ライフサイエンスコーパス: molecular mass

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

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

3 otopologues diffusion coefficients and their molecular mass.

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

5 with the corresponding metabolite compound's molecular mass.

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

7 and affects primarily OMM proteins of higher molecular mass.

8 pplication of proteins and fibres reduced PA molecular mass.

9 (TGE) device to separate intact proteins by molecular mass.

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

11 more than one aminopeptidase, having similar molecular mass.

12 are synthesized in excellent yields and high molecular masses.

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

14 each other by one or a few N-methyl groups (molecular mass 15 Da).

15 oxic factors: one, derived from macrophages (molecular mass 17 kDa), was named TNF, and the second, d

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

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

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

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

20 amines of low mass (m/z < 200), compounds of molecular masses above 1000 Da were observed in the plas

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

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

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

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

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

26 )(600E) resides in large complexes of higher molecular mass and activity, while BRAF(WT) is confined

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

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

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

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

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

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

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

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

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

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

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

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

39 s; (ii) comparison of their changes in their molecular masses and fragment ions with those of the par

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

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

42 radation products were derived from accurate molecular masses and multistage mass spectrometry.

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

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

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

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

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

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

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

50 25-kDa rab17 is responsible for the shift in molecular mass, and that rab17 prenylation is required f

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

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

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

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

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

56 nate and Western blotting, PCFT species with molecular masses approximating those of the PCFT dimer a

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

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

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

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

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

62 vious gel permeation data that estimated the molecular mass as a tetramer.

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

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

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

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

67 ee neurofilament subunits different in their molecular mass assemble to form heteropolymers that prod

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

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

70 gh molecular mass band of 23 kDa and one low molecular mass band of 19 kDa.

71 g p21 is expressed as two isoforms, one high molecular mass band of 23 kDa and one low molecular mass

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

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

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

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

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

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

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

79 This high-molecular mass biopolymer consists mainly of poly(cis-1,

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

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

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

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

84 rget proteins, where the modification alters molecular mass, charge, and structure/function and/or pr

85 n of the isolated SAM domain as well as high molecular mass complex formation of EN and abrogates the

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

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

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

89 Target of Rapamycin (TOR) kinase forms high molecular mass complexes and is a major regulator of cel

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

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

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

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

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

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

96 gies are discussed in detail leading to high molecular mass compounds showing appropriate redox (ioni

97 hat are covalently coupled to haptens (small molecular mass compounds) activate the immune system, el

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

99 Many of these low molecular masses corresponded to molecular formulas of p

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

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

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

103 O-xylosylation was discovered as a result of molecular mass determination, peptide mapping analysis,

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

105 -PAGE was 93 kDa for both strains, while the molecular masses determined by MALDI-TOF for wild and mu

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

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

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

109 Comparison of the molecular mass distribution of the commercial enological

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

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

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

113 The subunit molecular mass estimated by SDS-PAGE was 93 kDa for both

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

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

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

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

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

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

120 cells with hypoxic stress suppressed a high molecular mass form of CTCF (150 kDa), but not a lower m

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

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

123 Electron microscopy reveals that high-molecular-mass Gle1 oligomers form ?26 nm diameter disk-

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

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

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

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

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

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

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

131 This high-molecular-mass HA accumulates abundantly in naked mole-r

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

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

134 noacyl-tRNA synthetase complex (MARS), whose molecular mass has been proposed to be between 1.0 and 1

135 Low-molecular mass heparin-induced chemical shift perturbati

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

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

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

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

140 Low molecular mass hyaluronans are known to induce inflammat

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

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

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

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

145 Components of identical molecular mass in the polysorbate formulations have been

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

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

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

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

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

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

152 4 proteins of 22,000- and 33,000-Da apparent molecular mass (L4-22K and -33K proteins) that are expre

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

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

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

156 The low molecular mass (LMM) extract of Cichorium intybus var. s

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

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

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

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

161 nge of low molecular weight (LMW) molecules (molecular mass < 150 Da) that differ from each other by

162 mall organic and metal-containing molecules (molecular mass <1,000) can catalyse synthetically useful

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

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

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

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

167 s after surgery, the 1) HA concentration and molecular mass (M(r) ) distribution in the SF, 2) endoge

168 deuterium ((2)H) with the highest abundance molecular mass (M) at M(beta-C)+(2)H(1)(0).

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

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

171 Despite a lower molecular mass, MEnd ligase-DNA had a lower electrophore

172 es the partitioning into vacuoles of the low molecular mass metal chelator nicotianamine and leads to

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

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

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

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

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

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

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

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

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

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

183 MALDI-TOF revealed a molecular mass of 13,221 Da, and 12-23 aa sequences of O

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

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

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

187 SmCI is a 165-residue glycoprotein with a molecular mass of 19.69 kDa (mass spectrometry) and 18 c

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

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

190 tracellular Ig V-type domain and a predicted molecular mass of 21.5 kDa.

191 ecrease of an LHCII protein with an apparent molecular mass of 22 kDa, whereas silencing/lack of LHCB

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

193 Apolipoproteins E3 and E4, proteins with a molecular mass of 34.15 kDa, differ by a single amino ac

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

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

199 of TL1A trimers in solution with an apparent molecular mass of 516 kDa.

200 protein of 505 amino acids with a predicted molecular mass of 57.44 kDa.

201 all hydrophobic polypeptide with an apparent molecular mass of 6 to 7 kDa.

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

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

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

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

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

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

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

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

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

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

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

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

214 The purified enzyme showed a single band at molecular mass of approximately 25 kDa on 12% sodium dod

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

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

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

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

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

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

221 Molecular mass of contrast agents affected diffusivities

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

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

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

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

228 glycans, which constitute almost half of the molecular mass of the external Env domains, produce cons

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

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

231 ion mass spectrometry was used to obtain the molecular mass of the resulting products, which is helpf

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

233 PC1 has a predicted molecular mass of ~460 kDa comprising a long multidomain

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

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

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

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

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

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

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

244 itional primase subunits does not change the molecular mass or helicase activity of the primosome, bu

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

246 ion, are required for expression of the high molecular mass p21 isoform through phosphorylation at se

247 The high-molecular mass penicillin binding proteins of bacteria c

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

249 dazole- and benzoxazole-pyrimidones as small molecular mass PI3Kbeta-selective inhibitors.

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

251 ta2, and beta5 by the inducible subunits low molecular mass polypeptide (LMP) 2 (beta1i), multicataly

252 nhibitor of the immunoproteasome subunit low molecular mass polypeptide (LMP) 7 (beta5i) that attenua

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

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

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

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 By contrast, cytosolic Bax exhibits a slight molecular mass shift on SDS-PAGE as compared with recomb

269 This molecular mass shift was shown to contain SUMO moieties

270 eins photolabeled by [(32)P-5N(3)]NAADP have molecular masses smaller than the sea urchin TPCs, and a

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

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

273 Molecular mass spectra can be obtained from the same sou

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

275 Molecular mass spectrometry has been applied to simultan

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

277 FPLC column, which is in agreement with the molecular mass suggested by mass spectroscopy to be 83 k

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

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

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

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

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

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

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 ero-oligomers in vitro, which had an average molecular mass that was intermediate of each of the homo

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

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 Molecular mass was determined to be 85 kDa by Superose-1

297 Increasing molecular mass was shown to decrease the adhesion force

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

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

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