ライフサイエンスコーパス: agglutinin

1 acers (choleratoxin subunit B and wheat germ agglutinin).

2 e-containing form, as detected by wheat germ agglutinin.

3 ) and GL7 (52%), and bound the lectin peanut agglutinin.

4 njugates reacting with the lectin wheat germ agglutinin.

5 t decreasing biofilm formation than salivary agglutinin.

6 g to the holdfast-specific lectin wheat germ agglutinin.

7 nti-deacetylated PNAG antibody or wheat germ agglutinin.

8 yed reduced binding to the lectin wheat germ agglutinin.

9 the glycoprotein may function as a bacterial agglutinin.

10 losely related, less toxic Abrus precatorius agglutinin.

11 cular-weight salivary mucin MG2 and salivary agglutinin.

12 e of S. mutans to immobilized human salivary agglutinin.

13 ed by the nuclear pore inhibitor, wheat germ agglutinin.

14 e readily aggregated by fluid-phase salivary agglutinin.

15 nding to Vicia villosa agglutinin and peanut agglutinin.

16 they may have evolved from primitive mating agglutinins.

17 Heat-resistant agglutinin 1 (Hra1) is an accessory colonization factor

18 n-containing receptor; and 3) Ulex europaeus agglutinin 1, and were able to form cord/tube-like struc

19 5) and K14, but fails to bind Ulex europaeus agglutinin-1 (UEA-1) lectin.

20 ress CD80 and bind the lectin Ulex europaeus agglutinin-1, leading to a significant decrease in the e

21 v beta 3, and bind the lectin ulex europaeus agglutinin-1.

22 le export sites, but not with Lens culinaris agglutinin, a marker for cortical granules.

23 We demonstrate that peanut agglutinin, a minor peanut allergen, is a novel ligand f

24 By using Wisteria floribunda agglutinin, a specific marker for PNN, PV-MP interneuron

25 Peanut agglutinin activates DCs to induce the expression of cos

26 nts revealed that MG1, MG2, and the salivary agglutinin also present Lewis blood group antigens, the

27 h the sugar and the lectin (here, wheat germ agglutinin and a single hevein domain) and cannot always

28 Immunohistochemical analyses with peanut agglutinin and an antibody specific for cone transducin

29 integrity was determined by IHC using peanut agglutinin and an M-opsin-specific antibody.

30 ctin columns with immobilized Sambucus nigra agglutinin and concanavalin A.

31 pulmonary lymphoid aggregates express peanut agglutinin and GL7, two markers of GC B cells, as well a

32 Binding affinities to peanut agglutinin and human galectin-3 were measured by isother

33 inished alpha-dystroglycan binding to peanut agglutinin and inhibited neuraminidase-induced AChR clus

34 Seven ANF's corresponding to soybean agglutinin and Kunitz trypsin inhibitor were identified

35 utant protein is considerably less active as agglutinin and less sensitive to low-level ligand presen

36 clonal antibody 6B4 and the lectins soy bean agglutinin and Maackia amurensis indicated that the pred

37 e sialic acid-binding lectins Sambucus nigra agglutinin and Maackia amurensis lectin-I, which are rou

38 ans, as revealed by binding to Vicia villosa agglutinin and peanut agglutinin.

39 s as well as improved avidity for wheat germ agglutinin and phytohemagglutinin.

40 nding to the specific lectins Sambucus nigra agglutinin and Polysporus squamosus lectin and confirmed

41 r length slightly reduces lectin capacity as agglutinin and slows down aggregate formation at low lig

42 Interactions between salivary agglutinin and the adhesin P1 of Streptococcus mutans co

43 bly by liposomes was inhibited by wheat germ agglutinin and thus required active nuclear transport, s

44 ddition, the prevalence of receptors such as agglutinin and ubiquitinated proteins in ciliary ectosom

45 ainst two plant lectins, Glycine max soybean agglutinin and Vicia villosa.

46 Fluid-phase salivary agglutinin and, to a lesser extent, immobilized agglutin

47 We have previously purified the agglutinins and analyzed their structural organization u

48 ism underlying the collective requirement of agglutinins and Fig2p for mating.

49 the Sag1 and Sad1 genes that encode the two agglutinins and relate their derived amino acid sequence

50 ssic germinal center markers, peanut lectin (agglutinin) and GL-7.

51 ract, including a known toxin (Proteus toxic agglutinin) and the high pathogenicity island of Yersini

52 he expression of the tracer, WGA (wheat germ agglutinin), and used these in combination with LepRb(cr

53 etide synthesis system), hra (heat-resistant agglutinin), and vat (vacuolating toxin) were significan

54 , positive for binding of the lectin, peanut agglutinin, and an antibody to the carbohydrate epitope,

55 e-type lectin, a plant lectin, Pisum sativum agglutinin, and the bacterial Gal-/Glc-binding protein f

56 e of biocytin, labeled the cones with peanut agglutinin, and then used antibodies against blue cone o

57 ia, immunoglobulin M [IgM] paraprotein, cold agglutinins, and disialosyl antibodies) is a rare syndro

58 by combining a retrograde tracer (wheat-germ agglutinin apo-horseradish peroxidase colloidal gold) wi

59 njection of the retrograde tracer wheat germ agglutinin-apo (inactivated) horseradish peroxidase conj

60 labeled after focal injections of wheat germ agglutinin-apo (inactivated) horseradish peroxidase conj

61 We chose wheat germ agglutinin as a candidate lectin with clinical potential

62 Using the lectin wheat germ agglutinin as a probe, we show that the matrix on C. ele

63 tear film gp340 may function as a bacterial agglutinin as it does in saliva, tears were incubated wi

64 n assay using both soybean and Vicia villosa agglutinins as model lectins.

65 Dextran- and wheat-germ agglutinin-associated signals were correlated in the t-s

66 molytic anemia in which autoantibodies (cold agglutinins) bind to red blood cells (RBCs) at low tempe

67 rix sheets, IRBP colocalized with the peanut agglutinin binding matrix glycans.

68 a direct correlation between reduced soybean agglutinin binding to 63- and 68-kDa midgut glycoprotein

69 sphatase activity detection, reduced soybean agglutinin binding to HvALP from Cry1Ac resistant larvae

70 We observed that Wisteria floribunda agglutinin-binding PNNs develop around DCN neurons from

71 e samples were analyzed with a Vicia villosa agglutinin biosensor that has specificity for the cancer

72 combining retrograde transport of wheat germ agglutinin-bound gold after injections into the VTA with

73 inished in adherence to immobilized salivary agglutinin but remained immunoreactive and were readily

74 nhibit bacterial adherence to human salivary agglutinin by a BIAcore surface plasmon resonance assay.

75 by the lectins Datura stramonium and peanut agglutinin (by approximately 74 and approximately 43%, r

76 ents induction of in vitro hemolysis by cold agglutinins (CA).

77 Sequential use of wheat germ agglutinin chromatography, Sephacryl S300 gel filtration

78 y to inhibit bacterial adherence to salivary-agglutinin-coated hydroxyapatite beads.

79 y a tetravalent model lectin: the leguminous agglutinin Con A, which is structurally related to endog

80 n of IRBP, as well as glycans binding peanut agglutinin (cone matrix) and wheat germ agglutinin (rod/

81 to fluorescein or, alternatively, wheat-germ agglutinin conjugated to an Alexa fluor dye.

82 Injections of wheat germ agglutinin conjugated to horseradish peroxidase were pla

83 CS terminations were traced using wheat germ agglutinin conjugated to horseradish peroxidase.

84 of the retrograde pathway tracer wheat germ agglutinin conjugated with horseradish peroxidase (WGA-H

85 beta (CTB), Fluoro-ruby (FR), and wheat germ agglutinin conjugated with horseradish peroxidase (WGA-H

86 y labeled following injections of wheat germ agglutinin-conjugated horseradish peroxidase (WGA-HRP) i

87 Unilateral intravitreal wheat germ agglutinin-conjugated horseradish peroxidase (WGA-HRP) i

88 l Vi/Vc, or MDH) or peripherally (wheat germ agglutinin-conjugated horseradish peroxidase or cholera

89 vivo using ductal-specific Dolichos biflorus agglutinin (DBA) lectin labeling followed by magnetic be

90 paeus agglutinin (UEA) and Dolichos biflorus agglutinin (DBA), to determine whether they exhibit diff

91 However, wheat germ agglutinin-detectable N-acetyl-glucosamine (GlcNAc) epit

92 ariant on MUC5AC using the lectin wheat-germ agglutinin discriminated mucin-producing cystic tumors (

93 trospectively studied 232 patients with cold agglutinin disease (CAD) at 24 centers in 5 countries.

94 Primary chronic cold agglutinin disease (CAD) is a well-defined clinicopathol

95 One such disorder is cold agglutinin disease (CAD), an autoimmune hemolytic anemia

96 In cold agglutinin disease (CAD), immunoglobulin M autoantibodie

97 n fludarabine and rituximab for chronic cold agglutinin disease (CAD).

98 d 89 patients from our institution with cold agglutinin disease from 1970 through 2012.

99 Cold agglutinin disease is a difficult-to-treat autoimmune he

100 Cold agglutinin disease is a rare and poorly understood disor

101 Ten patients with cold agglutinin disease participated in the phase 1b componen

102 Seven of 10 patients with cold agglutinin disease responded with a hemoglobin increase

103 n erythrocytes and B lymphocytes, cause cold agglutinin disease, and are carried by 5% of naive B cel

104 de paroxysmal nocturnal hemoglobinuria, cold agglutinin disease, hemolytic uremic syndrome, nephropat

105 mmune thrombocytopenic purpura, chronic cold agglutinin disease, IgM-mediated neuropathies and mixed

106 ropathy, amyloidosis, cryoglobulinemia, cold-agglutinin disease, or evidence of disease transformatio

107 ropathy, amyloidosis, cryoglobulinemia, cold-agglutinin disease, or transformed disease should be con

108 ent-mediated hemolysis in patients with cold agglutinin disease, significantly increasing hemoglobin

109 tion and treatment improves outcomes in cold agglutinin disease.

110 encode the mating-type plus and minus sexual agglutinins, displayed only by gametes, and we document

111 pore formation with microinjected wheat germ agglutinin does not inhibit the nuclear localization of

112 edicted to encode a chimeric lectin with two agglutinin domains and an ETX/MTX2 toxin domain.

113 for rapid differentiation between ricin and agglutinin done in real time.

114 ing CP activation, TNT003 also prevents cold agglutinin-driven generation of anaphylatoxins.

115 The results showed that MG1 and the salivary agglutinin express the MECA-79 epitope, an unusual sulfa

116 Pretreatment with wheat germ agglutinin followed by etoposide treatment induces DNA d

117 with similarity with Pterocarpus angolensis agglutinin from the same tribe.

118 Lectin-binding analyses were performed with agglutinins from Arachis hypogaea, Maackia amurensis, an

119 We cloned and sequenced the full-length agglutinin gene from strain 60A and have designated it h

120 ycolylneuraminic acid, and Dolichos biflorus agglutinin glycans recognized by human preexisting antib

121 The adhesins that bind salivary agglutinin glycoprotein (gp340) and human cell surface r

122 ge of host molecules, in particular salivary agglutinin glycoprotein (SAG or gp340), and with ligands

123 to other oral bacteria and also to salivary agglutinin glycoprotein, a constituent of the salivary f

124 binant Spy1325 bound purified human salivary agglutinin glycoprotein.

125 cans that bind the lectins Galanthus nivalis agglutinin (GNA), Pisum sativum agglutinin (PSA), and Le

126 is detected by the lectin Galanthus nivalis agglutinin (GNA).

127 tis, confers binding to immobilized salivary agglutinin gp-340.

128 s to assess the interaction of Helix aspersa agglutinin (HAA) and Helix pomatia agglutinin (HPA) with

129 Helix pomatia agglutinin (HGA) distinguished epithelial regions contai

130 We used Wisteria Floribunda agglutinin histochemistry to visualize PNNs to investiga

131 Oscillatoria agardhii agglutinin homolog (OAAH) proteins belong to a recently

132 Here, we show that wheat germ agglutinin horse radish peroxidase (WGA-HRP) chemically

133 Wheat germ agglutinin-horseradish peroxidase (0.5-1.0 mul) was inje

134 ctions of fluorescent tracers and wheat germ agglutinin-horseradish peroxidase (WGA-HRP) in dorsal (P

135 monkeys by means of injections of wheat germ agglutinin-horseradish peroxidase into the appropriate L

136 The lectin Helix pomatia agglutinin (HPA) has been shown to bind aggressive metas

137 x aspersa agglutinin (HAA) and Helix pomatia agglutinin (HPA) with Gal-deficient IgA1.

138 ort that EAEC 042 carries the heat-resistant agglutinin (hra1) gene, also known as hek, which encodes

139 Ricinus communis agglutinin I (RCA I), a galactose-binding lectin from ca

140 However, the binding of Ricinus communis agglutinin I (RCA) to sCJD and vCJD samples was signific

141 ding specificity of lectins Ricinus communis agglutinin I (RCA), peanut (Arachis hypogaea) agglutinin

142 simplicifolia II (GS II) and Ulex europaeus agglutinin I (UEA I) selectively bind to rat fibroblast

143 rensis lectin II (MALII), and Ulex europaeus agglutinin I (UEA) was utilized in force spectroscopy me

144 Ulex Europaeus Agglutinin I (UEA-I) lectin has been used to label and i

145 belling by the fucose-binding Ulex europaeus agglutinin I (UEA-I) was completely abrogated, GDP-Fuc w

146 luorescently labeled lectin Ricinus communis agglutinin I detected polysaccharides secreted by F. joh

147 parenchymal infiltration of Ricinus communis agglutinin I(+) microglia/macrophages, but never associa

148 as competitively inhibited by Ulex europaeus agglutinin-I (UEA-I), a lectin specific for Fucalpha1-2

149 of human endothelial specific Ulex europaeus agglutinin-I demonstrated an increased number of perfuse

150 eration) were evaluated using Ulex europaeus agglutinin-I labeling to discriminate between vessels wi

151 ressing the trans-synaptic tracer wheat germ agglutinin in LepRb neurons reveal the innervation of Ce

152 c with the apical membrane marker wheat germ agglutinin in T84WT cells.

153 rmation are analogous to the roles of sexual agglutinins in mating reactions.

154 ure, and suggest a conserved role for sexual agglutinins in mediating mating, cell cohesion and biofi

155 etically expressed lectin tracer, wheat germ agglutinin, in Na(V)1.8-expressing nociceptors of the no

156 Enrichment of a protein, soybean agglutinin, in the dextran-rich phase improves from 2.3-

157 various glycosidases and binding to soybean agglutinin indicated that the structure of the glycan pr

158 ffonia simplicifolia lectin I and wheat germ agglutinin induced serum IgM Abs in mice that mediated t

159 Whole saliva- and salivary agglutinin-induced aggregation of S. mutans was adversel

160 lutinin and, to a lesser extent, immobilized agglutinin inhibited biofilm development by S. mutans in

161 liferation and differentiation (amylase, DBA-agglutinin, insulin, glucagon, beta-catenin, E-cadherin,

162 Apart from the well-known agglutinin interaction between Aga2p and Sag1p, three mo

163 l participate in or influence a well-studied agglutinin interaction mediated by Aga1p-Aga2p complexes

164 say targeting the gene encoding for the germ agglutinin isolectin A protein (Tri a 18 allergen), usin

165 pulation, and associated Wisteria floribunda agglutinin-labeled perineuronal nets (WFA/PNNs) are alte

166 Wheat germ agglutinin labels all olfactory axons uniformly during m

167 sativum agglutinin (PSA), and Lens culinaris agglutinin (LCA) but not lectins binding Golgi-modified

168 ts, using the fucose-specific Lens culinaris agglutinin (LCA).

169 vasculature was labeled using Ulex europaeus agglutinin lectin and examined using confocal microscopy

170 Intravenous injection of wheat germ agglutinin lectin and its adsorption onto the endothelia

171 lpha2,6-linkages, as shown by Sambucus nigra agglutinin lectin blotting.

172 ariv reagent but interacting with the peanut agglutinin lectin was proposed.

173 d CD31 binding to Arachis hypogaea or peanut agglutinin lectin, indicating CD31 desialylation.

174 rface detected by enhanced binding of peanut agglutinin lectin.

175 ecific glycocalyx stained by the PNA (peanut agglutinin) lectin marker.

176 detected by staining with jacalin and peanut agglutinin lectins after 30 min of treatment; no reducti

177 Blotting with Maackia amurensis and peanut agglutinin lectins established epidermal growth factor r

178 Furthermore, FGR23, which encodes an agglutinin-like protein, was found to enhance both matin

179 n of the eight genes in the Candida albicans agglutinin-like sequence (ALS) family was studied by rev

180 bicans and Candida glabrata express the ALS (agglutinin-like sequence) and EPA (epithelial adhesin) f

181 The C. albicans ALS (agglutinin-like sequence) gene family encodes eight larg

182 cells, expressing members of the C. albicans Agglutinin-Like-Sequence (ALS) cell wall protein family.

183 era agglutinin (MPA), and Limulus polyphemus agglutinin (LPA), suggesting the presence of an O-linked

184 ffonia simplicifolia lectin I and wheat germ agglutinin mediate the apoptosis of tumor cells.

185 amples and showed that TNT003 prevented cold agglutinin-mediated deposition of complement opsonins th

186 by peanut agglutinin (PNA), Maclura pomifera agglutinin (MPA), and Limulus polyphemus agglutinin (LPA

187 Oscillatoria agardhii agglutinin (OAA) is a recently discovered cyanobacterial

188 he signal peptide of cell wall protein alpha-agglutinin of S. cerevisiae, the serine-threonine-rich r

189 Strikingly, the central regions of the agglutinins of both mating types have diverged completel

190 protease C1s, on CP activity induced by cold agglutinins on human RBCs.

191 hat C2C12 alpha-dystroglycan bound to peanut agglutinin only after digestion with neuraminidase.

192 colocalized with dextran (but not wheat germ agglutinin or transferrin), and uptake of AF-ALN or [14C

193 ults suggest that MG1, MG2, and the salivary agglutinin play important roles in governing leukocyte a

194 kinetics of the multivalent proteins peanut agglutinin (PnA) and cholera toxin B subunit (CTB) to a

195 A galactose-binding peanut agglutinin (PNA) and sialic acid-binding Sambucus nigra

196 cell types, and found that UEA-I and Peanut agglutinin (PNA) have a specific affinity for acinar cel

197 Cone photoreceptors were stained by peanut agglutinin (PNA) lectin in the flatmounted retina.

198 the area of the future IVD contained peanut agglutinin (PNA) staining cartilage.

199 with TF-antigen for binding sites on peanut agglutinin (PNA) that is immobilized on magnetic beads.

200 -enhancing effect of beta-Lact toward peanut agglutinin (PNA), a lectin strongly binding multivalent

201 gglutinin I (RCA), peanut (Arachis hypogaea) agglutinin (PNA), Maackia amurensis lectin II (MALII), a

202 ts showed positive lectin staining by peanut agglutinin (PNA), Maclura pomifera agglutinin (MPA), and

203 a characteristic increased binding of peanut agglutinin (PNA), reflecting an increased expression of

204 Flow cytometry sorted peanut agglutinin (PNA)-labeled cones from dissociated mouse re

205 ched by their affinity for the lectin peanut agglutinin (PNA).

206 ned remained intact and positive with peanut agglutinin (PNA).

207 ing the lectin from Arachis hypogaea (peanut agglutinin, PNA) as the recognition element.

208 he levels of AMPK in succinylated wheat germ agglutinin precipitates correlated with hexosamine flux

209 f fluid-phase or adsorbed saliva or salivary agglutinin preparations.

210 rome oxidase, Nissl, and Wisteria floribunda agglutinin preparations.

211 Both agglutinin proteins are organized into three distinct do

212 rombin, and the bacterial surface display of agglutinins, proteins that bind polymerized fibrin, are

213 thus nivalis agglutinin (GNA), Pisum sativum agglutinin (PSA), and Lens culinaris agglutinin (LCA) bu

214 Proteus toxic agglutinin (Pta) represents a novel autotransported cyto

215 sin, a secreted cytotoxin, and proteus toxic agglutinin (Pta), a surface-associated cytotoxin, mutant

216 injecting the toxic lectin Ricinus communis agglutinin (RCA) I into the sciatic nerve.

217 gglutinin type I (SNA), and Ricinus communis agglutinin (RCA) on polycrystalline gold electrodes was

218 s from 1 fM (Con A), 10 fM (Ricinus communis agglutinin (RCA), or 100 fM (SNA) with a linear range sp

219 A N-glycosidases, including Ricinus communis agglutinin (RCA), saporin, and abrin II.

220 solectin B4 (VVL-B(4)), and Ricinus communis agglutinin (RCA120).

221 des-gamma carboxyprothrombin, lens culinaris agglutinin-reactive AFP, human hepatocyte growth factor,

222 Lin-Sca-1+c-Kit+ cells with reduced S. nigra agglutinin reactivity.

223 structure of the fucose-binding European eel agglutinin revealed a novel lectin fold (the "F-type" fo

224 anut agglutinin (cone matrix) and wheat germ agglutinin (rod/cone matrix), was defined by confocal mi

225 ites on AgI/II to the host receptor salivary agglutinin (SAG) were identified by surface plasmon reso

226 the putative tooth surface receptor salivary agglutinin (SAG), as monitored by surface plasmon resona

227 conformational epitopes as well as salivary agglutinin (SAG)-binding activity.

228 Salivary agglutinin [SAG, encoded by the deleted in malignant bra

229 The salivary scavenger and agglutinin (SALSA), also known as gp340 and dmbt1, is an

230 alNAc residues (Tn-PSM) binds to the soybean agglutinin (SBA) with a K(d) of 0.2 nm, which is approxi

231 high affinity (K(d) = 0.2 nM) of the soybean agglutinin (SBA), a tetrameric GalNAc specific lectin, f

232 e evaluated a panel of four lectins (Soybean agglutinin (SBA), Wisteria floribunda lectin (WFL), Vici

233 ) IgD+ IGHV4-34+ B cells and removal of cold agglutinin self-reactivity by hypermutation, often accom

234 oscopy with fluorescently labeled wheat germ agglutinin showed a paucity of PNAG in S. lugdunensis bi

235 modifications, we focused on Sambucus nigra agglutinin (SNA) and Aleuria aurantia lectin (AAL), lect

236 ding were characterized using Sambucus nigra agglutinin (SNA) and other lectins including Maackia amu

237 A lectin column prepared from Sambucus nigra agglutinin (SNA) was used to select and compare the conc

238 (PNA) and sialic acid-binding Sambucus nigra agglutinin (SNA) were covalently surface-immobilized on

239 the carbohydrate-binding protein wheat germ agglutinin specifically stains colonies and the slow swi

240 Confocal microscopy of peanut agglutinin-stained sections showed dose-dependent FeSO(4

241 and length were measured on FITC-wheat germ agglutinin-stained sections.

242 Cone density was assessed by peanut agglutinin staining and confocal microscopy.

243 Cone morphology was assessed by peanut agglutinin staining in retinal flatmounts and cryosectio

244 t followed a reduction in jacalin and peanut agglutinin staining.

245 ction with the glycoprotein complex salivary agglutinin that is comprised primarily of the scavenger

246 oproteins (HRGPs), the plus and minus sexual agglutinins, that are displayed on their flagellar membr

247 d the highly toxic mistletoe Viscum album L. agglutinin, the bacterial lectin PA-IL from Pseudomonas

248 to the fucose recognition domain of the eel agglutinin, their C-terminal domain exhibits changes tha

249 ing experiments with Trichosanthes kirilowii agglutinin (TKA), a galactose-specific lectin, and AFM o

250 The binding of wheat germ agglutinin to human tissue was determined to be specific

251 Here Vanover et al. use labeled soybean agglutinin to selectively label RSV G protein and show h

252 ort the use of fluorescently labeled soybean agglutinin to selectively label the respiratory syncytia

253 -/-) retina, and was colocalized with peanut agglutinin to the Irbp(-/-) cone outer segments.

254 Peripheral routes are blocked by wheat germ agglutinin to yield 2-fold lower permeability for 17 nm-

255 ntroduce the lectin Tetragonolobus purpureas agglutinin (TPA) as a novel cell surface marker that all

256 ed on Concanavalin A (Con A), Sambucus nigra agglutinin type I (SNA), and Ricinus communis agglutinin

257 ntigen was developed by using Sambucus nigra agglutinin type I (SNA-I) as the recognition element.

258 two different plant lectins, Ulex europaeus agglutinin (UEA) and Dolichos biflorus agglutinin (DBA),

259 neurons that were labeled with Vicia villosa agglutinin (VVA), a parvalbumin neuron-selective marker,

260 a floribunda lectin (WFL), Vicia villosa-B-4 agglutinin (VVA), and Helix pomatia agglutin (HPA)) with

261 nhibition of biofilm development by salivary agglutinin was differently influenced by particular muta

262 me-linked immunosorbant assay, and titers of agglutinin were determined.

263 Cold agglutinins were identified in 15 (34%) patients.

264 ryzae lectin [AOL] and binding of wheat germ agglutinin) were assessed in paraffin-embedded tissue sa

265 Wisteria floribunda agglutinin (WFA) is a legume lectin that recognizes term

266 of PNNs, as detected by Wisteria floribunda agglutinin (WFA) labeling, has been reported to be lower

267 mal human amygdala using wisteria floribunda agglutinin (WFA) lectin histochemistry.

268 ng with the plant lectin Wisteria floribunda agglutinin (WFA) to identify compounds that altered musc

269 r matrix (PNNs/ECM) with Wisteria floribunda agglutinin (WFA), and critically contributes to the acqu

270 shed by dense binding of Wisteria floribunda agglutinin (WFA).

271 ment of two PNN markers (Wisteria floribunda agglutinin [WFA] and Cat-315) and the effect of neonatal

272 between binding sites is ca. 9 A, wheat germ agglutinin (WGA) (shortest distance between binding site

273 Further, coexpression of wheat germ agglutinin (WGA) and an axon-targeted beta-gal supports

274 n adeno-associated virus encoding wheat germ agglutinin (WGA) and by immunoelectron microscopy determ

275 Wheat germ agglutinin (WGA) binds to the glycosylated extracellular

276 ents accessible to HRP-conjugated wheat germ agglutinin (WGA) disrupted delivery of HA but not endoly

277 Wheat germ agglutinin (WGA) reactive glycans on fibronectin and thr

278 Wheat germ agglutinin (WGA) showed significantly decreased binding

279 Further, abnormal phalloidin and wheat germ agglutinin (WGA) staining of Tdrd7-/- fiber cells, parti

280 ed the transneuronal tract tracer wheat germ agglutinin (WGA) to nonpeptidergic nociceptive neurons.

281 ding of concanavalin A (ConA) and wheat germ agglutinin (WGA) to their target monosaccharides indicat

282 ody-like reagent against mycosis, wheat germ agglutinin (WGA) was linked to the effector Fc region of

283 ession of a transneuronal tracer, wheat germ agglutinin (WGA), in the 5HT neurons so as to study the

284 ession of a transneuronal tracer, wheat germ agglutinin (WGA), is induced in primary sensory neurons,

285 ycophorin A, and the more general wheat germ agglutinin (WGA), were selected to label REVs.

286 an approximately 50% decrease in wheat germ agglutinin (WGA)-labeled components of the GCX under DF

287 alin A (ConA), jacalin (JAC), and wheat germ agglutinin (WGA).

288 MAL), concanavalin A (Con A), and wheat germ agglutinin (WGA).

289 le by carbohydrate affinity using wheat germ agglutinin (WGA).

290 from the highly homologous Ricinus communis agglutinin which is currently not feasible using immunol

291 ns and the transganglionic tracer wheat germ agglutinin which, after sciatic nerve injection, labels

292 m using the lectins Helix aspersa and peanut agglutinin, which bind to alternative forms of O-glycan

293 duct/tubule marker, Lectin Dolichos biflorus Agglutinin, which correlates with the site of Cre-mediat

294 reactivity with the lectin Maackia amurensis agglutinin, which recognizes alpha2,3-linked sialic acid

295 Among a panel of seven lectins, soybean agglutinin, which recognizes N-acetyl-d-galactosamine, g

296 Interestingly, another plant lectin, peanut agglutinin, which shares the same carbohydrate specifici

297 PK was recognized by succinylated wheat germ agglutinin, which specifically binds O-GlcNAc.

298 specific legume lectin Erythrina cristagalli agglutinin with several sugars has been characterized in

299 influenza hemagglutinin, and Sambucus nigra agglutinin) with sialylated glycans on the same cell sur

300 hain and for distinction of ricin from ricin agglutinin within a single analytical run.