ライフサイエンスコーパス: glutathione S-transferase

1 heat-induced amorphous aggregation of human glutathione S-transferase.

2 e formation of thioether products similar to glutathione S-transferase.

3 modium falciparum antigen EXP1 is a membrane glutathione S-transferase.

4 2 dynamic range for detecting target antigen glutathione-S-transferase.

5 (SWA), tegument allergen-like 1, and 28-kDa glutathione-S-transferase.

6 transport and detoxification, in particular glutathione S-transferases.

7 oxidant enzymes (lactoperoxidase, microsomal glutathione S-transferase 2 and 3, glutathione S-transfe

8 gh polyunsaturated fat liquid diet to female glutathione-S-transferase 4-4 (Gsta4(-/-))/peroxisome pr

9 hod for lipid aldehyde detoxification is via glutathione S-transferase A4 (GSTA4) dependent glutathio

10 murine adipose tissue and is metabolized by glutathione S-transferase A4 (GSTA4), producing glutathi

11 f antioxidant genes such as cytochrome b561, glutathione s-transferase a4 and protein kinase C-epsilo

12 TDC WB can specifically detect the extrinsic glutathione-S-transferase added in the Escherichia coli

13 Using glutathione-S-transferase affinity chromatography, AgmU

14 stigate the cross-reactivity between a major glutathione-S transferase allergen of cockroach (Bla g 5

15 Glutathione S-transferase alpha 4 (GSTA4) is a phase II

16 target genes, such as lipoprotein lipase and glutathione S-transferase alpha-2, which are implicated

17 tion enzymes, such as lipoprotein lipase and glutathione S-transferase alpha-2.

18 eine ligase catalytic and modifier subunits, glutathione S-transferases Alpha-1 and Mu-1, haem oxygen

19 ular enzymes fructose-1,6-bisphosphatase and glutathione-S-transferase-alpha Additionally, we quantif

20 n of urinary fructose-1,6-bisphosphatase and glutathione-S-transferase-alpha release exclusively with

21 Silencing glutathione S-transferase alpha4, a scavenger of 4-HNE,

22 ose and up-regulated the gene expressions of glutathione S-transferase and antioxidant enzymes.

23 astic foci in the liver (increased placental glutathione S-transferase and cytokeratin 8-18 activity;

24 de dismutase, but minimal inhibition against glutathione S-transferase and glutathione peroxidase.

25 vity of recombinant human K(ATP) channels or glutathione S-transferase and NBD2 fusion proteins conta

26 in vitro (purified GST-PH-PLD2, where GST is glutathione S-transferase and PH is pleckstrin homology)

27 These data demonstrate that helminth glutathione-S transferase and the aeroallergen Bla g 5 s

28 ts, alteration in reduced glutathione level, glutathione-s-transferase and catalase activity, malondi

29 Six fusion proteins made up of glutathione-S-transferase and each of the Bcl-2 members

30 Cell lysates were prepared and reacted with glutathione-S-transferase and the fluorescent labeling c

31 y between tagged versions of glutathione and glutathione S-transferase, and via the determination of

32 uch as genes coding for heat shock proteins, glutathione S-transferases, and peroxidases.

33 50 monooxygenases, carboxyl/cholinesterases, glutathione-S-transferases, and ATP-binding cassette tra

34 roups of proteins (i.e. heat shock proteins, glutathione-S-transferases, and carbohydrate metabolic p

35 ely damaged biomolecules, i.e., haptoglobin, glutathione-S-transferases, and possibly manganese super

36 tones, tubulin, and lumican and (ii) reduced glutathione S-transferase, annexin, and dermatopontin, a

37 450 monooxygenase, glycosyl transferase, and glutathione S-transferase are often implicated in herbic

38 Using oxidized glutathione S-transferase as a model substrate, we showe

39 immunosorbent assay, using JCV-VP1 fused to glutathione S-transferase as antigen.

40 encoding cytochrome P450 monooxygenases and glutathione S-transferases associated with detoxificatio

41 Here, we report that a glutathione S-transferase chimera bearing the cytoplasmi

42 In CHO-IR cell lysates, a glutathione S-transferase chimera of the cargo-binding C

43 atorial libraries with two isozymes from the glutathione S-transferase class of enzyme, and observed

44 hepatic catalase, glutathione peroxidase and glutathione S transferase compared with the control, and

45 KN1C blocks their ability to phosphorylate a glutathione S-transferase-CTD fusion protein in vitro.

46 whereas those with various polymorphisms in glutathione S-transferase demonstrated increased perform

47 NKCC1), and the N terminus of NKCC1 fused to glutathione S-transferase demonstrated that PP1 dephosph

48 omonas putida CBB5 utilizes an unprecedented glutathione-S-transferase-dependent Rieske oxygenase for

49 For example, glutathione S-transferases detoxify polycyclic aromatic

50 Fusion of Ubc4' with the more stable glutathione-S-transferase domain demonstrates that QSOX

51 regulated genes related to diapause included glutathiones-S-transferase et al., and down-regulated ge

52 glutathione binding site architecture of the glutathione S-transferase family.

53 CALI ([FP]-CALI), the activities of purified glutathione-S-transferase-FP (GST-EXFP) fusions were mea

54 In vitro studies using glutathione S-transferase fused to the delta subunit int

55 Association of the PDHK2 and GST-L2 (glutathione-S-transferase fused to the inner lipoyl doma

56 In this study, we used glutathione S-transferase-fused Eps15 (GST-Eps15) fusion

57 f this study was to determine the effects of glutathione-S-transferase-fused recombinant biglycan (GS

58 cDNA was expressed in Escherichia coli as a glutathione S-transferase fusion protein and was purifie

59 experiments with rat brain extracts using a glutathione S-transferase fusion protein encompassing am

60 ta(2)-AR physically interacted with Rab8 and glutathione S-transferase fusion protein pulldown assays

61 Importantly, coimmunoprecipitation and glutathione S-transferase fusion protein pulldown experi

62 in vitro ((32)P-phosphorylation assays with glutathione S-transferase fusion proteins) experiments t

63 coexpressed in COS-7 cells or using purified glutathione S-transferase fusion proteins.

64 Glutathione S-transferase fusion pulldown and receptor m

65 Furthermore, a novel glutathione-S-transferase fusion protein (MMP-9-PEX), wh

66 Glutathione-S-transferase fusion proteins containing two

67 Glutathione-S-transferase fusion proteins containing wil

68 Polymorphisms in the glutathione S-transferase gene are a potential genetic c

69 ntrol of a pathogen-inducible promoter, from glutathione S-transferase gene from potato.

70 omologous gene GPXH/GPX5 and the sigma-class glutathione-S-transferase gene GSTS1.

71 sive genes, including heat shock protein and glutathione S-transferase genes, whose expression is fur

72 ese associations are modified by variants in Glutathione S-Transferase genes.

73 Glutathione S-transferase (GST) affinity pulldowns also

74 e actions were related to the stimulation of glutathione S-transferase (GST) and superoxide dismutase

75 he activities of superoxide dismutase (SOD), glutathione S-transferase (GST) and total glutathione pe

76 inhibitor mode of action was evaluated using glutathione S-transferase (GST) as a model enzyme that u

77 al genotoxicity occurs predominantly through glutathione S-transferase (GST) conjugation and bioactiv

78 esection for stage I NSCLC were subjected to glutathione S-transferase (GST) E-cadherin pulldown and

79 leyl pyruvate isomerase (MPI) is a bacterial glutathione S-transferase (GST) from the pathway for deg

80 ressed and purified from Escherichia coli as glutathione S-transferase (GST) fused to the CNGA3 C-ter

81 lly phosphorylated a full-length SAP97 and a glutathione S-transferase (GST) fusion protein containin

82 signated CR1 and CR2, were used to construct glutathione S-transferase (GST) fusion proteins (GST-CR1

83 he interaction in vitro, we incubated Ptp52F-glutathione S-transferase (GST) fusion proteins with per

84 Using a multivariate test statistic, a glutathione S-transferase (GST) gene was found to be ass

85 Glutathione S-transferase (GST) genes as well as heme ox

86 Considering that glutathione S-transferase (GST) is a broadly employed en

87 nce of SLBP (amino acids 51 to 108) fused to glutathione S-transferase (GST) is sufficient to mimic S

88 ue and/or species availability of functional glutathione S-transferase (GST) metabolic activity, the

89 Y was identified as a member of the glutathione S-transferase (GST) protein family and Z fou

90 as confirmed by co-immunoprecipitation and a glutathione S-transferase (GST) pull-down assay.

91 Using glutathione S-transferase (GST) pull-down assays, we fou

92 on as determined by mammalian two-hybrid and glutathione S-transferase (GST) pull-down assays.

93 noprecipitation experiments, as well as with glutathione S-transferase (GST) pull-down experiments.

94 Glutathione S-transferase (GST) pulldown assays demonstr

95 Coimmunoprecipitation/mass spectrometry and glutathione S-transferase (GST) pulldown assays identifi

96 Coimmunoprecipitation and glutathione S-transferase (GST) pulldown assays revealed

97 lying mechanism of this differential effect, glutathione S-transferase (GST) pulldown assays were per

98 ls, yeast two-hybrid interaction assays, and glutathione S-transferase (GST) pulldown assays, we show

99 n through coimmunoprecipitation and in vitro glutathione S-transferase (GST) pulldown assays.

100 By using glutathione S-transferase (GST) pulldowns, we identified

101 In particular, enzymes in the glutathione S-transferase (GST) superfamily function in

102 In these studies, we explore the use of the glutathione s-transferase (GST) to anchor the bactericid

103 MBP) fusions, MBP::NaPCCP or MBP::NaSBP1 and glutathione S-transferase (GST), GST::AGP CTD fusions.

104 x), small ubiquitin-related modifier (Sumo), glutathione S-transferase (GST), maltose-binding protein

105 In this study, we utilized glutathione S-transferase (GST)- and green fluorescent p

106 m or preincubating mammalian host cells with glutathione S-transferase (GST)-Asp14 significantly inhi

107 Purified PLCbeta3 bound directly to glutathione S-transferase (GST)-fused M3R intracellular

108 As expected, GP binding to glutathione S-transferase (GST)-G(L)tr was reduced, wher

109 ubunit of MLCP, at Thr-696 and Thr-853 using glutathione S-transferase (GST)-MYPT1 fragments having t

110 Active PKBalpha phosphorylated in vitro a glutathione S-transferase (GST)-NHE1 fusion protein comp

111 Binding of NoV VLPs, P particles, and glutathione S-transferase (GST)-P domain fusion proteins

112 lyzed the in vitro methylation products of a glutathione S-transferase (GST)-PRMT7 fusion protein wit

113 Glutathione S-transferase (GST)-RP2 pulled down Gbeta fr

114 Bacterially expressed glutathione S-transferase (GST)-Smads 1, 5 or 8, but not

115 a strain of Synechocystis 6803 expressing a glutathione S-transferase (GST)-tagged derivative (FtsH2

116 Glutathione S-transferase (GST)-tagged versions of OmpA

117 bstrates and the impassable reporter protein glutathione S-transferase (GST).

118 d the redox homeostasis, and the activity of glutathione S-transferase (GST).

119 phosphorylation, and rhythmic translation of glutathione S-transferase (GST-3) from constitutive mRNA

120 ins of the hepatitis C virus E2 protein with glutathione S-transferase (GST-E2) or FLAG peptide (FLAG

121 Glutathione S-transferases (GST) were evaluated as bioma

122 CLICs resemble the omega class of Glutathione S-transferases (GST), yet differ from them i

123 eroxidase (GPx), glutathione reductase (GR), Glutathione-S-Transferase (GST) activities, and reduced

124 superoxide dismutase (SOD), catalase (CAT), glutathione-s-transferase (GST) and non-enzymatic antiox

125 a proof of concept, a reversible label-free glutathione-S-transferase (GST) biosensor is demonstrate

126 easures the nucleotide binding properties of glutathione-S-transferase (GST) chimeras for prototypica

127 nique trimer of subunits each containing two glutathione-S-transferase (GST) domains.

128 (ELR) that can bind different members of the glutathione-S-transferase (GST) enzyme family.

129 Here, we report on activities of bacterial glutathione-S-transferase (GST) enzymes that cleave beta

130 gs by modifying carbon paste electrodes with glutathione-s-transferase (GST) enzymes.

131 Hlike-1 were isolated, and when expressed as glutathione-S-transferase (GST) fusion proteins, were ca

132 Our use of the common dimeric glutathione-S-transferase (GST) fusion tag allowed two C

133 Glutathione-S-transferase (GST) is known to protect endo

134 have determined that Nrf2 and members of the glutathione-S-transferase (GST) mu family are extensivel

135 detecting 90-6000 ng of purified recombinant glutathione-S-transferase (GST) proteins and could parti

136 Reciprocal glutathione-S-transferase (GST) pulldown experiments usi

137 s of ethoxyresorufin-O-deethylase (EROD) and glutathione-S-transferase (GST), and (ii) the metabolic

138 ion of insecticide and fungus, activities of glutathione-S-transferase (GST), general esterases (ESTs

139 stressors on biomarkers of oxidative stress (glutathione-S-transferase (GST), superoxide dismutase (S

140 trigger (in vitro) the catalytic activity of glutathione-s-transferase (GST), which is not its natura

141 echanism involving the catalytic activity of glutathione-S-transferase (GST).

142 ex composed of NdmC, NdmD, and NdmE, a novel glutathione-S-transferase (GST).

143 The two proteins (a 50-kDa Fab and a 60-kDa glutathione S-transferase [GST] antigen) form a relative

144 s using different purification tags (biotin, glutathione S-transferase [GST], and His) placed at eith

145 rthermore, we found that the expression of a glutathione S-transferase, GstD1, which utilizes GSH in

146 e P450s AfCYP6Z1, AfCYP6Z3, AfCYP6M7 and the glutathione-s-transferase GSTe2 with respective fold cha

147 of alpha-ketoglutarate dehydrogenase and the glutathione S-transferases GSTF2, GSTF8, GSTF10 and GSTF

148 deletion polymorphism in the M1 gene loci of glutathione S-transferase (GSTM1-null) in addition to ta

149 The glutathione S-transferase GSTP is overexpressed in many

150 he analysis of progression of the persistent glutathione S-transferase (GSTP)(+) focal lesions to ful

151 nthin and meso-zeaxanthin, the pi isoform of glutathione S-transferase (GSTP1), only human and monkey

152 Biotransformation enzymes such as Glutathione S-Transferases (GSTs ) detoxify mutagenic an

153 Glutathione S-transferases (GSTs) are a superfamily of e

154 Hookworm glutathione S-transferases (GSTs) are critical for paras

155 Glutathione S-transferases (GSTs) are involved in the me

156 Although glutathione S-transferases (GSTs) are thought to play ma

157 Glutathione S-transferases (GSTs) are ubiquitous enzymes

158 Glutathione S-transferases (GSTs) comprise a diverse fam

159 Glutathione S-transferases (GSTs) detoxify environmental

160 Glutathione S-transferases (GSTs) form a superfamily of

161 Moreover, the roles of glutathione S-transferases (GSTs) in the glutathione con

162 ether cross-reactivity or cosensitization to glutathione S-transferases (GSTs) occurs in tropical and

163 asured by the activity of monooxygenases and glutathione S-transferases (GSTs) was detected in popula

164 nked to increased expression and activity of glutathione S-transferases (GSTs).

165 is reveals sequence similarities of GDAP1 to glutathione S-transferases (GSTs).

166 Glutathione S-transferases (GSTs: EC2.5.1.18) are a supe

167 curonosyltransferase (AAEL014279-RA) and the glutathione-S transferases GSTS1 and GSTT3.

168 ylation and demonstrate a role for the yeast glutathione S-transferase Gtt1p in glutathionylation.

169 rette smoke and is the most highly expressed glutathione S-transferase in lung tissue.

170 s and with the cytosolic tail of gD fused to glutathione S-transferase in rabbit reticulocyte lysates

171 nes that were different are cytochrome P450, glutathione S-transferase, Indian hedgehog, and solute c

172 g glutathione reductases, glutaredoxins, and glutathione S-transferases, indicated a key role for asc

173 for the prediction of interhelical angles in glutathione S-transferase, intracellular chloride channe

174 onfirmation of the expression array results: Glutathione S-transferase isoform mu1 (GSTM1) and mu5 (G

175 urally similar glutathione transferase (GST, glutathione S-transferase) isoforms with high specificit

176 ng purified Gga2p VHS-GGA and TOM1 (GAT) and glutathione S-transferase-Kex2p C-tail fusions show that

177 gnostic accuracy of the perfusate biomarkers glutathione S-transferase, lactate dehydrogenase (LDH),

178 gnostic accuracy of the perfusate biomarkers glutathione S-transferase, LDH, heart-type fatty acid bi

179 nd to correlate with the conformation of the glutathione S-transferase ligands glutathione, s-hexylgl

180 Glutathione S-transferase M1 (GSTM1) is a multifunctiona

181 Glutathione S-transferase M1 (GSTM1) is a phase II enzym

182 scordant angiotensin I-converting enzyme and glutathione S-transferase M1 alleles.

183 The glutathione S-transferase M1-null phenotype has been lin

184 , and RNA interference knockdown to identify glutathione S-transferase M4 (GSTM4) as a critical EWS/F

185 We produced a glutathione S-transferase-mA3 fusion protein in insect c

186 e Httex1 is fused to large proteins, such as glutathione S-transferase, maltose-binding protein, or t

187 tivation was artificially maintained through glutathione S-transferase-mediated dimerization, there w

188 dneys from naive Mrp2-null mice had elevated glutathione S-transferase mRNA levels, which could incre

189 Glutathione S-transferase mu 1 (GSTM1) encodes an enzyme

190 ion of NAD(P)H dehydrogenase, quinone 1, and glutathione S-transferase Mu 1 was increased, indicating

191 Glutathione-S-transferase mu 1 (GSTM1) gene polymorphism

192 rotein L-1 (APOL1) high-risk alleles and the glutathione-S-transferase-mu1 (GSTM1) null allele have b

193 rase allergen of cockroach (Bla g 5) and the glutathione-S transferase of Wuchereria bancrofti (WbGST

194 Glutathione S-transferase omega 1 (GSTO1) is an atypical

195 rostate stem cell antigen, DnaJC, member 15, glutathione S-transferase omega-1, and thymidine kinase

196 wild-type E-cadherin or E-cadherin fused to glutathione S-transferase or green fluorescent protein w

197 of proteins, including cytochrome P450 2A6, glutathione S transferase P, and alcohol dehydrogenases

198 iR-29B1, and elevated levels of antioxidants glutathione S-transferase P (GSTP) and superoxide dismut

199 the hypothesis that removal of aldehydes by glutathione S-transferase P (GSTP) diminishes I/R injury

200 ade in determining the in vivo regulation of glutathione S-transferase P (GSTP), particularly the hum

201 usion were delayed in hearts of mice lacking glutathione S-transferase P (GSTP).

202 NAD(P)H dehydrogenase (quinone 1) (NQO1) and glutathione S-transferase P (GSTP).

203 o-way gene-air pollution interaction between glutathione S-transferase P (GSTP1) and PM10 on the risk

204 Catalysis of both the forward (glutathione S-transferase P) and reverse (glutaredoxin)

205 (who may also have polymorphic expression of glutathione S-transferase P) exposed to agents that caus

206 ticulin, protein disulfide-isomerase A3, and glutathione-S-transferase P.

207 for the detection of hypermethylation of the glutathione S-transferase P1 (GSTP1) gene, a specific ma

208 Glutathione S-transferase P1 (GSTP1) is of importance fo

209 Under normal physiologic conditions, the glutathione S-transferase P1 (GSTP1) protein exists intr

210 ously demonstrated by using tumor cells that glutathione S-transferase P1 (GSTP1) sequesters NO as di

211 =77, P-value=0.0001), similar to the rate of glutathione S-transferase P1 (GSTP1) silencing.

212 Elevated glutathione S-transferase P1 (GSTP1), a major drug-metab

213 by glutathione in a reaction accelerated by glutathione S-transferase P1 (GSTP1), an enzyme frequent

214 gulation of the phase II detoxifying enzyme, glutathione S-transferase P1 (GSTP1).

215 The glutathione S-transferase P1 Ile105Val polymorphism has

216 The glutathione S-transferase P1 Ile105Val polymorphism mark

217 t the regulation of allergic inflammation by glutathione S-transferase P1 in human asthmatics.

218 Glutathione S-transferase P1 is a Phase II cytoprotectiv

219 nistic explanation for regulatory effects of glutathione S-transferase P1 polymorphism on airway path

220 )/Val(105) compared with asthmatics with the glutathione S-transferase P1 Val(105)/Ile(105) and Ile(1

221 Asthmatics with glutathione S-transferase P1 Val(105)/Val(105) compared

222 h model thiols, as well as the model protein glutathione S-transferase P1, in vitro.

223 Recently, glutathione S-transferase P1-1 (GST P1-1) was shown to b

224 Phase 1 testing of ezatiostat, a glutathione S-transferase P1-1 inhibitor, for the treatm

225 ated with NO-aspirin 2 showed an increase in glutathione S-transferase-P1 (GST-P1), glutamate-cystein

226 Using glutathione S-transferase-PABP pull-down and proteomic a

227 antioxidant metabolites and upregulation of glutathione S-transferase pathway genes, including Gstp1

228 icrosomal glutathione S-transferase 2 and 3, glutathione S-transferase peroxidase kappa 1, and glutat

229 y induced associations of Fas with ERp57 and glutathione S-transferase pi (GSTP), a protein disulfide

230 Glutathione S-transferase pi (GSTP1) detoxifies polycycl

231 egions of two prostate cancer-related genes: glutathione S-transferase pi (GSTPi) and retinoic acid r

232 Glutathione S-transferase pi 1 (GSTP1) is frequently ove

233 s of six markers (p53, thymidylate synthase, glutathione s-transferase pi [GST-pi], Bcl 2, beta tubul

234 the first time, suggested that the levels of glutathione S-transferase Pi may play an important role

235 sexually dimorphic cytochrome P 450 Cyp2d9, glutathione S-transferase pi, Cyp2a, Cyp2b, and Cyp3a ge

236 One of the confirmed proteins, glutathione S-transferase Pi, was further investigated i

237 was mechanistically linked to alterations in glutathione S-transferase-pi expression and function.

238 Glutathione S-transferases play an important role in cel

239 S-transferase pull downs were performed, and glutathione S-transferase-PLCgamma1 showed binding of Gr

240 response genes, such as cytochrome P-450 and glutathione S-transferases, potentially involved in the

241 mopressin increased the translation of seven glutathione S-transferase proteins and enhanced protein

242 Pull-down assays with GST (glutathione S-transferase) proteins revealed that the cy

243 rotin biosynthetic enzymes revealed that the glutathione S-transferase PsoE requires participation of

244 Glutathione S-transferase pull downs were performed, and

245 Glutathione S-transferase pull-down and coimmunoprecipit

246 Glutathione S-transferase pull-down and immunoprecipitat

247 on was further demonstrated by both in vitro glutathione S-transferase pull-down and in vivo co-immun

248 Using a glutathione S-transferase pull-down approach, we identif

249 Immunoprecipitation experiments and glutathione S-transferase pull-down assay showed a direc

250 interacting domains of Nrf2 and RAC3 using a glutathione S-transferase pull-down assay.

251 putative myrosinase-associated protein, and glutathione S-transferase pull-down assays demonstrated

252 Glutathione S-transferase pull-down assays demonstrated

253 Most importantly, glutathione S-transferase pull-down assays identified th

254 Immunofluorescence results and glutathione S-transferase pull-down assays revealed an a

255 In glutathione S-transferase pull-down assays, TDP-43 bound

256 rect protein interactions were determined by glutathione S-transferase pull-down assays.

257 Coimmunoprecipitation and glutathione S-transferase pull-down experiments demonstr

258 ed in a variety of coimmunoprecipitation and glutathione S-transferase pull-down experiments.

259 Glutathione S-transferase pull-down studies indicate tha

260 Yeast two-hybrid, in vitro glutathione S-transferase pull-down, and coimmunoprecipi

261 ction between LOG2 and GDU1 was confirmed by glutathione S-transferase pull-down, in vitro ubiquitina

262 Glutathione S-transferase pull-downs identified distinct

263 Additionally, glutathione S-transferase pull-downs show that E1B-AP5 a

264 Forster resonance energy transfer (FRET) and glutathione S-transferase pulldown analyses identified A

265 nally antagonistic proteins was confirmed by glutathione S-transferase pulldown assay and co-immunopr

266 are sufficient to interact with pU(L)6 in a glutathione S-transferase pulldown assay in the absence

267 Co-immunoprecipitation and glutathione S-transferase pulldown assays confirm the co

268 In this study, glutathione S-transferase pulldown assays indicated that

269 Glutathione S-transferase pulldown assays revealed bindi

270 iption factors was subsequently confirmed by glutathione S-transferase pulldown assays.

271 f renal tissue lysate with ROMK antibody and glutathione S-transferase pulldown experiments demonstra

272 Glutathione S-transferase pulldown experiments revealed

273 Using glutathione S-transferase pulldown experiments, chemical

274 ion of epitope-tagged IFNAR1 constructs, and glutathione S-transferase pulldown experiments, we demon

275 inding between RelB and G9a was confirmed by glutathione S-transferase pulldown in vitro and coimmuno

276 Co-immunoprecipitation, glutathione S-transferase pulldown, and luciferase assay

277 The E2-MEK2 interaction was confirmed by glutathione S-transferase pulldown, coimmunoprecipitatio

278 regulating cell movement, yeast 2-hybrid and glutathione-S-transferase pulldown analyses show Robo4 b

279 subunits of PP2A (PP2A-A or PP2A-B) using a glutathione S-transferase-pulldown assay.

280 However, glutathione S-transferase pulldowns and intragenic compl

281 ollowed by acidic residues, we have utilized glutathione S-transferase pulldowns, two-hybrid analysis

282 cids of PduD to green fluorescent protein or glutathione S-transferase resulted in the association of

283 We showed previously that glutathione S-transferase S1 (gstS1), an enzyme with con

284 The labeling reaction of purified glutathione S-transferase tagged AGT with ZP1BG and the

285 ous NKCC1 from Calu-3 total cell lysates and glutathione S-transferase-tagged NT-NKCC1 pulls down end

286 ed this hypothesis by generating full-length glutathione-S-transferase-tagged DUSP5 and serine 147 pr

287 several genes such as ASCORBATE PEROXIDASE2, GLUTATHIONE S-TRANSFERASE TAU9, and several SMALL AUXIN

288 A possible association between glutathione S-transferase theta 1 gene (GSTT1) polymorph

289 5068) in the promoter/enhancer region of the glutathione S-transferase theta 1 gene (GSTT1, encoding

290 we report the molecular characterization of glutathione s-transferase-theta (GST-theta) from freshwa

291 Adding glutathione S-transferase, thioredoxin, or maltose bindi

292 A chimeric protease precursor, glutathione S-transferase-transframe region (TFR)-PR-FLA

293 rted that Arabidopsis (Arabidopsis thaliana) GLUTATHIONE S-TRANSFERASE U17 (AtGSTU17; At1g10370) part

294 ing SOD1 (superoxide dismutase 1), catalase, glutathione S-transferase, uncoupling protein-1, or tran

295 cCPE.GST or GST (GST is glutathione S-transferase) was conjugated to the metal i

296 ncluding glutamate-cysteine ligase (GCL) and glutathione S-transferase, was measured by quantitative

297 The proteome analysis revealed that Glutathione S-transferases were induced in the shoot and

298 romes P450, one glycosyl-transferase and one glutathione-S-transferase) were NTSR markers which combi

299 topic expression of hGSTA4-4, the isozyme of glutathione S-transferase with high activity for 4-HNE.

300 ase-1, NAD(P)H quinone oxidoreductase 1, and glutathione-S transferase, with inhibition of transformi