ライフサイエンスコーパス: CD spectroscopy

1 nalysis combined with Br(2) footprinting and CD spectroscopy.

2 oenriched and monitoring its racemization by CD spectroscopy.

3 ed by crystallography, Fe removal rates, and CD spectroscopy.

4 the gp120 molecule, as also demonstrated by CD spectroscopy.

5 pported by size-exclusion chromatography and CD spectroscopy.

6 ds, does it show a chiral excess measured by CD spectroscopy.

7 y structure of the proenzyme, as revealed by CD spectroscopy.

8 n solution at pH 4.7-7.8 by far- and near-UV CD spectroscopy.

9 fully unfolded protein were investigated by CD spectroscopy.

10 /P50L as observed by both the cGMP assay and CD spectroscopy.

11 typical cysteine-knot fold, as evidenced by CD spectroscopy.

12 also a disturbed structure as determined by CD spectroscopy.

13 s of ubiquitin, has been examined by NMR and CD spectroscopy.

14 lained by thermal denaturation studies using CD spectroscopy.

15 This was verified by CD spectroscopy.

16 g urea-induced unfolding monitored by far-UV CD spectroscopy.

17 mutant (P34-hNPY) have been characterized by CD spectroscopy.

18 , with DNA have been investigated by NMR and CD spectroscopy.

19 a centrifugation assay, Tm measurements, and CD spectroscopy.

20 anganese Stabilizing Protein as monitored by CD spectroscopy.

21 similar secondary structures on the basis of CD spectroscopy.

22 hods, and their interactions were studied by CD spectroscopy.

23 of betaAPP have been investigated by NMR and CD spectroscopy.

24 respectively) were characterized by NMR and CD spectroscopy.

25 alpha-helix propensities varied as shown by CD spectroscopy.

26 el, which is undetectable using conventional CD spectroscopy.

27 ATR, human SMG-1, and human TRRAP by NMR and CD spectroscopy.

28 shed by single crystal X-ray diffraction and CD spectroscopy.

29 substitutions and analyzed by using NMR and CD spectroscopy.

30 ized, and helical content was assessed using CD spectroscopy.

31 g the information previously obtainable from CD spectroscopy.

32 olabile in the absence of NADPH as judged by CD spectroscopy.

33 mer, as determined using circular dichroism (CD) spectroscopy.

34 NA-bending assays and by circular dichroism (CD) spectroscopy.

35 ng calorimetry (DSC) and circular dichroism (CD) spectroscopy.

36 etic resonance (NMR) and circular dichroism (CD) spectroscopy.

37 (T(m)) measurements and circular dichroism (CD) spectroscopy.

38 h TnsD were monitored by circular dichroism (CD) spectroscopy.

39 f recombinant ERalpha by circular dichroism (CD) spectroscopy.

40 rements and using far-UV circular dichroism (CD) spectroscopy.

41 esicles, were studied by circular dichroism (CD) spectroscopy.

42 s divalent cations using circular dichroism (CD) spectroscopy.

43 ow-frequency S-band) and circular dichroism (CD) spectroscopy.

44 ce infrared (ATR-IR) and circular dichroism (CD) spectroscopy.

45 ored by fluorescence and circular dichroism (CD) spectroscopy.

46 with P4, as confirmed by circular dichroism (CD) spectroscopy.

47 an fluorescence (FL) and circular dichroism (CD) spectroscopy.

48 as determined by optical circular dichroism (CD) spectroscopy.

49 tercalated ethidium, and circular dichroism (CD) spectroscopy.

50 s aqueous solution using circular dichroism (CD) spectroscopy.

51 r magnetic resonance and circular dichroism (CD) spectroscopy.

52 variable-temperature variable-field magnetic CD spectroscopies.

53 ide denaturation curves monitored by ESR and CD spectroscopies.

54 apid-mixing stopped-flow, high-pressure, and CD spectroscopies.

55 were monitored by DSC and far-UV and near-UV CD spectroscopies.

56 form infrared (FT-IR) and circular dichroic (CD) spectroscopies.

57 Circular dichroism (CD) spectroscopy (263 nm) clearly detects two transition

58 Using CD spectroscopy, a competitive zinc binding assay, and a

59 Herein, we demonstrate that CD spectroscopy, a technique that is used primarily to e

60 the dG adducts was unequivocally assigned by CD spectroscopy after separation of each individual dias

61 The receptors were characterized by CD spectroscopy, analytical ultracentrifugation, and bin

62 iochemically using X-ray crystallography, UV-CD spectroscopy, analytical ultracentrifugation, and ITC

63 By the use of light-scattering, CD spectroscopy, analytical ultracentrifugation, and try

64 UV-vis absorbance, CD spectroscopy, analytical ultracentrifugation, redox p

65 k, resonance Raman and UV-visible absorption/CD spectroscopies and MS were used to characterize the i

66 eries of tryptophan zippers by static IR and CD spectroscopies and the IR temperature jump method.

67 We applied CD spectroscopy and (125)I radioprobing to determine the

68 elix formed by the host, as shown by NMR and CD spectroscopy and a solid-state structure.

69 CD spectroscopy and amide HDX of the UBI-SDS(n) complexe

70 ies of each individual EF-hand peptide using CD spectroscopy and analytical ultracentrifugation.

71 ary structures were similar as determined by CD spectroscopy and both proteins bound at multiple site

72 s an i-motif structure in vitro, as shown by CD spectroscopy and chemical footprinting.

73 We combine these measurements with visible CD spectroscopy and cross-linking experiments to demonst

74 For the present paper, CD spectroscopy and DMS methylation techniques were used

75 lix (HTH) motifs was investigated by NMR and CD spectroscopy and found to retain the same overall sol

76 CD spectroscopy and guanidine hydrochloride denaturation

77 By using AFM, leakage assays, CD spectroscopy and in silico tools, we found that Pa-MA

78 CD spectroscopy and limited proteolysis experiments defi

79 The duplexes were investigated by CD spectroscopy and MD simulations.

80 crystallization from CHCl3/acetonitrile, and CD spectroscopy and optical rotation show that the resol

81 CD spectroscopy and second-derivative UV spectra indicat

82 Data from CD spectroscopy and solution phase structure probing wit

83 ned using more established techniques (e.g., CD spectroscopy and SUPREX).

84 CD spectroscopy and the structure of an engineered disul

85 Moreover, CD spectroscopy and thermally induced unfolding studies

86 equential arrangements and investigated with CD spectroscopy and UV melting curve analysis.

87 tic resonance (EPR), and circular dichroism (CD) spectroscopies and thermal denaturation studies.

88 Circular dichroism (CD) spectroscopy and (1)H-(15)N heteronuclear single-qua

89 pc72 was demonstrated by circular dichroism (CD) spectroscopy and a fluorescence resonance energy tra

90 The method utilizes circular dichroism (CD) spectroscopy and a sensing ensemble composed of 2-fo

91 Circular dichroism (CD) spectroscopy and analytical ultracentrifugation indi

92 e protein as assessed by circular dichroism (CD) spectroscopy and biological activity.

93 ructure and stability by circular dichroism (CD) spectroscopy and differential scanning calorimetry (

94 Circular dichroism (CD) spectroscopy and electron microscopy show that the Q

95 r KCl using two methods: circular dichroism (CD) spectroscopy and electrophoretic mobility shift assa

96 ructure was indicated by circular dichroism (CD) spectroscopy and enzymatic footprinting with RNase T

97 structure and function, circular dichroism (CD) spectroscopy and homology modeling were used to dete

98 mal melting experiments, circular dichroism (CD) spectroscopy and plasmid unwinding assays.

99 esponse element (ERE) by circular dichroism (CD) spectroscopy and polyacrylamide gel electrophoresis.

100 Circular dichroism (CD) spectroscopy and RNA thermal denaturation revealed a

101 physical methods such as circular dichroism (CD) spectroscopy and sedimentation velocity analytical u

102 In the present report, circular dichroism (CD) spectroscopy and transmission electron microscopy (T

103 plexes were evaluated by circular dichroism (CD) spectroscopy and UV absorption melting studies of tr

104 mal aggregation assay, gel filtration study, CD spectroscopy, and bis-ANS interaction studies.

105 size-exclusion chromatography (SEC), far-UV CD spectroscopy, and catalytic activity measurements, an

106 Thermal denaturation, CD spectroscopy, and gel filtration experiments showed t

107 racentrifugation, fluorescence spectroscopy, CD spectroscopy, and guanidine-HCl denaturation were use

108 Site-directed mutagenesis, CD spectroscopy, and immunocytochemistry reveal that a p

109 nzymes as determined by fluorescence, far-UV CD spectroscopy, and incubation-induced rest activity sh

110 s in the intrinsic fluorescence of profilin, CD spectroscopy, and isothermal titration calorimetry to

111 ated and characterized using metal analyses, CD spectroscopy, and kinetic studies.

112 repeat-containing regions by gel filtration, CD spectroscopy, and negative-staining electron microsco

113 nova have been probed by Raman spectroscopy, CD spectroscopy, and nondenaturing gel electrophoresis.

114 by using nanoESI- and IM-mass spectrometry, CD spectroscopy, and protein chemical modification react

115 icroscopy, attenuated total reflection-FTIR, CD spectroscopy, and SDS-PAGE.

116 nactive (AApep; G's replaced by A's) TMDs by CD spectroscopy, and then their effects on the kinetics

117 of DNAs and oligonucleotides was measured by CD spectroscopy, and this allowed determination of a DNA

118 ing EI by sedimentation velocity, by near UV CD spectroscopy, and with a nonphosphorylatable active s

119 by 1H NMR spectroscopy, circular dichroism (CD) spectroscopy, and agarose gel electrophoresis.

120 matography (SEC), far-UV-circular dichroism (CD) spectroscopy, and catalytic activity measurements ov

121 RetGC1, characterized by circular dichroism (CD) spectroscopy, and investigated for protease resistan

122 on chromatography (SEC), circular dichroism (CD) spectroscopy, and stopped-flow kinetic analyses.

123 ature (Tm) measurements, circular dichroism (CD) spectroscopy, and the ethidium bromide (EB) displace

124 CD spectroscopy, appropriately designed peptide controls

125 The assets of CD spectroscopy are that the signal is directly linked t

126 Here, NMR and CD spectroscopy are used to characterize the role of imi

127 ation, fluorescence, and circular dichroism (CD) spectroscopy as a function of pH.

128 noncanonical helix were conducted by NMR and CD spectroscopy, as well as by X-ray crystallography and

129 e and cocoa were studied by fluorescence and CD spectroscopy at pH values of the gastrointestinal tra

130 l stability monitored by circular dichroism (CD) spectroscopy at 222 nm of 100 heterodimers that cont

131 ractions were studied by circular dichroism (CD) spectroscopy at pH 7 and 2.

132 be determined from spectra is a testament to CD spectroscopy being a very powerful technique.

133 lify how the advantages offered by automated CD spectroscopy can be exploited to quantify protein sta

134 CD spectroscopy confirmed the alpha-helical content of s

135 Circular dichroism (CD) spectroscopy confirmed that a substantial fraction o

136 Structural analysis by CD spectroscopy coupled with molecular dynamics simulati

137 the global thermodynamic analysis of DSC and CD spectroscopy data, which led to a detailed descriptio

138 CD spectroscopy demonstrated that the TMAO-induced struc

139 CD spectroscopy demonstrates that the conformation of rh

140 CD spectroscopy did not detect any optical activity in t

141 s, such as intrinsic fluorescence and far-UV CD spectroscopy did not show significant conformational

142 Data from CD spectroscopy, dynamic light scattering, analytical ul

143 At pH 7, CD spectroscopy, dynamic light scattering, and different

144 by kinetic and thermodynamic methods, using CD spectroscopy, dynamic light scattering, and scanning

145 Circular dichroism (CD) spectroscopy experiments indicated that bacterial me

146 opy, depth-dependent fluorescence quenching, CD-spectroscopy experiments, and MD simulations indicate

147 optical methods such as circular dichroism (CD) spectroscopy, fibrillogenesis is typically measured

148 ogeneity, and studied by circular dichroism (CD) spectroscopy, fluorescence spectroscopy, and initial

149 up2p structure by far-UV circular dichroism (CD) spectroscopy, Fourier transform infrared (FTIR) spec

150 estimation of protein secondary structure by CD spectroscopy from 29 to 37 proteins by including 3 ad

151 Circular dichroism (CD) spectroscopy gave ellipticity minima and maxima at 2

152 ecyl phosphocholin (DPC) micelles by UV-vis, CD spectroscopy, gel electrophoresis, and analytical ult

153 Magnetic CD spectroscopy has been used due to its established abi

154 However, CD spectroscopy has remained a low-throughput method bec

155 CD spectroscopy has special relevance for the study of m

156 Circular dichroism (CD) spectroscopy has become established as a key method

157 f the I1 intermediate by circular dichroism (CD) spectroscopy has shown that I1 retains a significant

158 the thermal unfolding curve (as measured by CD spectroscopy) hint at a well ordered stable fold.

159 Sedimentation and CD spectroscopy identified that phosphorylation of Thr(1

160 s demonstrated by mass spectrometry, NMR and CD spectroscopy in combination with quantum chemical cal

161 CD spectroscopy in solution and a crystal structure of a

162 ) were characterized by multinuclear NMR and CD spectroscopy in solution and by X-ray crystallography

163 ndent conformational transitions detected by CD spectroscopy in the far UV indicate a more ordered st

164 ntitative agreement with circular dichroism (CD) spectroscopy in detecting the domain melting transit

165 FTIR and CD spectroscopy indicate all six peptides adopt a stable

166 In vitro kinetic studies monitored by CD spectroscopy indicate that [2Fe-2S] clusters on GrxS1

167 NMR and CD spectroscopy indicate this small fusion module compri

168 sults of fluorometry and circular dichroism (CD) spectroscopy indicate that the main phase of thermal

169 the secondary structures of the variants by CD spectroscopy indicated significant random-coil format

170 CD spectroscopy indicated that association with ATCase d

171 CD spectroscopy indicated that the peptide adopted a str

172 Far-UV CD spectroscopy indicated that the secondary structure o

173 Near-UV CD spectroscopy indicated that these impairments are cau

174 CD spectroscopy indicated that wild-type AQP2 and the ph

175 orescence quenching, and circular dichroism (CD) spectroscopy indicated that the high solubility was

176 er normal physiological conditions; however, CD spectroscopy indicates that in the presence of hydrox

177 CD spectroscopy indicates that N-218 MLN64 is largely al

178 CD spectroscopy indicates that rHb (alphaH87G) and rHb (

179 Circular dichroism (CD) spectroscopy indicates that Notch ankyrin polypeptid

180 Circular Dichroism (CD) spectroscopy is a long-established technique for stu

181 Circular Dichroism (CD) spectroscopy is a powerful method for investigating

182 Circular dichroism (CD) spectroscopy is a powerful method for monitoring con

183 Circular dichroism (CD) spectroscopy is a well-established technique for stu

184 Circular dichroism (CD) spectroscopy is a widely used method for examining t

185 Circular dichroism (CD) spectroscopy is extensively utilized for determining

186 Circular dichroism (CD) spectroscopy is one of the most useful techniques fo

187 Circular dichroism (CD) spectroscopy is widely used in structural biology as

188 a, designated PLDalpha C2 and PLDbeta C2, by CD spectroscopy, isothermal titration calorimetry, and p

189 Here, using CD spectroscopy, isothermal titration calorimetry, and s

190 ation dependence of alpha-helix formation in CD spectroscopy, it is likely that these oligomers assem

191 By CD spectroscopy, K16-OA-Abeta and K28-OA-Abeta had incre

192 tudies using analytical ultracentrifugation, CD spectroscopy, limited proteolysis, and (1)H NMR show

193 Circular dichroism (CD) spectroscopy measured the thermal stability of eight

194 CD spectroscopy measuring the thermal unfolding of NKX3.

195 vation of low-melting ferritin subdomains by CD spectroscopy (melting midpoint 53 degrees C), account

196 UV-visible, EPR, and CD spectroscopies, metal analysis, and x-ray crystallogr

197 ssembly was confirmed by circular dichroism (CD) spectroscopy, microscopic images, and crystal struct

198 Circular dichroism (CD) spectroscopy monitored the thermal denaturation of 3

199 e complexes using steady-state fluorescence, CD spectroscopy, NMR, and native gel mobility shift assa

200 y structure content from circular dichroism (CD) spectroscopy, obtained using synchrotron light, show

201 Characterization by 1H NMR and CD spectroscopies of the resulting aptamers, TBA-T7b and

202 CD spectroscopy of a 37-mer model of alpha4 (residues 24

203 Far-UV CD spectroscopy of decorin and biglycan proteoglycans in

204 CD spectroscopy of DHFR and G121V-DHFR indicated that th

205 Conformational analysis using CD spectroscopy of purified, recombinant ECD2 protein de

206 Far-UV CD spectroscopy of StAR in PC membranes show more beta-s

207 the native sequence, was explored by NMR and CD spectroscopy of the 31-residue and 16-residue peptide

208 he two 11-mer migration products followed by CD spectroscopy of the isolated adducted nucleosides ind

209 CD spectroscopy of the peptide in dodecyl phosphocholine

210 CD spectroscopy of TMX-1 in oriented multilayers formed

211 s estimated using far-UV circular dichroism (CD) spectroscopy of all but Phe variants at position 30

212 tructure, as revealed by circular dichroism (CD) spectroscopy of recombinant proteins.

213 Circular dichroism (CD) spectroscopy of the apoE CT domain reveals spectra c

214 tron microscopy (EM) and circular dichroism (CD) spectroscopy of the nonmotor region shows characteri

215 gh each 32-mer formed stable triple helices (CD) spectroscopy, only 1a and 1b self-assembled into mic

216 c bases for these observations, here we used CD spectroscopy, photo-induced cross-linking of unmodifi

217 d physiological urea (1 mm) and monitored by CD spectroscopy, protein crystallography, and Fe2+ relea

218 Circular dichroism (CD) spectroscopy proves that these peptides are highly a

219 Circular dichroism (CD) spectroscopy provides rapid determinations of protei

220 asurements of the D-Arg peptide monitored by CD spectroscopy reveal an apparent two-state helix-coil

221 UV-vis and CD spectroscopy reveal that a stable hybrid possessing G

222 UV-vis and CD spectroscopy reveal that the quadruplex structure of

223 In addition, protein fingerprinting and CD spectroscopy reveal the flexibility of 3betaHSD2, a n

224 CD spectroscopy revealed a series of sequential conforma

225 CD spectroscopy revealed that a conformational change oc

226 However, CD spectroscopy revealed that the addition of certain tr

227 EPR and CD spectroscopy revealed that the membrane restrains rho

228 CD spectroscopy revealed that the mutant receptors have

229 Biophysical studies using NMR and CD spectroscopy revealed that UBXD1-N can be classified

230 lymerase stop assay, and circular dichroism (CD) spectroscopy revealed that the G-quadruplex containi

231 ral analysis of duplexes with DNA and RNA by CD-spectroscopy revealed a shift from B- to A-type confo

232 CD spectroscopy reveals that mitochondrial malate dehydr

233 CD spectroscopy reveals that, in the presence of the sma

234 CD spectroscopy showed that the 33-mer peptide P3W folds

235 nary estimations of secondary structure from CD spectroscopy showed that the channel exists mostly in

236 in the presence of vesicles, and difference CD spectroscopy showed that the transmembrane regions of

237 modifications were identified using MS, and CD spectroscopy showed the receptor to be approximately

238 Circular dichroism (CD) spectroscopy showed that the detergent-solubilized p

239 Surprisingly, CD spectroscopy shows a stable parallel G-quadruplex str

240 enatured ferrous protein, fast time-resolved CD spectroscopy shows a submillisecond folding process t

241 i, and i + 1, i + 2, or i + 3 arrangements, CD spectroscopy shows that As(III) coordination causes h

242 CD spectroscopy shows that it is approximately 45% alpha

243 CD spectroscopy shows that the structure is unimolecular

244 CD spectroscopy shows that these structures' helical sen

245 idinium unfolding of myoglobin, monitored by CD spectroscopy, shows destabilization at less than 1.3

246 that was high in alpha-helix as measured by CD spectroscopy, similar to the normal cellular isoform

247 ared and characterized using metal analyses, CD spectroscopy, steady-state kinetics, stopped-flow flu

248 NMR and CD spectroscopy studies demonstrated that [F9A]AuIB reta

249 Structural analysis of Atm1-C by CD spectroscopy suggested a similarity of secondary stru

250 CD spectroscopy suggests that Rv2302 partially unfolds u

251 se previously undescribed photosensors using CD spectroscopy supports a structurally heterogeneous ch

252 the C 499D mutant protein by absorbance and CD spectroscopy supports the conclusion that its bilin c

253 etic resonance (NMR) and circular dichroism (CD) spectroscopy supports the hypothesis that increasing

254 Circular dichroic (CD) spectroscopy supports this folding and self-assembly

255 Here, we show by NMR and CD spectroscopy that LcrG lacks a tertiary structure and

256 Here we show using NMR and CD spectroscopy that the C9orf72 hexanucleotide expansio

257 luding heterocomplex pulldown assays, far-UV CD spectroscopy, the thioflavin T binding assay, transmi

258 Using circular dichroism (CD) spectroscopy, the thermal stability of these protein

259 action with the G4DNA has been obtained from CD spectroscopy, thermal denaturation, and UV-vis titrat

260 tertiary structure as determined by near UV CD spectroscopy, thermal denaturation, sedimentation equ

261 , and then studied by using a combination of CD spectroscopy, Thioflavin T fluorescence, EM, atomic f

262 metry, in conjunction with UV absorbance and CD spectroscopy to detect and to characterize the confor

263 sidue 133) long overhand loops were found by CD spectroscopy to have helical contents similar to that

264 ) were purified to homogeneity and judged by CD spectroscopy to have structures similar to that of th

265 nalysis of AlkB using NMR, fluorescence, and CD spectroscopy to show that AlkB is a dynamic protein e

266 infrared (ATR-FTIR) and circular dichroism (CD) spectroscopies to identify secondary and dynamic str

267 etic resonance (NMR) and circular dichroism (CD) spectroscopy to analyze the structural integrity and

268 on calorimetry (ITC) and circular dichroism (CD) spectroscopy to characterize the binding of soluble

269 ve used fluorescence and circular dichroism (CD) spectroscopy to characterize the effects of calcium

270 e (Tm) measurements, and circular dichroism (CD) spectroscopy to evaluate the effects of these novel

271 ry dispersion (ORD), and circular dichroism (CD) spectroscopy together with density functional theory

272 blish the versatility of circular dichorism (CD) spectroscopy toward understanding aggregation of mon

273 Circular dichroism (CD) spectroscopy, Triton X-114 (TX-114) phase partitioni

274 Based on results of CD spectroscopy, trypsin treatment, and MS, we propose a

275 changes in the DNA molecule were detected by CD spectroscopy upon protein-DNA complex formation.

276 In contrast to CD spectroscopy, UV absorbance spectroscopy shows only a

277 wed its characterization by EPR, UV-vis, and CD spectroscopies, validating spin-delocalization throug

278 ariable-temperature, variable-field magnetic CD spectroscopies was applied to HmaS and compared with

279 Moreover, CD spectroscopy was applied to the mutant NP7(E27Q) and

280 Far-UV CD spectroscopy was employed for detection of conformati

281 A combination of HPLC, optical rotation and CD spectroscopy was employed to distinguish stereoisomer

282 Steady-state CD spectroscopy was utilized to characterize the peptide

283 Circular dichroism (CD) spectroscopy was employed to show that the alcohol s

284 Circular dichroism (CD) spectroscopy was used to monitor the urea-induced un

285 Using CD spectroscopy, we find that approximately 1 mol eq of

286 Using UV-visible and CD spectroscopy, we found that P450 21A2 thermal stabili

287 n using Thioflavin T fluorescence and far-UV CD spectroscopy, we have found that the aggregation of A

288 Using CD spectroscopy, we provide evidence that hSloRCK2 under

289 revious study using peptide design, EPR, and CD spectroscopy, we showed that the HGGGW segment within

290 Using circular dichroism (CD) spectroscopy, we demonstrate that urea promotes form

291 By employing circular dichroism (CD) spectroscopy, we demonstrated that the lipopeptides,

292 Using on-surface circular dichroism (CD) spectroscopy, we have investigated the structure of

293 tweezers instrument and circular dichroism (CD) spectroscopy, we provide compelling evidence that hi

294 both 1H NMR and visible-circular dichroism (CD) spectroscopy, we show that two Ni2+ ions bind to His

295 Folding experiments of T1-892 using CD spectroscopy were carried out at varying concentratio

296 with Trp fluorescence and near-UV and far-UV CD spectroscopy were performed on variants with Lys-66,

297 ogues, conformation-specific antibodies, and CD spectroscopy were used to evaluate the basis of the e

298 n lipid membrane environments, using NMR and CD spectroscopy with lipid micelle and lipid bilayer sam

299 was further indicated in circular dichroism (CD) spectroscopy with a positive (A) or negative (B) Del

300 red (FTIR) spectroscopy, circular dichroism (CD) spectroscopy, X-ray diffraction (XRD), and solid-sta