ライフサイエンスコーパス: filtrate

1 l and were not detected in the extracellular filtrate.

2 mal catabolism of proteins captured from the filtrate.

3 us suppresses the re-uptake of P(i) from the filtrate.

4 s), from environmental samples and a biofilm filtrate.

5 tinocytes (HKs) are in contact with a plasma filtrate.

6 ecular weight substances into the glomerular filtrate.

7 proximal tubules reclaim from the glomerular filtrate.

8 tuberculosis (SapM) localized to the culture filtrate.

9 ular weight polypeptides from the glomerular filtrate.

10 ntrifugation, O-glycans are recovered in the filtrate.

11 noparticles synthesized by B. cereus Nem 212 filtrate.

12 ling the nephron to sequentially process the filtrate.

13 n the bacterial community composition in the filtrate.

14 s of metagenomes recovered from geyser water filtrate.

15 d that filters blood to form primary urinary filtrate.

16 ation and remodelling compared to WT culture filtrate.

17 L1 uptake from the circulation or glomerular filtrate.

18 ction was two-times higher than that of whey filtrate.

19 tant reclamation of solutes from crude blood filtrate.

20 cytosing urinary albumin from the glomerular filtrate.

21 rier to macromolecular flow into the urinary filtrate.

22 nd is mainly present as a monomer in culture filtrates.

23 ts were autoclaved or converted into sterile filtrates.

24 y commonly observed in S. marcescens culture filtrates.

25 doenzyme from Diplococcus pneumoniae culture filtrates.

26 cted diverse bacterial DNA signatures in the filtrates.

27 ls analysis of fabric digests and wash water filtrates.

28 The 3 kDa filtrate (1 mg/ml), that demonstrated highest ACE-I inhi

29 Subsequent HPLC fractionation of plasma filtrate (10-kd MWt cutoff) by sequential column chromat

30 tric monitoring of the concentrations of the filtrates (214 nm).

31 ing activity in Rhizobium meliloti cell-free filtrates, a plant response dependent on the bacterial n

32 Furthermore, sonication of the filtrates abolished their ability to elevate [Ca(2+)](i)

33 fumigatus vaccine preparations (sonicate and filtrate) administered intranasally and subcutaneously w

34 The condensed materials in the filtrated aerogel particles can be squeezed and washed o

35 e protective immunogen (cryptococcal culture filtrate Ag + heat-killed cryptococci-CFA), or controls,

36 th shed cryptococcal products (C. neoformans filtrate Ag) but not other nonspecific stimuli.

37 e protective immunogen (cryptococcal culture filtrate Ag-CFA), in contrast to the nonprotective immun

38 The C. albicans culture filtrates also induced migration of PMNs across confluen

39 ges of carbohydrates were identified in whey filtrate and in all second fractions, where galactose wa

40 itinase enzyme activity found in SEs culture filtrate and in cellular extracts of developing SE and h

41 ration of Aspergillus fumigatus cell culture filtrate and OVA.

42 lbumin, which were secreted into the primary filtrate and reabsorbed by proximal tubular cells, resul

43 rved on light microscopy from 10 mL of urine filtrate and the proportion who had self-reported initia

44 igh molecular weight proteins into the blood filtrate and urine, a condition called proteinuria.

45 trated that Sepp1 passed into the glomerular filtrate and was specifically taken up by proximal tubul

46 Lake deposits, plant-based ashes, filtrates and evaporites or alkaline salts are used trad

47 LC-MS metabolomic analysis of the extracted filtrates and mycelium from 15 blueberry isolates of thi

48 g of the three chlorobenzenes in the 1.5 mum filtrate, and the partitioning behavior did not follow t

49 The hydrolysate was ultra-filtrated, and the fractions were evaluated for antioxid

50 (85-kDa antigen complex, "short-term culture filtrate," and peptides from the ESAT-6 protein), as wel

51 ity (DTH) reactivity to cryptococcal culture filtrate antigen (CneF) can be either protective or nonp

52 mmunized with a soluble cryptococcal culture filtrate antigen (CneF) emulsified in complete Freund's

53 antigen preparations, one a soluble culture filtrate antigen (CneF) in complete Freund's adjuvant (C

54 showed that GXM or the cryptococcal culture filtrate antigen CneF directly induces L-selectin loss f

55 ing heat-killed whole C. neoformans, culture filtrate antigen, C. neoformans lysate, and purified cry

56 tion of genes encoding several early culture filtrate antigens (ESAT-6-like proteins), ribosomal prot

57 s, there is a well-defined subset of culture filtrate antigens that elicits antibodies during noncavi

58 Since this IMS was reactive to culture filtrate antigens, several of these proteins were cut fr

59 were prepared against the 10 x -concentrated filtrate antigens.

60 chemoattractant in Candida albicans culture filtrates appeared to act through the formyl peptide rec

61 The carbohydrates in the filtrate are then derivatized with 1-phenyl-3-methyl-5-p

62 lbumin-sized nanoparticles reach the primary filtrate, are captured by proximal tubule cells, and are

63 Using mouse brain filtrate as substrate, both brain sulfotransferases were

64 We found that crude ETEC culture filtrates, as well as purified ETEC toxins, did potentia

65 nd hyphae in response to serum or to a serum filtrate but does form pseudohyphae.

66 ied MnP proteins in C. subvermispora culture filtrates, but none in P. chrysosporium cultures.

67 Analysis of culture filtrate by double immunodiffusion yielded a single line

68 ron are reabsorbed daily from the glomerular filtrate by kidney proximal tubule cells (PT), requiring

69 Analysis of the filtrate by SDS-PAGE showed a major band at approximatel

70 reabsorption of proteins from the glomerular filtrate by the renal proximal tubule.

71 by active reabsorption of nearly 99% of that filtrate by the tubules creates vulnerability in both co

72 To prevent recontamination of the filtrate by zinc in this type of experiment, Candida alb

73 urified to apparent homogeneity from culture filtrates by ammonium sulfate precipitation and ion-exch

74 These filtrates caused no damage to mouse small intestinal epi

75 a 32-kDa putative glyoxalase in the culture filtrate (CF) of growing M. tuberculosis (originally ann

76 testing including measurement of MTB culture filtrate (CF)-stimulated interferon gamma (IFN-gamma) an

77 ntigens (whole-cell [WC] antigen and culture filtrate [CF] antigen) of B. pseudomallei The ELISAs wer

78 study, we found that a cryptococcal culture filtrate (CneF), when injected into the bloodstream of m

79 oformans strain B3501, we prepared a culture filtrate (CneF-Cap67) similar to that used for preparing

80 retention changes were demonstrated by large filtrate concentration reductions at all temperatures te

81 mbrane surface area or membrane fouling, the filtrate concentrations behaved according to a barrier b

82 tures for C. difficile and cytotoxin B fecal filtrate concentrations.

83 The filtrate contained pure streptavidin.

84 The particle free filtrate containing the growth media is suitable for rec

85 We demonstrate that the presence of the filtrate containing these enzymes prevents ATP-induced m

86 We investigated whether sterile fecal filtrates (containing bacterial debris, proteins, antimi

87 tron microscopy (IEM) in an infectious stool filtrate derived from an outbreak of gastroenteritis in

88 fatty acids at the same concentration as the filtrates did not.

89 into the distal tubule and establishes blood filtrate drainage.

90 us: high levels of glucose in the glomerular filtrate drive increased reabsorption of glucose and sod

91 inaceous elicitor called sclerotinia culture filtrate elicitor1 (SCFE1) from the necrotrophic fungal

92 chiral pores of the AAO membrane leaving the filtrate enriched with the other enantiomer.

93 s are concentrated inside the oral cavity as filtrate exits between the rakers, but particles are not

94 The culture filtrate exponentially decreased the viscosity of a pect

95 ndicated that the major component in culture filtrate extracts of the mutant was less polar and small

96 ative gene disruption construct, and culture filtrate extracts of the mutant were assayed for the pre

97 graphic fractionation of S. meliloti culture filtrate extracts revealed at least three peaks with AHL

98 Filtrate flow exerted a mean wall shear stress of 39 Pa

99 Furthermore, increasing filtrate flow velocity by 50% increased wall shear stres

100 size-exclusion HPLC analysis of the ethanol filtrate for low molecular weight components.

101 obulin binding proteins, we examined culture filtrates for their ability to induce endothelial cell a

102 E in renal structure and regulation of renal filtrate formation, single-nephron GFR, proximal tubular

103 Analysis of virus-like particles from a filtrate found to reduce symptoms of CDI showed a comple

104 ed lipids from the cell envelope and culture filtrate from 52 isolates of Mycobacterium species, anal

105 w cell densities, was rescued by the culture filtrate from a high cell density tup1Delta culture and

106 When mice are vaccinated with a culture filtrate from Cryptococcus neoformans (CneF), they mount

107 Thrombin, trypsin, tryptase, a filtrate from degranulated mast cells, and peptides corr

108 Microbiota analysis was performed on fecal filtrate from donors and stool samples from FT recipient

109 the presence of an intestinal content fluid filtrate from gnotobiotic pigs.

110 hyperfiltration, hypertrophy, and outflow of filtrate from subpodocyte spaces.

111 o P13 the pigs were inoculated with a tissue filtrate from the corresponding pig in the previous pass

112 ferns, their enriched leaf pockets and water filtrate from the surrounding ditch established that bac

113 Filtrate from toxic strains of Pfiesteria spp. in bacter

114 osed over the course of 5 weeks with culture filtrate from wild-type (WT), Asp f 5 null (5) or Asp f

115 ovine leukocytes were incubated with culture filtrates from a mutant strain of P. haemolytica that do

116 y and validated the assays using (i) culture filtrates from a panel of clinical C. difficile isolates

117 ents with CDI shows that transfer of sterile filtrates from donor stool (FFT), rather than fecal micr

118 Culture filtrates from Helicobacter pylori promote the transfer

119 33 but not at 37 degrees C, and only culture filtrates from infected monolayers incubated at 33 degre

120 The culture filtrates from isogenic mutants were devoid of hemolytic

121 ass spectrometer for the analysis of culture filtrates from Mycobacterium marinum.

122 Culture filtrates from selected M. ovis field isolates demonstra

123 Furthermore, colonic luminal filtrates from the mice transplanted with patients' feca

124 harveyi but exhibited no response to culture filtrates from V. harveyi mutants defective in BAI-2 syn

125 ined by electron microscopy, whereas culture filtrates from wild-type Aeromonas caused complete destr

126 osensor responded to the addition of culture filtrates from wild-type Vibrio harveyi but exhibited no

127 lly, 29%; sonicate given subcutaneously, 0%; filtrate given intranasally, 75%; and filtrate given sub

128 y, 0%; filtrate given intranasally, 75%; and filtrate given subcutaneously, 50%.

129 The filtrated gum showed a higher concentration of phenolics

130 essed form of MTB12 protein found in culture filtrates has a molecular mass of 12.5 kDa.

131 Serratia marcescens culture filtrates have been reported to be cytotoxic to mammalia

132 erived results are used to study the flow of filtrate in a flat plat hemodialyzer.

133 reabsorption of Me-4FDG from the glomerular filtrate in wild-type mice and the absence of reabsorpti

134 nd that bovine S. aureus M60 and its culture filtrates induce a 3- to 10-fold increase in urokinase-t

135 Culture filtrates induced similar levels of endothelial cell apo

136 en deleted strains, in particular 13 culture filtrate, induced significantly less airway inflammation

137 sistent with transtubular backleak of 57% of filtrate (inulin) in sustained ARF.

138 adium catalyst is removed by filtration, the filtrate is blown dry with an inert gas, and the dried p

139 tration, and a renal tubule, along which the filtrate is modified.

140 ugal filtration, and digested HA left in the filtrate is quantified by electrospray ionization mass s

141 of piGC, the force opposing the formation of filtrate, is predominantly or uniquely responsible for t

142 rovides a paracellular pathway through which filtrate leaks back in sustained allograft ARF.

143 c intranasal exposure to the three different filtrates led to comparable airway hyper-reactivity and

144 oxic incubation of sulfate-reducing culture filtrates led to further degradation of the major anaero

145 te, leading to poor size cut-off properties, filtrate loss within the membranes, and low transport ra

146 ation of ultrafiltration and flow-associated filtrate modification that is central to CKD etiology is

147 Instead, a filtrate (molecular mass, <1 kDa) devoid of serum albumi

148 three distinct urinary spaces through which filtrate must pass before reaching the proximal convolut

149 te (NOMr, Mw = 691,000 g/mol) and 98 wt % of filtrate (NOMf, Mw = 12,800 g/mol).

150 m Pseudomonas fluorescens SBW25 with sterile filtrate obtained from garden compost communities.

151 Manganese oxide formation in cell-free filtrates occurred via reaction with the oxygen radical

152 reabsorption of insulin from the glomerular filtrate occurs by binding to as yet unidentified sites

153 Purification of the enzymes from the culture filtrate of 7H9-grown M. bovis BCG cells and determinati

154 nd only 1 nM of thiamine was obtained in the filtrate of a 100 nM thiamine stock passed through a bor

155 incubation with trypsin or with the culture filtrate of a P. aeruginosa lasAdelta mutant.

156 From the culture filtrate of a P. palmivora strain isolated from papaya,

157 in relevant biological samples, the culture filtrate of A. niger grown on wheat straw.

158 enged intranasally on days 0, 3 and 6 with a filtrate of Alternaria alternata.

159 alactosidase A was purified from the culture filtrate of an over-producing strain of Aspergillus nige

160 tethered ligand), mast cell tryptase, and a filtrate of degranulated mast cells stimulated a prompt

161 Interestingly, a cell culture filtrate of FB17 suppressed flg22-induced MAMPs-activate

162 pure solvent and spiked into fungal culture filtrate of Fusarium graminearum respectively.

163 urifying polypeptides present in the culture filtrate of M. tuberculosis and evaluating these molecul

164 ow here that *MtCM secretes into the culture filtrate of M. tuberculosis.

165 Polypeptide Ags present in the culture filtrate of Mycobacterium tuberculosis were purified and

166 on was illustrated by demonstrating that the filtrate of plasma (10-kd MWt cutoff) could supply compo

167 rioferritin was more abundant in the culture filtrate of the live vaccine strain.

168 xidase was much more abundant in the culture filtrate of the virulent clinical isolate, whereas bacte

169 blood of infected mice, we used a cell-free filtrate of their blood to immunize congenic naive mice.

170 Culture filtrates of a MAT1-1 strain contained an activity that

171 nferred a cytotoxic phenotype on the culture filtrates of a nonpathogenic Escherichia coli strain.

172 cterized the proteins present in the culture filtrates of a virulent recent clinical isolate and the

173 rotease activity on external substrates, and filtrates of AAV virus preparations also showed no prote

174 undertaken to define the antigens in culture filtrates of actively replicating Mycobacterium tubercul

175 inity purification studies were performed on filtrates of bacteria incubated in human serum and plasm

176 It has been reported that culture filtrates of clinically derived strains of B. cepacia ar

177 chitinase had been isolated from the culture filtrates of Coccidioides immitis endosporulating spheru

178 n Circumdati, ochratoxin was not detected in filtrates of cultures grown in various media.

179 Gnotobiotic calves inoculated with fecal filtrates of each group B rotavirus developed diarrhea,

180 Interestingly, while filtrates of fatty acid solutions evoked CCK secretion a

181 11 ng of trans-zeatin per liter from culture filtrates of four PPFM leaf isolates (from Arabidopsis,

182 mpare the repertoires of antigens in culture filtrates of in vitro-grown Mycobacterium tuberculosis t

183 ntibodies detected no antigen in the culture filtrates of M. avium and other nontuberculous mycobacte

184 tected Rv1681 protein in lysates and culture filtrates of M. tuberculosis and immunoprecipitated it f

185 Fractionation of filtrates of M. tuberculosis cultures has yielded an abu

186 To identify and purify novel proteins in the filtrates of M. tuberculosis cultures, a bacteriophage l

187 stimulated by whole cell lysates and culture filtrates of Mycobacterium tuberculosis and Mycobacteriu

188 orobenzene to COC for both 1.5 mum and 1 kDa filtrates of PE was investigated using the gas-stripping

189 Serum-free culture filtrates of six Candida species and Saccharomyces cerev

190 Furthermore, cell-free filtrates of some isolates produced Mn oxides at specifi

191 h those from rapidly prepared noncentrifuged filtrates of sputum (r(s) = 0.94).

192 ive proteins partially purified from culture filtrates of strain N4-7.

193 Culture filtrates of strains expressing HopPtoD2 were able to de

194 ixty-five Gn pigs were inoculated with fecal filtrates of the NoV/GII/4/HS66/2001/US strain or with p

195 amined for inflammatory responses to culture filtrates of the outbreak strain.

196 lucanase, pectinase, and xylanase in culture filtrates of the Tox2(+) ccsnf1 mutant were reduced by 5

197 The g-C(3) N(4) film is filtrated on the separator in air using a common alcohol

198 contaminants so far unknown to occur in bank filtrate or in natural waters at all, such as tetramethy

199 cine formulations prepared as either culture filtrate or partially purified toxoid.

200 overed from the factory, warehouse, solution filtrate, or unopened solution bottles; production of im

201 lp determine the water profile direction and filtrate outlets for different food materials based on t

202 Heat inactivation of H. somnus culture filtrates partially reduced the apoptotic effect on endo

203 As the glomerular filtrate passes through the nephron and into the renal m

204 icity was significantly reduced when culture filtrates prepared from wild-type strains were pretreate

205 nsisted of 2-week-old fission arthroconidial filtrates produced in Pine's broth at 37 degrees C.

206 A fumigatus culture filtrates profoundly inhibited the differentiation, migr

207 ed Mycobacterium tuberculosis 10-kDa culture filtrate protein (CFP)10 is a potent T cell Ag that is r

208 The 10-kDa culture filtrate protein (CFP-10) and 6-kDa early secretory anti

209 tigenic target (ESAT-6) and a 10-kDa culture filtrate protein (CFP-10), that is essential for virulen

210 ic target 6-kDa (ESAT-6) protein and culture filtrate protein 10 (CFP-10) antigens via the Salmonella

211 we confirm the DND captured antigen is cell filtrate protein 10 (CFP-10) because its Mascot analysis

212 Culture filtrate protein 10 (CFP-10) from Mycobacterium tubercul

213 ic target 6-kDa protein (ESAT-6) and culture filtrate protein 10 (CFP-10), was therefore investigated

214 00-amino-acid protein referred to as culture filtrate protein 10 (CFP-10).

215 ic target 6-kDa (ESAT-6) protein and culture filtrate protein 10 (CFP-10).

216 ic target 6-kDa (ESAT-6) protein and culture filtrate protein 10 (CFP10).

217 ese clones, the Ag was identified as culture filtrate protein 10 (CFP10)/Mtb11, a 10.8-kDa protein no

218 rived macrophages (BMDM) compared to culture filtrate protein 10 kDa (CFP10) and antigen 85A.

219 agnitude of ex vivo reactivity, with culture filtrate protein 10 kDa being most dominant, followed by

220 rly secreted antigenic target 6 kDa, culture filtrate protein 10 kDa, Rv2031c, Rv2654c, and Rv1038c.

221 rly secretory antigenic target 6 and culture filtrate protein 10, for 18 mo after cessation of tuberc

222 y compatible with current ESAT-6 and culture filtrate protein 10-based diagnostics.

223 he secreted proteome of Histoplasma, culture filtrate protein 4 (Cfp4) is a heavily glycosylated fact

224 A native 37-kDa culture filtrate protein and a 55-kDa mycelial glycoprotein (gp5

225 The mycobacterial culture filtrate protein MPT64 was expressed as a chimeric prote

226 ESAT-6 and its molecular chaperone, culture filtrate protein of 10 kDa (CFP10), on the capacity of h

227 e of one of the new genes encoding a culture filtrate protein of 310 amino acid (aa) residues.

228 mulated ex vivo with M. tuberculosis culture filtrate protein was delayed in ApoE(-/-) HC mice, and t

229 ith Mycobacterium tuberculosis H37Rv culture filtrate protein was higher than that of CD4(+) T cells

230 1 prevented secretion of the CFP-10 (culture filtrate protein, 10 kilodaltons)/ESAT-6 virulence facto

231 with the M. tuberculosis-specific Ag culture filtrate protein-10 (CFP-10).

232 CD8(+) T cells specific for culture filtrate protein-10 (CFP10) are found in purified protei

233 early secretory antigenic target-6, culture filtrate protein-10, and PPD as stimulatory antigens wer

234 Culture filtrate proteins (CFP) of Mycobacterium tuberculosis ha

235 ained and recall immune responses to culture filtrate proteins (CFP) of Mycobacterium tuberculosis we

236 in M. tuberculosis lysate but not in culture filtrate proteins (CFP), indicating that it is not a sec

237 ion of mice with Mycobacterium bovis culture filtrate proteins (CFP), prepared in a variety of adjuva

238 mild adjuvant admixed with purified culture filtrate proteins and enhanced by the cytokine interleuk

239 s confirmed by using M. tuberculosis culture filtrate proteins and fractions from infected macrophage

240 sis, are among the bacterium's major culture filtrate proteins in actively growing cultures.

241 lectrophoresis, detailed maps of the culture filtrate proteins of M. tuberculosis H37Rv were generate

242 Lipoarabinomannan-free culture filtrate proteins of M. tuberculosis were fractionated b

243 nary antibodies directed against the culture filtrate proteins of M. tuberculosis, MPT 32, and the 81

244 e with Leishmania major promastigote culture filtrate proteins plus Corynebacterium parvum confers re

245 Normal reabsorption of glomerular filtrate proteins probably requires recycling of the end

246 A number of the culture filtrate proteins secreted by Mycobacterium tuberculosis

247 terogeneous, our studies with native culture filtrate proteins show that the antibody responses in TB

248 Finally, we expressed the major culture filtrate proteins that are promising vaccine candidates

249 B patients recognized 26 of the >100 culture filtrate proteins, and the repertoire changed with disea

250 as several other well-characterized culture filtrate proteins, including members of the 85B complex.

251 all extract, and Mycobacterium bovis culture filtrate proteins.

252 s were obtained for three additional culture filtrate proteins; however, these did not yield signific

253 he effectiveness of DNA-HSP65 or CpG/culture filtrated proteins (CFP) immunotherapy.

254 Filtrate PRP collected from an optimally-designed CIF de

255 responses that were triggered by crude ETEC filtrates, purified STa, and the peptide hormone guanyli

256 r (h), instantaneous volumetric flow rate of filtrate (Q), and cumulative volume of water produced (V

257 was immunoscreened by using an anti-culture filtrate rabbit antiserum.

258 8 years): age >=75 years, anemia, glomerular filtrate rate <60 mL/min/1.73 m(2), left ventricular eje

259 ference in the slope of estimated glomerular filtrate rate, 0.01 mL/min per 1.73 m [-0.06 to +0.09]).

260 ofile direction and the anolyte to catholyte filtrate ratio.

261 s and times of Staphylococcus aureus culture filtrate revealed a single dose- and time-dependent diff

262 ivated sludge process (ASP)), tertiary (sand filtrated (SF)), or advanced (chlorine dioxide (ClO(2)),

263 model was proposed to estimate critical bank filtrate shares resulting in exceedances of monitoring t

264 Parent WT and 5 culture filtrates showed high protease activity, whilst protease

265 Proteome analyses of selected FFT filtrates showed no obvious protein candidates associate

266 Chemical analysis of low-pH culture filtrates showed that the proteins encoded by the ompATb

267 tRNA hydrolysates in addition to the culture filtrates, suggesting that secreted trans-zeatin resulte

268 is protective antigens released into culture filtrate supernatant (CFS), a bacterial growth system wa

269 as abundant proteins in Phytophthora culture filtrates that have the capacity to elicit hypersensitiv

270 or two known components of the early culture filtrate, the secreted 45/47-kDa antigen complex and the

271 on artifacts; and (2) the direct delivery of filtrate to dedicated bottle sets for specific analytes.

272 ognized in the glomerulus conducting primary filtrate to the proximal convoluted tubule has been Bowm

273 protein components of mycobacterial culture filtrates to develop subunit vaccines and immunodiagnost

274 n that the ability of C(10), C(12) and C(14) filtrates to elevate [Ca(2+)](i) decayed with time was c

275 ed the cytotoxicity of S. marcescens culture filtrates towards HeLa cells, suggesting the involvement

276 e series to investigate the effects of fecal filtrate transfer (FFT) in 5 patients with symptomatic c

277 bridizations, immunoblot analyses of culture filtrates using both CTS1-specific murine antiserum and

278 omotes retrieval of iron from the glomerular filtrate via its ferrireductase activity and modulates k

279 ing from application of F. oxysporum culture filtrate was also reduced in lbd20 leaves relative to th

280 aked in acidified ethanol, filtered, and the filtrate was cleaned by solid phase extraction using sil

281 ield through samples between two electrodes, filtrate was discharged mainly towards the anode in OJ s

282 nto the SPRi chip surface covalently and the filtrate was flowed over the sensor surface.

283 and the most abundant protein in the culture filtrate was identified as the only family 7 glycoside h

284 ture and the active molecule in this culture filtrate was identified to be an oligopeptide composed o

285 The response to tryptase and the mast cell filtrate was inhibited by the tryptase inhibitor BABIM,

286 vity, whilst protease activity in 13 culture filtrate was low.

287 nd chemotaxis toward the C. albicans culture filtrate was not inhibited by an FPR antagonist (t-butox

288 ignificant HOC-COC partitioning to the 1 kDa filtrate was observed with organic carbon-normalized par

289 to remove small particles and bacteria; the filtrate was transferred to patients in a single adminis

290 oGastro Cd assay and 200 microl of the stool filtrate was used for the TOX-B CCCNA.

291 The hemolytic activity of the culture filtrates was attenuated after heat treatment.

292 fter stimulation with Pseudomonas aeruginosa filtrates was not greater in CF cells in the absence of

293 ulations, but reappearance of toxin in fecal filtrates was observed in 28% of vancomycin-treated pati

294 efense eliciting activity present in culture filtrates was recovered and purified by ultrafiltration

295 Using GII.4 huNoV positive stool filtrates, we demonstrated limited huNoV replication in

296 FH), and the generated 3 kDa and 10 kDa MWCO filtrates were assessed for their in vitro ACE-I inhibit

297 order to better define these anomalies, the filtrates were collected in sequential fractions of 7.5

298 activity was restored when the same culture filtrates were incubated with zinc divalent cations, whi

299 MPT63, purified from M. tuberculosis culture filtrates, were indistinguishable in serological assays.

300 us humor is a clear fluid, primarily a blood filtrate, which circulates through the anterior chamber