ライフサイエンスコーパス: copurify

1 able complex with Rev7, and the two proteins copurify.

2 ains inner and outer membranes and that they copurify.

3 says, A-AC4 protein and miRNA complexes were copurified.

4 The virions and exosomes copurified.

5 observed that collectin liver 1 (CL-L1) was copurified.

6 Both hSSB1 mutants copurified a subset of Integrator complex subunits and t

7 Copurified ABCG5/G8 displayed low but significant ATPase

8 The catalytic activity of copurified ABCG5/G8 was characterized in detail, demonst

9 ins is required for telomere maintenance and copurifies active RNP.

10 cerebellum and choroid plexus: the proteins copurified after detergent treatment and co-immunoprecip

11 is consistent with the equivalent complexes copurified after they had been co-expressed in Escherich

12 Upon immunoisolation, NflD and NflH copurified, along with three other proteins whose functi

13 ntial importance of previously unappreciated copurified and/or contaminating TLR ligands in PPS vacci

14 CTIP2 copurifies and interacts with an inactive P-TEFb complex

15 otein huntingtin-associated protein-1 (HAP1) copurify and colocalize with autophagosomes in neurons.

16 but find that the response is dependent upon copurified APC expressing class II MHC that are autologo

17 Nodal, Gdf1, and their cleaved propeptides copurified as a heterodimeric low molecular weight compl

18 apparatus of polarized epithelial cells and copurify as a tight complex during IF-cobalamin affinity

19 dily interconvert, this isomeric mixture was copurified by HPLC away from the other isomeric products

20 density membranes on a Nycodenz gradient and copurify by affinity isolation using native but not Trit

21 To overcome this obstacle, we copurified disulfide-linked Ig heavy and light chains fr

22 The PdxS and PdxT proteins copurified during affinity chromatography and apparently

23 ing partners, including SOX2 and SALL4, that copurified during immunoprecipitation.

24 olipids, specifically cardiolipin, bound the copurified EpsE/cyto-EpsL complex and stimulated its ATP

25 In biochemical preparations, CARMIL copurified extensively with two polypeptides that were s

26 at the different DBHS proteins are typically copurified from mammalian cells, and suggesting that the

27 both the membrane and cytoplasm and could be copurified from the latter fraction.

28 fact that RNase E and PNPase can be readily copurified from Y. pseudotuberculosis cell extracts, sug

29 studies showed that these proteins could be copurified from yeast.

30 We have found that Def1 copurifies from yeast whole-cell extract with TFIIH, the

31 ting proteins within the growing leaf, since copurified GROWTH-REGULATING FACTORs (GRFs) varied throu

32 We copurified HISTONE DEACETYLASE19 (HDA19) with MSI1 and t

33 NrdE and NrdF were copurified in a 1:1 ratio from this engineered B. subtil

34 smD, CsmE, CsmF, CsmH, CsmI, CsmJ, and CsmX) copurified in a constant proportion together with bacter

35 with punctate structures within neurons and copurified in part with mitochondria.

36 Cadherins, NPRAP, GRIP, and GluR2 copurified in the fractionation of synaptosomes and the

37 not a factor, because all of these proteins copurify in caveolin-3-enriched vesicles isolated from a

38 tein S1 and nucleic acid-binding protein Hfq copurify in molar ratios with RNA polymerase (RNAP).

39 the kinase Bur1, and that both Sub1 and Spt5 copurify in the same complex, likely during early transc

40 oteins, Sra, Nap, Wave-2, Abi, and Hspc, are copurified, indicating that they form a tight complex.

41 is known to be phosphorylated in vitro by a copurifying kinase, and it has been demonstrated recentl

42 ting the possibility of contamination with a copurifying kinase.

43 Here, we identify a set of 10 copurifying kinetochore proteins from Caenorhabditis ele

44 cleavage, and a native structure containing copurified ligands, modeled as DHAP and glycerol.

45 omponents including native PrP(C) molecules, copurified lipid molecules, and a synthetic polyanion.

46 reparation containing only native PrP(C) and copurified lipid molecules.

47 and TLR2/TLR1 by LPS is in large part due to copurifying molecules that are sensitive to the action o

48 eIF3k from transiently transfected COS cells copurifies other eIF3 subunits.

49 matography coupled with mass spectrometry to copurify otoferlin interaction partners in the mammalian

50 phosphatase and phosphodiesterase activities copurify over several steps; inorganic phosphate, a stro

51 Nup2 localizes with a copurifying partner termed NupA, a highly divergent yet

52 er that correlates with the concentration of copurified PL.

53 inhibition was due to calreticulin and not a copurifying protein in the native calreticulin preparati

54 e-microtubule attachments, we show that this copurifying protein network plays a central role at the

55 plex and identified an approximately 120 kDa copurifying protein that is the plant homolog of UV-Dama

56 , a deubiquitinating enzyme, was a prominent copurifying protein.

57 Mass spectrometry analyses of copurified proteins revealed that BAP1 is associated wit

58 inase (RSK) proteins, we found several other copurified proteins, including prominent ones of approxi

59 genetic analysis of 592 mitotic microtubule copurifying proteins (MMCPs).

60 ed subunit was purified from infected cells, copurifying proteins included the other RdRP subunits (P

61 Copurifying proteins suggest that the APs interact with

62 Additional copurifying proteins were identified by Western blot ana

63 n and mass spectrometry analysis to identify copurifying proteins, two-hybrid analysis to identify in

64 mily, from a background of approximately 900 copurifying proteins.

65 cription complex within a high background of copurifying proteins.

66 suspension cell culture and characterize the copurified proteome, identifying 37 high-confidence cand

67 conditions used in the purification allowed copurifying PSBS with its interactors, which were identi

68 Unexpectedly, Y5 RNA uniquely copurified ribosomal protein L5 and its binding partner

69 , RNase P was rapidly affinity-purified, and copurified RNAs were identified by using a genome-wide m

70 r matrix, and some intracellular components, copurified specifically with IgG from RA and OA tissues.

71 We also show that Fdh copurifies specifically with VhuD in the absence of othe

72 into a heteroheptameric ring, only a subset copurifies telomerase and Cajal body ribonucleoproteins.

73 The ability to copurify this protein by transferrin affinity was depend

74 I/IV/V and fushi tarazu localization signals copurified through multiple fractionation steps, suggest

75 SSIII, SSIIa, SBEIIa, and SBEIIb copurified through successive chromatography steps, and

76 detectably enrich active telomerase but did copurify ubiquitin ligase machinery.

77 lly differentiate ubiquitinated species from copurified unmodified components.

78 li, two complexes of different stoichiometry copurified with 40 and 72 nt crRNA species, respectively

79 n addition to RENT components and Fob1, Tof2 copurified with a two-subunit complex composed of Lrs4 a

80 zyme, SPTLC1, but not subunit 2 (SPTLC2), is copurified with ABCA1 and negatively regulates its funct

81 results from cross-linking, GRIFIN subunits copurified with alpha-crystallin complexes during size e

82 The alpha2 protein copurified with alpha1 and beta in a complex with an ove

83 Both transcripts could be copurified with an Ab against the nascent hERG 1a N term

84 d protein-1) as a cofactor that specifically copurified with an NR2C1/NR2C2 (TR2/TR4) orphan nuclear

85 16 inhibitory sera, and inhibitory activity copurified with anti-double-stranded DNA in the immunogl

86 ssion system, secreted recombinant UGRP1 was copurified with apolipoprotein A-I.

87 homologues of UreD, UreF, and UreG have been copurified with apourease, it remains unclear specifical

88 signalosome in intact cells and in addition copurified with ASK1 following treatment for 3 min.

89 PI4KIIalpha copurified with BLOC-1 and AP-3 in neuronal cells.

90 H4 that copurified with CAF-1 was a mixture of isoforms acetylat

91 that REST and nine REST-associated proteins copurified with Cbx family PcG proteins from mouse embry

92 Recently, LMP1 was shown to be copurified with CD63, a conserved tetraspanin protein en

93 ibitable by cysteine protease inhibitors was copurified with Cpl immunoreactivity, and purified Cpl a

94 Many of the transcripts that copurified with CsrA were previously determined to respo

95 e found among 721 different transcripts that copurified with CsrA.

96 Furthermore, FAP163 copurified with D1bIC(FAP133) and the LC8 dynein light c

97 EFs SPT4/SPT5, SPT6, FACT, PAF1-C, and TFIIS copurified with each other and with elongating RNAPII, w

98 en telomerase was affinity purified, primase copurified with enzyme from mated cells but not with the

99 of this enzyme, we identified proteins that copurified with epitope-tagged Rsp5.

100 In addition, FtsZ copurified with FLAG-FtsE.

101 Importantly, both gI and Us9, but not KIF1A, copurified with gE-GFP.

102 Examining membrane-associated proteins that copurified with GOA-1 Galpha, we found that the transmem

103 and other extracellular matrix proteins that copurified with gp120.

104 l heat shock proteins Ssb1 and Ssb2 are also copurified with HA(3)-TAP-tagged Reg1.

105 sing anti-HDAC3, transcription factor TFII-I copurified with HDAC3.

106 CpcS-I copurified with His(6)-tagged (HT) CpcU as a heterodimer

107 tive gel electrophoresis, and Psb27 could be copurified with histidine-tagged PSI isolated from the w

108 ng yeast CENP-C homologue Mif2p specifically copurified with histones H2A, H2B, and H4, and with the

109 g their own BAF." Supporting this model, BAF copurified with HIV-1 virions that were digested with su

110 Sse1/2 copurified with Hsp70 and other proteins comprising the

111 Forty-six proteins that copurified with ICP4 were identified by mass spectrometr

112 subunit of PP2A, microtubule star (MTS), is copurified with INAD, and an elevated phosphorylation of

113 tic cells, and an unknown 55 kDa protein was copurified with it.

114 11, but not the non-DAF-using EV11, could be copurified with lipid raft components during infection a

115 at identical perinuclear locations, and both copurified with M proteins, but E.T was entirely incompe

116 enriched in intestinal IEL preparations and copurified with markers of Talphabeta and Tgammadelta IE

117 unofluorescence analysis showed that SOK was copurified with membrane fractions and was exposed on th

118 cond alternative exon (x01) localized to and copurified with microtubule bundles as dynamic polymers

119 vertebrate kinetochore protein CENP-H, also copurified with Mif2p and a variety of central kinetocho

120 nsmembrane AMPAR regulatory proteins (TARPs) copurified with neuronal AMPARs, but we found negligible

121 total nonmuscle myosin II in axoplasm, 43.2% copurified with organelles in the 15% sucrose fraction,

122 reviously uncharacterized proteins were also copurified with OST.

123 We also found that DRD1 copurified with Pol V subunits and that RDM1, like DRD1

124 haeon Methanocaldococcus jannaschii that was copurified with prolyl-tRNA synthetase (ProRS).

125 d not exclusive, although the major proteins copurified with PSBS were components of the LHCII trimer

126 Factor activity copurified with Rad50, Mre11 and NBS1, three proteins th

127 Bud8p and Bud9p could also be copurified with Rax1p, and localization studies provided

128 o E3 ligases, Arf-bp1 and Pam (Myc-bp2), are copurified with Rev-erb alpha and required for its ubiqu

129 Bovine PDEdelta was originally copurified with rod cGMP phosphodiesterase (PDE) and sho

130 nti-nucleosome IgG2a(a) mAb, termed 3F7.A10, copurified with self-histones and was a potent immunogen

131 Pnn colocalized and copurified with serine-arginine (SR) proteins.

132 Spt5 also copurified with several previously unstudied proteins; w

133 In addition, SigD was specifically copurified with SigE-His(6) on a nickel column.

134 Specifically, both LC3-II and Rab11 proteins copurified with some infectious VZV particles.

135 ogenous NADH oxidase activity from rat heart copurified with SR enriched with RyR2.

136 Additional proteins that copurified with SSIII in multiple biochemical methods in

137 Endogenous MtrC copurified with tagged OmcA in wild-type Shewanella, sug

138 The majority of miRNAs studied copurified with the Ago2 ribonucleoprotein complex, but

139 extract found that the PP1 catalytic subunit copurified with the anchoring protein.

140 ASF/SF2 splicing factor-associated protein, copurified with the CBF complex.

141 cts, 25 and 18 kDa; only the 18-kDa fragment copurified with the Cdt complexes.

142 Interacting proteins were copurified with the epitope-tagged crystallin complexes

143 Heat shock cognate protein 70 (HSC70) also copurified with the GST-PDZ1-containing fragment but lac

144 All three Cdt peptides copurified with the His-tagged Cdt peptide.

145 Because Rap1a was previously copurified with the human neutrophil NADPH oxidase, we a

146 Although CikA is copurified with the Kai proteins that constitute the cir

147 cluding components of the Nup82 complex that copurified with the mutant Nmd3.

148 -like protein present in the spliceosome and copurified with the Prp43p DExD/H-box ATPase.

149 We identified 374 different proteins that copurified with the PSD structure and discovered thirtee

150 tein components of the H/ACA sno/scaRNP also copurified with the pseudouridylase activity.

151 In addition, the E. coli GroEL chaperonin copurified with the recombinant NodD proteins.

152 Three sperm mitochondrial proteins copurified with the recombinant, ubiquitin-associated do

153 vious RNA-seq analyses showed that moaA mRNA copurified with the RNA binding protein CsrA (carbon sto

154 ospho-IC and the total amount of dynein that copurified with the signaling endosomes.

155 The eighth polypeptide copurified with the subcomplex at all stages, is strongl

156 YscP-GST copurified with the type III ATPase complex (YscN, YscL,

157 a coli, the prokaryotic hsp70 chaperone DnaK copurified with the VP1 C-terminal domain that links pen

158 virion tegument phosphoprotein, specifically copurified with UL97 during TAP, as shown by mass spectr

159 polypeptides of approximately 110 and 66 kDa copurified with VITF-2 activity through multiple chromat

160 A sequences by cloning fragments of DNA that copurified with XCENP-A by chromatin immunoprecipitation

161 Here we show that MDMX copurifies with 14-3-3, and DNA damage stimulates MDMX b

162 ound that NML is an RNA binding protein that copurifies with 5S, 5.8S, and 28S rRNA.

163 Here we report that Swi1 copurifies with a 181-amino-acid protein encoded by swi3

164 This activity copurifies with a proliferating cell nuclear antigen-dep

165 enzyme from Saccharomyces cerevisiae (THI4) copurifies with a set of strongly bound adenylated metab

166 lyses confirm that the wild-type THI2 enzyme copurifies with a thiazole precursor to thiamine, wherea

167 We find that AAK1 copurifies with adaptor protein (AP)2 and that it direct

168 re, we find that triple Myc-tagged Aha1/Myc3 copurifies with all noninducible Mal63 mutant activators

169 PTIP copurifies with ALR, MLL3, and other components of a his

170 UBE2S copurifies with APC; dominant-negative Ube2S slows down

171 data suggest that a minor lipid species that copurifies with beta-GlcCer in mammals functions as a li

172 n 1 (HIP1), a binding partner of huntingtin, copurifies with brain clathrin-coated vesicles and assoc

173 protein required for cell size control that copurifies with Bre1.

174 that Mps1 is the major kinase activity that copurifies with budding yeast kinetochore particles and

175 approximately 200 nt) of cellular TERRA and copurifies with CD63- and CD83-positive exosome vesicles

176 We show that the LIC subunit copurifies with cDHC1b during flagellar isolation, dynei

177 Furthermore, Pin1 localizes to and copurifies with centrosomes in interphase but not mitoti

178 A small portion of C1beta3Gal-T copurifies with Cosmc from cell extracts, demonstrating

179 The TtCmr complex copurifies with crRNA species of 40 and 46 nt, originati

180 ously identified FUS12 locus and that AtCSN2 copurifies with CSN, confirming that AtCSN2 is an integr

181 The finding that N-RAP copurifies with detergent-extracted intercalated disk fr

182 Our results demonstrate that HOS copurifies with HAS and that HAS copurifies with HOS, in

183 te that HOS copurifies with HAS and that HAS copurifies with HOS, indicating that HOS and HAS interac

184 the identification of a TUTase activity that copurifies with in vitro editing and is catalyzed by the

185 Tctex2b copurifies with inner arm I1 after both sucrose gradient

186 tracts that completely lack outer arms, LC7b copurifies with inner arm I1, whereas in ida1 extracts t

187 We found that DinB(C66A) copurifies with its interacting partners, RecA and UmuD,

188 The PRV Us9 protein copurifies with KIF1A, recruiting the motor to transport

189 sucrose gradients with 43S/40S subunits, and copurifies with late 43S particles.

190 Finally, we found that US28 copurifies with mature virions and is expressed in HPCs

191 ultipotent adult progenitor cell (MAPC) that copurifies with mesenchymal stem cells from postnatal hu

192 Moreover, HtrA1 cosediments and copurifies with microtubules.

193 Also, Swi6 copurifies with Mis4 protein, a cohesin loading factor e

194 The DNA topoisomerase II copurifies with mitochondria and directly associates wit

195 Additionally, UNC-96 copurifies with native thick filaments.

196 ms a stable complex with the chromosome that copurifies with nucleoids following gentle cell lysis.

197 ependent biochemical methods found that YdeI copurifies with OmpD/NmpC, a member of the trimeric beta

198 omplemented by the recent report that Mdm20p copurifies with one of three acetyltransferases in yeast

199 LC9 copurifies with outer arm dynein in sucrose density grad

200 The signalosome copurifies with Pcu4 (cullin 4).

201 eceptors and upstream of PDK1 and mTORC2 and copurifies with PI3K in immunoprecipitation assays.

202 Nonmuscle myosin copurifies with polysomes, and there is a subset of poly

203 nti-His-tag antibodies, and recombinant PrtP copurifies with PrcB-6xHis in nickel affinity chromatogr

204 Cag3 is membrane associated and copurifies with predicted inner and outer membrane Cag T

205 Moreover, LdpA copurifies with proteins previously shown to be integral

206 Sqs1p copurifies with Prp43p and is shown to bind Prp43p and S

207 n arms) and pf17 axonemes with 0.5 M KI, and copurifies with radial spokes in sucrose density gradien

208 M-RIP copurifies with RhoA and Rho kinase, colocalizes on acti

209 Here, we show that dMCRS2 copurifies with RNA polymerase II (RNAP II) complexes an

210 wever, following in vivo cross-linking, RAF1 copurifies with Rubisco large subunit, suggesting that t

211 d proteomic analysis revealed that PSMA1-GFP copurifies with several acrosomal membrane-associated pr

212 Interestingly, CgtA(E) copurifies with SpoT, a ribosome-associated ppGpp hydrol

213 Here, we found that DGCR8 copurifies with subunits of the nuclear exosome, prefere

214 , unlike other class I HDACs, HDAC3 uniquely copurifies with the catalytic and regulatory subunits of

215 ovalent complex is due to unreacted CcP that copurifies with the covalent complex.

216 Nbl1p colocalizes and copurifies with the CPC, and it is essential for CPC loc

217 The ADP ligand copurifies with the enzyme, and its presence does not in

218 rmline-specific RNA-containing particles and copurifies with the essential RNA helicase, CGH-1, in an

219 acellular, 130-kD, leucine-rich protein that copurifies with the fibroblast growth factor receptor fr

220 r3, and Hpc2 comprise the HIR complex, which copurifies with the histone deposition protein Asf1.

221 ing that the heterochromatin protein HP1beta copurifies with the macroH2A1-containing chromatin fragm

222 We show that CTCF copurifies with the nucleolar protein nucleophosmin and

223 of the Hat1p/Hat2p complex and find that it copurifies with the product of the uncharacterized open

224 resence of endogenous nuclease activity that copurifies with the replication complex.

225 Because a portion of YidC copurifies with the Sec translocase, this interaction mi

226 ein required for the production of 18S rRNA, copurifies with the snR30/U17 processing snoRNP but is a

227 dentified as a large multimeric complex that copurifies with the thyroid hormone receptor (TR) from H

228 ost plant homeodomains [PHDs] of Trr), which copurifies with the Trr complex.

229 In budding yeast, Ndc80 copurifies with three additional interacting proteins: N

230 When overexpressed in E. coli, PPAT copurifies with tightly bound CoA, suggesting a feedback

231 lization with Rab11a and VAMP8 and partially copurifies with ZG fractions.

232 sion in Escherichia coli, TrpRS II binds to, copurifies with, and dramatically enhances the solubilit

233 ages of purification, AcMNPV AN was found to copurify with a 44-kDa polypeptide which was identified

234 ansion of tumor-initiating cells (TICs) that copurify with a CD24(med)CD49f(hi) population from prema

235 uantitative analysis indicates that vesicles copurify with a low number of stably bound motors: one t

236 rimeric PP2A containing B' and B' ' subunits copurify with alpha(1)1.2.

237 inity purified TINA and found it to uniquely copurify with An-WDR8, a WD40-domain protein conserved f

238 ee proteins (kette, Abi, and Sra-1) known to copurify with and inhibit SCAR in vitro leads to SCAR de

239 Autophagosomes copurify with anterograde and retrograde motors, suggest

240 utarate dehydrogenase complexes specifically copurify with both LipB and LipA.

241 sRNA, helicase, polymerase, and protease p29 copurify with C. parasitica trans-Golgi network (TGN) ma

242 Although alpha2delta subunits copurify with CaV2 channels, it has recently been sugges

243 spectrometry data to identify proteins that copurify with components of the budding yeast TFIID tran

244 hDcp1a and hDcp2 copurify with decapping activity, an activity sensitive

245 ISTEM SILENCING 3 (DMS3), we found that they copurify with each other and with a novel protein, RNA-D

246 Characterization of cellular proteins that copurify with ectopically expressed measles virus V prot

247 ther RGG domain-containing proteins in yeast copurify with eIF4E/G and we demonstrate that two such p

248 imately 30% of its outer arms, LC7b fails to copurify with either dynein, suggesting that it interact

249 glycine cleavage system H protein, does not copurify with either LipA or LipB.

250 the ability of mutant 4.5S RNA molecules to copurify with Ffh.

251 However, SCAR has recently been found to copurify with four other proteins in a complex.

252 ein-1 (Aup1) as one of several proteins that copurify with gp78.

253 nsistent with these observations, Mn did not copurify with Gpm.

254 ulgaris and M. barkeri enzyme complexes both copurify with haem, whose redox state influences the act

255 ent expression in planta, HopQ1 was shown to copurify with host 14-3-3 proteins.

256 ne deacetylase 2 (HDAC2) corepressor complex copurify with hSWI/SNF complexes.

257 ected HeLa cells was found to colocalize and copurify with hyperphosphorylated forms of Pol II (Pol I

258 y, an unusually large number of granulocytes copurify with low density PBMCs on a density gradient ra

259 orates into functional dynein complexes that copurify with membranous organelles.

260 demonstrated that a subset of cellular mRNAs copurify with mitotic microtubules in egg extracts of Xe

261 In biochemical assays, Pms1p failed to copurify with mlh1-2, and two-hybrid studies indicated t

262 (i) uracil-DNA glycosylase activity did not copurify with Ndk activity; (ii) Ndk purified from E. co

263 ly associate with interphase chromosomes and copurify with nuclear scaffold, indicating that RNAs mig

264 recently showed that flagellar ODA8 does not copurify with ODA5 or ODA10.

265 In addition, BiP and pp28 copurify with other assembly compartment components on s

266 Both ubiquitin and Smt3p copurify with Pac1p.

267 Three polypeptides copurify with PBP-1 activity, suggesting that PBP-1 is c

268 xsackievirus B3, and human rhinovirus 14 all copurify with PI4KIIIbeta.

269 We have found that these two proteins copurify with Pol I and associate with the rDNA in vivo.

270 inent approximately 45-kDa band was found to copurify with processive polymerase activity.

271 ue to show that one or more tyrosine kinases copurify with rat brain phospholipase C-gamma1.

272 Enzymes that copurify with RNA polymerase include those associated wi

273 nucleolar RNAs (snoRNAs), because these both copurify with RNase P and accumulate larger forms in the

274 nce of low molecular mass (LMM) species that copurify with tAFP and function equivalently to the LMM

275 Although both TER1 and TER2 copurify with telomerase activity and serve as templates

276 Both PAF49 and PAF53 copurify with that fraction of the RNA polymerase I mole

277 entrate at costameres of striated muscle and copurify with the dystrophin-glycoprotein complex, perha

278 together, but these larger oligomers did not copurify with the functional F(o)F(1) complex and were c

279 first sugar, GlcNAc, was previously shown to copurify with the GnT51 polypeptide whose gene has now b

280 found that multiple picornavirus 3A proteins copurify with the Golgi adaptor protein acyl coenzyme A

281 S-1 is found to colocalize and biochemically copurify with the microtubule organizing complex (MTOC)

282 ass B synthetic multivulva (synMuv) protein, copurify with the Myb complex components to form the Myb

283 te NRPS systems, we show that these proteins copurify with the NRPSs and influence amino acid activat

284 tive transcription factor, was discovered to copurify with the Nup107-160 complex in Xenopus interpha

285 ex of approximately 450 kDa and was found to copurify with the Rpd3 histone deacetylase protein durin

286 confirmed that vesicles containing cryparin copurify with the same fractions previously shown to con

287 CUL4A and its paralog, cullin 4B (CUL4B), copurify with the UV-DDB complex, but it is unclear whet

288 We previously showed that seven proteins copurify with the yeast (Saccharomyces cerevisiae) SF3b

289 ain protein, named Atac1 (ATAC component 1), copurify with this complex.

290 Previously Isw1p was shown to copurify with three other proteins.

291 It has been shown that the polypeptides copurify with two homopolymers, poly[(R)-3-hydroxybutyra

292 The H-CT domain does not copurify with V(1) when expressed in yeast, but the bact

293 iated neuronal protein, one of many proteins copurifying with Cdk5/p35 in membrane-bound multimeric c

294 perones involved in ER-quality control, were copurifying with Cf-4-enhanced green fluorescent protein

295 and 46 human cellular proteins specifically copurifying with extracellular HCV virions.

296 (OH), is isolated as a native RNA-DNA hybrid copurifying with mtDNA.

297 ce proteomics, we identified 850 interactors copurifying with nine NPHP/JBTS/MKS proteins and discove

298 PRESSOR OF PHYA-105 (SPA) family as proteins copurifying with UVR8(W285A).

299 We previously found that one protein copurifying with Yta7 is the yFACT member Spt16.

300 nherent to NH(2)Y-RNRs and not the result of copurifying wt enzyme.