ライフサイエンスコーパス: reticulocyte lysate

1 heterocomplexes has been reconstituted from reticulocyte lysate.

2 length HRI synthesized de novo in the rabbit reticulocyte lysate.

3 he heme-regulated eIF2 alpha kinase (HRI) in reticulocyte lysate.

4 ient mRNA-protein fusion formation in rabbit reticulocyte lysate.

5 proteasome-dependent N-end rule pathway in a reticulocyte lysate.

6 atalytic protein subunit expressed in rabbit reticulocyte lysate.

7 refold luciferase in the presence of rabbit reticulocyte lysate.

8 ation of ornithine decarboxylase in a rabbit reticulocyte lysate.

9 ard ubiquitination and degradation in rabbit reticulocyte lysate.

10 mally denatured firefly luciferase in rabbit reticulocyte lysate.

11 ver, these proteins inhibited translation in reticulocyte lysate.

12 s in the GR.hsp90 heterocomplex assembled in reticulocyte lysate.

13 to bind eIF4E and to inhibit translation in reticulocyte lysate.

14 n-vitro transcription-coupled translation in reticulocyte lysate.

15 e potent inhibitors of translation in rabbit reticulocyte lysate.

16 ut with the protein-folding system in rabbit reticulocyte lysate.

17 e to fold into globular proteins in a rabbit reticulocyte lysate.

18 embranes (95% rhodopsin) were incubated with reticulocyte lysate.

19 proteins by in vitro translation in a rabbit reticulocyte lysate.

20 to degradation in both lens fiber lysate and reticulocyte lysate.

21 xpression of the downstream reporter gene in reticulocyte lysate.

22 he effect of novobiocin on Hsp90 function in reticulocyte lysate.

23 n translating target proteins with mammalian reticulocyte lysate.

24 aturation of luciferase and bind to Hsp70 in reticulocyte lysate.

25 ssa in vitro translation system or in rabbit reticulocyte lysate.

26 e-regulated eIF2alpha kinase (HRI) in rabbit reticulocyte lysate.

27 tes that it binds to other factors in rabbit reticulocyte lysate.

28 d from budding yeast, wheat germ, and rabbit reticulocyte lysates.

29 rticoid receptors (GR) synthesized in rabbit reticulocyte lysates.

30 ranscription, translation and prenylation in reticulocyte lysates.

31 e translation assays carried out with rabbit reticulocyte lysates.

32 itiation step of protein synthesis in rabbit reticulocyte lysates.

33 ion of nsP4 produced in infected cells or in reticulocyte lysates.

34 ing that YY1 is readily polyubiquitinated in reticulocyte lysates.

35 proglobulins were synthesized from cDNAs in reticulocyte lysates.

36 utant (Q227L) activated Galphas expressed in reticulocyte lysates.

37 CAT inhibited translation in vitro in rabbit reticulocyte lysates.

38 the eta PKC isoenzyme synthesized in rabbit reticulocyte lysates.

39 east and with in vitro translation in rabbit reticulocyte lysates.

40 peptides produced by in vitro translation in reticulocyte lysates.

41 hifting by 30-fold compared with 2.5-fold in reticulocyte lysates.

42 and eta PKC isoenzymes synthesized in rabbit reticulocyte lysates.

43 ctions are not known or cannot be assayed in reticulocyte lysates.

44 porter gene and assayed their translation in reticulocyte lysates.

45 hepatoblastoma cells) or in vitro in rabbit reticulocyte lysates.

46 tallin to degradation in both lens fiber and reticulocyte lysates.

47 by an endogenous methyltransferase in rabbit reticulocyte lysates.

48 degrees C than 30 degrees C, when tested in reticulocyte lysates.

49 oteolytic degradation in both lens fiber and reticulocyte lysates.

50 promoted the degradation of rMGMT in rabbit reticulocyte lysates.

51 n by the purified kinase as well as by crude reticulocyte lysates.

52 lation of this mRNA both in cells and rabbit reticulocyte lysates.

53 r than the endogenous eIF4G concentration in reticulocyte lysates.

54 ed into an active complex in vitro in rabbit reticulocyte lysates.

55 sing chimeric reporter transcripts in rabbit reticulocyte lysates.

56 th an efficiency similar to that measured in reticulocyte lysates (40%), there were important qualita

57 e bound to alpha-crystallin was treated with reticulocyte lysate, a rich source of chaperones, up to

58 lation among TPMT half-life values in rabbit reticulocyte lysate, aggresome formation in COS-1 cells,

59 s degraded moderately in both lens fiber and reticulocyte lysates, alpha A(1-168)-crystallin was resi

60 tion of the in vitro oxidized mRNA in rabbit reticulocyte lysate also led to formation of SPs.

61 inding activity after incubation in a rabbit reticulocyte lysate also was substantially lower than th

62 Immunoadsorption of FKBP52 from reticulocyte lysate also yields co-immunoadsorption of c

63 of HspBP1 on renaturation of luciferase in a reticulocyte lysate and a defined system were examined.

64 which was post-translationally modified by a reticulocyte lysate and ATP-generating system.

65 h lacZ-CTA and ner-ACC were tested in rabbit reticulocyte lysate and E. coli to select UTRs that were

66 to greater than 80% homogeneity from rabbit reticulocyte lysate and has been given the name eIF4H.

67 and oxidized luciferase mRNA in both rabbit reticulocyte lysate and human HEK293 cells.

68 process, both in the complex environment of reticulocyte lysate and in a purified system.

69 is phosphorylated on Ser13 in situ in rabbit reticulocyte lysate and in cultured K562 cells and that

70 Mdm-2 in rabbit reticulocyte lysate and in normal, non-transformed 3T3 c

71 newly translated cyclin E, both in vitro in reticulocyte lysate and in vivo in human cells in cultur

72 onent of this assembly machinery in vitro in reticulocyte lysate and in vivo in Sf9 cells is p23.

73 of two reporter proteins, in vitro in rabbit reticulocyte lysate and in vivo in transfected BT7-H cel

74 e dimer is dependent upon factors present in reticulocyte lysate and other cytosols.

75 [3H]FK506, we found that both rabbit PP5 in reticulocyte lysate and purified rat PP5 were specifical

76 e RNA specificity of onconase in vitro using reticulocyte lysate and purified RNA substrates indicate

77 o assay combining a ribosome-depleted rabbit reticulocyte lysate and ribosomes prepared from HeLa or

78 ation/translocation experiments using rabbit reticulocyte lysate and rough microsomes revealed that t

79 GCF2 expressed in vitro using reticulocyte lysates and Escherichia coli migrates as a

80 n vitro assembly systems derived from rabbit reticulocyte lysates and human cell extracts.

81 h the RNA subunit hTR in two systems (rabbit reticulocyte lysates and human cell lines) with respect

82 d a procedure for purifying eIF6 from rabbit reticulocyte lysates and immunochemically characterized

83 d/or assembly of proglobulin trimers both in reticulocyte lysates and in seeds.

84 dthrough in vitro in wheat germ extracts and reticulocyte lysates and in vivo in oat protoplasts.

85 bited Mos-mediated MAPK activation in rabbit reticulocyte lysates and repressed MKK activation by v-M

86 sufficient to inhibit translation in rabbit reticulocyte lysates and sufficient to inhibit reporter

87 e resulting mutants were expressed in rabbit reticulocyte lysates and their interaction with HBcAg wa

88 es, occurred with equal efficiency in rabbit reticulocyte lysates and was much enhanced over that exh

89 0-2 AGG interruptions, both in vitro (rabbit reticulocyte lysates) and in cell culture (HEK-293 cells

90 exes at an intermediate stage of assembly in reticulocyte lysate, and Hip is also thought to be an in

91 -ACC) enhanced protein synthesis in a rabbit reticulocyte lysate, and it was compared to a lacZ-CTA,

92 nsisting of in vitro-transcribed RNA, rabbit reticulocyte lysate, and microsomal membranes on the bas

93 igo(A) tail are translated equally well in a reticulocyte lysate, and their translation is stimulated

94 DAPK suppresses translation in rabbit reticulocyte lysate, and treatment of neuroblastoma cell

95 by incubating immunopurified p53 with rabbit reticulocyte lysate, and we show by peptide competition

96 bition of eRF1 enhanced PRF in yeast, rabbit reticulocyte lysates, and mammalian cells.

97 eta-Tubulin mutants were expressed in rabbit reticulocyte lysates, and the effect of C-terminal, N-te

98 ncated s4 mRNAs were translated using rabbit reticulocyte lysates, and translation product sigma3 was

99 ly, in a degradation system utilizing rabbit reticulocyte lysate, antizyme 1 (AZ1) accelerates protea

100 nsistent with the effects observed in rabbit reticulocyte lysate, application of geldanamycin to fibr

101 st that these two conjugated proteins of the reticulocyte lysate are specific substrates for isopepti

102 haracteristics to eIF4H purified from rabbit reticulocyte lysate as described previously.

103 determined using both lens fiber lysate and reticulocyte lysate as sources of ubiquitinating and pro

104 determined using both lens fiber lysate and reticulocyte lysate as sources of ubiquitinating and pro

105 order Q70E/Q162E>Q162E> Q70E=WT betaB2 using reticulocyte lysate as the source of degradation machine

106 of translational repression, we used rabbit reticulocyte lysates as an in vitro translation system t

107 translation of the target mRNA in the rabbit reticulocyte lysate assay, but not in the cell-based ass

108 of protein synthesis in the cell-free rabbit reticulocyte lysate assay, degrading tRNA at concentrati

109 BAG-1 was present in reticulocyte lysate at a BAG-1:hsp70/hsc70 molar ratio o

110 70, RPS3, and NF45) were expressed in rabbit reticulocyte lysate, bacteria, and MCF-7 cells.

111 70, we purified a 38-kDa protein from rabbit reticulocyte lysate based upon its ability to stimulate

112 The DGD protein expressed in rabbit reticulocyte lysates bound truncated DHBV pre-S protein

113 Pr55(gag) was synthesized in reticulocyte lysates, bound to membranes, and incubated

114 t SBP2 is the only limiting factor in rabbit reticulocyte lysate but not in transfected rat hepatoma

115 04 cooperates with the chaperones present in reticulocyte lysates but not with DnaK of E. coli.

116 ptor-hsp90 heterocomplex is brought about in reticulocyte lysate by a preformed protein-folding compl

117 firefly luciferase readily occurs in rabbit reticulocyte lysate by an ATP-dependent process.

118 The addition of recombinant PEK to reticulocyte lysates caused a dose-dependent inhibition

119 n in each variant was quantified in a rabbit reticulocyte lysate cell-free translation system supplem

120 RNA and to inhibit translation in the rabbit reticulocyte lysate compared to its counterpart containi

121 cription/translation system utilizing rabbit reticulocyte lysates confirmed the interaction of NQO1 a

122 itro experiments using proteins generated in reticulocyte lysates confirmed this interaction and indi

123 d that GR.hsp90 heterocomplexes assembled in reticulocyte lysate contain cytoplasmic dynein in a mann

124 tory complex subunits, S2, was translated in reticulocyte lysate containing [(35)S]methionine and use

125 of these putative ATPases was synthesized in reticulocyte lysate containing [35S]methionine, and the

126 length p56(lck) molecules produced in rabbit reticulocyte lysate containing active chaperone machiner

127 e expressed these chimeras by translation in reticulocyte lysate containing canine pancreatic microso

128 biquitination relative to its translation in reticulocyte lysates containing 125I-ubiquitin.

129 ncreased when translation was carried out in reticulocyte lysates containing high K+ concentrations,

130 vitro degradation of a target mRNA in rabbit reticulocyte lysates containing in vitro-translated Vhs.

131 Reticulocyte lysate contains a chaperone system that ass

132 Rabbit reticulocyte lysate contains a multiprotein chaperone sy

133 Rabbit reticulocyte lysate contains a multiprotein chaperone sy

134 Rabbit reticulocyte lysate contains a multiprotein system that

135 0, is imported by isolated mitochondria in a reticulocyte lysate-dependent manner.

136 B59 protein synthesized in vitro in a rabbit reticulocyte lysate dephosphorylated rat ERK1 and ERK2 p

137 ized seven members of the family in a rabbit reticulocyte lysate, determined their Stokes radius, sed

138 ranslation of these fusion vectors in rabbit reticulocyte lysate +/- dog pancreatic microsomes follow

139 tive of whether it was synthesized in rabbit reticulocyte lysate, Escherichia coli or Trichoplusia ni

140 parately synthesized in vitro using a rabbit reticulocyte lysate expression system.

141 In assays using Hop-depleted rabbit reticulocyte lysate for the cell-free assembly of recept

142 , by the endogenous ubiquitinating system in reticulocyte lysate fraction II, and by intact HEK293 ce

143 ked to an unidentified protein in the rabbit reticulocyte lysate, generating a product slightly large

144 In the presence of rabbit reticulocyte lysate, grp170 can refold and partially res

145 We show that rabbit reticulocyte lysate harbors enzymatic components that ca

146 tein synthesizing system that employs rabbit reticulocyte lysates has been employed for protein produ

147 in that wheat hsp70 functions in the rabbit reticulocyte lysate heterocomplex assembly system and hu

148 Originally characterized in rabbit reticulocyte lysates, HRI was shown in 1976 to phosphory

149 ed in an expression system coupled to rabbit reticulocyte lysate in the presence or absence of dog pa

150 ous v-Mos mutants were expressed in a rabbit reticulocyte lysate in vitro translation system and in C

151 rboxyl-terminal domain of ICP0 to the rabbit reticulocyte lysate in vitro translation system resulted

152 ties of RSV mutants translated in the rabbit reticulocyte lysate in vitro translation system.

153 accumulation of heavy polymeric ribosomes in reticulocyte lysates in vitro.

154 tin in a cell-free expression system (rabbit reticulocyte lysate) increased by 40%.

155 d-type Pak2 in cells and addition of Pak2 to reticulocyte lysate inhibit translation, while kinase-in

156 his work, we separate the proteins of rabbit reticulocyte lysate into three fractions by DEAE chromat

157 epressed ferritin synthesis 4-fold in rabbit reticulocyte lysates (IRP1 + IRP2), confirming differenc

158 ge activity of NS2/3 protease synthesized in reticulocyte lysate is ATP-dependent, as evidenced by AT

159 thase by the native ubiquitinating system of reticulocyte lysate is dependent upon both Hsp70 and the

160 impression by showing that all of the Hop in reticulocyte lysate is present in an hsp90.Hop.hsp70 com

161 When a rabbit reticulocyte lysate is programmed with uncapped lucifera

162 The apo-nNOS activating activity of reticulocyte lysate is retained in a pool of fractions c

163 Furthermore, translation activity in rabbit reticulocyte lysate is strongly inhibited by RNAs exceed

164 f full-length Gag synthesized in vitro using reticulocyte lysates is inhibited when RNAs that contain

165 in, G beta, synthesized in vitro in a rabbit reticulocyte lysate, is unable to fold into a native str

166 After its in vitro synthesis in rabbit reticulocyte lysate, it can also be efficiently imported

167 translation of intact sIL-1Ra cDNA in rabbit reticulocyte lysates led to both pro-sIL-1Ra and icIL-1R

168 Use of reticulocyte lysates manipulated to deplete them of eIF4

169 M-AS inhibited translation in vitro (rabbit reticulocyte lysate) of target mRNA at concentrations as

170 e have isolated a protein kinase from rabbit reticulocyte lysates on the basis of its ability to phos

171 We isolated a protein kinase from rabbit reticulocyte lysates on the basis of its ability to phos

172 ependent translation when used to supplement reticulocyte lysate; one of these activities was identif

173 ere we show that immunodepletion of Hip from reticulocyte lysate or addition of high levels of Hip to

174 ) complex of chaperone proteins is formed in reticulocyte lysate or from purified proteins.

175 n then be refolded by the addition of rabbit reticulocyte lysate or hsc70 and Hdj-1, whereas Hdj-1 do

176 nthesized substrate proteins bound to CCT in reticulocyte lysate or intact Xenopus oocytes.

177 novo in cell-free systems containing rabbit reticulocyte lysate or wheat germ extracts assembles int

178 nterestingly, we find that pre-incubation of reticulocyte lysates or ribosomal salt wash fractions wi

179 we found that an activity present in rabbit reticulocyte lysates phosphorylates and activates Chk2.

180 fied VHL-CCT complexes, when added to rabbit reticulocyte lysate, proceeded to form VCB and VCB-Cul2.

181 Rabbit reticulocyte lysates programmed with monocistronic RNAs

182 in the translation mixture by the endogenous reticulocyte lysate proteasome.

183 h a source of ubiquitination enzymes (rabbit reticulocyte lysate), purified ubiquitin, and ATP reveal

184 e detected by electron microscopy within the reticulocyte lysate reaction mixtures and appeared essen

185 An in vitro assay with reticulocyte lysate recapitulated the release of intact

186 Expressed in rabbit reticulocyte lysate, recombinant p133 and telomerase RNA

187 Using an eIF4G-depleted reticulocyte lysate, reconstitution with mock-phosphoryl

188 in vitro translation of the mRNAs in rabbit reticulocyte lysate reflected differences in the positio

189 erminal variants of RGS4 that were stable in reticulocyte lysate remained unstable in L cells.

190 ression of the ORF 3 coding region in rabbit reticulocyte lysates resulted in the production of a sin

191 In vitro translation of rabbit reticulocyte lysate ribosomes was inhibited by the C-ter

192 incubated with both exogenous ATP and rabbit reticulocyte lysate (RRL) as a source of ubiquitin-prote

193 We used a rabbit reticulocyte lysate (RRL) cell-free system to examine tr

194 iation factor 2 (HRI) is activated in rabbit reticulocyte lysate (RRL) in response to a number of env

195 ha kinase (HRI) in hemin-supplemented rabbit reticulocyte lysate (RRL) in response to heat and oxidat

196 la, was translated in vitro in either rabbit reticulocyte lysate (RRL) or wheat germ extract (WGE).

197 mally denatured firefly luciferase in rabbit reticulocyte lysate (RRL) requires hsp90, hsc70, and oth

198 d prey proteins (probes) in cell-free rabbit reticulocyte lysate (RRL) systems.

199 In a rabbit reticulocyte lysate (RRL) translation system, a mutant A

200 inhibit Hsc70-dependent processes in rabbit reticulocyte lysate (RRL) was examined.

201 expressed in a mammalian cell lysate, rabbit reticulocyte lysate (RRL), was able to assemble into cap

202 ver, it did not affect translation in rabbit reticulocyte lysate (RRL).

203 (HRI) interacts with hsp90 in situ in rabbit reticulocyte lysate (RRL).

204 ent in mock and Ric-8A-immunodepleted rabbit reticulocyte lysate (RRL).

205 activated not only in heme-deficient rabbit reticulocyte lysates (RRL), but also in hemin-supplement

206 f the 750-kD keratin complex, we used rabbit reticulocyte lysates (RRL).

207 cription/translation system employing rabbit reticulocyte lysates (RRLs).

208 Translation of RNAs in reticulocyte lysates showed that cleavage at the nsP3/ns

209 The binding of AIP to AhR in reticulocyte lysate shows several of the characteristics

210 1 and STAT2 or STAT1 and STAT3 translated in reticulocyte lysate spontaneously form heterocomplexes w

211 lation of in vitro translated Rab5 in rabbit reticulocyte lysate, suggesting that it competes for lip

212 fused to glutathione S-transferase in rabbit reticulocyte lysates, suggesting a role for the pU(L)34/

213 ram a cell-free translation system of rabbit reticulocyte lysates supplemented with canine pancreas m

214 ation by using purified Pr55(Gag) and rabbit reticulocyte lysate-synthesized Tsg101, and (iii) in viv

215 nslation products of these fusion vectors in reticulocyte lysate system +/- microsomal membranes were

216 n was performed using [(35)S]methionine in a reticulocyte lysate system +/- microsomes, and the trans

217 hBVR translated by the rabbit reticulocyte lysate system appears on a nondenaturing ge

218 ts from control and diabetic adipocytes to a reticulocyte lysate system demonstrated the inhibition o

219 antigen can rescue protein synthesis in the reticulocyte lysate system from inhibition by low concen

220 ag proteins synthesized in vitro in a rabbit reticulocyte lysate system in the absence of exogenous l

221 pitation of proteins in vitro expressed in a reticulocyte lysate system showed an interaction between

222 In the reticulocyte lysate system the W RNAs shut off protein s

223 Using a cell-free reticulocyte lysate system we have examined the relation

224 ng translation in vitro in a standard rabbit reticulocyte lysate system, although all of the other vi

225 c proteins with a substrate synthesized in a reticulocyte lysate system, before its posttranslational

226 Using a rabbit reticulocyte lysate system, E2EPF was shown to support t

227 Thus, in the rabbit reticulocyte lysate system, the c-jun 5' UTR likely impe

228 imeric and truncated proteins expressed in a reticulocyte lysate system, we have identified two topog

229 Through the use of an eIF4G-depleted reticulocyte lysate system, we show that this presumptio

230 opomyosin 3'UTR RNA was observed in a rabbit reticulocyte lysate system, which is known to contain en

231 pe and mutant proteins incubated in a rabbit reticulocyte lysate system.

232 with masses of 26 and 17 kDa) formed in the reticulocyte lysate system.

233 ells and Rep78 produced in vitro in a rabbit reticulocyte lysate system.

234 a and in a coupled transcription/translation reticulocyte lysate system.

235 anslation was assessed in an in vitro rabbit reticulocyte lysate system.

236 nhibition of protein synthesis in the rabbit reticulocyte lysate system.

237 The proteins were expressed in vitro in a reticulocyte lysate system.

238 on in both the wheat germ extract and rabbit reticulocyte lysate systems.

239 minimal chaperone system reconstituted from reticulocyte lysate that forms glucocorticoid receptor (

240 When added to rabbit reticulocyte lysate that has been depleted of endogenous

241 inant telomerase requires a factor in rabbit reticulocyte lysate that promotes ribonucleoprotein asse

242 iated with a kinase endogenous to the rabbit reticulocyte lysate that was identified as PAK-2, (ii) N

243 are Gbeta isoform-specific factors in rabbit reticulocyte lysates that determine the efficacy of Gbet

244 pitulated in an in vitro system using rabbit reticulocyte lysates that had been largely depleted of e

245 Protein complexes in reticulocyte lysates that specifically interact with the

246 We find, using rabbit reticulocyte lysates, that the presence of the c-jun 5'

247 rative support of p56lck structure in rabbit reticulocyte lysate, the specific occurrence of complexe

248 , we utilized pulse-chase analyses in rabbit reticulocyte lysate to demonstrate that hsp90-bound inte

249 nly in the templating region and used rabbit reticulocyte lysates to reconstitute telomerase activity

250 stress from studies of protein synthesis in reticulocyte lysates to the regulation of glutathione me

251 In a rabbit reticulocyte lysate transcription/translation system, th

252 nts co-migrated with fragments formed in the reticulocyte lysate translation mixture used for GAP-43

253 In this study, a rabbit reticulocyte lysate translation reaction was used to rec

254 ing frame is highly efficient in both rabbit reticulocyte lysate translation reactions and in culture

255 lenocysteines can be reconstituted in rabbit reticulocyte lysate translation reactions.

256 Rs can be synthesized in vitro with a rabbit reticulocyte lysate translation system supplemented with

257 oring translation to a PABP-dependent rabbit reticulocyte lysate translation system.

258 and inhibit globin translation in the rabbit reticulocyte lysate translation system.

259 nto an immature capsid when synthesized in a reticulocyte lysate translation system.

260 Western blot analysis of rabbit reticulocyte lysate using polyclonal antibody against th

261 protein synthesis, was purified from rabbit reticulocyte lysates using an assay that specifically me

262 mobility of GR recovered on incubation with reticulocyte lysate was inhibited by geldanamycin, a dru

263 The inhibition of translation observed in reticulocyte lysates was prevented by the addition of ad

264 ere was efficient reinitiation in a standard reticulocyte lysate, when initiation would be largely dr

265 2A10, recognises a protein present in rabbit reticulocyte lysate which binds murine p53 translated in

266 ent homogeneity a 66-kDa protein from rabbit reticulocyte lysate which is associated with hsp 70.

267 ated by the DE52-retained fraction of rabbit reticulocyte lysate, which also assembles nNOS.hsp90 het

268 ate investigation of these questions, rabbit reticulocyte lysate, which contains the cytoplasmic chap

269 tion substrates in fraction II of the rabbit reticulocyte lysate with an efficiency parallel to their

270 When PABP was depleted from the reticulocyte lysate with anti-human PABP antibody, the c

271 90.p60.hsp70 foldosome complex isolated from reticulocyte lysate with antibody against p60.

272 Mutant NQO1 incubated in rabbit reticulocyte lysate with MG132 resulted in the accumulat

273 Supplementation of rabbit reticulocyte lysate with nucleolin decreased APP mRNA st

274 radation of ubiquitinated proteins in rabbit reticulocyte lysates with an IC50 of 52 microM.

275 al inhibition of brain poly(A) RNA in rabbit reticulocyte lysate without accelerated mRNA degradation

276 ted their translation efficiencies in rabbit reticulocyte lysates, Xenopus oocytes, and primary cultu