ライフサイエンスコーパス: binding capacity

1 quences have confirmed function (e.g. target binding capacity).

2 nsactivation ability and upregulation of DNA binding capacity.

3 l ties, we could maintain ThreeFoil's glycan-binding capacity.

4 monary fibrosis (IPF) exhibit enhanced FXIIa binding capacity.

5 nd transcriptional activity, through its RNA-binding capacity.

6 asomes are asymmetric in their polyubiquitin binding capacity.

7 with WT, presumably due to enhanced membrane-binding capacity.

8 proteins showed significantly decreased IgE binding capacity.

9 of HCAs may significantly contribute to the binding capacity.

10 S100B homodimers do not exhibit such Mn(II)-binding capacity.

11 fic anti-HLA antibodies and their complement-binding capacity.

12 basic motif, causes the loss of p17 heparin-binding capacity.

13 , also could be highly promiscuous in its GF-binding capacity.

14 to integrins, thereby enhancing their ligand binding capacity.

15 ion associated with loss of activity and DNA binding capacity.

16 lected since it provided the highest protein binding capacity.

17 essitates knowledge of the precise metal-ion binding capacity.

18 lysis, cysteine activation, and metal (zinc) binding capacity.

19 ut antibody leakage or reduction in antibody binding capacity.

20 king density is used to achieve high protein binding capacity.

21 t in SpoVAD essentially abolish its DPA(2,6)-binding capacity.

22 ues is diminished in the absence of FcgammaR binding capacity.

23 aracterized several VHHs that retain antigen binding capacity.

24 strates, a result stemming from impaired DNA binding capacity.

25 t the attack of RNS while preserving its DNA-binding capacity.

26 ate APCs, despite retaining full ganglioside-binding capacity.

27 in slices, the PPM capillaries offer greater binding capacity.

28 rotein interaction, independent of SPDEF DNA binding capacity.

29 iption factor, exclusively requiring its DNA-binding capacity.

30 wed an allelic difference in nuclear protein binding capacity.

31 e the reason for the observed differences in binding capacity.

32 tains its protein stability and tetrapyrrole binding capacity.

33 ond domain, without compromising its calcium binding capacity.

34 orbed to a porous membrane with high protein binding capacity.

35 recipitate pri-miRs, suggesting possible RNA-binding capacity.

36 ut hydroxyprolines displayed a very weak IgE-binding capacity.

37 s is consistent with a change in the maximum binding capacity.

38 tophosphorylation abolished its carbohydrate-binding capacity.

39 en screened for clones with restored antigen binding capacity.

40 an acetylation mimic, reduces NDPK-A FBXO24 binding capacity.

41 which results in maintenance of their ligand-binding capacities.

42 l the isolates and MR and VOR had high metal binding capacities.

43 /DP heteromers without altering their ligand-binding capacities.

44 nanoparticles exhibited high His-tag protein binding capacity (0.21 and 0.58 mg/mg for His-tagged gre

45 Cationic MBs (+15.8 mV; DNA binding capacity, 0.03 pg per MB) partially protected bo

46 significantly changing the apparent maximal binding capacity; (2) CLIC2 reduced the maximal Ca2+ eff

47 it immunoglobulin G [IgG]), with the highest binding capacities (71-77 mg IgG/g silica) being obtaine

48 a dissociation constant of 3 nM and maximum binding capacity 83 fmol/10(6) SKOV3 cells.

49 cell wall hydrolytic activity and ampicillin binding capacity, a characteristic of most bacterial CWM

50 AR function was highly dependent upon strong binding capacity across a broad range of tumor-associate

51 cence intensity, DSA IgG3 positivity and C1q binding capacity adequately reclassified patients at low

52 anges in serum ferritin level and total iron-binding capacity, adverse effects.

53 ious micro-organisms, we assessed whether HS-binding capacity affects MHC class II-restricted present

54 matin similarly in mitosis and how different binding capacities among them relate to function.

55 pproach utilizing crystal structures, Ca(2+) binding capacities, analytical ultracentrifugation, and

56 Detergent-binding capacities and phospholipid contents of the mode

57 rking temperature during the synthesis, high binding capacity and affinity.

58 tructural homolog and suggest that its lipid-binding capacity and association with COQ7 are key featu

59 resident peritoneal cells exhibited reduced binding capacity and biologic responses to the CCR1 liga

60 The changes in functional binding capacity and BP(ND) were less than the near-comp

61 -alphaPEG, hybrid-type cells) to improve the binding capacity and detection limit for free PEG and PE

62 ity through measurements of iron solubility, binding capacity and dialyzability.

63 e mass of protein present in blood, both DNA binding capacity and extraction efficiency were signific

64 types of peel flour showed interesting water binding capacity and fat absorption capacity.

65 of CRT2 is responsible for its high calcium-binding capacity and function in regulating the endogeno

66 amily can diversify while maintaining ligand-binding capacity and identifies features that should be

67 amino acids 43 and 67 showed promiscuous HLA-binding capacity and induced memory CD4(+) T-cell respon

68 stronger T cell-stimulatory and reduced IgE-binding capacity and induced murine Bet v 1-specific ant

69 ermembrane space domain of Mic60 has a lipid-binding capacity and induces membrane curvature even in

70 t non-competing receptors, albeit with lower binding capacity and markedly reduced phagocytosis.

71 The calcium buffering power, binding capacity and non-linear binding properties of th

72 (2)O(2)-oxidized p53 (10(-3) M) enhances DNA binding capacity and prevents ONOO(-)-induced abrogation

73 How does unliganded HIV-1 maintain CD4-binding capacity and regulate transitions to the CD4-bou

74 GLUT1 retained cytochalasin B and d-glucose binding capacity and released full-length transmembrane

75 d (palmitic acid analog) to Uox with the HSA binding capacity and retained enzyme activity.

76 allenge model of inflammation, Treg selectin binding capacity and the molecular basis of Treg rolling

77 ters (serum iron, serum ferritin, total iron-binding capacity and transferrin saturation), serum hepc

78 fic adsorption typically accompanies loss of binding capacity and vice versa for many surface coating

79 ility (pH 7.4-9), emulsificant capacity, oil binding capacity and water adsorption capacity.

80 njugating enzymatic activities but high heme-binding capacities, and they may be involved in the deto

81 Diabetic albumin showed impaired NEFA binding capacity, and both structural and functional alt

82 vitro cholesterol and 25-hydroxycholesterol-binding capacity, and cholesterol extraction from liposo

83 esins could saturate the resin, decrease its binding capacity, and displace weakly bound proteins suc

84 tein family, originally defined by their RNA binding capacity, and forms a complex with SLIRP that ha

85 by site-directed mutagenesis, loss of copper-binding capacity, and resultant loss of enzymatic activi

86 Pancreatic BP(ND), functional binding capacity, and stimulated insulin secretion measu

87 condary structure, DNA binding ability, iron binding capacity, and the ability to form higher-order s

88 d that RAP has an intrinsic and specific RNA binding capacity, and the RAP binding site was mapped to

89 However, BP(ND) and functional binding capacity appear to overestimate beta-cell mass g

90 The SMZ-MIPs had SMZ binding capacity approximately more than eight times hig

91 vation states possessing differential myosin binding capacities are also visible.

92 volume ratios and subsequently large protein binding capacities are of interest for advanced immunoso

93 :CD1b tail chimeras, that retain the same Ag-binding capacity as CD1a but traffic based on the cytopl

94 Fermentation increased water- and oil-binding capacity as well as protein solubility at pH 4.0

95 ed large ranges of affinity, specificity and binding capacity as well as substantial lot-to-lot varia

96 There was no effect on water binding capacity assessed by centrifuge, however, low-fi

97 cessive variants were enriched in nucleotide binding capacity, ATPase activity, and the dynein heavy

98 for in vitro biofilm formation, fibronectin-binding capacity, autolysis, and protease and nuclease a

99 horetic mobility shift assays, with some DNA-binding capacity being retained in the presence of 2 mol

100 evels of functional protein, with the ligand-binding capacity (Bmax) typically 20-fold higher than th

101 of 1 mM ACh with Kd, 4.23 nM, and saturable binding capacity (Bmax), 6.38 pmol/mg protein.

102 , electrostatic interactions affect membrane-binding capacity, but do not appear to affect the curvat

103 These results suggest that FcgammaR binding capacity by anti-HA antibodies was dependent on

104 of chemical and physical stability and high binding capacity combined with the intrinsic advantages

105 significantly higher swelling power and fat binding capacity compared to other fractions (F1, F2 and

106 ndependent in vivo; the presence of FcgammaR-binding capacity compromises their anti-tumor activity.

107 The metal binding capacities, conditional stability constants, and

108 use of processed walnuts with decreased IgE binding capacity could be a potential strategy for walnu

109 noclonal antibody (mAb) effectively, but the binding capacity decays over repeated purification cycle

110 Mean total iron-binding capacity decreased from 501 to 389 mug/dL (ferro

111 he cross-linked surface retained the antigen binding capacity demonstrating its robustness in being r

112 ncated CDC37 (DeltaC-CDC37) that lacks HSP90 binding capacity did not affect kinase client expression

113 s that lack either alpha-actinin or Ena/VASP-binding capacity display compromised response to mechani

114 A carried J chain and displayed selective SC binding capacity either in a mixture with monomeric IgA

115 Thus, PCM size and binding capacity emerge from the regulated polymerizatio

116 This study shows that removal of receptor binding capacity enhances potency of the subunit HCR vac

117 umic colloids lost up to 50% of their copper-binding capacity, expressed as a molar ratio to organic

118 The binding capacities for fluorescein and for fluorescently

119 The columns exhibited excellent binding capacities for microaffinity enrichment: Con A w

120 pho-deficient mutant has significantly lower binding capacity for 14-3-3 when compared with the phosp

121 main-engineered bNAb variants with selective binding capacity for activating FcgammaRs displayed augm

122 rihydrite at a ratio of 1:2 has the greatest binding capacity for arsenic (As), cadmium (Cd), copper

123 ly, hLrp1(-/-) hepatocytes displayed reduced binding capacity for extracellular cathepsin D, resultin

124 ation between LARGE-glycan extension and its binding capacity for extracellular matrix ligands.

125 nding as dendritic cells exhibited the lower binding capacity for fungi and HIV protein gp-120 when t

126 that controls muscle growth by altering the binding capacity for myostatin.

127 tios were optimised in order to maximise the binding capacity for phosphate.

128 or histocompatibility complex (MHC) class II-binding capacity for rapid production as synthetic poly-

129 higher surface densities, yielding a higher binding capacity for the analyte.

130 periplasmic Zn(2+) by ZnuA may free up TroA binding capacity for the importation of Fe and Mn(2+).

131 This can be attributed to a loss of binding capacity for the microRNAs (miRNAs) Let-7e and L

132 uired to be stored at 4 degrees C) with high binding capacity for the separation and purification und

133 ed MMSNs were highly effective and had large binding capacity for U sequestration from high salt wate

134 g motif of Mamu-A2*05:01, and elucidated the binding capacity for virus-derived peptides.

135 Vaccines that lack receptor binding capacity have the added property of limited off-

136 llergenic activity in terms of patients' IgE-binding capacity, human basophil activation, and positiv

137 d to adsorb via a Langmuir model and to have binding capacities in the order Zn(++)>Co(++)>Ni(++).

138 ion constants, point to the loss of integrin-binding capacity in case of the Pro943Leu (Kd=5+/-3 micr

139 k showing low midbrain serotonin transporter binding capacity in depressed suicides and may partially

140 s showed that BCR ligation up-regulates BLyS binding capacity in mature B cells, reflecting increased

141 a CADD score of 29.6, and increases protein binding capacity in silico.

142 ations lead to significant reduction in Ca2+-binding capacity in spite of the similarity of their sec

143 an 17 beta-estradiol (betaE2), but lacked ER binding capacity in vitro and feminizing effects in vivo

144 that LRPPRC displays a broad and strong RNA binding capacity in vitro in contrast to SLIRP that asso

145 mutant showed only a modest decrease in cell binding capacity in vitro, the KIM5 Deltaail mutant exhi

146 Addition of DSA IgG3 positivity or C1q binding capacity increased discrimination performance of

147 -labeled tBid(G94E) also confirmed that tBid binding capacity increased upon PLS3 overexpression and

148 an Rbd2 mutant with diminished PtdIns(4,5)P2-binding capacity indicates that this interaction is nece

149 HHP treatment decreased the IgE and IgG-binding capacities, indicating a significant decrease in

150 a fragment of RACK1 that retains G betagamma-binding capacity inhibits cell migration.

151 ion of Fox-1 by WNK3 does not change its RNA binding capacity; instead, WNK3 increases the cytoplasmi

152 The results show that absolute binding capacity is a better predictor of immunogenicity

153 In contrast, its DNA-binding capacity is enhanced on IgM stimulation in respo

154 iation constant of ~30 muM, and its arginine-binding capacity is required for arginine to activate mT

155 rA mispairs is fully inhibited, although its binding capacity is retained.

156 eron-stimulated gene (ISG) with possible RNA-binding capacity, is an important restriction factor for

157 ssay-regeneration cycles without significant binding capacity loss.

158 rum ferritin level >15 ng/mL, and total iron-binding capacity <425 mug/dL at the 12-week visit), chan

159 Moreover, we demonstrate altered sugar-binding capacities of 6 recombinant galectins in the clu

160 in by two purification circuits altering the binding capacities of albumin by biochemical (changing o

161 Amino acid substitutions may disrupt binding capacities of dystrophin and have a major impact

162 Bile acid (BA)-binding capacities of in vitro digested samples and nutr

163 p120 (surface HIV-1 glycoprotein of 120 kDa) binding capacities of isolated Lg-CRD.

164 erms, we obtained dissociation constants and binding capacities of the membranes.

165 To further examine peptide-binding capacities of these two allelic variants, we use

166 The BA-binding capacities of WFB and FBSC were 1.94 and 37.50mu

167 ndicated an imprinting factor, IF, of ~10, a binding capacity of 0.5-2 mg/g, and the ability to rebin

168 brushes (60 nm thick) have a phosphopeptide binding capacity of 0.6 microg/cm(2) and exhibit phospho

169 a dissociation constant of 2 nM and maximum binding capacity of 18 fmol/10(6) cells, and (18)F-FES h

170 Additionally, the overall binding capacity of 293T/SL-alphaPEG cells for PEGylated

171 tudy was developed in order to determine the binding capacity of 4-EG by PANI materials in 12% ethano

172 Substitution of E45 reduces the binding capacity of 6H4, confirming that it is critical

173 this study, we demonstrate that the protein binding capacity of a surface modified matrix-assisted l

174 g to the high selectivity and cost-effective binding capacity of affinity resins for capture of the F

175 with its tensile strength, whereas the water-binding capacity of aggrecan provides compressibility an

176 ctive metabolites in platelets when the NEFA binding capacity of albumin is blunted by glycoxidation.

177 levant levels of fatty acids modulate the Zn-binding capacity of albumin, with far-reaching implicati

178 In summary, these data show that glycogen-binding capacity of AMPKbeta is regulated by Thr-148 aut

179 Equilibrium constant (KD) and maximum binding capacity of analyte (Bmax) values for the intera

180 brium dissociation constant (KD) and maximum binding capacity of analyte (Bmax) values for the intera

181 We investigated whether the complement-binding capacity of anti-HLA antibodies plays a role in

182 The IgE-binding capacity of Ara h 2 was then recapitulated with

183 blocks and then used to saturate the biotin binding capacity of avidin coated wells.

184 analogous results, suggesting that the dsRNA binding capacity of B2 somehow played a role in coat pro

185 In this study, metal binding capacity of barley protein hydrolysates and thei

186 The water and fat binding capacity of beta-chitosan presently studied was

187 a h 6, Ara h 6 immune complexes, and the IgE binding capacity of breast milk samples were measured us

188 aggressively than MgCl2 and NaCl due to the binding capacity of Ca(2+) ions with hydroxyl and carbon

189 oxOL binding to CSQ2 reduced both the Ca(2+) binding capacity of CSQ2 (by 48%-58%) and its aggregatio

190 The ICAM-1-binding capacity of DC4 was mapped to the C-terminal thi

191 vity with and cross-inhibition of the ICAM-1 binding capacity of domain cassette 4 PfEMP1s.

192 Assessment of the complement-binding capacity of donor-specific anti-HLA antibodies a

193 We conclude that assessment of the C3d-binding capacity of DSA at the time of AMR diagnosis all

194 d within this region negatively affected the binding capacity of each fimbria.

195 tavidin is used to quantify the streptavidin binding capacity of each mesh type through confocal micr

196 bound E. coli LPS mutants, and the properdin-binding capacity of each strain correlated with its resp

197 the inter-RRM interaction or the loss of RNA binding capacity of either RRM impairs splicing repressi

198 We show that this requires DNA binding capacity of EVI1, suggesting that downstream tar

199 described that Ala258Ser leads to increased binding capacity of ficolin-2 to N-acetylglucosamine.

200 cytometry examination revealed the specific binding capacity of fluorescein isothiocyanate-RamAb to

201 In vitro bile acid-binding capacity of FVJ was about 4.30times higher than

202 This PSD-95 binding capacity of GPR30 is specific and determined by

203 However, the overall Pu binding capacity of HA (particulate + colloidal-Pu) decr

204 The affinity and binding capacity of heparin can be significantly diminis

205 ans as an important determinant of the FXIIa binding capacity of HLF.

206 The binding capacity of HMF to casein was about 10% but did

207 The binding capacity of hybrid-type cells for PEG-like molec

208 SA surface expression, leading to higher C4S-binding capacity of infected erythrocytes.

209 acid increased the affinity and the maximum binding capacity of LPMO for cellulose.

210 ntenance function uses a common G-quadruplex binding capacity of LR1 and LR2, which may be targetable

211 tofusins (Mfns) 1 and 2-and enhances the GTP-binding capacity of Mfn2, suggesting that IHG-1 acts as

212 e' form of arrestin, increasing the arrestin-binding capacity of microtubules while readily dissociat

213 Binding capacity of N8-GP on human monocyte-derived dend

214 Activity and binding capacity of nuclear factor (NF)-kappaB were conf

215 IgE-binding capacity of oleosins derived from in-shell roast

216 s UBAN domain at S473, thereby expanding the binding capacity of OPTN to diverse Ub chains.

217 We found that the vitronectin-binding capacity of PAI-1 was the primary determinant re

218 nction, we measured the zinc content and DNA-binding capacity of PARP-1 immunoprecipitated from arsen

219 The phosphatidylinositol 4,5-bisphosphate-binding capacity of PBP10 was not in its own sufficient

220 0min, produces a significant decrease of IgE-binding capacity of peanut allergens.

221 study was to investigate the changes in IgE binding capacity of peanut proteins produced by thermal-

222 It is possible that the binding capacity of pica substances explains the associa

223 Importantly, the double-stranded DNA-binding capacity of protein p6 is essential for its relo

224 ds, which we named regacin, disrupts the DNA binding capacity of RegA by interacting with amino acid

225 nduced activation of mTORC1 requires the SAM binding capacity of SAMTOR.

226 nduction of T3S, it was evident that the Tir-binding capacity of SepL is important to delay the relea

227 The leucine-binding capacity of Sestrin2 is required for leucine to

228 ting titer to determine the infectious prion binding capacity of SLS and Mte.

229 Our data reveal significant prion-binding capacity of soil and the utility of BASICS to es

230 oil has complicated attempts to quantify the binding capacity of soil for prion infectivity.

231 , but not hydrogen peroxide, inhibit the DNA-binding capacity of SsrB, demonstrating the selectivity

232 Thus, the antigen binding capacity of the attached Abs was enhanced by up

233 HLA restriction of the specific TCLs and the binding capacity of the epitope-containing peptides to c

234 The ubiquitin-binding capacity of the FAAP20 UBZ is required for recru

235 time did not affect the carbon specific iron-binding capacity of the humic substances which was [L]/[

236 ino acid sequences double the carbon dioxide binding capacity of the previously reported fiber formed

237 The maximum binding capacity of the protein G-coupled membrane was 4

238 The antibody binding capacity of the protein G-coupled membrane was e

239 While the microtubule-binding capacity of the protein tau has been known for m

240 OH was synthetically deleted, and the sterol binding capacity of the resulting derivative, C2'deOAmB,

241 The microtubule-binding capacity of the SAH domain is important for mito

242 arted by this particular region inhibits the binding capacity of the tri-domain protein for GPIbalpha

243 gulated molecule, SULF2, normalizes the VLDL-binding capacity of their hepatocytes and abolishes post

244 The protein binding capacity of this architectured target is compare

245 tivation of TTP by MK2, whereas retained RNA-binding capacity of TTP-AA to 3'UTRs caused profound cha

246 In uninfected cells, the impaired RNA-binding capacity of Y315A was evident by a shift of A3G

247 ing pathway, an effect dependent on the SMAD-binding capacity of Zfp423.

248 ced oxidative complexation with an estimated binding capacity of ~3.5 mumol Hg/g HA and a partitionin

249 xhibited distinct activity patterns, various binding capacities on cellulosic substrates, and differe

250 Determination of the tBid binding capacity on the mitochondrial surface by FITC-la

251 or allergen, Der p 13 may, through its lipid-binding capacity, play a role in the initiation of the H

252 metals in non bioavailable forms, the metal-binding capacity provided by OC and iron and manganese o

253 Maximum IgG binding capacities, Qm of 6.7, 3.8, and 4.1mgm(-2) were

254 Equilibrium constant (KD), maximum binding capacity (Rmax) and Gb values for interaction of

255 h include incomplete template removal, small binding capacity, slow mass transfer, and irregular mate

256 ulting in soluble Shh clusters with their HS binding capacities strongly reduced.

257 e-relevant non-canonical Wnt ligands lack HS binding capacity, suggesting that Sulfs indirectly repre

258 ut lipid addition and had much greater lipid-binding capacity than the recombinant alpha-synuclein st

259 Hg(2+) ion from all other metal ions, and a binding capacity that is >/=18 times that of thio-crown

260 ex of total pancreatic VMAT2, the functional binding capacity (the sum of voxel BP(ND) x voxel volume

261 imulator (BLyS) receptor expression and BLyS binding capacity, these cells do not rely on BLyS for su

262 transferrin saturation (SAT) and total iron binding capacity (TIBC) in 2347 AAs participating in the

263 association study of serum iron, total iron binding capacity (TIBC), transferrin saturation, and fer

264 protein isolates (CPIs) revealed the highest binding capacity to all aldehydes followed by wheat glut

265 A high-throughput screen to analyse TINCR binding capacity to approximately 9,400 human recombinan

266 eveals that non-neurotransmitter Abeta has a binding capacity to beta(2)AR and induces PKA-dependent

267 dent, comprehensive functional assays of DNA-binding capacity to explore the evolution of DNA-binding

268 r MoS2 nanosheets also exhibit a much higher binding capacity to pesticides and a much larger specifi

269 B-CK shows high binding capacity to selective I(2) ligands; [(3)H]-2-BFI

270 VIM1-binding capacity to target genes was significantly reduc

271 etalg aggregation, which in turn affects its binding capacity to the FA.

272 rface-exposed epitope conferring optimal IgE-binding capacity to the folded allergen.

273 ENaC-alpha, displayed significantly reduced binding capacity to TIP peptide and to TNF.

274 its function in cancer, even while retaining binding capacity to WBP2.

275 patient samples (median, 2.3 x 10(5) antigen-binding capacity units/cell) and hT-NHL cell lines (3.4

276 hT-NHL cell lines (3.4 x 10(5) CD45 antigen-binding capacity units/cell).

277 e 45 min process and is capable of achieving binding capacities up to 1 000 000 times greater than si

278 at the NA of the zoonotic H7N9 viruses has a binding capacity via both the secondary binding site and

279 functional properties and in vitro bile acid-binding capacities was performed.

280 The average functional binding capacity was decreased by at least 40% in patien

281 High cobalamin-binding capacity was found in trout stomach (210 pmol/g)

282 rmocomp/glass substrates in terms of protein binding capacity was observed for at least two months.

283 nt of STAT-1 tyrosine phosphorylation or DNA-binding capacity was observed in IFN-gamma-treated mouse

284 A higher antibody binding capacity was observed on the GalCer-diluted flui

285 on (DOC) concentration above ca. 250 muM the binding capacity was only 50% of the theoretical value o

286 C4S binding, and at the 32nd generation, the binding capacity was only approximately 31% of that of I

287 The MIP with the highest binding capacity was selected.

288 olic Ca binding affinity, whereas maximal Ca binding capacity was unchanged.

289 Based on its nucleic acid binding capacity, we propose a dual location and functio

290 th differing (defined) heparin- and integrin-binding capacities were applied directly to resistance a

291 of anti-HLA antibodies and their complement binding capacity were associated with increased severity

292 ies such as the swelling power and bile acid binding capacity were increased by acetylation.

293 , H2B supported approximately 50% of the Plg binding capacity, whereas the other Plg-Rs contributed l

294 PPW showed interesting water-holding and fat-binding capacities which were 4.097 +/- 0.537 g/g and 4.

295 , such boron-selective resins have a limited binding capacity with a maximum free base content of 0.7

296 Our results suggest that the loss of copper-binding capacity with increasing residence time is cause

297 linker protein, periplakin, and shares that binding capacity with the other major lens IF protein, v

298 rial, we show that there is plasticity in ER-binding capacity, with distinct combinations of cis-regu

299 hat lipid membranes have substantial calcium-binding capacity, with several types of binding sites pr

300 o a therapeutic protein resulting in the HSA binding capacity without compromising therapeutic activi