ライフサイエンスコーパス: violet

1 volumes as large as 461 A(3) (e.g., crystal violet).

2 blue and nickel complexation by pyrocatechol violet.

3 Adherent cells were quantified using crystal violet.

4 ative to the energy transfer to free crystal violet.

5 deoxycholate and the hydrophobic dye crystal violet.

6 ained with FJ and counterstained with cresyl violet.

7 ng glory, Ipo-moea (Pharbitis) nil Roth. cv. Violet.

8 r the dendritic marker MAP-2, or with cresyl violet.

9 ise was decreased in the presence of crystal violet.

10 udy was performed after injection of gentian violet.

11 assessed by visual experiments using crystal violet.

12 mpanied by a change of colour from orange to violet.

13 erified using a low concentration of crystal violet (10(-)(5)M) as the probe molecule.

14 ficiently and reversibly using, alternately, violet (400 nm) and blue (446 nm) light.

15 ophores were examined: Rhodamine 6G, crystal violet, a cyanine dye, and a cationic donor-acceptor sub

16 All brains were stained with Cresyl violet, a Nissl stain.

17 rgy transfer donors to the acceptor, crystal violet, a noncompetitive antagonist of the nAChR.

18 ce the amount of silver in relation to their violet absorbing predecessors.

19 encapsulates an ~11 silver atom cluster with violet absorption at 400 nm and with minimal emission.

20 The silver cluster has a single violet absorption band (lambda(max) = 400 nm), and its s

21 vely strong emission develops in lieu of the violet absorption.

22 red, re-yellow, and so forth, ending with si-violet, accompanied by a decrease in saturation.

23 some cationic and one neutral dye (methylene violet), also stiffened the Li(+) GB hydrogel.

24 res, which are stressed by intense prolonged violet and blue laser sources.

25 melanogaster larvae respond to ultraviolet, violet and blue light, and are major mediators of light

26 Cresyl violet and dimethylaminoazobenzene are Raman labels that

27 P3, were examined histologically with cresyl violet and iron stain to assess the degree of damage.

28 aining) leading to neurodegeneration (cresyl violet and neuronal nuclei staining) associated with inc

29 It is concluded that crystal violet and other dyes of similar structure bind to the h

30 Grains are white, black, yellow, and red-violet and plants are cultivated in vast areas of Peru,

31 Organic dyes such as crystal violet and Rhodamine B, the nucleobase cytosine, and nuc

32 Viability tests were performed with crystal violet and ROS tests with DCFH-DA.

33 itric, balsamic, spicy and above all floral (violet and rose) aromas than untreated wines or wines su

34 ning but extensive neurodegeneration (cresyl violet and silver staining) when evaluated 4 days later.

35 to several antimicrobials, including crystal violet and streptomycin (this phenotype could also be co

36 {the reduction of chloranil by leuco crystal violet and the reduction of morphinone reductase by NADH

37 ic fiber communication at short wavelengths (violet and ultra-violet), where a conventional laser is

38 The isolation and comparison of such violet and UV pigments in fish living in different ecolo

39 ght into the mechanism of tuning between the violet and UV.

40 Betalains are tyrosine-derived red-violet and yellow pigments, found in plants only of the

41 Betalains are tyrosine-derived red-violet and yellow plant pigments known for their antioxi

42 erivatives to form a variety of betacyanins (violet) and betaxanthins (yellow), respectively.

43 Cryosections of LG were stained with cresyl violet, and acinar cells and ductal epithelial cells wer

44 ched P. gingivalis were stained with crystal violet, and attachment was expressed based on dye absorp

45 pathologies associated with exposure to UVA, violet, and blue light.

46 stabilize and modulate (in particular blue, violet, and red) colors in flowers, berries, and food pr

47 mixture composed of methylene blue, crystal violet, and rhodamine 6G for positive ion mode detection

48 er Malpighiales, which includes poinsettias, violets, and passionflowers.

49 lecular bases of spectral tuning in the UV-, violet-, and blue-sensitive pigments are not well unders

50 Nearly all flowering plants produce red/violet anthocyanin pigments.

51 The ESR spectra of red and violet anthocyanins was predominantly g approximately 2.

52 techniques to fabricate a pattern of crystal violet as a standard reticle slide for assessing spatial

53 scent NCIs ethidium, quinacrine, and crystal violet as well as [(3)H]thienylcyclohexylpiperidine was

54 ifferent dye molecules (pyranine and crystal violet) as well as avidin through melittin induced membr

55 We used a crystal violet assay and confocal laser scanning microscopy to d

56 nhibitors, estimated cell numbers by crystal violet assays, measured caspase activity by cleavage of

57 ell survival, as measured by MTT and crystal violet assays, regardless of IGF1 pre-treatment.

58 xed tissues using stains for neurons (cresyl violet), astrocytes (GFAP), microglia (Iba1), glutamater

59 es of resistance versus sensitivity to ultra-violet B radiation.

60 rosis factor-alpha, to account for the ultra-violet B-susceptible phenotype.

61 Ultra- violet-B or pTpT treatment of cultured dermal fibroblast

62 also extend to visible and potentially ultra-violet bands.

63 cessary for biofilm development in a crystal violet-based assay involving 24-well tissue culture plat

64 these M. catarrhalis strains in the crystal violet-based assay.

65 transposon insertion mutants in the crystal violet-based biofilm assay system yielded six mutants th

66 from unfermented, slaty, and underfermented, violet, beans, independently of the variety or geographi

67 The zebrafish mutant violet beauregarde (vbg) can be identified at two days p

68 Crystal violet binding blocked agonist-induced 22Na ion efflux f

69 2 negative charges within 8 A of the crystal violet binding site.

70 Following crystal violet biofilm assays for single metal ion solutions, an

71 nd have been shown to strongly absorb in the violet, blue, and/or green regions of the visible spectr

72 he color index of silver (Ag) nanoparticles (violet, blue, green, and red) is used as the sized index

73 aging (MRI) contrast with green (500 nm) and violet-blue (435 nm) light.

74 Solid-state films exhibit intense violet-blue emission (lambda(PL) = 398-415 nm) with high

75 A pH-independent violet-blue emission band is due to the addition of nucl

76 minescence from all four naphthalimides have violet-blue fluorescence and phosphorescent bands betwee

77 All are efficient violet-blue fluorophores with emission maxima at approxi

78 Violet-blue light is toxic to mammalian cells, and this

79 In this report, we show that violet-blue light, as well as UVA, stimulated H2O2 produ

80 n to a red fluorescent form upon exposure to violet-blue light.

81 KATP channel activity following exposure to violet-blue light.

82 ting group that absorbs visible light in the violet-blue range.

83 rt a previously unnoticed duplication of the violet-blue short wavelength-sensitive 2 (SWS2) opsin, w

84 aled a wide spectrum of colors, ranging from violet-blue to red with excitation through a single filt

85 5 to 420 nm (corresponding to ultraviolet to violet/blue emission).

86 sure binding, we determined that one crystal violet bound per receptor with a dissociation constant o

87 me flavin (and hence to iodonitrotetrazolium violet) but not from flavin to heme (or not between the

88 ed in the visible spectral range of green to violet by varying the indium mole fraction of the InxGa1

89 rains were harvested and stained with cresyl violet, caspase-3, and TUNEL to detect morphological and

90 The flux of the crystal violet cation across the membrane is simultaneously meas

91 The Raman spectra obtained from cresyl fast violet (CFV) deposited on substrates with differing mean

92 sts that unpaired nucleobases coordinate the violet cluster and favor the single-stranded sensor.

93 directly link single-stranded hosts for the violet cluster and their hybridized analogs for the blue

94 When the two monomeric DNA/violet cluster conjugates transform to one dimeric DNA/n

95 with complementary oligonucleotides, and the violet cluster converts to an emissive near-infrared clu

96 arget analytes transform the weakly emissive violet cluster to a new chromophore with blue-green abso

97 ter size, and DNA structure of the precursor violet cluster-DNA complex.

98 rong enhancement of a 405 nm band giving the violet color of bioluminescence.

99 The reddish-violet complex formed showed lambdamax at 540nm.

100 is(2-pyridyl)-s-triazine, which forms a blue-violet complex ion in the presence of ferrous ions.

101 oxy-3-naphthoic acid (BTAHNA) to give a deep violet complex with high molar absorptivity (7.05x10(6)L

102 Xenopus violet cone opsin (VCOP) and its counterion variant (VCO

103 d 140 K, the photochemical excitation of the violet cone opsin at 425 nm generates the batho intermed

104 Extended illumination of the violet cone opsin at 75 K, however, generates a red-shif

105 The batho intermediate of the violet cone opsin generated at 45 K has an absorption ma

106 FTIR spectroscopy of violet cone opsin indicates conclusively that the chromo

107 oughly 75% of the observed blue shift of the violet cone pigment relative to rhodopsin.

108 In the presence of sbeta-CD, the crystal violet-containing buffer was blue and was deflected anod

109 In the absence of sbeta-CD, the crystal violet-containing buffer was reddish/purple and the crys

110 ing site location for the fluorophor crystal violet (CrV), a noncompetitive antagonist of the nicotin

111 ied in numerous plant species of the coffee, violet, cucurbit, pea, potato, and grass families.

112 be logarithmically divergent with the ultra-violet cut-off, but physically meaningful regularized po

113 (C343)-TiO(2) nanoparticles (NP) and Cresyl Violet (CV(+))-TiO(2) NP systems, using time-correlated

114 s well as bactericidal activity with crystal violet (CV) coated polyurethane.

115 SC4) interacts with the aromatic dye crystal violet (CV) to form complexes with stoichiometries rangi

116 am-negative strains by staining with crystal violet (CV).

117 N-methyl mesoporphyrin IX (NMM) and Crystal Violet (CV).

118 action of a benzo-phenoxazine ligand (Cresyl Violet, CV) with antiparallel and (3 + 1) hybrid G-quadr

119 gh-pressure liquid chromatography with ultra-violet detection (HPLC-UV) is one of the most commonly u

120 olor of the colloidal suspension from red to violet due to coupling of surface plasmons in aggregated

121 Lysine, peptides, crystal violet dye, and a biotin conjugate are found to survive

122 Anionic I3(-) reacts with cationic crystal violet dye, and the product is extracted into 1-hexyl-3-

123 Brilliant green and crystal violet dyes were the molecular probes, and the experimen

124 Fos activity in a territorial finch, the violet-eared waxbill (Estrildidae: Uraeginthus granatina

125 apid increase of hard and soft X-rays, ultra-violet emission with large Doppler blue shifts associate

126 hane dyes (rose bengal, rhodamine B, crystal violet, ethyl violet, fast green fcf, and brilliant gree

127 In our search for new violet-excitable dyes with improved photophysical and ph

128 provided by resonance enhancement with deep violet excitation.

129 Such dark state engineering enables violet-excited blue emission to be increased upon lower

130 e bengal, rhodamine B, crystal violet, ethyl violet, fast green fcf, and brilliant green) have been a

131 highly conductive black powder or dark blue-violet films.

132 Test results with blue-violet filter, a short-pass yellow filter and with no fi

133 st results increased significantly with blue-violet filters for all patients.

134 of Viola pubescens Aiton, a yellow-flowered violet found in the temperate forests of eastern North A

135 ion, a hierarchy with [red, (magenta)-red], [violet], [green/yellow], [blue], [orange], and [cyan], a

136 sensitivities are malachite green > crystal violet > quinaldine red > ascorbate reduction > antimony

137 Gentian violet (GV) is a cationic triphenylmethane dye with pote

138 s and the long wavelength fluorophore cresyl violet, has been used for the determination of coenzyme

139 y of methodologies: cytoarchitecture (cresyl violet), histochemistry (peanut agglutinin), immunocytoc

140 performance liquid chromatography with ultra violet (HPLC-UV) detection.

141 A-type chromophores are sensitive only to violet illumination and are phototransformed either into

142 its beautiful blue fluorescence under ultra-violet illumination.

143 chemical imaging of the cationic dye crystal violet in inked lines on glass and for lipid distributio

144 nce and fluorescence spectroscopy of crystal violet in order to elucidate the binding mechanism of th

145 Ultra violet-inactivated CVB3 did not induce any response, sug

146 have applications that extend from the ultra-violet into the mid-infrared bands.

147 e topoisomerase poison etoposide, like ultra violet irradiation, inhibits Mdm2 synthesis.

148 azine methosulfate, and iodonitrotetrazolium violet, is added to the cultures.

149 ls by the bound acceptor fluorophore crystal violet, its binding site was first localized within the

150 color from orange (lambda(max) = 510 nm) to violet (lambda(max) = 583 nm) upon reaction with cyanide

151 de (orange, lambda(max) = 510 nm) changes to violet (lambda(max) = 583 nm) upon reaction with cyanide

152 e-sensitive cone, SWS1, has switched between violet (lambdamax > 400 nm) and ultraviolet (lambdamax <

153 field optical microscope coupled to an ultra-violet laser emitting light at a wavelength of 244 nm.

154 ion products are detected with leuco crystal violet (LCV) dye by eye without a need for instrumentati

155 reen LED (RG) lights; and combined red-green-violet LED (RGV) lights during the night.

156 sic fuchsin leuconitrile (BFCN), and crystal violet leucomethyl (CVMe) and leucobenzyl (CVBn), as wel

157 The photochemical reactions of crystal violet leuconitrile (CVCN) were investigated by the mean

158 ongly (epsilon450 = 43,000 M(-1) cm(-1)) and violet light 11-fold more weakly.

159 nverted from green to red in the presence of violet light and calcium.

160 on of photocromic lens with a selective blue-violet light filter showed functional benefit in all eva

161 ameters using photocromic and selective blue-violet light filtering spectacle lenses in patients affe

162 Violet light illumination of JF-NP-26 induces a photoche

163 ilament fusion protein were illuminated with violet light in a short segment of axon to create a puls

164 ially dark but becomes red fluorescent after violet light irradiation.

165 dark" but exhibits red fluorescence after UV-violet light irradiation.

166 eous exposure of the cervical lymph nodes to violet light permitted punctual tagging of immune cells

167 den changes of [Ca(2+)] and because it emits violet light rather than blue due to a prominent band wi

168 romatically orthogonal manner using blue and violet light so as to modulate the neuronal firing rate

169 o orange light and repellent responses to UV/violet light that were comparable to those produced by t

170 The pacemaker neurons respond to violet light, and this response depends on Rh7.

171 that can be activated or inhibited with deep-violet light, but respond normally to acetylcholine in t

172 By exposing Kaede transgenic mouse skin to violet light, we tracked the fate of cutaneous T cells.

173 so decrease after exposure of cells to ultra violet light, which correlate with increase in the level

174 g out the betaME or through irradiation with violet light, with up to 80% total recovery.

175 A violet light-emitting diode (LED) excitation source and

176 - is tunable and depends on the intensity of violet light.

177 ctivated with a short burst of low-intensity violet light.

178 ence of bacteria was attained with green and violet light.

179 issociates in cyan light and reassociates in violet light.

180 tially dark but become red fluorescent after violet-light irradiation.

181 e biosensors, we also introduce a deep ultra-violet lithography technique to simultaneously pattern t

182 by the presence of skin findings such as red-violet macular atrophy, platyspondyly and metaphyseal os

183 saceae p.p.), saxifrages (Saxifragales), and violets (Malpighiales).

184 medical grade silicone incorporating crystal violet, methylene blue and 2 nm gold nanoparticles.

185 by measuring the areal densities of crystal violet molecules embedded in an ultrathin spin-on-glass

186 and these particles when illuminated in the violet-near UV range produce cumulative toxicity.

187 these treatments were evaluated using cresyl violet (Nissl) staining.

188 trite based on the immobilisation of Lauth's violet on triacetyl cellulose membrane using absorption

189 At room temperature, the X. laevis violet opsin has an absorption maximum at 426 nm when ge

190 with rhodopsin, red opsin, green opsin, and violet opsin reporters, we have identified hundreds of d

191 and brain sections were stained with cresyl violet or immunolabeled with NeuN (for neuronal counts),

192 cells (flat preparations stained with cresyl violet or retrograde labeling with a neurotracer), the n

193 sues with metachromatic dyes such as crystal violet or with the cotton dye Congo red (particularly un

194 lambda max) at approximately 360 nm, whereas violet (or blue) vision is mediated by orthologous pigme

195 tochrome oxidase (CO) histochemistry, cresyl violet, or demonstration of TCAs by placement of 1,1'-di

196 d was more susceptible to killing by crystal violet, osmotic shock, and select carbapenem antibiotics

197 nd CoQ10 causes the MLs lysis and the cresyl violet oxidation, obtaining a decrease in the fluorescen

198 itized trans-cis isomerization, using cresyl violet perchlorate as the sensitizer, also led to simila

199 In the avian lineage, the origin of the violet pigment and the subsequent restoration of UV pigm

200 ransformed the zebra finch UV pigment into a violet pigment by incorporating one amino acid change, C

201 ve constructed chimeric pigments between the violet pigment of African clawed frog (Xenopus laevis) a

202 constructed UV pigments from the orthologous violet pigments of the pigeon and chicken.

203 arisons of the tertiary structures of UV and violet pigments reveal that the distance between the cou

204 Anthocyanins are red and violet pigments that color flowers, fruits and epidermal

205 n TM II is narrower for UV pigments than for violet pigments, which may restrict the access of water

206 was expressed in all cases, and the blue and violet pigments, which were not detected in any of the s

207 s that many other fish also have orthologous violet pigments.

208 hnique using fiducial markers such as cresyl violet, Ponceau S, and bromophenol blue that possess a c

209 Like their violet predecessors, purified blue-green clusters have a

210 microextraction procedure using pyrocatechol violet (PV) as complexing reagent and 1-hexyl-3-methylim

211 Ultra-violet radiation (UVR)-induced skin melanin synthesis is

212 response to the selective pressure of ultra-violet radiation (UVR).

213 skin fibroblasts exposed to time-bound ultra-violet radiation has been performed using quantitative p

214 nion of 2-chloranthraquinone and the crystal violet radical, which display improved resolution at low

215 FP and its additional absorbance band in the violet range has allowed for designing a chimeric protei

216 ent fluorophores, emitting light in the blue-violet range.

217 The reaction produces intense violet-red color and can be easily used both for quantit

218 UV1C extends the DNAzyme's activity into the violet region of the spectrum.

219 The patterned crystal violet reticle was also used to diagnose issues with IMS

220 Retinas were stained with cresyl violet, retinal cell-specific markers, and a human nucle

221 One dye with high affinity, crystal violet, revealed a greater than 200-fold fluorescence en

222 corporated the addition of a dry ink gentian violet S-stamp to the stromal side of Descemet membrane.

223 es that correlate with spectral sensitivity, violet sensitive above 390 nm and ultraviolet sensitive

224 and, neutralizing this charge, converts the violet sensitive pigment into one that absorbs maximally

225 d in four genes: SWS1 (UV sensitive), SWS2B (violet sensitive), RH2Abeta (green sensitive), and LWS (

226 hat rod opsin positive cells were absent and violet-sensitive cone and green-sensitive cone opsin pos

227 Violet-sensitive pigments probably evolved from an ances

228 ultraviolet sensitivity has re-evolved from violet-sensitive pigments.

229 with a lambda(max) of 423 nm, an example of violet-sensitive SWS1 pigment in fish.

230 The finding of a violet-sensitive SWS1 pigment in scabbardfish suggests t

231 of the short-wave pigment and confirmed its violet sensitivity by expression and reconstitution of t

232 e can switch sensitivity from ultraviolet to violet sensitivity, but where such a change is not invol

233 echanical (QM/MM) computations show that the violet-sensitivity was achieved by the deletion of Phe-8

234 We obtain single-mode lasing in the blue-violet spectral region with a remarkable 60 nm of tuning

235 Cresyl violet stain demonstrated massive loss of neurons in the

236 Counting of cresyl violet stained sections showed an apparent increase in g

237 re evaluated for area of tissue loss (Cresyl-violet stained sections) and the number of GFAP immunore

238 image analysis system (BioQuant) and cresyl violet stained sequential sections from the forebrain re

239 wo adult rat spinal cords on adjacent cresyl violet-stained and in situ hybridization sections.

240 Molecular fingerprint comparison of cresyl violet-stained CA1 and CA3 pyramidal neurons microaspira

241 Using still images from cresyl-violet-stained material, we present an adaptation of the

242 diately after I/R injury and counting cresyl violet-stained retinal ganglion cell layer cells (RGCLCs

243 For both methods, Arc cresyl violet staining (cell density) and NPY and Y1 receptor-i

244 Brain tissue loss determined using cresyl violet staining and astrocyte hypertrophy and proliferat

245 d neurodegeneration, as visualized by cresyl violet staining and quantified in 20 serially stained si

246 ng a microtiter plate assay with the crystal violet staining method, and the presence of the putative

247 uous passaging at a 1:3 split and by crystal violet staining of confluent dishes.

248 ed a modified alcohol-based, buffered cresyl violet staining protocol that provides reproducible stai

249 C adhered strongly (quantified using crystal violet staining) to collagen IV and collagen I (P < 0.01

250 outgrowth ([3H]thymidine uptake and crystal violet staining) was also tested.

251 Crystal violet staining, acryflavin agglutination, and polymyxin

252 pendent measures: Congo red binding, crystal violet staining, and confocal laser scanning microscopy.

253 valuated by fluorescence microscopy, crystal violet staining, and the MTS assay.

254 s were identified and quantitated by crystal violet staining.

255 distal tubular cells, as observed by crystal violet staining.

256 monds, musks, ambers, woods, sandalwoods and violets strongly correlate with odor character.

257 allene function, leading to a conjugated and violet tertiary carbocation that returned immediately to

258 materials that reflect light from the ultra-violet, through the visible, to the near-infrared.

259 later at > or =6 months of age using cresyl violet, Timm, and rapid Golgi staining and immunocytoche

260 EB, BC and PC, pure blue colours devoid of a violet tint were exclusively observed for the phenolic e

261 ew seconds, to the formation of intense pink/violet to green colors that bleach completely in a few m

262 eotide phosphate, NADPH, reduces tetrazolium violet to its formazan, the color of which reflects the

263 ucture and silver stoichiometry underlie the violet to near-infrared cluster transformation.

264 376 to 633 nm, yielding apparent colors from violet to red, all of which can be visualized directly.

265 sistent with preferential binding of crystal violet to the desensitized conformation of the AChR.

266 and visualized with the addition of crystal violet to the separation buffer.

267 t surprisingly, we detected gene loss of the violet/ultraviolet-sensitive opsin (SWS1) in all owls we

268 to generate an unusual four-photon-promoted violet upconversion emission from Er(3+) with an intensi

269 Cell proliferation was monitored by crystal violet uptake, and pericyte migration was assessed in a

270 Ultra-Violet (UV) fluorescence from Chlorophyll present in the

271 on with a fluorescent dye, which under ultra violet (UV) illumination makes the fingermarks visible a

272 ects that were strongly potentiated by ultra violet (UV) irradiation, resulting in a dramatic loss of

273 zene chromophore which is sensitive to ultra-violet (UV) light works as "motor", and the UV light and

274 predominantly at body sites exposed to ultra violet (UV) radiation, pointing to a key role for UV in

275 ructures have a well-defined broadband ultra-violet (UV) to blue wavelength distribution; the corresp

276 u nano particles were characterized by Ultra Violet (UV), Fourier Transform Infrared (FTIR), Raman sp

277 ls from DNA-damaging agents, including ultra violet (UV)-induced apoptosis.

278 S; lambda=514.5 nm) or long wavelength ultra-violet (UVA; lambda=366 nm) light.

279 nd 47.4mmol Trolox/kg for the yellow and red-violet varieties analyzed respectively.

280 ion of the betacyanin pigment betanin in red-violet varieties is here further analyzed detecting the

281 f these pigments change from red to green to violet via systematic shifts in the position of the prim

282 (Zea mays), soybean (Glycene max) and field violet (Viola arvensis) at three time points in one seas

283 sion and scanning electron microscopy, ultra violet-visible and X-ray photoelectron spectroscopy, and

284 Many other species switched to violet vision and, then again, some avian species switch

285 These UV and violet vision are mediated by short wavelength-sensitive

286 rectly from the vertebrate ancestor, whereas violet vision in others has evolved by different amino a

287 Ultraviolet (UV) and violet vision in vertebrates is mediated by UV and viole

288 adaptations, but also the genetics of UV and violet vision.

289 vision in vertebrates is mediated by UV and violet visual pigments that absorb light maximally (lamb

290 ng buffer was reddish/purple and the crystal violet was deflected cathodically in the chamber.

291 neutral Tb3+ -chelate to nAChR-bound crystal violet was reduced 95% relative to the energy transfer t

292 This result indicated that crystal violet was strongly shielded from solvent when bound to

293 as much more rapid when iodonitrotetrazolium violet was used as electron acceptor than when oxygen al

294 us (DOF) of 15lambda using a planar SOL at a violet wavelength of 405 nm.

295 e, spectra of glucose, arginine, and crystal violet were obtained with no observed interferences in t

296 monitor assay progress by color change from violet when negative to sky blue when positive, and resu

297 ation at short wavelengths (violet and ultra-violet), where a conventional laser is difficult to real

298 , and to regulate binding to the dye crystal violet, whereas motility, flagellar secretion, and exter

299 r signal is based on the reaction of Lauth's violet with bromate as an oxidant in the presence of nit

300 catalytic effect on the oxidation of Lauth's violet with bromate in acidic media.