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 udy was performed after injection of gentian violet.

3 assessed by visual experiments using crystal violet.

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

5 blue and nickel complexation by pyrocatechol violet.

6 Adherent cells were quantified using crystal violet.

7 ative to the energy transfer to free crystal violet.

8 deoxycholate and the hydrophobic dye crystal violet.

9 ained with FJ and counterstained with cresyl violet.

10 f 10(11) of the signal detected from crystal violet.

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

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

13 for two American minks with Moyle (m/m) and Violet (a/a m/m /p/p) phenotypes.

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

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

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

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

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

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

20 zed a 12-year dataset (2004-2015), combining violet abundance, habitat physiognomy and fire history d

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

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

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

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

25 Degradation efficiency of crystal violet and commassie blue R250 after 6 h was assessed to

26 Cresyl violet and dimethylaminoazobenzene are Raman labels that

27 ivation of the vertebrate TRPA1 channel with violet and green light, respectively.

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

29 abolic activity were quantified with crystal violet and methyl thiazolyl tetrazolium staining methods

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

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

32 of detection for chemical sensing of Crystal Violet and Rhodamine 6G by the Al-QS was driven up to si

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

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

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

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

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

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

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

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

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

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

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

44 DASA exist normally in open form (blue/violet) and readily convert to cyclic (light yellow/colo

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

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

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

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

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

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

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

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

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

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 rmination of colony-forming units, a crystal violet assay, scanning electronic microscopy and live/de

57 Resazurin and crystal violet assays indicated that 8a decreases triple-negativ

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

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

60 phylococcal isolates was assessed by crystal violet assays.

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

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

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

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

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

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

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

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

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

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

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

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

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

79 shift value and emission color ranging from violet-blue through deep blue, green, yellow to red.

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

81 5 to 420 nm (corresponding to ultraviolet to violet/blue emission).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

101 photobactericidal polymer containing crystal violet (CV) and thiolated gold nanocluster ([Au(25)(Cys)

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

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

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

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

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

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

108 The article discusses the use of deep ultra violet (DUV) laser-induced fluorescence for detecting ca

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

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

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

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

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

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

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

116 provided by resonance enhancement with deep violet excitation.

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

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

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

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

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

122 tion step, and a liquid chromatography-ultra violet-fluorescence (HPLC-UV/FL) analysis.

123 The nature of the dodecaboride colors-violet for ZrB(12) and blue for YB(12)-can be attributed

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

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

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

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

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

129 its beautiful blue fluorescence under ultra-violet illumination.

130 Pyrocatechol violet impregnated magnetic graphene oxide hybrid materi

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

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

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

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

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

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

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

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

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

140 pacitance enhancement up to 21% under 405 nm violet laser irradiation has been observed, suggesting a

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

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

143 elease of white phosphorus using inexpensive violet LED sources.

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

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

146 These investigations identify violet light as a developmental timing cue that, via an

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

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

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

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

151 state Schiff base is unique, requiring only violet light in this instance.

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

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

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

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

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

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

158 adily upconvert 488-640 nm photons to 425 nm violet light with efficiencies as high as 7 +/- 0.9% and

159 conserved opsin that is sensitive to visible violet light(1,2).

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

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

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

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

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

165 This analysis thus identifies a violet light-sensitive deep brain photoreceptor that nor

166 tions that are effective for photolysis with violet light.

167 A neurons increase cAMP when stimulated with violet light.

168 ight, and the fluorescence can be reset with violet light.

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

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

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

172 issociates in cyan light and reassociates in violet light.

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

174 The reaction proceeds by violet-light photoinduced electron transfer between an N

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

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

177 hol blue, phenol red, calcein, leuco crystal violet, malachite green, and a fluorescent dye for visua

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

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

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

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

182 , whereas total anthocyanins were highest in violet, nerone, and black rice flours.

183 mplexes 5 and 6, on the other hand, are blue/violet neutral complexes, which carry an EWG-substituted

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

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

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

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

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

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

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

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

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

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

194 emonstrated for the exfoliation of black and violet phosphorus (yielding monolayers of "phosphorene"

195 ated compounds including P(4)S(3), Hittorf's violet phosphorus.

196 Moreover, violet photostimulation during cold exposure acutely sup

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

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

199 ains occur in two forms i.e. betacyanin (red-violet pigment) and betaxanthin (yellow-orange pigment)

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

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

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

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

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

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

206 ed the character of habitats associated with violet presence and abundance, in particular a strong po

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

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

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

210 s in South America, where exposures to ultra-violet radiation are high.

211 The ergosterol was exposed to ultra-violet radiation for conversion to ergocalciferol (vitam

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

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

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

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

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

217 Betalains are violet-red, natural food grade pigments with health bene

218 sible through the appropriate combination of violet/red light and temperature, results that highlight

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

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

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

222 Total phenolic content was highest in violet rice flours, whereas total anthocyanins were high

223 phenolic contents and found to be higher in violet rice flours.

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

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

226 A functional violet sensitive SWS1 with crucial Ser90 is presumed.

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

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

229 Violet-sensitive pigments probably evolved from an ances

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

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

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

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

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

235 olet (UV) sensitivity to the ancestral avian violet sensitivity, thus improving visual resolution.

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

237 0 nm polystyrene and 98.6 nm silica beads by violet side scatter (VSSC).

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

239 on-like modes occur in the visible and ultra-violet spectral regions, respectively.

240 Cresyl violet stain demonstrated massive loss of neurons in the

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

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

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

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

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

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

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

251 A crystal violet staining-based assay shows that tiny bacterial mi

252 s were identified and quantitated by crystal violet staining.

253 re in driving both presence and abundance of violets, suggesting management with prescribed fires can

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

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

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

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

258 slices and subsequently stained with cresyl violet to enable high-resolution spatial analysis of tra

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

260 Laser light from violet to infrared is coupled onto the chip via an optic

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

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

263 376 to 633 nm, yielding apparent colors from violet to red, all of which can be visualized directly.

264 n be systematically varied over 270 nm, from violet to red, through proper choice of the acceptor (ca

265 eO(3) (BLFO) ceramics has been studied under violet to UV irradiation.

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

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

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

269 ntribution of each has been unclear as ultra violet (UV) exposure also causes the generation of vitam

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 vignon blanc grapes were exposed to an ultra-violet (UV) light source post-hand harvest (whole bunche

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

274 eria and are known to be induced under ultra-violet (UV) light.

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

282 spatiotemporal distribution and abundance of violets (Viola spp.), the host plants of the threatened

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

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

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

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

294 nd its metabolite, crystal and leuco crystal violet, were extracted from spiked fish extracts and qua

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

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

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

298 The red color GO-AuNPs was changed to violet while adding 250 x 10(-5) M KMS whereas the absor

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.