ライフサイエンスコーパス: expression plasmid

1 VP2 was provided in trans from a eukaryotic expression plasmid.

2 488 after infection or transfection of a US3 expression plasmid.

3 was restored by cotransfection with a ChREBP expression plasmid.

4 rom Treponema pallidum were cloned into this expression plasmid.

5 s expressing Jak2 via the addition of a Jak2 expression plasmid.

6 ansfected with a wild-type androgen receptor expression plasmid.

7 ls transiently transfected with a human TLR5 expression plasmid.

8 se blue (S) opsin gene was cloned into a Cre-expression plasmid.

9 ATP-binding cassette transporter A1 (ABCA1) expression plasmid.

10 only in cells cotransfected with a human VDR expression plasmid.

11 rescent protein genes, and (iii) an envelope expression plasmid.

12 ugmented by cotransfection with Sp1 or EGR-1 expression plasmid.

13 inase I cDNA or a beta-galactosidase control expression plasmid.

14 dominant negative mutant vector and a c-jun expression plasmid.

15 in-producing renal As4.1 cells with LXRalpha expression plasmid.

16 pression plasmid, as well as to a C/EBPalpha expression plasmid.

17 ion alone or in combination with thioredoxin expression plasmid.

18 -infected Rael cells transfected with a LANA expression plasmid.

19 ms: a replication deficient adenovirus or an expression plasmid.

20 d 5-10-fold when cotransfected with a GATA-6 expression plasmid.

21 were enhanced by a co-transfected C/EBPdelta expression plasmid.

22 was observed upon injection of 10 mug of the expression plasmid.

23 ng chain polylysine and a beta-galactosidase expression plasmid.

24 ored by the transient transfection of a CD81 expression plasmid.

25 in MDA-MB-231 cells transfected with ZBTB10 expression plasmid.

26 ably transfected with an inducible protein A expression plasmid.

27 Amplified products were cloned into an expression plasmid.

28 ently constructed the DENV-1, -3, and -4 VLP expression plasmids.

29 lease of virus-like particles encoded by Gag expression plasmids.

30 B receptor mRNAs were designed and cloned in expression plasmids.

31 lowing stable transfection with TLR2 or TLR5 expression plasmids.

32 ecreted Frizzled receptor protein 1 (sFRP-1) expression plasmids.

33 gical response of HCV transgenic mice to HCV expression plasmids.

34 oter activity induced by IRF-1 and NF-kappaB expression plasmids.

35 anisms, we generated a series of bicistronic expression plasmids.

36 ic Cas9 lines and versatile guide RNA (gRNA) expression plasmids.

37 fibroblast-like Cos cells+/-HNF3beta or GATA expression plasmids.

38 d into uninfected cells by transfection with expression plasmids.

39 were introduced into the cell via multicopy expression plasmids.

40 pa 1c1c7 cells using antisense Arnt and Arnt expression plasmids.

41 ontrol expression plasmid and/or with mutant expression plasmids.

42 tinoic acid receptor and retinoid X receptor expression plasmids.

43 gradation-resistant HIF-1alpha or HIF-2alpha expression plasmids.

44 viruses together with the supporting protein expression plasmids.

45 0-fold compared to conditional selection for expression plasmids.

46 gene (clyA::t-csp) in genetically stabilized expression plasmids.

47 ds within the cross-reactive epitopes of VLP expression plasmids.

48 ter plasmid in combination with NOD1 or NOD2 expression plasmids; 2) by inhibiting DMXAA-induced chem

49 n C2C12 myoblasts carrying an inducible p204 expression plasmid) accelerated the fusion of myoblasts

50 Overexpression of PARP-1 with an expression plasmid activated expression of the alpha-SMA

51 e co-transfection of HeLa cells with a B-Myb expression plasmid activated the transfected SP-A promot

52 studies used prime/boost combinations of DNA expression plasmids alone or DNA priming and boosting wi

53 the current work we electroporated an I-SceI expression plasmid along with HaeIII fragments of φX

54 iver regeneration after injection of an LSP1 expression plasmid also led to decreased hepatocyte prol

55 Transient transfection of Pdcd4 expression plasmid and 4 x AP-1 reporter gene showed tha

56 Cotransfection of a CPF expression plasmid and a CYP7A reporter gene resulted in

57 One fragment was subcloned into a bacterial expression plasmid and a GST-fusion protein was produced

58 have been constructed in an Escherichia coli expression plasmid and added to the open-source BioBrick

59 When rPrP is mixed with an expression plasmid and Ca(2+), the rPrP.DNA complex is t

60 ne, beginning with the design of a pro-siRNA expression plasmid and ending with siRNA purification.

61 n the 2.0-kb LAT sequence, both within a LAT expression plasmid and in the context of the virus.

62 ragments were cloned into a xylose-inducible expression plasmid and transformed into S. aureus.

63 d in normal FLS by transfection with a Wnt-1 expression plasmid and was down-regulated in RA FLS by t

64 which are transfected with either a control expression plasmid and/or with mutant expression plasmid

65 The use of newly available expression plasmids and hosts has allowed the expression

66 nes, luciferase derivatives were made of the expression plasmids and introduced into Aedes albopictus

67 bait and prey thereby halving the number of expression plasmids and recombinant proteins required fo

68 Here, using extensive mutagenesis of expression plasmids and RNAi screening, we reveal that c

69 r single plasmids or cocktails of up to four expression plasmids and then challenged with sublethal d

70 quences for the VEGF-A gene were cloned into expression plasmids and transfected into HT1080 human fi

71 re permanently transfected with a luciferase expression plasmid, and C6 experimental brain tumors wer

72 Ang(-S)Exp/pSVL (or a corresponding control) expression plasmid, and mitotic indices were measured fo

73 f the DNA capture events involved the I-SceI expression plasmid, and several events involved retrotra

74 incorporated via mutagenesis into the fiber expression plasmid, and the resulting fiber proteins wer

75 omoter was about 50% in both orientations in expression plasmid, and two transcriptional factors were

76 e or by co-transfecting with Runx2 antisense expression plasmid, and was enhanced by overexpression o

77 th the NF-kappa B-Luc reporter, CD14 and MD2 expression plasmids, and expression plasmids for TLR2, T

78 of endogenous DeltaNp63alpha, DeltaNp63-EGFP expression plasmids, and p53 were assessed after treatme

79 enotype 1b genes were cloned into eukaryotic expression plasmids, and the immunogenicity was determin

80 These high- or low-copy yeast expression plasmids are then converted quickly into inte

81 ine phosphatase 1B (PTP1B), and PTP1B mutant expression plasmids as well as SirT1 small interfering R

82 activity in response to a cotransfected Sp1 expression plasmid, as well as to a C/EBPalpha expressio

83 We have enhanced the maintenance of expression plasmids at two independent levels.

84 caques were coimmunized intramuscularly with expression plasmids bearing genes encoding Th1 (interleu

85 Mammalian expression plasmids bearing mutations in these motifs (F

86 also stimulated by transfection with a STAT6 expression plasmid, but was inhibited by antisense oligo

87 SW480 colon cancer cells transfected with an expression plasmid (c-srcY527F) encoding a constitutivel

88 ltering the ratio of proviral genome and env expression plasmids can produce pseudovirions that are s

89 or ICAM-CAT, cotransfection with a CMV-IE72 expression plasmid caused promoter and CAT activation.

90 However, cotransfection of expression plasmids coding for MyoD and cTaxREB107 did n

91 formation of the iscS(-) strain with an iscS expression plasmid complemented all of the observed phen

92 Ntcp promoter, while a dominant negative JNK expression plasmid completely blocked IL-1 beta-mediated

93 a low copy arabinose-inducible pBAD/Myc-HisA expression plasmid constructed in our laboratory.

94 s, exchange is achieved by introducing a Cre-expression plasmid containing an equivalent cassette con

95 melanomas and HCCs were transfected with an expression plasmid containing argininosuccinate syntheta

96 D(+) cells transfected with an expression plasmid containing RARalpha cDNA had a 6- to

97 rol cells, HEK293T cells transfected with an expression plasmid containing the c.5098C>T (p.Pro1700Se

98 A new expression plasmid containing the fla operon promoter an

99 t murine IL-6 or intradermal injection of an expression plasmid containing the full-length murine IL-

100 verexpression of GSH by transfection with an expression plasmid containing the GCLC cDNA conferred se

101 FKBP52 was purified by using a prokaryotic expression plasmid containing the human cDNA.

102 A UL52 expression plasmid containing the mutation in the zinc f

103 We used microinjection to introduce expression plasmids containing Bcl-w and Bcl-x(L) cDNAs

104 strains require a GlcNAc supplement and that expression plasmids containing both exogenous components

105 sfection of Chinese hamster ovary cells with expression plasmids containing different V(H) and V(L) s

106 in the prior experiment with two individual expression plasmids containing gH and gL.

107 isubunit DNA binding protein (EcoR124I) with expression plasmids containing the EcoR124I recognition

108 ine repeats and reading frame when producing expression plasmids containing the Mig-7 sequence.

109 analysis of three in vivo-inducible promoter expression plasmids, containing pnirB, ppagC, and pkatG,

110 econstitution of ClC-3 expression with ClC-3 expression plasmids could rescue the cells from the cell

111 140,000 second-generation short hairpin RNA expression plasmids, covering a substantial fraction of

112 zed storage and distribution for the protein expression plasmids created by PSI researchers.

113 Cotransfection of LIP or c-Jun expression plasmids decreased the transcriptional activi

114 ould be restored by cotransfection of an env expression plasmid (DeltaGP).

115 ansfection with the kinase-defective pp90RSK expression plasmid demonstrated a statistically signific

116 ocedure including construction of redesigned expression plasmids, development of automated protein ex

117 e reporter construct plus dHAND or dHAND-E12 expression plasmids did not alter luciferase activity, w

118 Furthermore, boosting with recombinant NS3 expression plasmid DNA after priming with M-ISA720/CpG-a

119 se two derivatives were cloned separately on expression plasmids downstream from the CFA/I operon.

120 me system in which T7 RNA polymerase from an expression plasmid drove expression of RNA transcripts f

121 m cells transfected with Smad1 linker region expression plasmid effectively inhibited osteoclastogene

122 ntrolateral o blast cells by injection of an expression plasmid elicited the dorsolateral P cell fate

123 Dividing the insert between three high-copy expression plasmids enables the bulk purification of the

124 An expression plasmid encoding bacterial beta-galactosidase

125 perties, we favored the use of a bicistronic expression plasmid encoding both GFP and a beta subunit.

126 invasive i.v. administration of a 6- to 7-kb expression plasmid encoding either luciferase or beta-ga

127 onal and structural study of this enzyme, an expression plasmid encoding His-tagged human PMK has bee

128 ells and in cells transfected with a protein expression plasmid encoding PB2.

129 cancer cells transiently transfected with an expression plasmid encoding pd1EGFP and treated with FZ

130 HepG2) were transiently transfected with the expression plasmid encoding PPARalpha and a plasmid cont

131 The expression plasmid encoding the p53 mutant, with Lys-320

132 Shc-SH2, an expression plasmid encoding the SH2 domain of Shc, atten

133 ion-deficient adenovirus, poly-L-lysine, and expression plasmids encoding beta subunits could be opti

134 ansfection of a GAL reporter gene along with expression plasmids encoding c-Jun plus c-Fos, or the ca

135 were immunized by intradermal injection with expression plasmids encoding calcyclin or MIDA1.

136 Cells stably transfected with expression plasmids encoding either Bag1 or Bag1L displa

137 SRD-15 cells when they are transfected with expression plasmids encoding either Insig-1 or Insig-2.

138 tored when SRD-14 cells are transfected with expression plasmids encoding either Insig-1 or Insig-2.

139 Multicopy expression plasmids encoding essential MOB1 or CDC28 gen

140 ce system for the stabilization of multicopy expression plasmids encoding foreign antigens in a Salmo

141 Three expression plasmids encoding HIV(Ba-L) gp160, cytoplasmi

142 NVAX(R)-B DNA vaccine (PV) is a mixture of 3 expression plasmids encoding HIV-1 Clade B Env, Gag, and

143 ld be rescued by transfecting the cells with expression plasmids encoding HNF-1alpha or HNF-4.

144 Using expression plasmids encoding individual LCMV proteins, w

145 , model cells (HeLa) were cotransfected with expression plasmids encoding its mutant or wild-type (wt

146 uced by gene gun vaccination with eukaryotic expression plasmids encoding melanocyte differentiation

147 Expression plasmids encoding methionine at amino acids 5

148 investigated using a NF-kappaB inhibitor and expression plasmids encoding NF-kappaB subunits.

149 generated by cotransfecting 293T cells with expression plasmids encoding patient-derived Vif, human

150 ccidiosis both alone and in combination with expression plasmids encoding the interleukin 1 (IL-1), I

151 Transfection of this plasmid, along with the expression plasmids encoding the N, P, M2-1, and L prote

152 Transfection of expression plasmids encoding the novel PKC isoforms delt

153 Two expression plasmids encoding the reporter green fluoresc

154 A series of expression plasmids encoding Yop-GSK fusion proteins wer

155 Surprisingly, the expression plasmid failed to allow the closely related P

156 ells transiently transfected with a Rex cDNA expression plasmid failed to become persistently infecte

157 regimen with a Zaire ebolavirus glycoprotein expression plasmid followed by infection with a vesicula

158 when further transfected transiently with an expression plasmid for a known positive prey.

159 ncode a transforming gene by transfecting an expression plasmid for JSRV [pCMVJS21, driven by the cyt

160 using particle-mediated gene transfer of an expression plasmid for postsynaptic density 95-green flu

161 PRB levels were elevated by transfecting an expression plasmid for PRB, but not when the cells were

162 ctor (eIF) 4H was subcloned into a bacterial expression plasmid for purification of recombinant prote

163 nsfected transiently with an OriP-containing expression plasmid for the positive prey together with e

164 k, an engineered E. coli strain harboring an expression plasmid for the Umbellularia californica acyl

165 Expression plasmids for Ag2/PRA(1-18) DNA (signal sequen

166 broad range of t-Bu-DEX concentrations when expression plasmids for both receptors were cotransfecte

167 lls transfected with various combinations of expression plasmids for BRCA1, BRCA1 specific inhibitory

168 e pairs of 5'-flanking sequence of GSTA2 and expression plasmids for either GR, pregnane X receptor (

169 deoxycholic acid (CDCA) and transfected with expression plasmids for farnesoid X-receptor (FXR), shor

170 mbinant L. monocytogenes carrying eukaryotic expression plasmids for feline tumor necrosis factor (TN

171 ction studies using the FR-beta promoter and expression plasmids for the nuclear receptors retinoic a

172 orter, CD14 and MD2 expression plasmids, and expression plasmids for TLR2, TLR4, or TLR5.

173 Cotransfection experiments with CREB and PKA expression plasmids further supported our conclusions th

174 n YB-1 binding and co-transfection of a YB-1 expression plasmid had a repressive effect on UV-inducib

175 s overcome by increasing amounts of a K-bZIP expression plasmid in the cotransfection mixture or by d

176 nly when additional ORF50 was supplied as an expression plasmid in the transfection mixture, suggesti

177 ected with increasing amounts of selected TF expression plasmids in addition to LCR-luciferase vector

178 Co-transfection of KLF-4 and HDAC expression plasmids in breast cancer cells results in sy

179 H pylori strains, or transfected with a CagA expression plasmid, in the absence or presence of SMO sm

180 eficient cell line, MDA-MB-468, with an NQO1 expression plasmid increased apoptotic responses and let

181 e stimulated by cotransfection with an Hsp72 expression plasmid, indicating that hsp72 likely plays a

182 Co-transfection of a JNK expression plasmid inhibited RXR:RAR-mediated activation

183 The transfection of a p202a expression plasmid inhibited the c-Myc-dependent express

184 the present studies we transfected a Smurf1 expression plasmid into 2T3 osteoblast precursor cells a

185 We show first that transfection of an LMP1 expression plasmid into Ad-AH cells, an EBV-negative nas

186 pression as transient transfection of an AhR expression plasmid into AhR(-/-) fibroblasts significant

187 Cotransfection of an Sp1 expression plasmid into Drosophila SL2 cells with a -228

188 In contrast, transient transfection of MeCP2 expression plasmid into fibroblasts enhanced alpha-SMA g

189 Injection of SRF antisense expression plasmid into gastric ulcers in rats significa

190 e HBV replicative plasmid with RIG-I or MDA5 expression plasmid into Huh7 cells and found that MDA5,

191 -17, because transient transfection of TRAF6 expression plasmid into the TRAF6-deficient cells restor

192 n ulcer healing by local injection of an SRF expression plasmid into ulcers (gene therapy).

193 ty-two hours after the transfection of eight expression plasmids into cocultured 293T and MDCK cells,

194 kappa opioid receptors, by transfecting dual-expression plasmids into COS-7 cells, the full-length GA

195 Upon transfection of appropriate expression plasmids into COS1 cells, immunofluorescence

196 oter sequences, by transient transfection of expression plasmids into human kidney 293T cells.

197 f drug resistance genes for the selection of expression plasmids introduced into live vectors poses t

198 The expression plasmid is driven either by a broadly express

199 Thus, introduction of an ORF50 expression plasmid is sufficient to drive the lytic cycl

200 Microinjection of expression plasmids is an effective technique for introd

201 by multiple site mutagenesis on recombinant expression plasmids is sufficient to convert the kinetic

202 d the mutant protein was synthesized from an expression plasmid, it concentrated in punctate cytoplas

203 injection into mice of IL-15 and IL-15Ralpha expression plasmids led to significantly increased level

204 When Sp1 levels were increased through an expression plasmid, luciferase reporter gene expression

205 10 harbored a specific segment of the I-SceI expression plasmid mapping between two replication origi

206 Three injections of a recombinant eukaryotic expression plasmid of BDV p10 were needed to generate a

207 RESEARCH DESIGN AND An expression plasmid of plasminogen kringle 5 (K5), a natu

208 he introduction into bacteria carrying a Red expression plasmid of synthetic (PCR-generated) DNA.

209 accomplished this through incorporation into expression plasmids of a postsegregational killing syste

210 at were transiently transfected with various expression plasmids of CK2 (thereby expressing additiona

211 Cotransfection of expression plasmids of human or mouse BCO2 into Escheric

212 lowed by intravenous injections of naked HGF expression plasmid or control vector.

213 by recoded allotopic ATP8 (nATP8) in a high-expression plasmid or in a CEN plasmid in the presence o

214 of US3 kinase in cells transformed with US3 expression plasmids or infected with each virus results

215 entation was provided by cotransfection with expression plasmids or infection with MV helper virus.

216 , using transfected fusion and hemagglutinin expression plasmids or with syncytium-based assays in Ve

217 expression of dominant-negative mutant TAp73 expression plasmid (p73DD) counteracted the MLN8054-indu

218 were spiked with different dilutions of the expression plasmid pA-EGFP_B, a PCN from 1 to 64 could b

219 The expression plasmid pCB8SJ2, containing the premembrane a

220 FIV-pPPRDelta vif DNA and a feline IFN-gamma expression plasmid (pCDNA-IFNgamma).

221 SNB19 cells were transfected with an expression plasmid (pcDNA3-ATF) containing a cDNA sequen

222 When SK-BR-3 cells were transfected with the expression plasmid pCI-ER alpha, but not pCI-ER beta, ar

223 MEL sFv-rGel was produced in bacterial expression plasmid (pET-32), and the protein composition

224 deliver mucosally to cotton rats eukaryotic expression plasmid pGA3-mH and Sindbis virus-based DNA r

225 for cloning, and recombined into a universal expression plasmid (pGW_cfosEGFP).

226 he AMO genes into the thiostrepton-inducible expression plasmid pIJ6021.

227 In this study four murine IL-12 naked DNA expression plasmids (pIL-12), containing both the p35 an

228 cells cotransfected with PKA-Calpha and SOX9 expression plasmids, PKA enhanced the phosphorylation of

229 h injection of a dominant negative (DN) FoxO expression plasmid prior to inoculation with Lewis lung

230 anulocyte colony-stimulating factor (hG-CSF) expression plasmids produced high-level gene expression

231 and in vivo and that transfection of a DLX5 expression plasmid promotes the expression of MYC in a d

232 In control experiments with the HMGCL expression plasmid, protein is localized in the mitochon

233 letion of env sequences from a JSRV proviral expression plasmid (pTN3) abolished its ability to produ

234 S medical countermeasures, we constructed an expression plasmid, pWRG/AND-M, that contains the full-l

235 sfection of these cells with a gamma-catenin expression plasmid reduced the elevated TCF activity by

236 endrimer nanoparticles containing a TNFalpha expression plasmid regulated by telomerase gene promoter

237 Furthermore, cotransfection of Gfi-1B expression plasmid repressed reporter activity of wild-t

238 expression using a short hairpin RNA (shRNA) expression plasmid resulted in markedly reduced prolifer

239 n-mediated intramuscular injection of TIMP-4 expression plasmid resulted in sustained plasma TIMP-4 l

240 asmid simultaneously with C/EBPalpha and Sp1 expression plasmids resulted in an increase in luciferas

241 sfection of the MUC5AC-luc reporter with Sp1 expression plasmids resulted in significantly increased

242 Co-transfection experiments with a SOX9 expression plasmid revealed that a construct containing

243 3T cells transfected with TRbeta or LXRalpha expression plasmids show that TR, together with its liga

244 onstructs with a dominant-negative PKC-delta expression plasmid showed that suppression of this kinas

245 cert with PPARgamma, PPARalpha, or PPARdelta expression plasmids, showed dose-dependent activation of

246 ave demonstrated that transfection of a p300 expression plasmid significantly activated ferritin H-CA

247 onal level, transfection of SMCs with a Prx1 expression plasmid significantly increased their growth.

248 of autoantigen cDNAs to be incorporated into expression plasmids so as to generate tolerizing vaccine

249 Cotransfection with LXRalpha and RXRalpha expression plasmids strongly stimulated rat CYP7A1/lucif

250 We also generated a mutant Mect1-Maml2 expression plasmid that carried silent nucleotide change

251 amster ovary (CHO) cells transfected with an expression plasmid that contained cDNA coding for the ch

252 antly inhibited the expression of a reporter expression plasmid that contains the 3'-untranslated reg

253 pneumophila effectors was screened using an expression plasmid that produces low levels of each prot

254 was compared with that from a control, null-expression plasmid that was identical except for a frame

255 emA gene from C. vibrioforme was cloned into expression plasmids that added an N-terminal His(6) tag

256 able transfection of HEK293S-TetR cells with expression plasmids that contained the opsin gene downst

257 ed anti-RT antibodies and constructed HTLV-1 expression plasmids that express truncated or hemaggluti

258 Using expression plasmids that expressed either wild-type Jak2

259 l mice, were transfected with two mutant E1A expression plasmids that inactivate either p300/CBP or r

260 introduced into E. coli and induced from an expression plasmid, the mutant subunits act as a decoy i

261 is protocol (from the receipt of the QconCAT expression plasmid to the absolute quantification of the

262 t plasmid was transactivated by a C/EBPalpha expression plasmid to the same extent as wild-type LF-89

263 We also generated expression plasmids to ectopically express all 7 chitina

264 ruitment of pUL53 to the nuclear envelope in expression plasmid-transfected and human cytomegalovirus

265 Both proteins were encoded in two different expression plasmids under the control of different tight

266 We constructed the recombinant prokaryotic expression plasmid using prokaryotic expression vector (

267 When an integrase expression plasmid was co-injected, hFIX serum levels in

268 If TLR2 expression plasmid was ectopically expressed in dysfunct

269 fection of NLDeltaVpr proviral DNA and a Vpr expression plasmid was employed to analyze the virion in

270 o2 cells stably transfected with CARD15/NOD2 expression plasmid was lower than untransfected Caco2 ce

271 10T1/2 cells, but cotransfection with a SOX9 expression plasmid was sufficient to activate the enhanc

272 The NBD2 expression plasmid was used to generate a Leu2027Phe mut

273 sites (RBS) in the three promoter/C fragment expression plasmids was also performed.

274 a MORF (moveable ORF) library of 5854 yeast expression plasmids was constructed, each expressing a s

275 n-replicating Epstein-Barr virus (EBV)-based expression plasmids was developed.

276 f viral structural proteins from the protein expression plasmids was not required for virus rescue, w

277 Using a luciferase expression plasmid, we monitored plasmid gene expression

278 Using extensive mutagenesis of expression plasmids, we show that miniature introns cont

279 lated, a trcR-lacZ fusion plasmid and a TrcR expression plasmid were cotransformed into Escherichia c

280 Mammalian cells transfected with CeABF-1 expression plasmids were capable of blocking E2A-mediate

281 When M and N expression plasmids were cotransfected into human 293 re

282 Specialized expression plasmids were developed to facilitate express

283 Multicopy tRNA expression plasmids were directly injected into skeletal

284 A series of SSB-encoding multicopy expression plasmids were introduced into reengineered S.

285 ndividual DeltaNp63 isoforms, DeltaNp63-EGFP expression plasmids were transiently expressed in hTCEpi

286 e of a SapI substrate site designed into the expression plasmid, which allows for in vitro selection

287 occurring plasmid partition function in our expression plasmids, which eliminates random segregation

288 ssion, we engineered lentivirus-driven miRNA expression plasmids, which we tested in the mouse placen

289 tudy, we show that cotransfection of the SEF expression plasmid with an SAA3/luciferase reporter resu

290 ing site in a co-transfection assay of IRF-1 expression plasmid with CARD4/NOD1 promoter.

291 Cotransfection of a pp150 expression plasmid with DeltaUL32-BAC DNA led to complem

292 Cotransformation of an expression plasmid with pTara provides a low-cost method

293 Cotransfection of mutant I-kappaBalpha expression plasmids with BMP-2 promoter-luciferase repor

294 olated from cox10 deletion strains harboring expression plasmids with coxI and coxII or with coxI and

295 erol nanoparticles containing nonintegrating expression plasmids with Foxm1 or Foxf1 cDNAs were injec

296 nt gp120 sequences were subcloned into gp160 expression plasmids with identical cleavage motifs and g

297 5-HT(1A) receptor expression plasmids with or without mutation of a single

298 Interestingly, in most cell lines, JSRV expression plasmids with Rej deleted showed normal trans

299 A library of DsbC expression plasmids with the active-site dipeptide rando

300 transfection of ES cells with a pCS2/noggin expression plasmid, with differentiation peaking at 72 h