ライフサイエンスコーパス: concanavalin

1 8.6 kDa), and the tetrameric protein complex Concanavalin A (103 kDa).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

46 nsing through polydopamine (PDA)-immobilized concanavalin A (Con A).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

78 ide (LPS) plus D-galactosamine (D-Galn), and concanavalin A (ConA) to identify the function of extrac

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

112 Concanavalin A (ConA)-stimulated peripheral blood mononu

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

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

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

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

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

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

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

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

121 , nanogold particles (NGPs), antibodies, and Concanavalin A (ConA).

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

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

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

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

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

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

128 valent affinity capture using NeutrAvidin or concanavalin A agarose beads or directly via covalent co

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

153 ver, CD160(-/-) mice are more susceptible to Concanavalin A challenge, and display elevated serum AST

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

155 Concanavalin A chromatography effectively enriched and p

156 The lectin concanavalin A conjugated to colloidal gold particles wa

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

158 Blocking endocytosis with concanavalin A eliminated the accumulation of fluorescen

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

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

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

162 Leukocyte adhesion was assayed by concanavalin A labeling.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

178 ower than that of maize and potato starches (concanavalin A precipitation method).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

195 1.5-microm diameter microsphere coated with concanavalin A was inserted though an ablated hole in th

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

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

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

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

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

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

202 re observed for a larger multimeric complex (Concanavalin A).

203 Concanavalin A, a lectin selective for high mannose and

204 Concanavalin A, a lectin that binds glucose and mannose

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

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

207 tures of the protein complexes streptavidin, concanavalin A, and C-reactive protein under charge redu

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

248 Instead, concanavalin A-induced hepatitis was completely prevente

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

269 ssessed after perfusion with FITC-conjugated concanavalin A.

270 separate group of mice by administration of concanavalin A.

271 of the second through sixth generations and Concanavalin A.

272 pon aggregation of unilamellar vesicles with concanavalin A.

273 ssessed by labeling adherent leukocytes with concanavalin A.

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

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

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

277 th immobilized Sambucus nigra agglutinin and concanavalin A.

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

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

280 10 is inducible by interferons (IFNs) and by concanavalin A.

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

282 n of peripheral blood mononuclear cells with concanavalin A.

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

284 ho-proliferative response to alloantigens or concanavalin A.

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

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

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

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

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

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

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

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

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

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

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

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

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

298 transthyretin, avidin, bovine serum albumin, concanavalin, human serum amyloid protein, and Immunoglo

299 tional space presented by both Ubiquitin and Concanavalin; it appears that diverse conformational fam

300 tems such as human pancreatic alpha-amylase, concanavalin, Pichia pastoris lysyl oxidase, and Klebsie