the PCB

17 rtaken to determine the structural basis for far-red absorption by JSC1_58120g3, a frCBCR from the th

18 itical for its verdin-binding preference and far-red absorption.

19 During far-red acclimation, transcript levels increase more tha

20 netic characteristics suggest this pair of a far-red and a near-infrared fluorescent protein as an op

21 Moreover, far-red and blue light upregulate the expression of PCH1

22 Two fluorescent proteins that emit in the far-red and infrared range for imaging applications in c

23 Phytochrome photoreceptors absorb far-red and near-infrared (NIR) light and regulate light

24 cells, aptamer/ligand pairs that emit in the far-red and near-infrared (NIR) regions are still rare.

25 r-resolution microscopy, particularly in the far-red and near-infrared emission range.

26 A far-red and near-infrared fluorescent cell cycle indicat

27 Far-red and near-infrared fluorescent proteins (FPs) ena

28 Genetically encoded far-red and near-infrared fluorescent proteins enable ef

29 nsive colorimetric/fluorescent biosensor for far-red and near-infrared imaging of live cells.

30 opto-RTKs that are reversibly regulated with far-red and near-infrared light.

31 ptical window of tissue, specifically in the far-red and near-IR region.

32 tive organic molecules to realize preferable far-red and NIR fluorescence, well-controlled morphology

33 Red, far-red, and blue light lead to negative phototropism in

34 g BBX32 display elongated hypocotyls in red, far-red, and blue light, along with reduced cotyledon ex

35 of-function plants are hyposensitive to red, far-red, and blue light, and flower precociously.

36 ease is triggered by wavelengths in the red, far-red, and near-IR regions, which can be pre-assigned

37 ction may mediate cross-talk between the red/far-red- and blue/UV-sensing pathways, enabling fine-tun

38 However, Malcosteus niger produces far-red bioluminescence and its longwave retinal sensiti

39 Far-red cyanine fluorophores find extensive use in moder

40 ctive Pr (lambdamax = 660 nm) forms in a red/far-red-dependent fashion and regulates, as molecular sw

41 imaging agent, the DML was labeled with the far-red dye sulfonate cyanine 5 (sCy5), site-specificall

42 thesis, these studies provide a new class of far-red dyes with promising spectroscopic and chemical p

43 A is regulated by the transport facilitators far red elongated hypocotyl 1 (FHY1) and fhy1-like, an i

44 Here, we present a phyA pathway in which FAR-RED ELONGATED HYPOCOTYL1 (FHY1), an essential partne

45 tor to nuclear import facilitators FHY1 (for FAR-RED ELONGATED HYPOCOTYL1) and FHL (for FHY1-LIKE).

46 FAR-RED ELONGATED HYPOCOTYL3 (FHY3) and its homolog FAR-

47 The transposase-related transcription factor FAR-RED ELONGATED HYPOCOTYL3 (FHY3) promotes seedling de

48 These complexes exhibit far-red emission, with high quantum efficiencies and bri

49 th dual fluorescence excitation and a single far-red emission.

50 tion for labeling an octreotide peptide with far-red emitting coumarin-based COUPY dyes.

51 The advancement of far-red emitting variants of the green fluorescent prote

52 interaction of TOC1 with PHYTOCHROME B under far-red-enriched light suggests a connection between cir

53 l of plant immunity genes and confirmed that far-red enrichment indeed contrastingly affects resistan

54 om an orange (ex./em. at 546 nm/561 nm) to a far-red (ex./em. at 619 nm/651 nm) form.

55 ed PSmOrange has, to our knowledge, the most far-red excitation peak of all GFP-like fluorescent prot

56 ble near-infrared (NIR) molecular probe with far-red excitation, NIR emission, and high "turn-on" rat

57 ation, 548 nm; emission, 565 nm) but becomes far-red (excitation, 636 nm; emission, 662 nm) after irr

58 Imaging studies may benefit from this far-red excited reporter/probe system, which features ti

59 ectively, and complemented by intraoperative far-red fluorescence imaging using a clinical laparoscop

60 The far-red fluorescence of photoconverted PSmOrange results

61 rnet, a robust monomeric marker protein with far-red fluorescence peaking at 670 nm.

62 l-penetrating peptides, which contain Cy5 as far red fluorescent donor and Cy7 as near-infrared fluor

63 Herein, we present LUXendin645, a far-red fluorescent GLP1R antagonistic peptide label.

64 onal human tumor suppressor, p53, fused to a far-red fluorescent protein, eqFP650.

65 ansition from S to G2 phase and engineered a far-red fluorescent protein, mMaroon1, to visualize chro

66 roduce PAmKate, a monomeric photoactivatable far-red fluorescent protein, which facilitates simultane

67 Far-red fluorescent proteins (FPs) are desirable for in

68 rt comparative testing of available GFP-like far-red fluorescent proteins along with a modified prote

69 We demonstrate that the signals of various far-red fluorescent proteins can be spectrally unmixed b

70 n imaging and constitutes a new scaffold for far-red fluorogenic molecules.

71 ration of NeutrAvidin, labeled with either a far-red fluorophore or (111)In, there was a significant

72 roaches are discussed for conventional RFPs, far-red FPs, RFPs with a large Stokes shift, fluorescent

73 m yield of mGarnet, 9.1%, that is typical of far-red FPs.

74 However, the impact of far red (FR) light on MAA biosynthesis has not been stud

75 Phytochrome A (PHYA) is essential for the far-red (FR) high-irradiance responses (HIRs), which are

76 ed by a reduction in the ratio of red (R) to far-red (FR) light and results in the stabilization of a

77 FHY3 direct target genes in darkness (D) and far-red (FR) light conditions, respectively, in the Arab

78 s indicated that a dysfunctional red (R) and far-red (FR) light receptor, phytochrome B (phyB), cause

79 Far-red (FR) light-coupled jasmonate (JA) signaling is n

80 sparate hypocotyl elongation responses under far-red (FR) light.

81 Photobiomodulation (PBM) by far-red (FR) to near-infrared (NIR) light has been demon

82 onitoring changes in the ratio of red (R) to far-red (FR) wavelengths (R:FR) in ambient light.

83 The reversibly red (R)/far-red (FR)-light-responsive phytochrome (phy) photosen

84 is an efficient FRET donor that supports red/far-red FRET biosensing.

85 Compared with far-red GFP-like proteins, iRFP has a substantially high

86 tabilizes the bHLH protein LONG HYPOCOTYL IN FAR RED (HFR1), which can bind to and inhibit PIF4 funct

87 ATED HYPOCOTYL 5 (HY5) and LONG HYPOCOTYL IN FAR-RED (HFR1) proteins; and the epistatic relationships

88 phytochrome A (PHYA) is responsible for the far-red high-irradiance response and for the perception

89 nder far-red light and are impaired in other far-red high-irradiance responses.

90 eliminated through prior reduction of PSI by far-red illumination.

91 ELONGATED HYPOCOTYL3 (FHY3) and its homolog FAR-RED IMPAIRED RESPONSE1 (FAR1), two transposase-deriv

92 and metabolites, the increased abundance of FAR-RED IMPAIRED RESPONSE1-like transcripts in nitrogen-

93 (CPs) with absorbances ranging from green to far-red, including 2 that are photoconvertible.

94 demonstrated to increase in abundance under far-red-induced shade avoidance conditions either decrea

95 able labeling of biological membranes in the far-red/infrared and exhibit the furthest red-shifted fl

96 ch dissipate after Pfr reverts back to Pr by far-red irradiation or by temperature-dependent nonphoto

97 The red/far red light absorbing photoreceptor phytochrome-B (phy

98 ponse to the relative proportions of red and far red light was regulated by SIG5 through phytochrome

99 e reduction in the ratio of red light (R) to far-red light (FR) as a warning of competition with neig

100 Far-red light (FR) pretreatment and transfer to white li

101 ging plants have to adapt to a high ratio of far-red light (FR)/red light (R) light in the canopy bef

102 g responses to the ratio of red light (R) to far-red light (FR; an indicator of competition) by suppr

103 ococcidiopsis thermalis PCC 7203 grown under far-red light (FRL; >725 nm) contains both chlorophyll a

104 tointerconversion between red light (Pr) and far-red light (Pfr)-absorbing states.

105 oreceptors perceive reduced ratios of red to far-red light (R:FR) and initiate stem elongation to ena

106 hotoreceptor that senses the ratio of red to far-red light (R:FR) to regulate the shade-avoidance res

107 as a reduction in the ratio of red light to far-red light (R:FR).

108 exposure and to complete this process under far-red light (typical of dense vegetation canopies).

109 he Y263F change prevents a red light-induced far-red light absorbing phytochrome chromophore configur

110 transfer bands could be responsible for the far-red light absorption leading to PS I photochemistry

111 on mutants show an elongated hypocotyl under far-red light and are impaired in other far-red high-irr

112 Phytochromes sense red/far-red light and control many biological processes in p

113 hyposensitivity to continuous low-intensity far-red light and shows reduced very-low-fluence respons

114 and phyB2 tomato mutants and was reversed by far-red light applied immediately after the red or blue

115 ree organs in response to a 1-h treatment of far-red light are highly distinctive.

116 In aquatic environments, red and far-red light are rapidly attenuated with depth; therefo

117 Sensing of red and far-red light by bacteriophytochromes involves intricate

118 The absorption of red or far-red light by one domain affects the conformation of

119 ontaining photoreceptors that detect red and far-red light by photointerconversion between a dark-ada

120 s of cAMP and cGMP by up to sixfold, whereas far-red light can be used to down-regulate activity.

121 ying light intensities and ratios of red and far-red light caused by shading and neighbor proximity.

122 Finally we show that both shaded, low red/far-red light conditions and high temperature induce mor

123 gulation of photomorphogenesis under red and far-red light conditions involves both positively and ne

124 uadruple mutant pifq both in the dark and in far-red light conditions.

125 ngs of their contrasting growth responses to far-red light enrichment.

126 tal results confirmed that cells grown under far-red light form biofilms with a significantly increas

127 fted from white light D2O-seawater medium to far-red light H2O-seawater medium, the observed deuterat

128 ty, such that axillary buds growing in added far-red light have greatly increased receptor transcript

129 SCL21 transcript itself is down-regulated by far-red light in a phytochrome A- and PAT1-dependent man

130 n, apparently by sensing the ratio of red to far-red light in the environment.

131 ommunities because of the deep penetrance of far-red light into mammalian tissue and the small size o

132 Additionally, exposure to yellow but not far-red light leads to comparable increases in the expre

133 t changing R:FRs or lowering R:FRs by adding far-red light led to the appearance of small nuclear bod

134 ought cannot be attributed to changes in red/far-red light perception alone.

135 In addition, the long hypocotyl in far-red light phenotype of the laf6 mutant could not be

136 is part of an extensive acclimation process, far-red light photoacclimation (FaRLiP), which occurs in

137 Far-red light photoacclimation appears to be controlled

138 obiliproteins and minor amounts of Chl d via far-red light photoacclimation in a range of cyanobacter

139 Far-red light photoacclimation leads to substantial remo

140 Here we propose that the red/far-red light photoreceptor HvPHYTOCHROME C (HvPHYC), ca

141 Moreover, the red/far-red light photoreceptor phyB interacts with SPA1 thr

142 The red/far-red light photoreceptor phytochrome mediates photomo

143 The red/far-red light photoreceptor phytochrome participates in

144 rs that interact physically with the red and far-red light photoreceptors, phytochromes, are called P

145 g, far-red photosystem II (FR-PSII) supports far-red light photosynthesis.

146 Excitation of the holoproteins by red or far-red light promotes the photoconversion to their far-

147 under a light program of alternating red and far-red light pulses and were named eid (for empfindlich

148 -limited and super-resolution imaging in the far-red light range, is optimally excited with common re

149 ribution of light quality, including the red/far-red light ratio (R/FR) that informs plants about pro

150 Plants interpret a decrease in the red to far-red light ratio (R:FR) as a sign of impending shadin

151 Low red light/far-red light ratio (R:FR) serves as an indicator of imp

152 ow that both low blue light and a low-red to far-red light ratio are required to rapidly enhance phot

153 The influence of red/far-red light ratio on the fibre length prompted us to e

154 egetation-induced reduction in the red light:far-red light ratio provides a competition signal sensed

155 th light quality (as crowding and the red-to-far-red light ratio) and phosphate availability, such th

156 carpel development to spt mutants by low red/far-red light ratios, simulating vegetation shade, which

157 Phytochromes, red/far-red light receptors, are believed to regulate light-

158 Phytochrome-mediated detection of far-red light reflection from neighboring plants activat

159 mitted farther through seawater than the red/far-red light sensed by land plant phytochromes.

160 Phytochromes are red/far-red light sensing photoreceptors employing linear te

161 re dimeric proteins that function as red and far-red light sensors influencing nearly every phase of

162 on module in leaves strongly linking red and far-red light signaling to drought responses in a TOC1-d

163 he light-to-dark) switch, the blue, red, and far-red light signals, and UV-B irradiation.

164 nsive photoacclimative response to growth in far-red light that includes the synthesis of chlorophyll

165 rough reduction in the ratio between red and far-red light that triggers the shade avoidance syndrome

166 Land plant phytochromes perceive red and far-red light to control growth and development, using t

167 vely ablated tumors by the illumination with far-red light to the mice, presumably through the combin

168 bidopsis thaliana) mutants hypersensitive to far-red light were isolated under a light program of alt

169 Here we present clear evidence that even far-red light with wavelengths beyond 800 nm, clearly ou

170 of a unique CBCR called IflA (influenced by far-red light), demonstrating that a second CBCR called

171 liar shade or neighbor proximity (low red to far-red light), some plant species exhibit shade-avoidin

172 ng that blue, yellow, and red light, but not far-red light, are absorbed by the neutral radical state

173 Stromule formation was sensitive to red and far-red light, but not to blue light.

174 When stimulated by far-red light, the intense TTA upconversion blue emissio

175 However, once illuminated with far-red light, the prodrug effectively killed SKOV-3 ova

176 nsed through a reduced ratio between red and far-red light, we show here through computational modeli

177 L3 (FHY3) promotes seedling de-etiolation in far-red light, which is perceived by phytochrome A (phyA

178 sing tissue penetrable and clinically useful far-red light, which kills the cancer cells through the

179 oximity as a decrease in the ratio of red to far-red light, which triggers a series of developmental

180 erconversion of red light-absorbing (Pr) and far-red light-absorbing (Pfr) states.

181 red-light-absorbing ground state (Pr) and a far-red light-absorbing active state (Pfr).

182 light promotes the photoconversion to their far-red light-absorbing Pfr state or the red light-absor

183 e red light-absorbing Pr state and an active far-red light-absorbing Pfr state.

184 Photoreceptors, especially the far-red light-absorbing phytochrome A, play a crucial ro

185 Red/far-red light-absorbing phytochromes (phys) also play a

186 light-absorbing state and the photoactivated far-red light-absorbing state revealed a large scale reo

187 To overcome these problems, we prepared the far-red light-activatable prodrug of PTX by conjugating

188 However, normal far-red light-associated transcript accumulation pattern

189 ped; they can operate with low-power density far-red light-emitting diode light.

190 in 60 s of irradiation using green, red, and far-red light-emitting diodes.

191 oximity and shade (i.e. to the perception of far-red light-enriched light filtered through or reflect

192 Further analysis reveals that far-red light-induced phosphorylation and degradation of

193 eds display strong hyposensitive response to far-red light-mediated seed germination and light-regula

194 s of both phyB and PCH1 generate stable, yet far-red light-reversible PBs that persisted for days.

195 y because it enables plants to deetiolate in far-red light-rich environments typical of dense vegetat

196 multiple photoreceptors, among which the red/far-red light-sensing phytochromes have been extensively

197 photobleaching and constitutes the brightest far-red light-up aptamer system known to date owing to i

198 ectral range for photosynthesis by absorbing far-red light.

199 saI in darkness even after illumination with far-red light.

200 s of light (VLFR) and high fluences (HIR) of far-red light.

201 synthesis in two cyanobacteria that grow in far-red light.

202 nase assays, show hyposensitive responses to far-red light.

203 f cyanobacteria that is capable of utilizing far-red light.

204 ght above 700 nm and enable cells to grow in far-red light.

205 showed that some cyanobacteria could utilize far-red light.

206 nanometers) and enhances oxygen evolution in far-red light.

207 90/717 nm following a brief irradiation with far-red light.

208 important for phyA-mediated deetiolation in far-red light.

209 ected in seedlings grown under low-intensity far-red light.

210 clear import of phyA-5 under low fluences of far-red light.

211 ated with near-infrared and inactivated with far-red light.

212 ation of low-lying charge transfer states by far-red light.

213 ent photopolymerization driven by visible to far-red light.

214 switchable on and off with near-infrared and far-red light.

215 whereas rod divisions predominate in red or far-red light.

216 sferases accumulated the most in response to far-red light.

217 er white light to an immobilized state under far-red light.

218 permits them to thrive in niches enriched in far-red light.

219 in and abscisic acid treatments and enhanced far-red light/phyA-mediated photomorphogenesis.

220 en the red light-absorbing form, Pr, and the far-red-light-absorbing form, Pfr.

221 We demonstrate its application to far-red-light-activated prodrugs.

222 The same far-red limit for the P700 (+) formation was observed in

223 The far-red limit of photosystem I (PS I) photochemistry was

224 Despite notable efforts, far-red marker proteins still need further optimization

225 ter proteins, including UnaG (green), mRuby (far red), mKate (red), and TagBFP (blue).

226 g dual wavelength illumination with blue and far-red/near-infrared light.

227 We investigated five far-red/near-infrared proteins in zebrafish: TagRFP657,

228 A compelling application of far-red/near-IR absorbing photocages is their potential

229 ficient and up to 40% quantum yield, whereas far-red operation region enables both in vitro and in vi

230 edly hypersensitive to red light, but not to far-red or blue light, and are compromised in multiple p

231 ty of hypocotyl elongation to red but not to far-red or blue light.

232 bility and brightness, variants excited with far-red or near-infrared light suffer from poor performa

233 A far-red or near-infrared protein could be particularly s

234 n be induced in dark-grown seedlings by red, far-red, or blue light treatments.

235 e in leaf expansion under monochromatic red, far-red, or blue light, and interaction with phytochrome

236 canonical phytochromes between red (Pr) and far red (Pfr) light-absorbing states.

237 Phytochromes are red/far-red photochromic photoreceptors central to regulatin

238 Compared to another orange-to-far-red photoconvertable variant, PSmOrange2 has blue-sh

239 MvirPHY1 exhibits a red-far-red photocycle similar to those seen in other strept

240 less complex than those reported for the red/far-red photocycles of the related phytochrome photorece

241 cclimation appears to be controlled by a red/far-red photoreceptor, RfpA, as well as two response reg

242 Phytochromes are the red/far-red photoreceptors in higher plants.

243 Phytochromes function as red/far-red photoreceptors in plants and are essential for l

244 CAB repositioning is mediated by the red/far-red photoreceptors phytochromes (PHYs) and is inhibi

245 Plant phytochromes are photoswitchable red/far-red photoreceptors that allow competition with neigh

246 Phytochromes are red/far-red photoreceptors that are widely distributed in pl

247 Phytochromes (phys) are red and far-red photoreceptors that control plant development an

248 Phytochromes are red/far-red photoreceptors that play essential roles in dive

249 Phytochromes are red/far-red photoreceptors using cysteine-linked linear tetr

250 ulated by ambient light cues through the red/far-red photoreceptors, the phytochromes.

251 wn to be controlled by phytochromes, the red/far-red photoreceptors; however, transcriptome analyses

252 cently discovered, chlorophyll-f-containing, far-red photosystem II (FR-PSII) supports far-red light

253 21-gene cluster that includes a knotless red/far-red phytochrome and two response regulators.

254 icipation and kinetics of spectrally shifted far-red pigments are directly observable and separated f

255 d; CRY1 interacts specifically with the dark/far-red (Pr) state of phyB, but not with the red light-a

256 ignaling involves perception of incident red/far-red (R/FR) light by phytochromes (PHYs) and modulati

257 Reduction of the red/far-red (R/FR) light ratio that occurs in dense canopies

258 in a diverse collection of light-stable red/far-red (R/FR) sensing photoreceptors.

259 phototropic response is enhanced by the red/far-red (R/FR)-sensing phytochromes (phy) with a predomi

260 toreceptor phytochrome B (phyB) by a low red/far-red ratio (R:FR), which is a signal of competition i

261 responses are mediated by changes in the red/far-red ratio of the light, which is perceived by phytoc

262 tions of the solar spectrum and a low-red to far-red ratio.

263 ccurrence and perception of a reduced red to far-red ratio.

264 ile the most conspicuous response to low red/far-red ratios (R:FR) of shade light perceived by phytoc

265 y shade involve the perception of low red to far-red ratios (R:FRs) by phytochrome B (phyB), which le

266 weak charge transfer bands absorbing in the far-red region in the ensemble of excitonically coupled

267 nes, making it a versatile tool spanning the far-red region of the spectrum.

268 rt a new, monovalent probe that emits in the far-red region of the visible spectrum with properties d

269 s is limited, and they do not operate in the far-red region.

270 lgal phytochromes are not limited to red and far-red responses.

271 The 2.6-A crystal structure of its red/far-red responsive photosensory module in the Pr state r

272 Far-red sensing and verdin incorporation make this frCBC

273 ultraviolet protection and phytochromes for far-red sensing.

274 a, we show that the perception of low red to far-red shade by the cotyledons triggers hypocotyl cell

275 ve shown that hypocotyl growth in low red to far-red shade is largely dependent on the photoreceptor

276 ibit tunable photophysical properties in the far-red spectral region with moderate fluorescent quantu

277 uning" approach is generalizable, yielding a far-red targetable indicator to visualize Ca(2+) fluxes

278 ifying novel fluorophores that excite in the far red, thereby avoiding compound fluorescence.

279 ned to combine 1) dual-emission ratioing, 2) far red to infrared wavelengths for in vivo mammalian im

280 tegy to expand anti-Stokes shifting from the far-red to deep-blue region in metal-free triplet-triple

281 The probes exhibited promising far-red to near-infrared (NIR) emission, large Stoke shi

282 synthesized and tested the first dual-color, far-red to near-infrared (nIR) emitting analogue of beet

283 one fluorescent semiconducting polymer based far-red to near-infrared (NIR) Pdot nanoprobe for the ra

284 s the design and synthesis of a photostable, far-red to near-infrared (NIR) platform for optical volt

285 efficient synthetic route to xanthene-based far-red to near-infrared dyes is reported.

286 Both these fluorophores display far-red to near-infrared excitation and emission prior t

287 Studying Chlorobaculum tepidum cultures with far-red to near-infrared light-emitting diodes, we found

288 Treatment with light in the far-red to near-infrared region of the spectrum (photobi

289 Our analogue produces different far-red to nIR emission maxima up to lambda(max)=706 nm

290 HOCl sensing, such as high brightness, ideal far-red to NIR optical window, excellent photostability,

291 ging applications, including emission in the far-red to NIR region, large Stokes' shifts, and high ph

292 BeRST 1 is the first member of a class of far-red to NIR voltage sensitive dyes that make use of a

293 ls or to electricity in semiconductors using far red-to-near infrared (NIR) light, which accounts for

294 ncement, which originates from (1) Enhancing far red-to-NIR (700~1200 nm) harvesting, up to 25%.

295 Mother Nature has evolved to smartly capture far red-to-NIR light via their intelligent systems due t

296 emonstrate the structural effects on obvious far red-to-NIR photocatalysis enhancement, which origina

297 f a new strategy, based on adopting nature's far red-to-NIR responsive architectures for an efficient

298 riety of fluorescent proteins, including new far-red variants, to produce a comprehensive guide to ch

299 A far-red version of this flavivirus sensor had the best s

300 ess emission maxima that range from green to far red wavelengths, and enable sensitive biomolecule de