ライフサイエンスコーパス: concanavalin A

1 of the second through sixth generations and Concanavalin A.

2 pon aggregation of unilamellar vesicles with concanavalin A.

3 ssessed by labeling adherent leukocytes with concanavalin A.

4 d has a surface that is capped by the lectin concanavalin A.

5 which is only manifested in the presence of concanavalin A.

6 te and sodium azide, and one model biotoxin, concanavalin A.

7 th immobilized Sambucus nigra agglutinin and concanavalin A.

8 at were resistant to the cytotoxic action of concanavalin A.

9 - and bivalent ligands for the legume lectin concanavalin A.

10 10 is inducible by interferons (IFNs) and by concanavalin A.

11 after stimulation of cells with the mitogen, concanavalin A.

12 n of peripheral blood mononuclear cells with concanavalin A.

13 cation exchange column and was shown to bind concanavalin A.

14 ho-proliferative response to alloantigens or concanavalin A.

15 tic liver damage induced by the injection of concanavalin A.

16 ose-containing bath solution or treated with concanavalin A.

17 ting the enzyme's aggregation induced by the concanavalin A.

18 ction in response to either C. pneumoniae or concanavalin A.

19 d Th-2 cytokine responses to SME antigen and concanavalin A.

20 ion-induced programmed cell death induced by concanavalin A.

21 desensitization blockers, cyclothiazide and concanavalin A.

22 separate group of mice by administration of concanavalin A.

23 binding of the polymers to the plant lectin concanavalin A.

24 ssessed after perfusion with FITC-conjugated concanavalin A.

25 s not evident after 48-hour stimulation with concanavalin-A.

26 8.6 kDa), and the tetrameric protein complex Concanavalin A (103 kDa).

27 Pretreatment of HEK-hCaR cells with concanavalin A (250 microg/ml) to block CaR internalizat

28 GC-5 cells were differentiated with succinyl concanavalin A (50 microg/mL) and transferred to a press

29 Concanavalin A, a lectin selective for high mannose and

30 Concanavalin A, a lectin that binds glucose and mannose

31 ectin binding experiments using succinylated concanavalin A, a plant lectin with high affinity for ma

32 scriptional regulation of CSF-2 and CSF-3 in concanavalin A-activated MSCs requires MT1-MMP signaling

33 GPI-IL-12-induced the proliferation of concanavalin A-activated T cells and induced IFN-gamma s

34 ene (aSMase(-/-)), we found that thymocytes, concanavalin A-activated T cells, and lipopolysaccharide

35 Mannosidase digestion and concanavalin A adsorption indicate that the terminal res

36 eted cryptococcal antigens were separated by concanavalin A affinity chromatography into adherent (ma

37 tionation, diethylaminoethyl chromatography, concanavalin A affinity chromatography, and chromatofocu

38 APS was purified on concanavalin A affinity columns to minimize the loss of

39 was also lost when they were incubated with concanavalin A-agarose beads, suggesting that the inhibi

40 After binding to the concanavalin A-agarose beads, the inhibitor in BAL fluid

41 f oocytes with 20% sucrose and 250 microg/ml concanavalin A, agents that inhibit the endocytosis of R

42 ctional valency of a triantennary analog for concanavalin A and D. grandiflora lectin are observed.

43 rate analogs to the Man/Glc-specific lectins concanavalin A and Dioclea grandiflora lectin was invest

44 a of infected insect cells using immobilized concanavalin A and immobilized BACE inhibitor, P10-P4' S

45 B10.BR splenic lymphocytes stimulated with concanavalin A and interleukin 2 were infected with a re

46 from broccoli flower buds was purified using concanavalin A and ion-exchange chromatography.

47 Here, by using Concanavalin A and LC-MS analysis, we identified a novel

48 Concanavalin A and lectins from pea and lentil, also man

49 nt experimental hepatitis models, induced by concanavalin A and Listeria monocytogenes.

50 , T cell proliferation upon stimulation with concanavalin A and phytohemagglutinin A was only 40-50%

51 ion lymphocytes were examined in response to concanavalin A and purified protein derivative (PPD) in

52 or the ability to proliferate in response to concanavalin A and purified protein derivative (PPD) in

53 tely 100 kDa, contained sugars that bound to concanavalin A and ricin.

54 protein receptors such as the plant lectins concanavalin A and the highly toxic mistletoe Viscum alb

55 her mannose/glucose binding lectins, such as concanavalin A and the pea, lentil and Calystegia sepium

56 in C57BL/6 mice by intravenous injection of concanavalin A and then analyzed liver concentrations of

57 unction of DR signaling in T cell-dependent (concanavalin A) and independent (lipopolysaccharide/gala

58 superoxide dismutase, dimeric and tetrameric concanavalin A, and heptameric GroES and Gp31; ranging i

59 asurements were performed with cytochrome c, concanavalin A, and poly-L-lysine, biomolecules that exh

60 y from Escherichia coli lipopolysaccharides, concanavalin A, and Pseudomonas aeruginosa exotoxin A.

61 ulin and enolase), tetrameric (streptavidin, concanavalin A, and pyruvate kinase), and pentameric (C-

62 an inducible pattern on T cells activated by concanavalin A, anti-CD3 mAb in combination with anti-CD

63 r induction of selective EC injury using the concanavalin A/anti-concanavalin A model and after ische

64 nti-bovine serum albumin (BSA) antibody, and concanavalin A are embedded in distinct regions of a 7.5

65 that of the wild type and did not react with concanavalin A as did wild-type LAM.

66 ives supported the integration of the lectin concanavalin A as well as the enzymes alpha1-2,3 mannosi

67 MIPP co-localized with concanavalin A at the endoplasmic reticulum, suggesting

68 suggesting that the polymers bind the lectin concanavalin A at the same site as natural carbohydrates

69 investigated by bromelain IgE inhibition and concanavalin A binding assays using sera of cypress poll

70 th a putative sequence tract RYRY that mimic concanavalin A-binding glycans.

71 n chromium-release assays against a panel of Concanavalin A blast targets.

72 ffectors were also able to specifically lyse Concanavalin A blasts isolated from H-2(d) mice (BALB/c,

73 ng BiP/Grp78 messenger RNA (mRNA) in splenic concanavalin A blasts.

74 l activation, as stimulation of T cells with concanavalin A, but not phorbol 12-myristate 13-acetate

75 A model of reactive lymph nodes after concanavalin A challenge served as an additional control

76 ZM-INVINH1 with the glycoprotein fraction by concanavalin A chromatogaphy suggests that ZM-INVINH1 in

77 Concanavalin A chromatography effectively enriched and p

78 Finally, concanavalin A-coated colloids were allowed to adsorb on

79 The two gammaGTases were resolved by concanavalin A (Con A) affinity chromatography, indicati

80 s been created using Alexa Fluor 647-labeled concanavalin A (Con A) and a fourth-generation PAMAM Ale

81 e material was derivatized with two lectins, Concanavalin A (Con A) and Aleuria aurantia lectin (AAL)

82 monitoring the specific interaction between Concanavalin A (Con A) and D-(+)-mannose.

83 ion of the electrical synapse was blocked by concanavalin A (Con A) and dynamin inhibitory peptide (D

84 e data available on the binding constants of Concanavalin A (Con A) and glycogen and Con A-mannan usi

85 bohydrate platform for the immobilization of Concanavalin A (Con A) and is capable of LPS binding mea

86 ew as the sensing probes for lectins such as concanavalin A (Con A) based on the molecular recognitio

87 eral crystal structures of the legume lectin concanavalin A (Con A) bound to closely related carbohyd

88 set of serial lectin columns consisting of a concanavalin A (Con A) column coupled to an SNA column f

89 sed to measure the adhesive strength between concanavalin A (Con A) coupled to an AFM tip and Con A r

90 of alpha-Man to the mannose-specific lectin concanavalin A (Con A) even though homogeneous beta-Lact

91 el on their surfaces was probed using lectin concanavalin A (Con A) from Canavalia ensiformis.

92 Hepatitis induced by concanavalin A (Con A) in mice is well known to be a T-l

93 Injection of concanavalin A (Con A) into mice recapitulates the histo

94 Concanavalin A (Con A) kills procyclic (insect) forms of

95 vation and expansion were studied by using a concanavalin A (Con A) liver injury model followed by pa

96 g the direct pili-mannose binding as well as Concanavalin A (Con A) mediated lipopolysaccharides (LPS

97 ial, we have developed a nanoscale chelating Concanavalin A (Con A) monolithic capillary prepared usi

98 These sensors utilize Concanavalin A (Con A) protein hydrogels with a 2D PC em

99 ntaining 2-D photonic crystal sensor detects Concanavalin A (Con A) through shifts in the 2-D diffrac

100 ible binding of a mobile fluorophore-labeled Concanavalin A (Con A) to immobile pendant glucose moite

101 -SNPs with fluorescein isothiocyanate (FITC)-concanavalin A (Con A) was determined using a fluorescen

102 sembled monolayer in combination with lectin concanavalin A (Con A) was used as molecular recognition

103 Conformational structure changes in concanavalin A (Con A), a legume lectin protein which is

104 achite green (MG-dextran), was conjugated to concanavalin A (Con A), an enzyme with specific affinity

105 ns including Maackia amurensis lectin (MAL), concanavalin A (Con A), and wheat germ agglutinin (WGA).

106 were cultured in the absence or presence of concanavalin A (Con A), phorbol myristate acetate (PMA)/

107 Construction of biosensors based on Concanavalin A (Con A), Sambucus nigra agglutinin type I

108 excellent selectivity to its target lectin, concanavalin A (Con A), surpassing the formerly used lin

109 lines, we identify a plant-derived compound, Concanavalin A (Con A), which differentially kills p53-n

110 ran-coated nanoparticles are aggregated with concanavalin A (Con A), which results in a significant s

111 Concanavalin A (Con A), which selectively blocks KAR des

112 mmune or viral hepatitis, and of mice during concanavalin A (Con A)-induced hepatitis (CIH).

113 Concanavalin A (Con A)-induced injury is an established

114 We used concanavalin A (Con A)-induced liver injury to study the

115 dhesion of the alpha-mannose-specific lectin concanavalin A (Con A).

116 ramide (alphaGalCer), anti-CD3 antibody, and concanavalin A (Con A).

117 nsity on the clustering of a model receptor, concanavalin A (Con A).

118 nd clustering of a model protein, the lectin concanavalin A (Con A).

119 tive protein (CRP), transthyretin (TTR), and concanavalin A (Con A).

120 ell lymphoma cells (TIB 155) stimulated with concanavalin A (Con A).

121 ondrial O2 consumption) in mice treated with concanavalin A (Con A).

122 UV-vis spectroscopy during its binding with concanavalin A (Con A).

123 ) kainate receptors, two unrelated proteins, concanavalin-A (Con-A) and postsynaptic density protein

124 riefly, the well-known lectin macromolecule (concanavalin A, Con A) monolayer was functionalized on 3

125 -HIV antibody 2G12 (shortest distance 31 A), concanavalin A (ConA) (shortest distance 72 A), RCA120 (

126 The lectin concanavalin A (ConA) activates immune cells, resulting

127 rate, compared to wild-type (wt) mice, upon concanavalin A (ConA) administration.

128 y, including T/NKT cell hepatitis induced by concanavalin A (ConA) and alpha-galactosylceramide (alph

129 CM electrodes present a higher adsorption of Concanavalin A (ConA) and Bovine Serum Albumin (BSA) pro

130 arbohydrates to the Man/Glc-specific lectins concanavalin A (ConA) and Dioclea grandiflora lectin (DG

131 arbohydrates to the Man/Glc-specific lectins concanavalin A (ConA) and Dioclea grandiflora lectin (DG

132 binding of the carbohydrate-binding proteins concanavalin A (ConA) and jacalin to arrays composed of

133 cterized chemical inhibitors of endocytosis: concanavalin A (conA) and phenylarsine oxide (PAO).

134 UVL patients exhibited normal ATP release to Concanavalin A (ConA) and phytohemagglutinin (PHA; 190+/

135 K using the receptor internalization blocker concanavalin A (ConA) and the carboxyl terminus-truncate

136 The jack bean lectin concanavalin A (ConA) and the Dioclea grandiflora lectin

137 d from a detailed analysis of the binding of concanavalin A (ConA) and wheat germ agglutinin (WGA) to

138 on, cells treated with ICZ increased surface concanavalin A (ConA) binding, corroborating an increase

139 Concanavalin A (ConA) bound to PTP1 and to the polar tub

140 ated in T cell-mediated hepatitis induced by concanavalin A (ConA) but are less extensively elevated

141 Concanavalin A (ConA) causes immune cell-mediated liver

142 anisms in optical glucose sensors based upon Concanavalin A (ConA) has tended to prevent the sensors'

143 mpetitive binding assays based on the lectin Concanavalin A (ConA) have displayed significant potenti

144 Competitive binding assays utilizing concanavalin A (ConA) have the potential to be the basis

145 Concanavalin A (ConA) inhibited phi C31 infection of S.

146 peptide reacted strongly with both lotus and concanavalin A (ConA) lectins, it bound to lotus stronge

147 robe was designed by noncovalent assembly of concanavalin A (ConA) on gold nanoparticles (AuNPs).

148 ects of T cell-mediated hepatitis induced by concanavalin A (ConA) on the regenerative response in vi

149 ls of hepatitis, including administration of concanavalin A (ConA) or alpha-galactosyl-ceramide, whic

150 in unstimulated or lipopolysaccharide (LPS), concanavalin A (ConA) or phytohemagglutinin (PHA) stimul

151 The treatment of splenic cells with concanavalin A (ConA) plus CT enhanced the production of

152 pha-D-mannopyranoside residues to the lectin concanavalin A (ConA) show increasing negative cooperati

153 cells showed enhanced responses to in vitro concanavalin A (ConA) stimulation when compared with WT

154 ent of either type of mutant with the lectin concanavalin A (ConA) that cross-links surface receptors

155 Here, we show that treatment of mice with concanavalin A (ConA) to induce liver injury triggered a

156 The binding of Concanavalin A (ConA) to mannose-functionalized self-ass

157 l apoptosis induced by the administration of concanavalin A (ConA) to pregnant mothers.

158 Concanavalin A (ConA) was used as an activator of lympho

159 opaeus (gorse, furze), Triticum vulgaris and Concanavalin A (ConA) was used for probes to evaluate bi

160 coefficients that showed mannose to bind to concanavalin A (conA) with 3.7 times greater affinity th

161 e binding affinity of mannose and glucose to concanavalin A (ConA), a 106 KDa homotetramer protein, i

162 ension of macroporous hydrogel particles and concanavalin A (ConA), a glucose-specific lectin, that a

163 Starting from concanavalin A (ConA), a mannose (Man)-binding protein,

164 tein, PZR displays a strong association with concanavalin A (ConA), a member of the plant lectin fami

165 tal model of autoimmune hepatitis induced by concanavalin A (ConA), a process involving T cell activa

166 MSCs were activated with concanavalin A (ConA), a Toll-like receptor (TLR)-2 and

167 feration and IL-2 production induced by PHA, concanavalin A (conA), and anti-TCR MAb.

168 oteins, namely, transthyretin (TTR), avidin, concanavalin A (conA), and human serum amyloid P compone

169 In situ competition with concanavalin A (ConA), another high-mannose specific lec

170 By using concanavalin A (ConA), as a recognition template, peptid

171 This was followed by binding concanavalin A (ConA), glucose oxidase (GOx), and Au nan

172 which consists of three mixtures of lectins concanavalin A (ConA), jacalin (JAC), and wheat germ agg

173 ure induced by Fas-agonistic antibody (Jo2), concanavalin A (ConA), or D-galactosamine/lipopolysaccha

174 and lipopolysaccharide (LPS), or the lectin concanavalin A (ConA), suggesting that physiologic level

175 tested with several plant lectins, including concanavalin A (conA), Vicia villosa isolectin B4 (VVL-B

176 On the basis of the model system glucose-Concanavalin A (ConA), we explore the application of Tra

177 tosamine (GaIN)/lipopolysaccharide (LPS) and concanavalin A (ConA)-induced acute liver failure (ALF),

178 lated by natural killer T (NKT) cells during concanavalin A (ConA)-induced acute liver injury.

179 ore D-Gal/LPS-induced FH and before or after concanavalin A (ConA)-induced FH.

180 ated the effects of THC in a murine model of concanavalin A (ConA)-induced hepatitis.

181 o chronic choline-deficient diet exacerbates concanavalin A (ConA)-induced liver hepatitis, which is

182 of the molecular and cellular mechanisms of concanavalin A (ConA)-induced liver injury have provided

183 ) mice, germ-free (GF) mice are resistant to Concanavalin A (ConA)-induced liver injury.

184 y susceptible to liver destruction following concanavalin A (ConA)-induced T cell activation.

185 DTA mice) exhibited enhanced lymph node (LN) concanavalin A (ConA)-induced Th1 responses after tick i

186 ingly, NK cells mediated hypersensitivity to concanavalin A (ConA)-mediated hepatitis in GNMT(-/-) mi

187 to Fas-specific antibody or co-cultured with concanavalin A (ConA)-stimulated hepatic mononuclear cel

188 Concanavalin A (ConA)-stimulated peripheral blood mononu

189 increased production of interferon-gamma by concanavalin A (ConA)-stimulated spleen T cells and expr

190 d interferon-gamma (IFN-gamma) production in concanavalin A (conA)-stimulated spleen T cells, and dim

191 sensitive to apoptosis upon activation with concanavalin A (ConA).

192 from autoimmune hepatitis induced by mitogen concanavalin A (ConA).

193 P) and then with the Fas agonist Jo2 or with concanavalin A (ConA).

194 ere identified by perfusion with fluorescent concanavalin A (ConA).

195 cose- and mannose-specific binding protein - Concanavalin A (ConA).

196 chemical displacement sensor for the protein concanavalin A (ConA).

197 er injury in the lipopolysaccharide/GalN and concanavalin A (ConA)/GalN models, but not in a ConA-onl

198 Activation of CD8(+) T lymphocytes with concanavalin A (ConA)/interleukin-2 (IL-2), and activati

199 The lectin concanavalin A conjugated to colloidal gold particles wa

200 While no effect was observed with concanavalin A, cyclothiazide greatly enhanced the Glu-,

201 that treatment of OAT1-expressing cells with concanavalin A, depletion of K(+) from the cells, or tra

202 Circular dichroism, mass spectrometry, concanavalin A detection, immunoblotting, enzyme-linked

203 Blocking endocytosis with concanavalin A eliminated the accumulation of fluorescen

204 protease domain of MDC9, Western analysis of concanavalin A-enriched glomerular microsomal extracts d

205 uired for TNFalpha-induced injury induced by concanavalin A/GalN but not by ConA alone.

206 ulin G, avidin:biotin, antibody:antigen, and concanavalin A:glycoprotein interactions are used to dem

207 ivity of single auditory nerve fibres, while concanavalin A had no effect, suggesting that the functi

208 or LcL were compared with those obtained for concanavalin A i.e. lectin, which interacts with the car

209 Following enzymatic hydrolysis, concanavalin A, immobilized or soluble, was added to the

210 ttenuated the suppression of the response to concanavalin A in immunized mice, providing further evid

211 s attenuated by blockade of endocytosis with concanavalin A, indicating a critical role for internali

212 ruited iNKT cells were anergic and prevented concanavalin A-induced (ConA-induced) hepatitis by speci

213 imicrobial susceptibility assay based on the concanavalin A-induced clustering of dextran-coated gold

214 that myosin phosphorylation is critical for concanavalin A-induced gathering of surface receptors.

215 Instead, concanavalin A-induced hepatitis was completely prevente

216 endogenous Gal-1 protected the liver against concanavalin A-induced hepatitis with the B6 genetic bac

217 henotype of these cells, reduced severity of concanavalin A-induced hepatitis, and alterations in the

218 ver regeneration, and in the murine model of concanavalin A-induced liver inflammation.

219 Similarly, concanavalin A-induced liver injury, where type 2 cytoki

220 These findings were confirmed in mice with concanavalin A-induced liver injury.

221 vents and treats both IL12-, IFN-gamma-, and concanavalin A-induced liver toxicity.

222 ion in A549 human lung epithelial cells, and concanavalin A-induced monocyte proliferation.

223 K12-Fc inhibited in a dose-dependent manner concanavalin A-induced proliferation, but not anti-TcRal

224 mal (BLV-negative) cows and had no effect on concanavalin A-induced proliferation.

225 ot wild type RLC almost completely abolished concanavalin A-induced receptor cap formation.

226 y, IL-22TG mice were completely resistant to concanavalin A-induced T cell hepatitis with minimal eff

227 Neutralization of CXCL10 ameliorated concanavalin A-induced tissue injury in vivo, which was

228 The loss of the concanavalin A-induced, but not the lipopolysaccharide-i

229 Upon transplantation into mice with concanavalin-A-induced acute liver failure and fatal met

230 Concanavalin A inhibited surface attachment of conidia,

231 more, a non-selective endocytosis inhibitor, concanavalin A, inhibited the internalization of wild ty

232 Thymocyte proliferative responses to concanavalin A + interleukin-2 were also significantly d

233 nnosylated conjugated polymer (sugar-PPE) by Concanavalin A is positively dependent upon sugar-PPE co

234 Leukocyte adhesion was assayed by concanavalin A labeling.

235 were simultaneously quantified by combining concanavalin A lectin (ConA) perfusion labeling with a f

236 asured by fluorescein isothiocyanate-coupled concanavalin A lectin and acridine orange labeling.

237 res show surprisingly high affinities toward Concanavalin A lectin receptor in comparison to their ho

238 characterized member of its superfamily, the Concanavalin A-like lectins/glucanases.

239 n in guinea pig spleen cells stimulated with concanavalin A, lipopolysaccharide (LPS), phorbol myrist

240 lminant hepatitis, but was without effect on concanavalin A-mediated hepatitis.

241 tive EC injury using the concanavalin A/anti-concanavalin A model and after ischemia/reperfusion (I/R

242 nding site separation of the sugar sites for concanavalin A of 3.6-4.3 nm was determined and a critic

243 compared with that of commercially available concanavalin A on agarose beads.

244 urement of the toxic effect of 100 microg/mL concanavalin A on macrophages and hepatocytes, but not o

245 We have immobilized the protein Concanavalin A onto a self-assembled monolayer of multiv

246 nalized graphene indicate that adsorption of Concanavalin A onto graphene is accompanied by near-comp

247 no significant difference in the binding of concanavalin A or Aleuria aurantia lectin was detected.

248 n) and this was not blocked by agents (i.e., concanavalin A or hypertonic sucrose) that inhibit D1 re

249 , and the generation of activated T cells by Concanavalin A or L-PHA was also reduced in Fng tKO mice

250 Splenic T cells were then stimulated with concanavalin A or ovalbumin in vivo or in vitro, and CD2

251 hole spleen cells following stimulation with concanavalin A or PPD.

252 d apoptosis following activation either with concanavalin A or with antibodies to CD3 and CD28 and le

253 ion in response to the homologous immunogen, concanavalin A, or lipopolysaccharide was similar for al

254 ncluded: (a) reduced IFN-gamma production by concanavalin A- or antigen-stimulated T cells; and (b) h

255 Downregulation of chIL-17RA occurred in concanavalin A- or lipopolysaccharide-activated splenic

256 911) and cyclic peptide (D002) reactive with concanavalin A presented in a multiple antigen peptide (

257 interaction force between a polymer-tethered concanavalin-A protein (ConA) and a similarly tethered m

258 itogen-induced lymphoproliferative activity (concanavalin A, range: 74,218 dropping to 55,880 counts

259 arger than that of the wild type, had gained concanavalin A reactivity, and that the arabinan termini

260 ration in response to phytohemagglutinin and concanavalin A remained stable or increased for the Inte

261 -induced binding to rhodopsin immobilized on concanavalin-A resin.

262 A, avidin, monoclonal anti-BSA antibody, and concanavalin A, respectively.

263 of bacterial growth inhibition, addition of concanavalin A results in the formation of extensive dex

264 microbalance (QCM) to show that tripod-bound Concanavalin A retains its affinity for polysaccharides

265 ctra of the amide I region of poly-l-lysine, concanavalin A, ribonuclease A, and lysozyme show cross-

266 Given that Concanavalin A's tertiary structure is thought to be rel

267 , and Rac-1 coprecipitates with rhodopsin on Concanavalin A Sepharose.

268 e, phenyl-Sepharose hydrophobic interaction, concanavalin A-Sepharose affinity and Superose 12 gel fi

269 Moreover, in response to aoHGE extracts or concanavalin A, splenocytes from ehrlichia-infected mice

270 PG27 significantly increased concanavalin A-stimulated in vitro IL-4 production by da

271 However, neither inhibition of concanavalin A-stimulated spleen cells nor keyhole limpe

272 , trough) and for lymphocyte functions using concanavalin A-stimulated whole blood assays to measure

273 ve loss of T cells, compromised responses to concanavalin A stimulation, and absence of inflammatory

274 and interleukin (IL)-4 (Th2 cytokine) after concanavalin A stimulation.

275 nocytes from infected animals in response to concanavalin A, suggesting a role for NO in mediating th

276 -alpha(5)beta(1) interaction is inhibited by concanavalin A, suggesting that GT1b binds to mannose st

277 roteases and organic extraction but bound to concanavalin A, suggesting that IRI is a sulfated glycan

278 In DRG cells treated with concanavalin A the EC50 for ATPA was 341 nM.

279 Likewise, after treatment with concanavalin A, there was no change in either desensitiz

280 oclonal antibody (M1) and for the binding of concanavalin A to a glycoprotein have been determined.

281 Flipping was assayed by using the lectin Concanavalin A to capture M5-DLOs that had been transloc

282 icrotubules that normally follows binding of concanavalin A to leukocyte cell surface receptors.

283 endocytosis of transferrin and transport of concanavalin A to the lysosome are both impaired, confir

284 d targets (carbonic anhydrase, streptavidin, concanavalin A) to identify desired ligands.

285 This analysis implies that, although Concanavalin A tolerates the additional 6 arm GlcNAc pre

286 with BSA, and the affinity of photoattached concanavalin A toward ovalbumin was compared with that o

287 as there was no protection against CCl(4) or concanavalin A toxicity.

288 ran) and tetramethylrhodamine isothiocyanate concanavalin A (TRITC-Con A) chemically conjugated into

289 ies agrin-G3 as a functional analogue of the concanavalin A-type lectins, highlights functional simil

290 o O-linked N-acetylglucosamine or the lectin concanavalin A was detected.

291 1.5-microm diameter microsphere coated with concanavalin A was inserted though an ablated hole in th

292 n with fluorescein isothiocyanate-conjugated concanavalin A, was increased in the absence of Dp71.

293 By using a Sepharose-immobilized lectin, concanavalin A, we isolated a fraction enriched with LRV

294 . coli 2443 with a fluorescent derivative of concanavalin A, we observed a similar helical organizati

295 oglobulin, ribonuclease A, E-cadherin 5, and concanavalin A were co-lyophilized with carbohydrates (t

296 ol) cows stimulated with the general mitogen concanavalin A were highly similar (overall r = 0.84), s

297 or all seven lectins, and similar to that of concanavalin A which is also a member of the Diocleinae

298 genes after exposure to interferon-gamma or concanavalin A, which resulted in minimal HLA-B27 up-reg

299 ned a high amount of mannose, as detected by concanavalin A, while the UT-A1 in lipid rafts was the m

300 pha-Man-(1--> 6)]-Man to bind to the lectin, Concanavalin A, with almost the same affinity as the tri