ライフサイエンスコーパス: wheat germ

1 extracts from S. cerevisiae, N. crassa, and wheat germ.

2 f the dorsal horn, using nerve injections of wheat germ agglutin-horseradish peroxidase for transgang

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

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

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

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

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

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

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

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

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

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

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

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

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

16 Wheat germ agglutinin (WGA) reactive glycans on fibronec

17 Wheat germ agglutinin (WGA) showed significantly decreas

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

36 EGFR isolated by wheat germ agglutinin affinity chromatography from nontr

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

63 Tracers included wheat germ agglutinin conjugated to horseradish peroxida

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

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

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

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

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

69 Injections of wheat germ agglutinin conjugated to horseradish peroxida

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

71 Injections of wheat germ agglutinin conjugated to horseradish peroxida

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

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

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

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

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

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

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

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

80 Injections of wheat germ agglutinin conjugated to horseradish peroxida

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

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

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

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

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

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

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

88 Pretreatment with wheat germ agglutinin followed by etoposide treatment in

89 Wheat germ agglutinin fractionation of fluorescein 5-mal

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

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

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

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

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

95 Wheat germ agglutinin labeled vessels only after pretrea

96 Wheat germ agglutinin labels all olfactory axons uniform

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

138 Injections of wheat germ agglutinin-conjugated horseradish peroxidase

139 Unilateral intravitreal wheat germ agglutinin-conjugated horseradish peroxidase

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

174 Wheat germ agglutinin-Sepharose affinity chromatography

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

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

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

178 Binding was profoundly inhibited by wheat germ agglutinin.

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

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

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

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

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

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

185 of glycoconjugates reacting with the lectin wheat germ agglutinin.

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

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

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

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

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

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

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

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

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

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

196 In wheat germ and mouse ascites Krebs-2 in vitro translatio

197 been depleted of endogenous hsp70, purified wheat germ and mouse hsp70's are equally active in promo

198 wo other plant viruses as well as tRNAs from wheat germ and yeast were similarly active in the BMV vi

199 ately 10 mg of the pure protein from 4 kg of wheat-germ), and improved characteristics of stability a

200 operties of this enzyme, we used a cell-free wheat germ-based expression system in which mRNA encodin

201 nner membrane protein into liposomes using a wheat germ-based in vitro translation system.

202 nts to identify the structural properties of wheat germ calmodulin (CaM) bound to either the plasma m

203 Oxidation of either Met(145) or Met(146) in wheat germ calmodulin (CaM) to methionine sulfoxide prev

204 ative modification of methionine residues in wheat germ calmodulin (CaM), and prevent activation of t

205 However, phosphorylation at Tyr139 of wheat germ calmodulin had essentially no effect on its i

206 The concentrations of [F138]calmodulin and wheat germ calmodulin required for half-maximal activati

207 tant containing tyrosine at position 99, and wheat germ calmodulin which has tyrosine at position 139

208 e upon addition of fesselin to MIANS-labeled wheat germ calmodulin.

209 itions of oxidative stress, we have examined wheat germ CaM for the presence of highly reactive sites

210 trotyrosine139 in calcium binding loop IV on wheat germ CaM indicate that the average spatial separat

211 25, Pfs230, and PfHAP2 were expressed in the wheat germ cell-free expression system.

212 Here we describe a wheat germ cell-free platform for protein production tha

213 falciparum proteins prepared using the wheat germ cell-free system (WGCFS).

214 levels in animal myocytes, E. coli, and the wheat germ cell-free system than Mbs from terrestrial ma

215 falciparum topoisomerase II (PfTopoII) in a wheat germ cell-free transcription-translation system.

216 es in nuclear extracts prepared from pea and wheat germ, consistent with the hypothesis that the Arab

217 Second, antibodies raised against wheat germ cytosolic Hsp70 and Escherichia coli Hsp90 in

218 ants (Kd) for the binding of various RNAs by wheat germ EF-1alpha.GTP.

219 bably because of the low binding affinity of wheat germ eIF4A for mRNA.

220 The RNA duplex unwinding activity of wheat germ eIF4A is similar to other mammalian systems;

221 The kinetic effects of eIF4B, PABP, and wheat germ eIFiso4F with two mRNA cap analogues and the

222 The wheat germ eukaryotic translation initiation factor (eIF

223 degree of homology to the p82 subunit of the wheat germ eukaryotic translation initiation factor eIF-

224 ction between VPg of turnip mosaic virus and wheat germ eukaryotic translation initiation factors eIF

225 Dramatic results were obtained in wheat germ extract (WGE) that has no endogenous Ric-8 co

226 n either rabbit reticulocyte lysate (RRL) or wheat germ extract (WGE).

227 cate in oat protoplasts, indicating that the wheat germ extract accurately reflected control of BYDV

228 s strong cap-independent translation in both wheat germ extract and oat protoplasts through a novel,

229 xhibits translational inhibition in both the wheat germ extract and rabbit reticulocyte lysate system

230 We find that standard wheat germ extract contains Dicer-like enzymes that conv

231 We show that addition of VPg to wheat germ extract leads to enhancement of uncapped vira

232 unidentified proteins or small molecules in wheat germ extract prevented eIF4F binding to mutant BTE

233 d robust blocks to both Escherichia coli and wheat germ extract translation systems, whereas N2-methy

234 functional shifty site for frameshifting in wheat germ extract, while the stop codon was not require

235 Here, we report on an efficient wheat germ extract-based in vitro transcription/translat

236 , we developed an in vitro transcription and wheat germ extract-based translation assay to examine qu

237 f virion RNA to be translated in a cell-free wheat germ extract.

238 olfactory receptor 17-4 (hOR17-4) using the wheat germ extract.

239 , and the resulting mRNAs were translated in wheat germ extracts and radiolabeled with either [35S]me

240 for this programmed readthrough in vitro in wheat germ extracts and reticulocyte lysates and in vivo

241 ems containing rabbit reticulocyte lysate or wheat germ extracts assembles into HCV capsids.

242 In vitro experiments using wheat germ extracts confirmed that DCP5 is a translation

243 RegA69-His6 synthesized in E. coli S30 or wheat germ extracts displayed RNA-binding properties sim

244 ed in the presence of rabbit reticulocyte or wheat germ extracts in an ATP-dependent process.

245 The apparent formation of polysomes in wheat germ extracts suggests that subsequent uncoating i

246 In wheat germ extracts, coat protein synthesis was constant

247 is recovered by immuno-depletion of PKI from wheat germ fractions.

248 oxisomal proteins were immunoprecipitated by wheat germ Hsp70 antibodies.

249 identify their enzymatic properties using a wheat germ in vitro translation (IVT, also known as cell

250 d alfalfa mosaic virus (AMV) 4, were used in wheat germ in vitro translation assays to measure their

251 The discrimination against wheat germ initiator Met-tRNAMet was almost entirely due

252 fashion in both yeast two-hybrid assays and wheat germ interaction assays.

253 or aspartate transcarbamoylase (ATCase) from wheat-germ is reported, with an eightfold increase in sc

254 In previous studies, this wheat germ kinase was shown to phosphorylate eIF2alpha,

255 Sequential DEAE, wheat germ lectin affinity, and hydroxyapatite chromatog

256 KBP to plant hsp90 is prevented by adding to wheat germ lysate a purified fragment containing the TPR

257 Here, we ask if wheat germ lysate also contains immunophilins of the FK5

258 the JJ3 antibody to protein A-Sepharose, to wheat germ lysate and allow ATP-dependent formation of a

259 tent inhibitor of PAP depurination of RNA in wheat germ lysate and competes with structured RNA deriv

260 The hsp90/hsp70-based chaperone system of wheat germ lysate assembles complexes between mouse GR a

261 Wheat germ lysate contains a similar protein folding act

262 tion of known Sec incorporation factors in a wheat germ lysate does not permit multiple Sec incorpora

263 ibits the translation of multiple mRNAs in a wheat germ lysate, suggesting that Prbp acts to repress

264 o contain endogenous PKR but was not seen in wheat germ lysate, which is not responsive to a known ac

265 sembly system and human p23 functions in the wheat germ lysate.

266 co mosaic virus preferentially uses eIF4G in wheat germ lysate.

267 nding of high risk HPV E6 proteins to PKN in wheat-germ lysate in vitro and in 293T cells in vivo.

268 ls) and insect (Sf9) cells and also a plant (wheat germ) lysate fold the immunopurified glucocorticoi

269 ome mosaic virus RNA in vitro translation in wheat germ lysates by the addition of double-stranded RN

270 o under physiological buffer conditions with wheat germ methionyl-tRNA synthetase, required mutation

271 ly marine invertebrates ( approximately 1%); wheat germ or bran ( approximately 1%); and spinach ( ap

272 shown to occur in the presence of endogenous wheat germ or rabbit reticulocyte NAC.

273 Recent studies demonstrated that wheat germ poly(A)-binding protein (PABP) interacted wit

274 A previously described wheat germ protein kinase was identified unambiguously a

275 Previous kinetic binding studies of wheat germ protein synthesis eukaryotic initiation facto

276 Previous kinetic binding studies of wheat germ protein synthesis eukaryotic translational in

277 ng the mechanism of helicase activity in the wheat germ protein synthesis system, we have utilized di

278 quantitatively assessed using higher plant (wheat germ) proteins: aminoacylation, EF-1alpha*GTP bind

279 an in vitro translation lysate derived from wheat germ repressed translation, which was subsequently

280 Interestingly, we found that mammalian and wheat germ ribosomes differentially regulate the signal-

281 e discovered that when Pgp was translated by wheat germ ribosomes in vitro, TM3 could not reinitiate

282 ents of Pgp and that rabbit reticulocyte and wheat germ ribosomes may use different mechanisms to con

283 ncharged tRNA and initiator Met-tRNAMet from wheat germ, RNAs that are normally excluded from the rib

284 n of mRNA produced from this clone in both a wheat germ system and Xenopus oocytes showed expression

285 nction was analyzed in Neurospora crassa and wheat germ translation extracts using the transfer of na

286 d GroEL substrate rhodanese in bacterial and wheat germ translation extracts.

287 Trimer assembly was stimulated when wheat germ translation mixtures defective in supporting

288 abeled ppalphaF6H was affinity purified from wheat germ translation reactions (or Escherichia coli) t