ライフサイエンスコーパス: wheat germ agglutinin

1 ifferent tracers (choleratoxin subunit B and wheat germ agglutinin).

2 Binding was profoundly inhibited by wheat germ agglutinin.

3 rity to the secondary GlcNAc-binding site of wheat germ agglutinin.

4 carried out on a highly homologous protein, wheat germ agglutinin.

5 equired GTP hydrolysis, and was inhibited by wheat germ agglutinin.

6 that is unable to hydrolyze GTP and also by wheat germ agglutinin.

7 ontained the bulk of receptors that bound to wheat germ agglutinin.

8 lglucosamine-containing form, as detected by wheat germ agglutinin.

9 of glycoconjugates reacting with the lectin wheat germ agglutinin.

10 d in binding to the holdfast-specific lectin wheat germ agglutinin.

11 g with an anti-deacetylated PNAG antibody or wheat germ agglutinin.

12 and displayed reduced binding to the lectin wheat germ agglutinin.

13 was reversed by the nuclear pore inhibitor, wheat germ agglutinin.

14 not oriented as in the crystal structure of wheat germ agglutinin, a highly homologous protein ( app

15 EGFR isolated by wheat germ agglutinin affinity chromatography from nontr

16 ractionation, dye-ligand chromatography, and wheat germ agglutinin affinity chromatography.

17 tracted from brain membranes associated with wheat germ agglutinin-affinity columns, was [3H]galactos

18 ity purification steps on Ni-NTA agarose and wheat germ agglutinin agarose provided substantial enric

19 text of both the sugar and the lectin (here, wheat germ agglutinin and a single hevein domain) and ca

20 s demonstrated by blotting with succinylated wheat germ agglutinin and by probing with bovine milk be

21 ovascular endothelial cells was inhibited by wheat germ agglutinin and chitooligomers prepared from t

22 ents to NMC by using retrograde transport of wheat germ agglutinin and horseradish peroxidase (WGA-HR

23 Ecgp was partially purified by wheat germ agglutinin and Maackia amurensis lectin (MAL)

24 otting and were purified from bovine BMEC by wheat germ agglutinin and Maackia amurensis lectin (spec

25 both lectins as well as improved avidity for wheat germ agglutinin and phytohemagglutinin.

26 clear assembly by liposomes was inhibited by wheat germ agglutinin and thus required active nuclear t

27 s was temperature dependent and sensitive to wheat germ agglutinin and was blocked by a 20-fold exces

28 it was a glycoprotein in that it adhered to wheat germ agglutinin and was eluted with N-acetyl gluco

29 promotes the expression of the tracer, WGA (wheat germ agglutinin), and used these in combination wi

30 ia, peanut agglutinin, Ricinis communis, and wheat germ agglutinin, and by ATPase and ADPase enzymati

31 rs bind differentially to concanavalin A and wheat germ agglutinin, and lectin-affinity chromatograph

32 eiraea simplicifolia lectin II, succinylated wheat germ agglutinin, and peanut agglutinin were signif

33 ty with the chitin-binding domain of hevein, wheat germ agglutinin, and several class I chitinases.

34 nergy-dependent, was inhibited by the lectin wheat germ agglutinin, and showed an absolute requiremen

35 monoclonal antibodies 1218 (anti-alpha) and wheat germ agglutinin (anti-beta), the H+, K(+)-ATPase i

36 be inhibited by pretreating the nuclei with wheat germ agglutinin, anti-NPC antibodies, or antibodie

37 identified by combining a retrograde tracer (wheat-germ agglutinin apo-horseradish peroxidase colloid

38 Injection of the retrograde tracer wheat germ agglutinin-apo (inactivated) horseradish pero

39 trogradely labeled after focal injections of wheat germ agglutinin-apo (inactivated) horseradish pero

40 e thalamus with the retrograde axonal tracer wheat germ agglutinin-apo-HRP-gold.

41 We chose wheat germ agglutinin as a candidate lectin with clinica

42 Using the lectin wheat germ agglutinin as a probe, we show that the matri

43 nd to immobilized Concanavalin A (Con A) and wheat germ agglutinin, as well as to immobilized recombi

44 Dextran- and wheat-germ agglutinin-associated signals were correlated

45 domain is the site of glycosylation based on wheat germ agglutinin binding activity of polypeptides p

46 The lectin wheat germ agglutinin bound to the nucleus; however, it

47 emonstration that chitotriose-bound OmpA and wheat germ agglutinin-bound brain microvascular endothel

48 the VTA by combining retrograde transport of wheat germ agglutinin-bound gold after injections into t

49 ociation with the alpha2delta subunit during wheat germ agglutinin chromatography, repeat III by itse

50 Sequential use of wheat germ agglutinin chromatography, Sephacryl S300 gel

51 d membranes were solubilized and purified by wheat germ agglutinin chromatography.

52 Surface biotinylation followed by wheat germ agglutinin column chromatography and anti-CD4

53 grade transport after intranasal infusion of wheat germ agglutinin conjugated horseradish peroxidase

54 injections of biotinylated dextran amine and wheat germ agglutinin conjugated horseradish peroxidase

55 tion neurons (PN), retrogradely labeled with wheat germ agglutinin conjugated horseradish peroxidase

56 C57BL/6J) mice using the anterograde tracer, wheat germ agglutinin conjugated horseradish peroxidase.

57 projections were labeled with injections of wheat germ agglutinin conjugated to horseradish peroxida

58 rs biocytin, biotinylated dextran amine, and wheat germ agglutinin conjugated to horseradish peroxida

59 of several different fluorescent tracers and wheat germ agglutinin conjugated to horseradish peroxida

60 Injections of wheat germ agglutinin conjugated to horseradish peroxida

61 The retrograde tracer, wheat germ agglutinin conjugated to horseradish peroxida

62 Injections of wheat germ agglutinin conjugated to horseradish peroxida

63 After multiple injections of wheat germ agglutinin conjugated to horseradish peroxida

64 extran, fluorescent dextran, 3H-leucine, and wheat germ agglutinin conjugated to horseradish peroxida

65 d green fluorescent latex microspheres or of wheat germ agglutinin conjugated to horseradish peroxida

66 ction was further studied with injections of wheat germ agglutinin conjugated to horseradish peroxida

67 ted leucine, biotinylated dextran amine, and wheat germ agglutinin conjugated to horseradish peroxida

68 d spinal trigeminal nuclei were labeled with wheat germ agglutinin conjugated to horseradish peroxida

69 The retrograde tracer, wheat germ agglutinin conjugated to horseradish peroxida

70 orescent latex microspheres or injections of wheat germ agglutinin conjugated to horseradish peroxida

71 Injections of wheat germ agglutinin conjugated to horseradish peroxida

72 CS terminations were traced using wheat germ agglutinin conjugated to horseradish peroxida

73 injections of biotinylated dextran amine and wheat germ agglutinin conjugated to horseradish peroxida

74 e NRA-lumbosacral projection with the use of wheat germ agglutinin conjugated to horseradish peroxida

75 Tracers included wheat germ agglutinin conjugated to horseradish peroxida

76 body was investigated in adult cats by using wheat germ agglutinin conjugated to horseradish peroxida

77 dult cats using biotinylated dextran amines, wheat germ agglutinin conjugated to horseradish peroxida

78 in subunit beta (CTB), Fluoro-ruby (FR), and wheat germ agglutinin conjugated with horseradish peroxi

79 Injections of the retrograde pathway tracer wheat germ agglutinin conjugated with horseradish peroxi

80 ran linked to fluorescein or, alternatively, wheat-germ agglutinin conjugated to an Alexa fluor dye.

81 onodelphis domestica were investigated using wheat-germ agglutinin conjugated to horseradish peroxida

82 ement, we injected the bidirectional tracer, wheat germ agglutinin-conjugated horseradish peroxidase

83 retrogradely labeled following injections of wheat germ agglutinin-conjugated horseradish peroxidase

84 old: ventral Vi/Vc, or MDH) or peripherally (wheat germ agglutinin-conjugated horseradish peroxidase

85 Injections of wheat germ agglutinin-conjugated horseradish peroxidase

86 Unilateral intravitreal wheat germ agglutinin-conjugated horseradish peroxidase

87 modulin-dependent transport was inhibited by wheat germ agglutinin consistent with transport proceedi

88 However, wheat germ agglutinin-detectable N-acetyl-glucosamine (G

89 a glycan variant on MUC5AC using the lectin wheat-germ agglutinin discriminated mucin-producing cyst

90 ng nuclear pore formation with microinjected wheat germ agglutinin does not inhibit the nuclear local

91 Ac-containing glycoproteins using the lectin wheat germ agglutinin dramatically enriches for CTD110.6

92 A PTPase detected above 200 kDa in wheat germ agglutinin eluates from solubilized cells sug

93 Pretreatment with wheat germ agglutinin followed by etoposide treatment in

94 rneal ultrastructure and surface-labeling by wheat-germ agglutinin for TRPA1/TRPV1 knockout murine co

95 Wheat germ agglutinin fractionation of fluorescein 5-mal

96 naptic tracer, consisting of codon-optimized wheat germ agglutinin fused to mCherry, with single-cell

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

98 cate midbrain neurons projecting to the NRA, wheat germ agglutinin horseradish peroxidase (WGA-HRP) w

99 Wheat germ agglutinin-horseradish peroxidase (0.5-1.0 mu

100 t nodose ganglion with 3 microl of either 4% wheat germ agglutinin-horseradish peroxidase (to label s

101 e identified regions was determined by using wheat germ agglutinin-horseradish peroxidase (WGA-HRP) a

102 Injections of wheat germ agglutinin-horseradish peroxidase (WGA-HRP) a

103 Transport of wheat germ agglutinin-horseradish peroxidase (WGA-HRP) f

104 e labeled either by anterograde transport of wheat germ agglutinin-horseradish peroxidase (WGA-HRP) f

105 injected 18 weeks later with 3 microl of 4% wheat germ agglutinin-horseradish peroxidase (WGA-HRP) i

106 placed injections of fluorescent tracers and wheat germ agglutinin-horseradish peroxidase (WGA-HRP) i

107 bbit maxillary sinus were localized by using wheat germ agglutinin-horseradish peroxidase (WGA-HRP) o

108 neuronal transport of intraocularly injected wheat germ agglutinin-horseradish peroxidase (WGA-HRP) o

109 Injections of wheat germ agglutinin-horseradish peroxidase (WGA-HRP) p

110 To identify the NRA, wheat germ agglutinin-horseradish peroxidase (WGA-HRP) w

111 thesis, we have analyzed the distribution of wheat germ agglutinin-horseradish peroxidase (WGA-HRP)-l

112 ranch, and were injected with 3 microl of 8% wheat germ agglutinin-horseradish peroxidase in the left

113 adult owl monkeys by means of injections of wheat germ agglutinin-horseradish peroxidase into the ap

114 Injections of wheat germ agglutinin-horseradish peroxidase into the ce

115 They were double-labeled by placing wheat germ agglutinin-horseradish peroxidase into the le

116 were labeled via iontophoretic injections of wheat germ agglutinin-horseradish peroxidase into the LG

117 gastrointestinal tract, the authors injected wheat germ agglutinin-horseradish peroxidase into the no

118 sensory areas by making small injections of wheat germ agglutinin-horseradish peroxidase into the sp

119 imals received nodose ganglion injections of wheat germ agglutinin-horseradish peroxidase or dextran-

120 We, therefore, placed discrete injections of wheat germ agglutinin-horseradish peroxidase or fluoresc

121 ections of either of two retrograde tracers, wheat germ agglutinin-horseradish peroxidase or fluoresc

122 We used anterograde transport of wheat germ agglutinin-horseradish peroxidase to examine

123 animals were randomly assigned to afferent (wheat germ agglutinin-horseradish peroxidase) or efferen

124 ere labeled by nodose ganglion injections of wheat germ agglutinin-horseradish peroxidase, and a stan

125 stricted injections of fluorochrome tracers, wheat germ agglutinin-horseradish peroxidase, or biotiny

126 us injections of either tritiated proline or wheat germ agglutinin-horseradish peroxidase.

127 nsneuronally after intraocular injections of wheat germ agglutinin-horseradish peroxidase.

128 e conducted tract tracing experiments (using wheat-germ agglutinin-horseradish peroxidase (WGA-HRP),

129 Presynaptic K axons were labeled with wheat germ agglutinin-HRP, and presynaptic and postsynap

130 ic mice expressing the trans-synaptic tracer wheat germ agglutinin in LepRb neurons reveal the innerv

131 on of KCNN4c with the apical membrane marker wheat germ agglutinin in T84WT cells.

132 rt of a genetically expressed lectin tracer, wheat germ agglutinin, in Na(V)1.8-expressing nociceptor

133 ty with Griffonia simplicifolia lectin I and wheat germ agglutinin induced serum IgM Abs in mice that

134 luorescein, Lucifer Yellow or FluoroRuby, or wheat germ agglutinin) into discrete VA/VL, MD, and fron

135 Wheat germ agglutinin labeled vessels only after pretrea

136 Wheat germ agglutinin labels all olfactory axons uniform

137 The protein binds to concanavalin A and wheat germ agglutinin lectin affinity columns, and PNGas

138 b2 to endothelial ELK receptors recovered by wheat germ agglutinin lectin and immunoprecipitation.

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

140 ulfate-proteoglycan antibody reactivity, and wheat germ agglutinin lectin staining of the metanephros

141 ns like Griffonia simplicifolia lectin I and wheat germ agglutinin mediate the apoptosis of tumor cel

142 In comparison to protein-based (wheat germ agglutinin) membrane markers, new membrane pr

143 irE2-ssDNA complex import in the presence of wheat germ agglutinin or a nonhydrolyzable GTP analog, b

144 he import was ATP-dependent and inhibited by wheat germ agglutinin or by an antibody against p97, a c

145 horseradish peroxidase conjugated to either wheat germ agglutinin or cholera toxin subunit B reveale

146 lar AF-ALN colocalized with dextran (but not wheat germ agglutinin or transferrin), and uptake of AF-

147 Four lectins, wheat germ agglutinin, peanut lectin, concanavalin A, an

148 The levels of AMPK in succinylated wheat germ agglutinin precipitates correlated with hexos

149 ls, and addition of the nuclear pore blocker wheat germ agglutinin prevented nuclear import.

150 Intravascular staining with wheat germ agglutinin revealed diminished capillary area

151 binding peanut agglutinin (cone matrix) and wheat germ agglutinin (rod/cone matrix), was defined by

152 Wheat germ agglutinin-Sepharose affinity chromatography

153 zyme with neuraminidase prevented binding to wheat germ agglutinin-Sepharose, indicating the presence

154 nfocal microscopy with fluorescently labeled wheat germ agglutinin showed a paucity of PNAG in S. lug

155 overed that the carbohydrate-binding protein wheat germ agglutinin specifically stains colonies and t

156 te diameter and length were measured on FITC-wheat germ agglutinin-stained sections.

157 investigate these changes in myofiber size, wheat germ agglutinin staining and digital histopatholog

158 mma of infected myocytes evidenced by intact wheat germ agglutinin staining.

159 f free virus and that uptake was enhanced by wheat germ agglutinin, strongly suggesting that the enve

160 alent cation independent but is inhibited by wheat germ agglutinin, suggesting that the major recepto

161 The binding of wheat germ agglutinin to human tissue was determined to

162 Peripheral routes are blocked by wheat germ agglutinin to yield 2-fold lower permeability

163 ed with horseradish peroxidase conjugated to wheat-germ agglutinin were in asymmetric synaptic contac

164 pergillus oryzae lectin [AOL] and binding of wheat germ agglutinin) were assessed in paraffin-embedde

165 t distance between binding sites is ca. 9 A, wheat germ agglutinin (WGA) (shortest distance between b

166 ning method employing fluorophore-conjugated Wheat Germ Agglutinin (WGA) and a lipophilic blue fluoro

167 Further, coexpression of wheat germ agglutinin (WGA) and an axon-targeted beta-ga

168 PHA-L) or an adeno-associated virus encoding wheat germ agglutinin (WGA) and by immunoelectron micros

169 Here we use the lectin wheat germ agglutinin (WGA) as ligand; WGA inhibits nucl

170 Wheat germ agglutinin (WGA) binds to the glycosylated ex

171 Wheat germ agglutinin (WGA) binds with high affinity and

172 Wheat germ agglutinin (WGA) bound only to the outermost

173 Removal of residual PM by absorption on wheat germ agglutinin (WGA) did not deplete G alpha subu

174 ytic components accessible to HRP-conjugated wheat germ agglutinin (WGA) disrupted delivery of HA but

175 rum against purified cyst walls (PCWs) or to wheat germ agglutinin (WGA) inhibited excystation by > 9

176 DEAE Sephacel column chromatography and by a wheat germ agglutinin (WGA) lectin affinity column.

177 Wheat germ agglutinin (WGA) reactive glycans on fibronec

178 Wheat germ agglutinin (WGA) showed significantly decreas

179 Further, abnormal phalloidin and wheat germ agglutinin (WGA) staining of Tdrd7-/- fiber c

180 ally targeted the transneuronal tract tracer wheat germ agglutinin (WGA) to nonpeptidergic nociceptiv

181 of the binding of concanavalin A (ConA) and wheat germ agglutinin (WGA) to their target monosacchari

182 broad antibody-like reagent against mycosis, wheat germ agglutinin (WGA) was linked to the effector F

183 ly applicable segmentation protocol based on wheat germ agglutinin (WGA), a lectin that binds to N-ac

184 multivalent interactions (K(D) ~ 40 nM) with wheat germ agglutinin (WGA), a model lectin that exhibit

185 rgeted expression of a transneuronal tracer, wheat germ agglutinin (WGA), in the 5HT neurons so as to

186 which expression of a transneuronal tracer, wheat germ agglutinin (WGA), is induced in primary senso

187 cific to glycophorin A, and the more general wheat germ agglutinin (WGA), were selected to label REVs

188 ermined using a Texas Red-conjugated lectin, wheat germ agglutinin (WGA), which binds SA residues.

189 ity HPLC column charged by Co2+, followed by wheat germ agglutinin (WGA)-affinity HPLC or size-exclus

190 The retrograde tracer wheat germ agglutinin (WGA)-apoHRP-gold was used to iden

191 and-binding assay was developed by employing wheat germ agglutinin (WGA)-coated Flashplates.

192 By using wheat germ agglutinin (WGA)-coated scintillation proximi

193 esponded to an approximately 50% decrease in wheat germ agglutinin (WGA)-labeled components of the GC

194 ntisera and loses reactivity with the lectin wheat germ agglutinin (WGA).

195 ns concanavalin A (ConA), jacalin (JAC), and wheat germ agglutinin (WGA).

196 is lectin (MAL), concanavalin A (Con A), and wheat germ agglutinin (WGA).

197 serum sample by carbohydrate affinity using wheat germ agglutinin (WGA).

198 some reaction (AR), is blocked by the lectin wheat germ agglutinin (WGA).

199 bination initiates expression of the lectin, wheat germ agglutinin (WGA).

200 (N)/A to an alternative cell-binding ligand, wheat germ agglutinin (WGA).

201 port of horseradish peroxidase conjugated to wheat germ agglutinin (WGA-HRP) with biotinylated dextra

202 (HRP) fused to the glycan-binding domain of wheat germ agglutinin (WGA-HRP).

203 interneurons and the transganglionic tracer wheat germ agglutinin which, after sciatic nerve injecti

204 nuclear uptake of GFP-ERK2 was inhibited by wheat germ agglutinin, which blocks nuclear entry by bin

205 und that AMPK was recognized by succinylated wheat germ agglutinin, which specifically binds O-GlcNAc