ライフサイエンスコーパス: SDS

1 SDS scaffolds were toxic to repopulating human mesenchym

2 SDS was shown to stabilise the blue conformation of phyc

3 SDS, Brij-35, Brij-58, Triton X-100 and Span-40 were exp

4 SDS-PAGE analyses indicated the formation of hydrolysate

5 SDS-PAGE analysis showed that salt addition contributes

6 SDS-PAGE and immunoassay analysis with rabbit polyclonal

7 SDS-PAGE gels were used to determine abundance of the CO

8 SDS-PAGE patterns show distinctive bands for each kind o

9 SDS-PAGE showed that annonacinone inhibited formation of

10 SDS-PAGE showed that collagens extracted with different

11 SDS-PAGE showed that the molecular mass of purified enzy

12 SDS-PAGE showed that the protein bands corresponding to

13 SDS-PAGE showed that the purified protein had molecular

14 SDS-PAGE shows the presence of a well separated protein

15 SDS-PAGE was carried out for all collagens extracted und

16 SDS/PAGE, mass spectrometry, and Edman degradation ident

17 (95% CI: 0.01, 0.08 SDS); fruit juice: 0.04 SDS (95% CI: 0.01, 0.06 SDS)] of the 6-y-old children.

18 sociated with a higher FMI [total SCBs: 0.05 SDS (95% CI: 0.01, 0.08 SDS); fruit juice: 0.04 SDS (95%

19 core (SDS) [Standard Error (SE) 0.007], 0.05 SDS (SE 0.008) and 0.14 SDS (SE 0.025), for rs13253111,

20 lved in <22min using a mobile phase of 0.05M SDS - 7.5% 1-propanol - 0.5% triethylamine buffered at p

21 pretreatment was a 1:1 dilution with a 0.05M SDS at pH 3 solution, filtration and direct injection, t

22 ut interferences using mobile phase of 0.05M SDS/12.5% 1-propanol/0.5% triethylamine at pH 3, running

23 ); fruit juice: 0.04 SDS (95% CI: 0.01, 0.06 SDS)] of the 6-y-old children.

24 day: 0.04 SD score (SDS); 95% CI: 0.00, 0.07 SDS].

25 rage risk allele was associated with a 0.073 SDS (SE 0.011, P-value = 3.12 x 10(-10)) increase in chi

26 MI [total SCBs: 0.05 SDS (95% CI: 0.01, 0.08 SDS); fruit juice: 0.04 SDS (95% CI: 0.01, 0.06 SDS)] of

27 e observed that protein extraction with 0.1% SDS followed by extraction with a 30% ACN/urea resulted

28 Treatment of blood samples with 0.1% SDS or Triton X-100 does not inactivate EBOV.

29 atment of blood samples, in contrast with 1% SDS treatment.

30 or (SE) 0.007], 0.05 SDS (SE 0.008) and 0.14 SDS (SE 0.025), for rs13253111, rs8092503 and rs13387838

31 These patients presented with a mean of -3.2 SDS and some suggestive clinical characteristics.

32 RS) compared to a white bread control (0.2% SDS and 2.5% RS), but also provided an acceptable palata

33 milar to its native form ( approximately 25% SDS; approximately 60% RS).

34 rnal education, smoking, and parity) >/=0.27 SDSs and an average of 0.48 SDSs.

35 The 2D SDS-PAGE separation demonstrated the presence of a few p

36 t 15 degrees C using 11.3mM borax and 11.2mM SDS adjusted to pH 8.5 as BGE.

37 Large aggregates unable to enter a 4% SDS-PAGE gel were formed at pH 6.5 and 8.5, which became

38 th up to 3 alphaLA per particle and up to 43 SDS per alphaLA, both considerably larger than for RL.

39 parity) >/=0.27 SDSs and an average of 0.48 SDSs.

40 ly provided high SDS and RS fractions (23.9% SDS and 30.2% RS) compared to a white bread control (0.2

41 pid, simple and versatile Free-of-Acrylamide SDS-based Tissue Clearing (FASTClear) protocol specifica

42 uten fractions were also extracted by adding SDS.

43 In addition, SDS-electrophoresis of proteins under special preparatio

44 In the present study, MWCNTs adsorbed SDS during ultrasonication to form stable MWCNTs suspens

45 d a single polypeptide band of 83.1kDa after SDS-PAGE.

46 SDSs), and 8% of them had low height-for-age SDSs.

47 ntinuously inject SDS into the gel, allowing SDS molecules to be compiled within the focused bands.

48 he number of surfactant molecules in alphaLA-SDS complexes increases with surfactant concentration, a

49 The alphaLA-SDS complexes contain a prolate micelle with a core radi

50 Although SDS-PAGE did not show any differences for either the num

51 ple was to homogenise and heat samples in an SDS-containing phosphate buffer to dissolve major muscle

52 uous extraction of analyte molecules into an SDS-free solvent stream based on the free-flow zone elec

53 rfactants could sharply decreased alpha, and SDS was more effective to facilitate CeO2-NPs transport

54 Proteomic analysis and SDS-PAGE electrophoresis of the extracted proteome sugge

55 ultrahigh pressure liquid chromatography and SDS-PAGE gels.

56 aration, lectin affinity chromatography, and SDS-PAGE.

57 tatic), sodium caseinate (electrosteric) and SDS-Tween 80 (combined electrostatic-steric) emulsifiers

58 aluated through the degree of hydrolysis and SDS-PAGE profiles.

59 lyte, BGE (borax, acetonitrile, methanol and SDS concentrations), was studied and optimized using res

60 protease showed a single band on native and SDS-PAGE with a molecular weight of 24kDa on SDS-PAGE.

61 olecular weight estimated by NATIVE-PAGE and SDS-PAGE electrophoresis was approximately 60 kDa.

62 biotin, guanidinium thiocyanate, pepsin, and SDS, which makes it possible to immobilize new biotinyla

63 The epitope was sensitive to reduction and SDS denaturation in the isolated ricin domain and the la

64 The results highlight how RL and SDS follow similar overall rules of self-assembly and in

65 cyl sulfate (SDS), sodium caseinate (SC) and SDS-Tween 80 as the emulsifiers.

66 rick tests (SPTs), specific IgEs (sIgEs) and SDS-PAGE immunoblotting.

67 roscopy, secondary ion mass spectrometry and SDS-PAGE indicate that Cba. tepidum biogenic S(0) globul

68 Spectroscopic and SDS-PAGE binding assays of Sin a 2 and Ara h 1 with diff

69 ility to osmotic (salt, sorbitol) stress and SDS.

70 ontents of RDS: 48.4g/100g, (23.4-76.9) and, SDS: 10.9g/100g, (0.8-24.2).

71 ue) structure of phycocyanin and the anionic SDS micelles.

72 btained by electrophoretic technique such as SDS-PAGE.

73 to certain stressors, including polymyxin B, SDS, and hydrogen peroxide.

74 om the sera of patients with diabetes before SDS-PAGE.

75 differences at 12 months' follow-up between SDS and TAU for mean HDRS17 score (14.8 [SD 7.9] in the

76 Biochemical (SDS-PAGE, Size exclusion chromatography and LC-MS/MS) an

77 t, the samples were dialyzed and analyzed by SDS-PAGE and for OA content.

78 nion-exchange chromatography and analyzed by SDS-PAGE, native PAGE, and Western immunoblot analysis.

79 min and 2 h, the pellicles were analyzed by SDS-PAGE.

80 tion time-of-flight mass spectrometry and by SDS-PAGE using biotinylated PGA1 (PGA1-B).

81 litates the induction of social avoidance by SDS.

82 ysis of AS-48 digestion fragments in bulk by SDS-PAGE, RP-HPLC, and MALDI-TOF proves that the previou

83 at 37 degrees C, but not at 20 degrees C, by SDS-page and mass spectrometry analyses as well as elect

84 lyzed the structure of recombinant CLEC3A by SDS-PAGE and immunoblot, glycan analysis, matrix-assiste

85 d 6.64mgg(-1)) were analysed and compared by SDS-PAGE, showing differences in their electrophoretic p

86 ysates with high specificity as confirmed by SDS-PAGE analysis with a phosphoprotein-specific stain a

87 their triple-helical structure, confirmed by SDS-PAGE and FTIR.

88 itional major peptide bands were detected by SDS-PAGE treatments as compared to the solar or freeze d

89 llagen alpha1/alpha2 ratio was determined by SDS PAGE and by qRT-PCR in ex-vivo bone explants.

90 m (IV) and rhodamine 6G (Ce-R6G) enhanced by SDS) for the determination of the total phenolic content

91 adation during in vitro GID was evaluated by SDS-PAGE and by measuring the nitrogen content of ultraf

92 Examination by SDS-PAGE followed by protein staining revealed protein p

93 A covalently cross-linked dimer isolated by SDS-PAGE and mass analysis showed that dityrosine dimer

94 ntification of the small cleavage product by SDS-PAGE.

95 (1-2 h); investigate SMALP protein purity by SDS-PAGE analysis and estimate protein concentration (4

96 rporation into receptor subunits resolved by SDS-PAGE, there was etomidate-inhibitable labeling by [(

97 le enzymatic treatments under sonication, by SDS-PAGE, western blot and ELISA, with serum IgE of alle

98 flocculation in nanodispersion stabilized by SDS-Tween 80.

99 tigate whether globular proteins unfolded by SDS can be refolded upon addition of C12E8 and DDM.

100 ual specialist mental health secondary care, SDS might improve depression symptoms for patients with

101 on of USP20 correlates with a characteristic SDS-PAGE mobility shift of the protein, blocks its deubi

102 bread using different extracts and conducted SDS-polyacrylamide gel electrophoresis.

103 in the molecular weight of Sup35-containing SDS-resistant polymers and no significant decrease in av

104 It shares all the advantages of conventional SDS CGE (labor-saving, easy automation, and convenient q

105 ent was 0.0-0.8%, comparable to conventional SDS CGE utilizing 0.1-0.5 mg proteins.

106 vity enhancement as compared to conventional SDS CGE.

107 binatorial peptide ligand libraries (CPLLs), SDS-PAGE, nLC-ESI-MS/MS, and database search, permitted

108 ced by HPP, this processing modified the 1-D SDS-PAGE sarcoplasmic patterns in a direct-dependent man

109 Cations (Na(+), Ca(2+)) decreased SDS desorption from MWCNTs due to charge screening effec

110 titive topical applications of the detergent SDS or by high-dose UV B radiation, IR/IGF-1R(MKO) mice

111 rapidly digestible (RDS), slowly digestible (SDS), and resistant (RS) starch for nutrition and with r

112 sifying properties of sodium dodecylsulfate (SDS) based micellar system and thus making it appropriat

113 0) containing (1.0mM) sodium dodecylsulfate (SDS) using cyclic voltammetry (CV) and electrochemical i

114 rmation of complexes that were stable during SDS-PAGE.

115 varying sizes of two, four, or six to either SDS (collaborative care approach between psychiatrists a

116 l sulfate-polyacrylamide gel electrophoresis SDS-PAGE-immunoblotting with patient sera and rabbit ser

117 decyl sulfate capillary gel electrophoresis (SDS CGE) with head-column field-amplified sample stackin

118 Sulphate-Polyacrylamide Gel Electrophoresis (SDS-PAGE) analysis revealed the localization of phosviti

119 w proteins separated by gel electrophoresis (SDS-PAGE) to be detected as peptides by mass spectrometr

120 naturing polyacrylamide gel electrophoresis (SDS-PAGE) was used to separate proteins.

121 sulfate polyacrylamide gel electrophoresis (SDS-PAGE), which was eliminated by phosphatase treatment

122 sulphate-polyacrylamide gel electrophoresis (SDS-PAGE).

123 ulphate-polyaccrylamide gel electrophoresis (SDS-PAGE).

124 sulfate-polyacrylamide gel electrophoresis (SDS-PAGE).

125 sulphate polyacrylamide gel electrophoresis (SDS-PAGE).

126 illar proteins using OFFGEL electrophoresis, SDS-PAGE and protein identification by MALDI-TOF MS.

127 ssays carried out included sugar estimation, SDS-PAGE, GPC, color, FT-IR, DSC, thermal stability, sol

128 As expected, SDS-PAGE patterns were species-specific but differences,

129 utralize the FvTox1 toxin involved in foliar SDS development.

130 the pathogen may be the root cause of foliar SDS.

131 inty was 3.6g/100g for RDS and 1.9g/100g for SDS.

132 The SAXS data for SDS agree with oblate-shaped micelles with a core of 20

133 water ratio 1:2 were found to be optimum for SDS (slow digestible starch) product development.

134 icelle concentration for bile salts than for SDS.

135 t micelles is more hydrophobic than that for SDS micelles.

136 induced cultures indicates that newly formed SDS resistant oligomers change in size over time and lys

137 Moreover, 19 protein bands from SDS-PAGE were analyzed and a total of 45 different prote

138 were identified as type-I collagens by FTIR, SDS-PAGE, and molecular weight distribution analyses.

139 ional changes (surface hydrophobicity, FTIR, SDS-PAGE and thiol content) of gluten in relation to its

140 oasted MPS pea starch not only provided high SDS and RS fractions (23.9% SDS and 30.2% RS) compared t

141 tis made from the composite flour had higher SDS and resistant starch (RS) values demonstrating poten

142 Membrane proteins denatured in SDS can also be refolded by addition of NIS.

143 Infectious EBOV titers were determined in SDS-treated plasma and whole blood from EBOV-infected no

144 Cells are lysed in SDS, which is then exchanged for urea and ammonium bicar

145 No fragmentation was observed in SDS-PAGE while transmission electron micrographs showed

146 In particular, in SDS there is enormous selective pressure to expand TP53-

147 bovine serum albumin (BSA) from unfolding in SDS.

148 standard deviation score in body mass index [SDS-BMI]).

149 en the two dimensions to continuously inject SDS into the gel, allowing SDS molecules to be compiled

150 on of the PA oligomer from "pre-pore" to its SDS and heat-resistant "pore" conformation while not pre

151 content and gluten strength parameters like SDS sedimentation volume, dough stability and gluten ind

152 be more effective additive in order to make SDS micellar system better for its potential application

153 ition (pH = 2; amount of MIONPs = 87.15 mg; [SDS]/[MIONP] ratio = 2.9), showed that adsorption of bot

154 h molecular-weight complexes and Blue Native/SDS-PAGE and isoelectric focusing demonstrated that diff

155 gene sequencing in additional SBDS-negative SDS cases or molecularly undiagnosed IBMFS cases, we ide

156 e-exome sequencing (WES) in an sbds-negative SDS family and candidate gene sequencing in additional S

157 nd to the disruption of the subunits, but no SDS-insoluble aggregates were formed.

158 esonance energy transfer (FRET), nonreducing SDS-PAGE, and strategic mutation of the Ab hinge region

159 pubertal participants this was not observed (SDS, 0.06; 95% CI, -0.04 to 0.15; P = 0.24).

160 Proteomics tools based on image analysis of SDS-PAGE protein gels and protein identification by tand

161 on ability of mixed hemi/ad-micelle array of SDS molecules not only induce an effective electron tran

162 Desorption of SDS from MWCNTs surfaces was then investigated as a func

163 or by size using sieving electrophoresis of SDS complexes.

164 the development of the clinical features of SDS.

165 gregation phase and induced the formation of SDS-stable, non-amyloid LC aggregates.

166 29.90 to 44.36%, which led to an increase of SDS from 7.41 in HHB to 13.78% in LHB (bread basis).

167 ous micellar and thermodynamic parameters of SDS like critical micellar concentration (CMC), standard

168 ntributes to the haematological phenotype of SDS.

169 the unfolded polyprotein in the presence of SDS.

170 The incremental cost-effectiveness ratio of SDS versus TAU was pound43 603 per quality-adjusted life

171 goni effect, where the asymmetric release of SDS surfactant induces fluid convection and rapid disper

172 his method has been used as a replacement of SDS-PAGE for purity analysis of adeno-associated virus (

173 nts the fluoxetine (FLX)-induced reversal of SDS-induced social avoidance, suggesting that 5-HT defic

174 ACN/urea extraction, indicating the role of SDS to be beneficial for protein solubility.

175 as demonstrated by glycoprotein staining of SDS PAGE gels.

176 igh-detergent extracts revealed a variety of SDS-stable low-n species.

177 SDS-PAGE with a molecular weight of 24kDa on SDS-PAGE.

178 d by these fibroblasts was mildly delayed on SDS-PAGE gel, suggesting some overmodification of collag

179 t molecular mass of approximately 150 kDa on SDS-PAGE and did not contain Gbeta5 Mass spectrometry an

180 revealed the same abnormal chain pattern on SDS-PAGE with an overabundance of a gamma112 cross-linke

181 ely 13 degrees and 20 degrees in the optimal SDS product indicated the formation of V-type complexes

182 molecular order was observed in the optimal SDS product.

183 eagents like HCl, Na2CO3, glycine buffer, or SDS are employed.

184 ion is not sufficient for regular SDS CGE or SDS-PAGE assay.

185 enital neutropenia linked with various other SDS phenotypes.

186 Our SDS cohort was young (median age 6.3 years), and many of

187 Analyses by SEC, blue native PAGE, SDS-PAGE, and dynamic light scattering indicated that th

188 rocessed 12S globulin by 2D blue-native PAGE/SDS-PAGE indicated that the nhx5 nhx6 knockouts showed c

189 llected and freeze-dried in order to perform SDS-PAGE and immunoblotting tests.

190 Applied to data from the UK10K Project, SDS reflects allele frequency changes in the ancestors o

191 ed in extraction of the SDS from the protein-SDS complexes and refolding of betaLG, BSA, and lysozyme

192 proteins, the addition of NIS to the protein-SDS samples resulted in extraction of the SDS from the p

193 ish species were estimated by a quantitative SDS-PAGE.

194 Repeated social defeat stress (R-SDS) reduces the expression of D1 receptor subtype in mP

195 tor subtype in mPFC of mice susceptible to R-SDS.

196 Whereas R-SDS reduces dendritic lengths of mPFC layer II/III pyram

197 ) patients (two receiving TAU, one receiving SDS care).

198 Ds) to inhibit LHb activity leads to reduced SDS-induced social avoidance behavior in both WT and Tph

199 Non-reducing SDS-PAGE confirms assembly of the predicted Cys(820)-lin

200 Non-reducing SDS-PAGE shows two bands of about 38kDa exhibiting stron

201 Analyses by non-reducing SDS-PAGE, size exclusion chromatography, and sedimentati

202 DS, making it possible to release and refold SDS-denatured proteins by adding sufficient amounts of N

203 concentration is not sufficient for regular SDS CGE or SDS-PAGE assay.

204 The resulting SDS-wrapped MWCNTs are utilized in industrial applicatio

205 hs of mPFC layer II/III pyramidal neurons, S-SDS increases arborization and spines of apical dendrite

206 Single social defeat stress (S-SDS) induces D1 receptor-mediated extracellular signal-r

207 thioflavin T fluorescence, light scattering, SDS stability, and atomic force microscopy.

208 re we introduce the singleton density score (SDS), a method to infer very recent changes in allele fr

209 dex increased 0.04 Standard Deviation Score (SDS) [Standard Error (SE) 0.007], 0.05 SDS (SE 0.008) an

210 of age [per serving per day: 0.04 SD score (SDS); 95% CI: 0.00, 0.07 SDS].

211 fference in height standard deviation score [SDS], 0.18; 95% confidence interval [95% CI], 0.07-0.29;

212 d low (<-2) body mass index (BMI) SD-scores (SDSs), and 8% of them had low height-for-age SDSs.

213 tient-based, specialist depression services (SDS) versus treatment as usual (TAU) on depression sympt

214 e a genetic basis for improvement of soybean SDS resistance through breeding strategies based on addi

215 romatography coupled with mass spectrometry, SDS-PAGE and immunoassay.

216 5.0109, as documented by mass spectrometry, SDS-PAGE, isoelectric focusing, size-exclusion chromatog

217 In the presence of SRHA, SDS adsorbed on MWCNTs was displaced.

218 The sample stacking SDS CGE technique can be adopted for size-based analysis

219 also the high sensitivity of silver stained SDS-PAGE.

220 sensitivity is comparable to silver-stained SDS-PAGE.

221 e starch (RDS) and slowly digestible starch (SDS) along with the associated analytical methodology we

222 orrelation between slowly digestible starch (SDS) and insoluble beta-glucan and total arabinoxylan co

223 for enrichment of slowly digestible starch (SDS) and resistant starch (RS) content in pea bread were

224 The slowly digestible starch (SDS) correlated positively (R=0.816, p<0.05) with TPC an

225 96.81% increase of slowly digestible starch (SDS) from 75 to 45% dough hydration.

226 stive starch (RDS), slowly digestive starch (SDS) and resistant starch (RS) of native and gelatinized

227 hen oven roasting was applied to pea starch, SDS content increased triply compared to the fully boile

228 Using social defeat stress (SDS) in mice, here we identified a role of dopamine D1 r

229 ased susceptibility to social defeat stress (SDS), a model of psychosocial stress, and prevents the f

230 r comparison against sodium dodecyl sulfate (SDS) (electrostatic), sodium caseinate (electrosteric) a

231 surfactants [anionic sodium dodecyl sulfate (SDS) and nonionic poly(ethylene glycol)-poly(propylene g

232 ed polyprotein using sodium dodecyl sulfate (SDS) as an example.

233 aphy (MLC) employing sodium dodecyl sulfate (SDS) as surfactant, were determined.

234 BP underwent either sodium dodecyl sulfate (SDS) decellularization or stepwise, solubilization-based

235 e procedure included sodium dodecyl sulfate (SDS) denaturation and chemical reduction of serum protei

236 The AS sodium dodecyl sulfate (SDS) denatures and unfolds globular proteins under most

237 Sodium dodecyl sulfate (SDS) facilitates multiwalled carbon nanotube (MWCNT) deb

238 While the use of sodium dodecyl sulfate (SDS) in separation buffers allows efficient analysis of

239 ated with 0.1% or 1% sodium dodecyl sulfate (SDS) or 0.1% Triton X-100 and assayed for clinical chemi

240 d hemi/ad-micelle of sodium dodecyl sulfate (SDS) was designed for the magnetic immobilization of hem

241 chemical surfactant sodium dodecyl sulfate (SDS) were also investigated.

242 ared using Tween 80, sodium dodecyl sulfate (SDS), sodium caseinate (SC) and SDS-Tween 80 as the emul

243 ssue (FACT) is a new sodium dodecyl sulfate (SDS)-based clearing protocol for the chemical clearing a

244 t focusing (TGF) and sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis (PAGE) in a PDMS

245 x dissociation using sodium dodecyl sulfate (SDS).

246 mplex in presence of sodium dodecyl sulfate (SDS).

247 Sodium dodecyl sulphate (SDS) enhanced PPO activity, with pulp showing a stronger

248 abilising effect of sodium dodecyl sulphate (SDS) micelles on pH-induced colour variations of phycocy

249 ithin, Tween-20 and sodium dodecyl sulphate (SDS) were tested.

250 ing a cosurfactant (sodium dodecyl sulphate (SDS)).

251 anionic surfactant, sodium dodecyl sulphate (SDS), as template to control the size of synthesized nan

252 and 5 min) on total sodium dodecyl sulphate (SDS)-soluble and sarcoplasmic proteins in frozen (-10 de

253 ement was obtained for an anionic surfactant SDS or the cationic surfactant DTAB, in which cases the

254 tection of these common anionic surfactants (SDS/SDBS) as the color changes from blue to yellowish gr

255 pathogen that causes sudden death syndrome (SDS) in soybean plants.

256 Shwachman-Diamond syndrome (SDS) (OMIM #260400) is a rare inherited bone marrow fail

257 openia (SCN) and Shwachman-Diamond syndrome (SDS) are congenital neutropenia syndromes with a high ra

258 SBDS) gene cause Shwachman-Diamond Syndrome (SDS), a rare congenital disease characterized by bone ma

259 MWCNTs exhibit higher affinity for SRHA than SDS.

260 The SDS content can identify foods rich in slow release carb

261 The SDS content increased from 18.01+/-2.11% to 82.81+/-2.34

262 The SDS-PAGE pattern of A. mellifera proteins honey showed t

263 a model for soybean root defense against the SDS pathogen.

264 olonic fluids, and thus largely enriched the SDS and RS fractions in starch.

265 18 months was significantly improved in the SDS group compared with the TAU group (13.6 [SD 8.8] in

266 red with the TAU group (13.6 [SD 8.8] in the SDS group vs 16.1 [6.6] in the TAU group; mean change di

267 for mean HDRS17 score (14.8 [SD 7.9] in the SDS group vs 17.2 [7.3] in the TAU group, p=0.056) or GA

268 howed a loss of typical Maltese cross in the SDS product and revealed a reorientation of crystalline

269 st degree of hydrolysis of HPIs by HT in the SDS-PAGE profiles.

270 in-SDS samples resulted in extraction of the SDS from the protein-SDS complexes and refolding of beta

271 ion may contribute to the development of the SDS phenotype.

272 asing clearing time, adjusting the pH of the SDS solution, and using the appropriate temperature for

273 ortant for ribosome maturation and therefore SDS belongs to the ribosomopathies.

274 f C12E8, while DDM was additionally added to SDS-denatured alphaLA and betaLG.

275 ents were assigned to TAU and 93 patients to SDS, and were included in intention-to-treat analyses.

276 Acetone treatment of cocoa powder prior to SDS-PAGE led to losses of nitrogenous compounds.

277 nidiation but had increased sensitivities to SDS, Congo red, and hyperosmotic stress.

278 are indicated by increased sensitivities to SDS-mediated dissociation and dispase proteolysis.

279 Although total SDS-soluble fraction indicated no important changes indu

280 wed excellent photophysical responses toward SDS and SDBS with a detection limit of 0.12 muM/(34 ppb)

281 t neutral pH by high resolution Tris-Tricine SDS-PAGE and matrix-assisted laser desorption ionization

282 cation of the molecular mechanism underlying SDS resistance in soybean, and provide a genetic basis f

283 Proteins were studied by using SDS-PAGE and immunoblotting with sera from patients with

284 Hydrolysis profiles were displayed using SDS-PAGE.

285 its of equal molecular mass estimated, using SDS-PAGE and native-PAGE electrophoresis, to be 86kDa.

286 e hydrolysis profiles were illustrated using SDS-PAGE.

287 ed glycation endproducts were measured using SDS-PAGE gels and by ELISA whereas Amadori products were

288 he hydrolysis profiles were visualised using SDS-PAGE.

289 cause CSPalpha to form high molecular weight SDS-resistant aggregates, which are also present in post

290 ared between the two methods was higher when SDS/ACN/urea was used, compared to the 30% ACN/urea extr

291 2+) and beta-mercaptoethanol increased while SDS and EDTA inhibited the xylanase activity of both Xyl

292 ompetitive nature of both the additives with SDS for available positions at the air/water interface.

293 with globular proteins for association with SDS, making it possible to release and refold SDS-denatu

294 effect was seen in prepubertal children with SDS of 0.28 (95% CI, 0.14-0.41; P < 0.0001).

295 lue native (BN) electrophorese combined with SDS-PAGE yielded NOX4 to reside in macromolecular comple

296 All proteins and their complexes with SDS were attempted to be refolded by the addition of C12

297 ion by studying quercetin's interaction with SDS micelles.

298 was present in 48% (13/27) of patients with SDS but was not seen in healthy controls (0/17, P < .001

299 rome/acute myeloid leukemia in patients with SDS.

300 etected in healthy controls or patients with SDS.