ライフサイエンスコーパス: molecular mass

1 more than one aminopeptidase, having similar molecular mass.

2 n-associated proteins, which were shifted in molecular mass.

3 samples, especially those of relatively low-molecular mass.

4 work well for ~12 kDa as the lowest limit of molecular mass.

5 otopologues diffusion coefficients and their molecular mass.

6 scaling (power-law) behavior with respect to molecular mass.

7 with the corresponding metabolite compound's molecular mass.

8 tion to the exclusion of compounds with high molecular mass.

9 and affects primarily OMM proteins of higher molecular mass.

10 teoforms, each of which has a characteristic molecular mass.

11 taken as a model globular protein of similar molecular mass.

12 are synthesized in excellent yields and high molecular masses.

13 ss defects were calculated using theoretical molecular masses.

14 hich limits our ability to determine neutral molecular masses.

15 rtion of HS components that have the highest molecular masses.

16 st level of interfering substances with high molecular masses.

17 Low-molecular mass (10 kD) cytosolic acyl-coenzyme A-binding

18 and ethanol precipitation leading to similar molecular masses (200-300kDa).

19 resis separations for targets accross a wide molecular mass (25-289 kDa), yet within 1 mm separation

20 d as a recombinant protein, due to its large molecular mass (252 kDa in S. cerevisiae).

21 The molecular mass (33.214) and other structural features of

22 aa) protein, in accordance with its apparent molecular mass (~40 kDa) observed by immunoblotting.

23 r, APOBEC3G with accumulation into the lower molecular mass active form as characterized by FPLC.

24 They were glycoproteins and molecular mass after peptide-N-glycosidase F treatment w

25 ectrometry data, approximately 100% of lower molecular mass alkanes (C9-C21) were removed within 10 m

26 upport for metabolite discovery by measuring molecular masses, ambiguities in elemental formulas ofte

27 s on soil solution OM is visible from higher molecular masses, an increasing degree of oxygenation an

28 lations are easy to use analytical tools for molecular mass analysis and aggregation studies as well.

29 phenotypes correspond with changes in pectin molecular mass and abundance that can affect wall mechan

30 )(600E) resides in large complexes of higher molecular mass and activity, while BRAF(WT) is confined

31 MET-XAlign takes the deduced molecular mass and estimated compound retention time inf

32 ed permeability of the BBB to a range of low-molecular mass and high-molecular mass tracers.

33 lar hydrolases, F-Zn(ii) displays the lowest molecular mass and highest catalytic efficiency, in addi

34 ne the contribution of the GPI-anchor to the molecular mass and isoelectric point of PrP quasispecies

35 t Tmax of individual phytochemicals based on molecular mass and lipophilicity.

36 ct their plasma absorption maximum, based on molecular mass and lipophilicity.

37 xtures of organic compounds with low to high molecular mass and low to high polarity.

38 ntified this protein through both its intact molecular mass and peptide mass fingerprint (PMF) by mat

39 On the basis of the deduced neutral molecular mass and retention time, we have also develope

40 tryptophan intrinsic fluorescence, increased molecular mass and Ricinus communis lectin recognition.

41 sue autofluorescence and high contrasts, its molecular mass and size are far below the renal cutoff a

42 DI) mass spectrometry matrix is proposed for molecular mass and structural determination of glycans.

43 ility for direct identification of allergens molecular mass and structure, discovery of unusual aller

44 f alkali influenced the glycosidic linkages, molecular mass and thermal stability of the polysacchari

45 inhibitory peptides were isolated and their molecular masses and amino acid sequences were determine

46 ives, and flavonoid aglycones based on their molecular masses and fragmentation pattern.

47 nalytes, while simultaneously changing their molecular masses and improving their desorption and ioni

48 Matching the molecular masses and relative migration times of the ext

49 ated and could be assigned based on detected molecular masses and relative migration.

50 a absolute Rayleigh scattering ratios, their molecular masses and second, third, and fourth virial co

51 Accurate molecular masses and tandem mass (MS/MS) spectra interpr

52 ctive species at 25 kDa (the predicted rab17 molecular mass) and 40 kDa.

53 t B (UVB) exposure on hyaluronan content and molecular mass, and expression of genes involved in hyal

54 erometric contrast, which is proportional to molecular mass, and fast acquisition rates, we detect an

55 carboxylic groups with greater polarity and molecular mass, and later eluting sub-fractions had grea

56 25-kDa rab17 is responsible for the shift in molecular mass, and that rab17 prenylation is required f

57 glycans account for approximately 30% of its molecular mass, and the newly solved crystal structure o

58 tometry can accurately count, distinguish by molecular mass, and thereby reveal the relative abundanc

59 in total polygalacturonase activity, pectin molecular mass, and wall composition and also display hi

60 found functional effects of binding by a low-molecular-mass antibiotic to the megadalton ribosome.

61 hile permitting effective probing with large-molecular-mass antibodies.

62 unspecific elimination of ROS by use of low molecular mass antioxidant compounds was not successful

63 results revealed an aspartic peptidase with molecular mass approximately 38kDa, maximal activity at

64 Despite its apparent molecular mass ( approximately 100 kDa), Smac-DIABLO was

65 to be indistinguishable by MS because their molecular masses are exactly the same.

66 rum against all peptides in a database whose molecular masses are similar to the precursor mass of th

67 soil amendments with greater content of high molecular mass aromatic components may positively affect

68 that results in more than 60wt% yield of low-molecular-mass aromatics.

69 nic compound in cod liver followed by higher molecular mass arsenic-containing fatty acids and hydroc

70 the nuclear form of HMR has the same reduced molecular mass as plastidial HMR, support a retrograde p

71 ffect grows stronger for compounds of higher molecular mass as the effect of a single atom on the ove

72 iated by a zwitterionic species, of the same molecular mass as the epoxide, which transforms to an in

73 High-molecular mass ASC complexes were also detected, consist

74 in yeast Saccharomyces cerevisiae, a 2.6-MDa molecular mass assembly containing six protomers each of

75 detect absorption features from a high mean-molecular-mass atmosphere.

76 were similar, but more fragments and higher molecular mass bands were observed in the Gd-P gel image

77 Low molecular mass BAP sequences are less likely to be broke

78 cosylated, with approximately 50% of the Env molecular mass being contributed by N-glycans.

79 appearance of protein bands having apparent molecular mass below 20 kDa.

80 The fraction containing peptides with a molecular mass below 3kDa demonstrated a strong radical

81 sidues contained one nitrogen atom and had a molecular mass between 375 and 525 Da, which was 150 to

82 In each tissue, Trpm4b had a different molecular mass, between approximately 129 and approximat

83 Numerous low molecular mass bioactive peptides (BAPs) can be generate

84 e analysis and determination of the relative molecular mass by mass spectrometry.

85 acellular RoxA has evolved to have twice the molecular mass by successively accumulating extensions o

86 r detected, MISA was able to uncover neutral molecular masses by in-source fragment matching.

87 We identify higher molecular mass carboxy-terminal fragments (CTFs) of APP,

88 Capsular polysaccharides (CPSs) are high-molecular-mass cell-surface polysaccharides, that act as

89 The structure of the large molecular mass complex was dependent on RHA binding to a

90 ASK1 forms a high molecular mass complex whose activity is, under non-stre

91 Numb and p53 are the constituents of a high molecular mass complex, which is disintegrated upon acti

92 erestingly, TbTim17 was accumulated as lower molecular mass complexes in TbTim62 KD mitochondria.

93 accumulate during heat stress and form high molecular mass complexes.

94 mass spectrometry identified two major high-molecular-mass complexes with distinct sets of interacti

95 ular-mass ribonucleoprotein complexes to low-molecular-mass complexes.

96 maize revealed substantial changes to small molecular mass components of the matrix.

97 term flavonolignan that is used for the low-molecular mass compounds composed of flavonoid and ligna

98 ng this combination for analysis of the high-molecular mass compounds present in multi-component matr

99 were associated with biomolecules with high molecular mass compounds, such as immunoglobulins, album

100 exist, particularly for the emerging and low molecular mass congeners.

101 arent diameter of about 1.4 nm with a 400-Da molecular mass cut-off.

102 o an automated searching algorithm against a molecular mass database covering over 17000 potential PS

103 Daltonics), in terms of the distribution of molecular masses detected and the reproducibility of the

104 enic-selective detection and high resolution molecular mass detection of the arsenolipids.

105 Epitope peptides were identified by accurate molecular mass determinations or by partial amino acid s

106 fusion of fluorescently labeled low and high molecular mass dextran molecules or albumin.

107 istics together with tubular presence of low molecular mass dextran provide clear evidence of functio

108 fully resolved separations of proteins with molecular mass differences of just 4 kDa or 12% (GAPDH,

109 largely with a pI between 5.0 and 8.0 and a molecular mass distribution between 10 and 170 kDa.

110 Significant changes were observed in molecular mass distribution of pressurized waxy maize st

111 Comparison of the molecular mass distribution of the commercial enological

112 ostatic pressure processing (650MPa/9min) on molecular mass distribution, and hydrodynamic and struct

113 d with significantly high activities, narrow molecular mass distributions, and the possibility of cop

114 mulas for organic compounds of relative high molecular mass (e.g., between 400 and 900 Da) to less th

115 ge of energetic couplings in biology by high-molecular-mass electron bifurcating machineries.

116 ose it is a biosynthetic constituent of high molecular mass EPS polymer.

117 PepX comprises two subunits of equal molecular mass estimated, using SDS-PAGE and native-PAGE

118 we define the structure of both high and low molecular mass exopolysaccharide from R7A.

119 plant receptor-like kinase, EPR3, binds low molecular mass exopolysaccharide from strain R7A to regu

120 The low molecular mass exopolysaccharide produced by R7A is a mo

121 tic chemicals and/or provide a source of low-molecular-mass feedstocks suitable for downstream proces

122 (S1pr1(iECKO) ) showed BBB breach for small-molecular-mass fluorescence tracers (<3 kDa), but not la

123 To determine EYFP's molecular mass for MSI studies, we performed intact mass

124 lation of 50S ribosomal subunits in the high-molecular-mass fraction of chloroplast stromal extracts.

125 aled that most of the sHsp substrates have a molecular mass from 50 to 100 kDa and a slightly acidic

126 vealing it to be rich in peptides (107) with molecular masses from m/z 700 to 2369Da.

127 Hyaluronan, a high molecular mass glycosaminoglycan, has been shown by us t

128 ve intermediates in organic synthesis and in molecular mass growth processes leading eventually to ca

129 y at high temperatures leading through rapid molecular mass growth processes to complex aromatic stru

130 benchmarks contesting established ideas that molecular mass growth processes to PAHs transpire at ele

131 that can be repeated 20,000 or more times, a molecular mass >8 million Da, and a length >20 mum.

132 control cells and that activation of the low-molecular-mass GTP-binding protein Rab27a, involved in t

133 ribosylation factor (ARF)1p and ARF2p, small molecular mass GTPases that regulate cargo transport thr

134 conversion of high molecular mass HA to low molecular mass HA facilitated GAS phagocytosis by macrop

135 the bacterium and host and suggest that high molecular mass HA facilitates GAS deep tissue infections

136 In contrast, native high molecular mass HA significantly impaired internalization

137 We discovered that conversion of high molecular mass HA to low molecular mass HA facilitated G

138 However, once high-molecular-mass HA is removed by either knocking down HAS

139 ied residual lignin, especially for the (low molecular mass) hardwood lignosulfonate, revealing that

140 Y380A mutants did not show increases in high molecular mass (HMM) species after treatment with DPTA o

141 termine the role of the acetyl groups of low molecular mass hyaluronan in stimulating the production

142 Selectively N-butyrylated lower molecular mass hyaluronan shows promise as an example of

143 size was internalized more readily than high molecular mass hyaluronan.

144 mole-rat fibroblasts secrete extremely high-molecular-mass hyaluronan (HA), which is over five times

145 he longest-living rodent, produces very-high-molecular-mass hyaluronan (vHMM-HA), compared to other m

146 Low molecular mass hyaluronans are known to induce inflammat

147 e acetylated and partially butyrylated lower molecular mass hyaluronans exert their effects through t

148 The adsorption and transport of a 300-Da molecular-mass hydrophobic ion at the Escherichia coli m

149 n that intensifies gradually with increasing molecular mass in both the wild-type and mutant strains

150 or, clade A, member 1, resulting in a higher molecular mass in lung homogenate compared to pancreas h

151 ) and the other with high (117 kDa; RHBDD2H) molecular masses in mouse retinal extracts.

152 The DDs assemble into complexes displaying molecular masses in the range 130-158kDa and RAIDD-DD:PI

153 PLE yields protein molecular mass information without the need for ionic su

154 rolysates were fractionated according to the molecular mass into three fractions of >5 kDa, 3-5 kDa a

155 h the transfer and over-fragmentation of low molecular mass ions.

156 e found to shift to lower frequencies as the molecular mass is increased, as expected.

157 4 proteins of 22,000- and 33,000-Da apparent molecular mass (L4-22K and -33K proteins) that are expre

158 e measurement of the binding kinetics of low molecular mass ligands with nanodisc-encapsulated membra

159 that is essential for the assembly of higher molecular mass light-harvesting PORB::PORA complexes and

160 owever, that the preferred substrates of low-molecular mass (LMM) class B and C dd-peptidases contain

161 of tAFP is dependent on the presence of low molecular mass (LMM) species that copurify with tAFP and

162 Low molecular mass (LMM) thiols is a diverse group of compou

163 Hg(II)-complexes, combining either with low molecular mass (LMM) thiols like Cys, Hg(Cys)(Mem-RS), o

164 pled plasma mass spectrometer revealed a low-molecular-mass (LMM) Fe(II) pool consisting of two iron

165 es from the protein isolate of raw bean with molecular mass lower than 3kDa reduced 89% of the HMGCR

166 Permeate fractions with molecular masses lower than 3 kDa (LFH <3 kDa) were oral

167 with Esperase, and a peptide fraction with a molecular mass <3kDa (F3) was isolated by ultrafiltratio

168 is of 21% had 65% of peptide material with a molecular mass <500Da.

169 ase in the content of proteins and peptides (molecular masses <20kDa) was determined for breads with

170 tudy, an antioxidant peptide fraction with a molecular mass<30kDa (PF30) isolated from rainbow trout

171 e empirical variations of D as a function of molecular mass M that distinguish folded, intrinsically

172 Peptide charge (Z) and size (molecular mass, M) are the two major factors determining

173 Such polymers, both high-molecular-mass materials and waxes, are chemically inert

174 ica nanoparticles against targets of varying molecular mass (melamine, vancomycin and trypsin).

175 Although a range of low molecular mass molecular single crystals has been shown

176 ossess considerable heterogeneity in average molecular mass, molecular mass range, disaccharide compo

177 Small molecular mass molecules (His6) exhibit a high binding a

178 N-glycans that account for 1/4 of the total molecular mass; most of the N-glycans could be visualize

179 By correlating the EM diameter to the molecular mass (Mr) of standards, the Mr of analytes can

180 c processes and range in complexity from low molecular mass natural halocarbons (nHCs, mostly halomet

181 S-induced inclusions colocalize with the low-molecular-mass neurofilament subunit (NFL) or peripherin

182 Activated macrophages formed a high-molecular-mass NLRP3-NEK7 complex, which, along with ASC

183 ion mass spectrometry (MS) revealed that the molecular mass of (protonated) legiobactin is 437.140 Da

184 ulfide-bonded complex with beta-actin with a molecular mass of 110 kDa.

185 Purified enzyme with an apparent molecular mass of 116 kDa forms monomers in solution as

186 nceptually translated protein has a relative molecular mass of 128.8x10(3) and contains all signature

187 n cells corresponds to a glycoprotein with a molecular mass of 150 kDa.

188 The pentameric complex has a molecular mass of 160 kDa, a stoichiometry of 1:1:1:1:1,

189 OF analyses revealed that BacJ1 had an exact molecular mass of 1881.036 Da.

190 found to have 14.63+/-0.70% (w/w) protein, a molecular mass of 2.4kDa and low hemolytic activity (<50

191 le-associated serine/threonine kinase with a molecular mass of 205 kDa) as a new CFTR regulator.

192 s predominantly as (gH/gL)2 homodimer with a molecular mass of 220 kDa in solution, has a stoichiomet

193 The study showed that flavonoids with molecular mass of 250-320 g/mol have high potential of a

194 ynthesis of a FA-major product, exhibiting a molecular mass of 386 g/mol and a EF-major product with

195 y of 1.26 ppm, a number-average monoisotopic molecular mass of 40074.64 Da was determined for pegfilg

196 s of 386 g/mol and a EF-major product with a molecular mass of 442 g/mol.

197 th with an ORF that encodes 434 amino acids (molecular mass of 46.9 kDa).

198 bitors, namely inhibitor I and II, exhibited molecular mass of 47 and 52 kDa, respectively, based on

199 hromatography, EcChiP had an apparent native molecular mass of 50 kDa, as predicted by amino acid seq

200 ng frame (ORF) that encodes 539 amino acids (molecular mass of 62.7 kDa); dsRNA2 dsRNA is 1,524 bp in

201 paran sulfate proteoglycan, perlecan, with a molecular mass of 640 kDa as well as smaller molecular m

202 ylated and secreted as a stable dimer with a molecular mass of 70.7 kDa in its native form.

203 The holoenzyme is a homo-hexamer with molecular mass of 720 kDa.

204 Based on its relative molecular mass of 7287 and NH2-terminal sequence, the pr

205 DPP5 was composed of 684 amino acids with a molecular mass of 77,453, and existed as a dimer while m

206 cleave L1 to generate an L1 fragment with a molecular mass of 80 kDa (L1-80).

207 Measuring the molecular mass of a sugar, however, immediately poses a

208 The complex had a high molecular mass of about 300 kDa and was only composed of

209 Composed of ten subunits that add up to a molecular mass of about 500 kDa, TFIIH is also essential

210 al homodecameric quaternary structure with a molecular mass of about 500kDa.

211 its were confounded by an increased apparent molecular mass of all beta1 and beta2 subunit isoforms i

212 One of the products had the apparent molecular mass of approximately 150 kDa on SDS-PAGE and

213 cross-reactive grass pollen allergens with a molecular mass of approximately 25-30 kDa.

214 ain variable fragment (scFv) antibody with a molecular mass of approximately 26 kDa that inhibits VEG

215 reduction-sensitive oligomers with a nominal molecular mass of approximately 400 kDa.

216 s the impact of FK506-binding protein with a molecular mass of approximately 52 kDa (FKBP52), an immu

217 Although recombinant progranulin has a molecular mass of approximately 85 kDa by SDS-PAGE, it e

218 (oxy)hydroxide AFM tips suggesting that the molecular mass of aromatic WEOM molecules plays a critic

219 ent proteins ratio patterns, even though the molecular mass of collagen subunits were similar, 123 an

220 Molecular mass of contrast agents affected diffusivities

221 el, which utilizes the number of charges and molecular mass of each proteoform as the parameters.

222 To examine the impact of the molecular mass of HA on GAS infection, we established in

223 f superior temporal gyrus revealed a smaller molecular mass of immature N-glycans on the alpha1 subun

224 Sha differed from Ler in the apparent molecular mass of NCED3, indicative of altered NCED3 pro

225 Vc defines a ratio, QR, that determines the molecular mass of proteins or RNA ranging from 10 to 1,0

226 SDS-PAGE showed that the molecular mass of purified enzyme was 21.7 kDa.

227 CED3 but did differ from Ler in the apparent molecular mass of stromal NCED3.

228 can be a suitable method for estimating the molecular mass of ternary complexes.

229 The molecular mass of the enzyme was estimated to be approxi

230 inverse power-law relation between D and the molecular mass of the isotopologues.

231 ion chromatography showed an increase of the molecular mass of the modified residual lignin, especial

232 However, the molecular mass of the rubber was not affected by TbREF s

233 embrane-protected fragments with an apparent molecular mass of ~26 kDa (major component) and ~24 kDa

234 s with three or four disulfide bridges and a molecular mass of ~5 kDa.

235 that the O. formigenes-derived factors have molecular masses of 10-30 kDa.

236 t hLAMP-2 expressed in ldlD cells, both with molecular masses of 110 kD.

237 Disulfide-rich plant peptides with molecular masses of 2-6 kDa represent an expanding class

238 , four that were identified had protonotated molecular masses of 305, 331, 347, and 359 and have not

239 into three predominant protein species with molecular masses of approximately 34, 27/29, and 25/26 k

240 aracterization of large protein systems with molecular masses of hundreds of kilodaltons.

241 mit," and the uptake of bulky molecules with molecular masses of more than approximately 600 Da is th

242 mass spectrometers provides a tool to assess molecular masses of peptides with great precision and ac

243 wing database searching, the matching of the molecular masses of the fragment ions to the correct cro

244 The molecular masses of the TBR-POD and Turnip-POD were appr

245 argeted profiling aims at uncovering neutral molecular masses of underlying metabolites and assign th

246 ry electrophoresis (ICxCE) separation of low-molecular-mass organic acids as test analytes.

247 acid 271 was critical for the altered NCED3 molecular mass pattern, while the other Sha NCED3 polymo

248 l or combined mutations in genes for the low-molecular-mass penicillin-binding proteins PBP3 and PBP4

249 ation in the efficient identification of low molecular mass peptide sequences in food protein hydroly

250 sedimented in the presence of GTP as a high molecular mass polymer with a well defined size and tend

251 by the nuclear genome, synthesized as higher molecular mass preproteins with an N-terminal transit pe

252 ds and a decreasing contribution from higher molecular mass products.

253 ype in their brains, characterized by a high molecular mass protease-resistant PrP fragment (HMM PrPr

254 s of the amount of RNA and lipid used, had a molecular mass, protease resistance and insolubility sim

255 SDS-PAGE) analysis of the OM revealed a high molecular mass protein as 300-kDa.

256 Low-molecular mass protein-7 (LMP7) is a proteolytic subunit

257 ng (100 degrees C; 0-15 min) on the relative molecular mass, protein unfolding and secondary structur

258 Addition of macronutrients such as high molecular mass proteins restored endocytosis and Ag pres

259 potent inhibitors of MMP-9, particularly low molecular mass proteins.

260 uffer system suitable for analyses of a wide molecular mass range (6.5-116 kDa).

261 tic neighbor embedding of peaks in the lipid molecular mass range (m/z 700-850) distinguishes several

262 y possible structures that matched the lower molecular mass range (maximum of 10 carbon atoms) of the

263 ble heterogeneity in average molecular mass, molecular mass range, disaccharide composition and conte

264 315A was evident by a shift of A3G from high-molecular-mass ribonucleoprotein complexes to low-molecu

265 This work lays the foundation for molecular mass separation in biophysical and chemical sy

266 XNDC16 in the cytosol by in vitro synthesis, molecular mass shift assay, and flow cytometry.

267 The ESI-MS spectra showed a molecular mass shift between 183 and 366g/mol for fructo

268 This molecular mass shift was shown to contain SUMO moieties

269 ructure (i.e., hydrodynamic radius), than to molecular mass (size).

270 In-channel antibody probing of small molecular mass species is especially challenging, since

271 molecular mass of 640 kDa as well as smaller molecular mass species of 300 and 130 kDa.

272 Molecular mass spectra can be obtained from the same sou

273 Ion sources for molecular mass spectrometry are usually driven by direct

274 Molecular mass spectrometry has been applied to simultan

275 lute protein quantification methods based on molecular mass spectrometry usually require stable isoto

276 P43, as well as most of their associated low molecular mass subunits, and the assembly factor Psb27.

277 of stimulated neutrophils despite their low molecular mass, suggesting that the conformation and rea

278 obesity were positively associated with the molecular mass sum of the PAHs and the total sum of naph

279 associated with precipitates was of a higher molecular mass than that remaining in ethanolic solution

280 s was more related with the proanthocyanidin molecular mass than with their percentage of galloylatio

281 olygalacturonase activity and smaller pectin molecular masses than wild-type controls, supporting a f

282 TbREF is homologous to the TbSRPPs but has a molecular mass that is atypical for the family.

283 from carbon monoxide in the galaxy yields a molecular mass that is consistent with the estimate from

284 t the three proteins formed a complex with a molecular mass that is consistent with the formation of

285 A but requires a cytosolic factor of >10-kDa molecular mass that is resistant to N-ethylmaleimide and

286 Consistent with this binding profile and the molecular mass, the sec49K receptor was identified as th

287 duces and exports appreciable amounts of low molecular mass thiol (LMM-RSH) compounds reaching concen

288 d concentrations of MeHg, sulfide, eight low molecular mass thiols and thiol groups associated with n

289 hyaluronan chain causing a reduction of the molecular mass to 30-214 kDa.

290 phos-methyl (m/z=306.1) containing different molecular mass to charge ratios (m/z=278.1, 301.1 and 31

291 BB to a range of low-molecular mass and high-molecular mass tracers.

292 roteins and protein complexes with aggregate molecular masses under approximately 50 kDa.

293 s containing up to five Leu/Ile residues and molecular masses up to 3000 Da.

294 proximately 100 ng) samples of gold MPCs, of molecular masses up to approximately 40 kDa, and with si

295 parations contained laminarin although their molecular mass varied considerably (4400-34,400 Da).

296 Increasing molecular mass was shown to decrease the adhesion force

297 mponent analysis data model revealed that PA molecular mass was significant in defining the fining re

298 eration function, HA samples of various mean molecular masses were added to keratinocyte cultures tre

299 anes and haloethanes) to compounds of higher molecular mass which often contain oxygen and/or nitroge

300 rough a gel filtration column toward smaller molecular masses with a reduced propensity for dimer for