ライフサイエンスコーパス: microspectroscopy

1 canning microscopy as well as confocal Raman microspectroscopy.

2 Saos-2 and SW-1353 cells by utilizing Raman microspectroscopy.

3 in desiccated specimens using confocal Raman microspectroscopy.

4 activity and carbon uptake in situ via Raman microspectroscopy.

5 copic information obtained by FTIR and Raman microspectroscopy.

6 ried and spectra were collected by using MIR-microspectroscopy.

7 (DSC) and Fourier Transform InfraRed (FTIR) microspectroscopy.

8 y an improved approach of sensitive infrared microspectroscopy.

9 rovided by a combination of Raman macro- and microspectroscopy.

10 r transform infrared (FTIR) spectroscopy and microspectroscopy.

11 nformation or present confounding effects in microspectroscopy.

12 inside a somatic mammalian cell using Raman microspectroscopy.

13 and outflow events and analyzed using Raman microspectroscopy.

14 tion were followed in situ by Raman tweezers microspectroscopy.

15 Cimone, Italy, using multimodal microspectroscopy.

16 analysed using optical-photothermal infrared microspectroscopy.

17 microalgae) enabling interrogation by Raman microspectroscopy.

18 l infrared spectroscopy (AFM-PTIR) and Raman microspectroscopy.

19 The analysis was performed using Raman microspectroscopy.

20 ynchrotron-Fourier transform infrared (FTIR) microspectroscopy.

21 ine content to perform quantitative infrared microspectroscopy.

22 custom-designed set-up for magneto-infrared microspectroscopy.

23 cation of the detected particles using Raman microspectroscopy.

24 elected area electron diffraction, and Raman microspectroscopy.

25 using a label-free approach, confocal Raman microspectroscopy.

26 ted biomolecular specificity for vibrational microspectroscopy.

27 for "spectral" cytology of urine using Raman microspectroscopy.

28 ized using atomic force microscopy and Raman microspectroscopy.

29 with the high specificity and speed of Raman microspectroscopy.

30 ed S and von Kossa staining as well as Raman microspectroscopy.

31 zation mass spectrometric imaging, and Raman microspectroscopy.

32 ated nerve fiber by means of polarized Raman microspectroscopy.

33 Fourier transform infrared (FTIR) and Raman microspectroscopies.

34 Fluorescence microspectroscopy additionally supports the presence of

35 herent anti-Stokes Raman spectroscopy (CARS) microspectroscopy allowed us to locally identify acylgly

36 chrotron Fourier transform infrared (S-FTIR) microspectroscopy allows the label-free examination of m

37 Using Raman microspectroscopy, amorphous calcium carbonate (ACC) was

38 sis using Fourier-transform infrared (FT-IR) microspectroscopy, an evolving method that allows the no

39 Proteomic and Raman microspectroscopy analyses showed that the method of dec

40 a multimodal approach using XFM and infrared microspectroscopy analyses to demonstrate colocalization

41 Multimodal microspectroscopy analysis during the background case re

42 ding native dentine and alveolar bone, Raman microspectroscopy analysis is used.

43 ese observations, Fourier transform infrared microspectroscopy analysis revealed that the ech and yip

44 Here we employ quantitative Raman microspectroscopy and biomolecular component analysis (B

45 least fivefold faster than spontaneous Raman microspectroscopy and can be used to generate maps of bi

46 ascitic fluid is possible by means of Raman microspectroscopy and chemometrical evaluation with the

47 onalities of the SOA were probed using X-ray microspectroscopy and compared with other laboratory gen

48 Confocal Raman microspectroscopy and fluorescence imaging are two well-

49 applied synchrotron radiation-FTIR (SR-FTIR) microspectroscopy and focal plane array (FPA-FTIR) micro

50 on the provided data we conclude that Raman microspectroscopy and imaging are suitable tools for the

51 ted here should enable the routine use of IR microspectroscopy and imaging for the molecular analysis

52 Raman microspectroscopy and imaging revealed significant diffe

53 lved data, obtained e.g. by scanning mode IR microspectroscopy and IR imaging by focal plane array de

54 combining Fourier Transform Infrared (FTIR) microspectroscopy and Machine learning to comprehensivel

55 radiation-based techniques on both, infrared microspectroscopy and micro X-ray diffraction, with the

56 ation spectroscopy (SCNS) by combining Raman microspectroscopy and optical trapping induced crystalli

57 Here, we show that a combination of Raman microspectroscopy and partial least-squares discriminant

58 sults demonstrate a great potential of Raman microspectroscopy and Raman imaging as marker-independen

59 signed to investigate the potential of Raman microspectroscopy and Raman imaging as non-invasive, mar

60 Raman microspectroscopy and Raman imaging were established as

61 Bacillus cereus spores using confocal Raman microspectroscopy and Raman imaging.

62 a collected with portable FT-IR and FT-Raman microspectroscopy and subjected to metabolomics analysis

63 ated on aluminum foils and analyzed by Raman microspectroscopy and subsequently by electron microscop

64 ynchrotron Fourier transform infrared (FTIR) microspectroscopy and synchrotron micro-X-ray fluorescen

65 xidation characteristics obtained with Raman microspectroscopy and temperature programmed oxidation,

66 chrotron-Fourier transform infrared (S-FTIR) microspectroscopy and the cheese was softer.

67 rs of residual dentin were examined by Raman microspectroscopy and Vickers microhardness, while the s

68 ssion scanning electron microscopy, infrared microspectroscopy, and biochemical characterization of s

69 nation of compound-specific chemical assays, microspectroscopy, and electron microscopy to show that

70 ted Raman scattering (SRS) microscopy, Raman microspectroscopy, and histochemical staining, which rev

71 -ray diffraction, Fourier transform infrared microspectroscopy, and inelastic neutron scattering, cou

72 structively analyzed by laser tweezers Raman microspectroscopy, and information on their composition

73 ynchrotron radiation FTIR (S-FTIR) and Raman microspectroscopy are powerful complementary techniques

74 signatures in spectra, obtained by infrared microspectroscopy, are still not clear.

75 ttenuated total internal reflection infrared microspectroscopy as a detector for high-performance liq

76 this study, we present the ability of Raman microspectroscopy as a novel analytical technique for a

77 ing NYscFv as probe in combination with SERS microspectroscopy at a single laser excitation wavelengt

78 ing forward stable isotope (resonance) Raman microspectroscopy at the single-cell level to broaden th

79 pores were analyzed by using nonlinear Raman microspectroscopy based on coherent anti-Stokes Raman sc

80 ering submicron resolution, this vibrational microspectroscopy-based approach emerges as a promising

81 emonstrates the potential for confocal Raman microspectroscopy becoming an indispensable tool to obta

82 gorous theory is presented for IR absorption microspectroscopy by using Maxwell's equations to model

83 ular changes were analyzed by Raman confocal microspectroscopy, calcium dynamics by confocal microsco

84 uch as optical photothermal infrared (OPTIR) microspectroscopy can achieve <500 nm spatial resolution

85 thermal Fourier-transform infrared (PT-FTIR) microspectroscopy can also be employed using the same pr

86 However, the potential of Raman microspectroscopy can be fully realized only when novel

87 mentation, Fourier transform infrared (FTIR) microspectroscopy can now be used to capture thousands o

88 Results showed that MIR-microspectroscopy can provide an alternative methodology

89 Raman microspectroscopy can provide the chemical contrast need

90 However, Raman microspectroscopy combined with a chemometric analysis r

91 Near-infrared (NIR) Raman microspectroscopy combined with advanced statistics was

92 carbon electrode using synchrotron infrared microspectroscopy combined with protein film electrochem

93 Here, we report that Raman microspectroscopy, complemented by hydrodynamic modellin

94 Furthermore, synchrotron-based infrared microspectroscopy confirmed a two-dimensional microscale

95 cal photothermal infrared (O-PTIR) and Raman microspectroscopy confirmed collected particle compositi

96 mical images obtained using synchrotron-FTIR microspectroscopy confirmed that the TG-MD displayed the

97 sue using Fourier-transform infrared (FT-IR) microspectroscopy, confocal Raman microspectroscopy (CRM

98 n-based Fourier transform infrared (SR-FTIR) microspectroscopy coupled with multivariate analysis was

99 Here we demonstrate the use of Raman microspectroscopy coupled with multivariate spectral ana

100 SR-FTIR microspectroscopy coupled with PCA appears to enable the

101 We illustrate that single-cell Raman microspectroscopy, coupled with deuterium isotope probin

102 , inelastic neutron scattering, and infrared microspectroscopy, coupled with modeling, reveal a pore

103 Here, we used microspectroscopy-coupled X-ray crystallography to inter

104 ed (FT-IR) microspectroscopy, confocal Raman microspectroscopy (CRM), and matrix-assisted laser desor

105 tate NMR spectroscopy, FTIR spectroscopy and microspectroscopy, cryo-EM, and amide hydrogen/deuterium

106 ing accurate chemical information from in IR microspectroscopy data.

107 In addition, Raman microspectroscopy demonstrated that different cations af

108 Raman microspectroscopy detected congestion during WI by measu

109 In situ synchrotron-sourced IR microspectroscopy detected the evolution of the reactant

110 d in crystallo reactions monitored by UV-vis microspectroscopy, electron paramagnetic resonance (EPR)

111 hermal-Fourier transform-infrared (PT-FT-IR) microspectroscopy employs a thermal probe mounted in a s

112 powder diffraction and synchrotron infrared microspectroscopy enable the direct visualization of bin

113 e the concept of supervised compressive CARS microspectroscopy, enabling artifact-less high-speed qua

114 advent of automated algorithms, vibrational microspectroscopy excels in the field of spectropatholog

115 cornea were collected by using a synchrotron microspectroscopy facility at Daresbury Laboratory (Unit

116 nt two-dimensional multifocus confocal Raman microspectroscopy featuring the tilted-array technique i

117 rove of the diagnostic capabilities of FT-IR microspectroscopy for monitoring in real-time the bioche

118 We used infrared microspectroscopy for the automatic characterization and

119 A method using confocal Raman microspectroscopy for the detection of cellular proteins

120 demonstrate the capability of confocal Raman microspectroscopy for the discrimination and identificat

121 Fourier transform infrared microspectroscopy (FTIRM) is a widely used method for ma

122 (SEM) analysis, a Fourier-transform infrared microspectroscopy (FTIRM) method was employed to monitor

123 CARS microspectroscopy further indicated lower lipid fluidity

124 Using a combination of Raman microspectroscopy, genome mining, and mutational analysi

125 Polarized Raman microspectroscopy has been employed to determine the ori

126 f microbiological samples with optical Raman microspectroscopy has been the inability to acquire pre-

127 Raman microspectroscopy has been used to monitor changes in th

128 Synchrotron radiation (SR) IR microspectroscopy has enabled determination of the therm

129 monstrates for the first time that NIR Raman microspectroscopy has the potential for the reagentless

130 s of samples of different types, obtained by microspectroscopy, have been performed.

131 FT-IR microspectroscopy holds great promise not only as a meth

132 Imaging mass lipidomics and Raman microspectroscopy identified conformational changes of l

133 ternal reflection Fourier-transform infrared microspectroscopy identified the mineral as apatite.

134 In this report, we employ coherent Raman microspectroscopy in a combination with a hierarchical c

135 coherent anti-stokes Raman scattering (CARS) microspectroscopy in a microfluidic device.

136 n-based Fourier transform infrared (SR-FTIR) microspectroscopy in a set of three GBM cell lines, incl

137 Raman microspectroscopy in combination with fluorescence in si

138 dent identification procedure by using Raman microspectroscopy in combination with innovative chemome

139 These results demonstrate that Raman microspectroscopy in combination with support vector mac

140 ctance Fourier transform infrared (SR FT-IR) microspectroscopy in conjunction with discriminant analy

141 n vivo by mixed stable isotope-labeled Raman microspectroscopy in conjunction with multivariate curve

142 e way toward novel approaches to apply Raman microspectroscopy in environmental process studies.

143 stigated by Synchrotron deep UV fluorescence microspectroscopy in order to characterize the change of

144 monstrate here by synchrotron based infrared microspectroscopy in transmission and attenuated total r

145 trochemical microcell for in situ soft X-ray microspectroscopy in transmission, dedicated for nonvacu

146 ration gradient over time via operando Raman microspectroscopy, in tandem with potentiostatic electro

147 The FT-IR microspectroscopy indicated that spatial accumulation of

148 Quantification using XRF and XANES microspectroscopy indicated up to 0.5 wt % of As(-I) in

149 Until nowadays most infrared microspectroscopy (IRMS) experiments on biological speci

150 Mid-infrared (IR) microspectroscopy is a non-invasive tool that allows in

151 Fourier transform infrared (FTIR) microspectroscopy is a powerful technique for label-free

152 Infrared microspectroscopy is a powerful tool in the analysis of

153 Raman microspectroscopy is a prime tool to characterize the mo

154 Infrared microspectroscopy is a tool with potential for studies o

155 Infrared (IR) vibrational spectroscopy/microspectroscopy is an established analytical method th

156 the combination with microscopy, vibrational microspectroscopy is currently emerging as an important

157 Raman chemical imaging microspectroscopy is evaluated as a technology for water

158 nce (ATR) Fourier transform infrared (FT-IR) microspectroscopy is presented.

159 thermal IR coupled with Raman (O-PTIR+Raman) microspectroscopy is used to classify MPs by polymer typ

160 Midinfrared (IR) microspectroscopy is widely employed for spatially local

161 Infrared microspectroscopy is widely used for the chemical analys

162 photon microscopy (MPM), and line scan Raman microspectroscopy (LSRM) for multiparametric assessment

163 spectroscopy in combination with synchrotron microspectroscopy measurements was used to differentiate

164 ial resolution, when compared to synchrotron microspectroscopy measurements.

165 s by indirect TBARS and direct in situ Raman microspectroscopy measurements.

166 mark method in pollen analysis, the infrared microspectroscopy method offers better taxonomic resolut

167 morphological and Fourier transform infrared microspectroscopy (mFTIR) analyses of intact sediments a

168 of attenuated total reflectance mid-infrared microspectroscopy (MIR-microspectroscopy) was evaluated

169 scopy (mu-Raman), Fourier-transform infrared microspectroscopy (mu-FTIR), and pyrolysis-gas chromatog

170 disposable gloves were analyzed using Raman microspectroscopy (mu-Raman), Fourier-transform infrared

171 We then used Fourier transform infrared microspectroscopy (muFTIR) to detect deuterium in larvae

172 opy (LDIR) and optical photothermal infrared microspectroscopy (O-PTIR).

173 ly-observed scattering phenomena in infrared microspectroscopy of cells and tissues.

174 ypes using Fourier transform infrared (FTIR) microspectroscopy of leaves.

175 determined experimentally by polarized Raman microspectroscopy of oriented fd fibers, using the amide

176 ions of Tyr 21 and Tyr 24 by polarized Raman microspectroscopy of oriented Ff fibers, utilizing a nov

177 ntroduce a novel sampling setup for infrared microspectroscopy of pollens preventing strong Mie-type

178 in hardening using uniaxial tensile loading, microspectroscopy of polymer chain alignment, and theory

179 first time directly, urine samples by Raman microspectroscopy on a single-cell level.

180 investigated by synchrotron radiation FT-IR microspectroscopy on connective tissue and in muscle fib

181 lysis of the solid surface by confocal Raman microspectroscopy performed at a constant focal distance

182 d have implications for the utility of Raman microspectroscopy process analysis for the generation of

183 ed that synchrotron FTIR and synchrotron XRF microspectroscopies provide complementary information on

184 Raman microspectroscopy provides for high-resolution non-invas

185 determination, Fourier-transformed infrared microspectroscopy, quantitative reverse transcription-PC

186 emonstrate the power of synchrotron infrared microspectroscopy relative to conventional infrared meth

187 Fourier transform infrared (FT-IR) microspectroscopy revealed a reduction in the a-helix co

188 Fourier transform infrared (FT-IR) microspectroscopy revealed a reduction in the alpha-heli

189 emical imaging by Fourier transform infrared microspectroscopy revealed large differences in the dist

190 Infrared microspectroscopy revealed that PMCA of native hamster 2

191 t the single-cell level using confocal Raman microspectroscopy (RM) and atomic force microscopy (AFM)

192 Raman microspectroscopy (RM) is a marker-independent, noninvas

193 n multidetector (AF4-MD) platform with Raman microspectroscopy (RM) represents a significant advancem

194 uisition times compared to spontaneous Raman microspectroscopy (RM).

195 uent chemical identification by online Raman microspectroscopy (RM).

196 ive was to develop and test a combined Raman microspectroscopy (RMS) and micro-optical coherence tomo

197 We present an application of Raman microspectroscopy (RMS) for the rapid characterization a

198 Raman microspectroscopy (RMS) is a chemical imaging technique

199 Raman microspectroscopy (RMS) was used to detect and image mol

200 Raman microspectroscopy (rms) was used to identify, image, and

201 Techniques employed include Raman microspectroscopy, scanning electron microscopy with ene

202 label-free and noninvasive single-cell Raman microspectroscopy (SCRM) platform was able to identify n

203 SR-FTIR microspectroscopy shows that GBM live cells of different

204 and the limitations of stable isotope Raman microspectroscopy (SIRM), resonance SIRM, and SIRM in co

205 Raman microspectroscopy, solution state (31)P NMR, and (31)P M

206 radiation-based Fourier Transformed Infrared microSpectroscopy (SR u-FTIR) to characterize organic re

207 Confocal Raman microspectroscopy, stimulated Raman scattering (SRS) and

208 niques including scanning transmission X-ray microspectroscopy (STXM), scanning electron microscopy (

209 Raman microspectroscopy subsequently revealed that polarized a

210 onant scattering spectrum using a dark-field microspectroscopy system.

211 emonstrated using synchrotron-based infrared microspectroscopy that the striatum and the cortex of pa

212 scently guided optical photothermal infrared microspectroscopy, that simultaneously exploits epifluor

213 gans plants using Fourier transform infrared microspectroscopy, that TE lignification occurs postmort

214 itored by Fourier transform-infrared (FT-IR) microspectroscopy the response of live breast cancer MCF

215 Applying Fourier transform infrared microspectroscopy, the cutin mutants long-chain acyl-coe

216 By Fourier-transform infrared microspectroscopy, the orientation of macromolecules in

217 This study highlights the potential of FTIR microspectroscopy to acquire useful structural informati

218 te the applicability of synchrotron infrared microspectroscopy to adsorbed proteins by reporting pote

219 We used Raman microspectroscopy to characterize four important stages

220 pectroscopy and focal plane array (FPA-FTIR) microspectroscopy to characterize periductal fibrosis an

221 We have employed polarized Raman microspectroscopy to determine the orientation of trypto

222 Hence, we demonstrate the potential of Raman microspectroscopy to directly sort pellets containing L.

223 For the first time, we apply Raman microspectroscopy to identify such chemotaxis-related af

224 of high-resolution bench top-based infrared microspectroscopy to investigate the microstructure of T

225 We also used confocal Raman microspectroscopy to map the presence and location of me

226 We have employed polarized Raman microspectroscopy to obtain further details of PH75 arch

227 nced catalytic conversion, as detected by IR microspectroscopy, to areas with high concentration of A

228 orce microscopy, x-ray tomography, and Raman microspectroscopy, to assess the properties of bone matr

229 We then used Fourier transform infrared microspectroscopy (uFTIR) to detect deuterium in larvae

230 of surface-enhanced Raman scattering (SERS) microspectroscopy using glass-coated, highly purified SE

231 imaging by fluorescence microscopy and Raman microspectroscopy, using externally fluorescence-labeled

232 Here, S-FTIR microspectroscopy was applied to observe the microstruct

233 The method of surface-enhanced Raman microspectroscopy was developed for direct detection of

234 emical digestion, Fourier-transform infrared microspectroscopy was used to analyze the presence and s

235 Raman microspectroscopy was used to determine biochemical mark

236 ation of NIR spectroscopy and FTIR and Raman microspectroscopy was used to elucidate the effects of d

237 zation (DMB), and Fourier transform infrared microspectroscopy was used to evaluate the physicochemic

238 chrotron-Fourier transform infrared (S-FTIR) microspectroscopy was used to investigate the effect of

239 Raman microspectroscopy was used to quantify freezing response

240 Confocal Raman microspectroscopy was utilized at cryogenic temperatures

241 In this proof-of-concept study, Raman microspectroscopy was utilized for gender identification

242 lectance mid-infrared microspectroscopy (MIR-microspectroscopy) was evaluated as a rapid method for d

243 Using synchrotron based infrared microspectroscopy we demonstrate that the brains of pati

244 e field-effect transistor (FET) and infrared microspectroscopy, we demonstrate a gate-controlled, con

245 Using Raman microspectroscopy, we estimated the trehalose and residu

246 Raman and Fourier Transform Infrared (FTIR) microspectroscopies were applied to assess the impact of

247 , and synchrotron Fourier-transform infrared microspectroscopy were used to measure bone vascular can

248 ods of high-resolution mass spectrometry and microspectroscopy were utilized for molecular analysis o

249 using confocal spontaneous Raman scattering microspectroscopy, which exploits the intrinsic vibratio

250 ng microfluidics, optical tweezing and Raman microspectroscopy, which yields live cells suitable for

251 resh-frozen donors were compared using Raman microspectroscopy with DuoScan technology.

252 . compared Fourier transform infrared (FTIR) microspectroscopy with histological pathology to evaluat

253 , bleaching-corrected polarized fluorescence microspectroscopy with nanometer spectral peak position

254 ynchrotron Fourier-transform infrared (FTIR) microspectroscopy with powerful discrimination tools, su

255 coherent anti-Stokes Raman scattering (CARS) microspectroscopy with simplex maximization and entropy-

256 By combining fluorescent staining and microspectroscopy with software-based spectral analysis,

257 beta-turn structures, as detected by S-FTIR microspectroscopy, with longer tempering leading to stru

258 impetus for this approach was that SR FT-IR microspectroscopy would offer several advantages over co