戻る
「早戻しボタン」を押すと検索画面に戻ります。

今後説明を表示しない

[OK]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1  to be a homotrimeric protein as assessed by gel filtration chromatography.
2 omere restriction fragments were purified by gel filtration chromatography.
3 onuclease 1 (APE1) over phosphocellulose and gel filtration chromatography.
4 ring IF-cobalamin affinity and nondenaturing gel filtration chromatography.
5 apientum (MSP) were isolated and purified by gel filtration chromatography.
6 ncentration following detergent exchange via gel filtration chromatography.
7 n the extracellular medium were separated by gel filtration chromatography.
8  associated and can be partially purified by gel filtration chromatography.
9 ultiple intermediates that are detectable by gel filtration chromatography.
10 ative polyacrylamide gel electrophoresis and gel filtration chromatography.
11 was estimated to be approximately 125 kDa by gel filtration chromatography.
12 exchange chromatography, ultrafiltration and gel filtration chromatography.
13 were analyzed for interactions by analytical gel filtration chromatography.
14 ied by sequential metal chelate affinity and gel filtration chromatography.
15 sugar residues were produced, as measured by gel filtration chromatography.
16 127Delta NifH with NifNE was investigated by gel filtration chromatography.
17 uilibrium analytical ultracentrifugation and gel filtration chromatography.
18 ely 270-300 and 400-450 kDa as determined by gel filtration chromatography.
19 e that can be purified by anion-exchange and gel filtration chromatography.
20 fied using ultrafiltration, ion exchange and gel filtration chromatography.
21 e and separated by tandem anion exchange and gel filtration chromatography.
22 FIID preparation was further fractionated by gel filtration chromatography.
23 e purified complex was 90 kd as estimated by gel filtration chromatography.
24      The hydrolysate was further purified by gel filtration chromatography.
25 native enzyme was estimated to be 160 kDa by gel filtration chromatography.
26 pitation with ammonium sulphate, followed by gel filtration chromatography.
27 eneity in two steps by DEAE ion exchange and gel filtration chromatography.
28 decamer in solution has been demonstrated by gel filtration chromatography.
29 nd activity measurements in combination with gel filtration chromatography.
30 ein still elutes in the void upon analytical gel filtration chromatography.
31 ing agents, and anomalous retardation during gel filtration chromatography.
32  sequences, and analyzing the products by P2 gel filtration chromatography.
33 ntibody complexes which could be isolated by gel filtration chromatography.
34  homogeneity by sequential metal-chelate and gel filtration chromatography.
35 y hydrophobic interaction, ion exchange, and gel filtration chromatography.
36 ad a molecular mass of nearly 2 MDa based on gel filtration chromatography.
37 ence of DNA by sedimentation equilibrium and gel filtration chromatography.
38 f GGT-deficient mice by papain treatment and gel filtration chromatography.
39 lei using ammonium sulfate fractionation and gel filtration chromatography.
40 eneity from strain DNT by anion exchange and gel filtration chromatography.
41 ss (32 kDa) forms that could be separated by gel filtration chromatography.
42 kd for the binding complex was determined by gel filtration chromatography.
43 ow density lipoprotein particles observed by gel filtration chromatography.
44 eneity using ion-exchange, DNA-affinity, and gel filtration chromatography.
45 -cell line MLA 144 by ionic, hydrophobic and gel filtration chromatography.
46 tion from HeLa cell extracts fractionated by gel filtration chromatography.
47 f the YABP was determined to be 74 300 using gel filtration chromatography.
48 d from partially constructed basal bodies by gel filtration chromatography.
49 d value was also obtained at 37 degrees C by gel filtration chromatography.
50  was stable during affinity purification and gel filtration chromatography.
51  measurements below the polymer's LCST using gel filtration chromatography.
52 metal affinity, hydrophobic interaction, and gel filtration chromatography.
53 ueous hydrogen fluoride (HF) and purified by gel filtration chromatography.
54 roteins were purified by Ni-NTA affinity and gel filtration chromatography.
55 s p50 were found to co-fractionate following gel filtration chromatography.
56 navalin A-Sepharose affinity and Superose 12 gel filtration chromatography.
57 were studied by dynamic light scattering and gel filtration chromatography.
58 4-DNA affinity beads and further purified by gel filtration chromatography.
59 heY3-P in vitro and eluted as a homodimer in gel filtration chromatography.
60 ies, neither of which could be restored upon gel-filtration chromatography.
61 hexamers were purified by anion-exchange and gel-filtration chromatography.
62 olumn and from elution steps in conventional gel-filtration chromatography.
63 s by a combination of hydrophobic column and gel-filtration chromatography.
64 ivum L. cv Alaska) epicotyls was examined by gel-filtration chromatography.
65 orresponding to approximately 170-180 kDa by gel-filtration chromatography.
66 eity using a combination of ion-exchange and gel-filtration chromatography.
67 alpha-synuclein by sedimentation followed by gel-filtration chromatography.
68 d by both analytical ultracentrifugation and gel-filtration chromatography.
69 nant protein purified by heparin-agarose and gel-filtration chromatography.
70 from pigments and larger protein material by gel-filtration chromatography.
71 ve molecular mass of approximately 18 kDa by gel-filtration chromatography.
72 ricted to oligomer-containing fractions from gel-filtration chromatography.
73 dentical subunits) that the complex survives gel-filtration chromatography.
74 pharose, Source 15Q, DEAE2, and Superdex 200 gel filtration chromatographies.
75 5 kD fraction (Ara h 2/6; 20 kD fraction) on gel filtration chromatography, account for the majority
76 sonance spectroscopy, titration calorimetry, gel-filtration chromatography, affinity chromatography,
77 or, AmiC, immobilized on a solid support and gel filtration chromatography, an AmiC-AmiR complex has
78                                           In gel filtration chromatography analyses of BC-3 cell lysa
79                              Sephacryl S-100 gel filtration chromatography analysis of the cytosolic
80 inary approach, including live cell imaging, gel filtration chromatography analysis, split ubiquitin
81 TS co-migrated exclusively with USP9X during gel filtration chromatography analysis.
82 ta-Pol-gapped DNA complex were determined by gel filtration chromatography and a gel mobility shift a
83 urified to near homogeneity then analyzed by gel filtration chromatography and analytical ultracentri
84                       Using a combination of gel filtration chromatography and analytical ultracentri
85                                              Gel filtration chromatography and analytical ultracentri
86                                  Analyses by gel filtration chromatography and analytical ultracentri
87              Tear proteins were separated by gel filtration chromatography and analyzed for bound lip
88 brium in the absence of DNA when examined by gel filtration chromatography and atomic force microscop
89 recursor cleaving activity by Sephacryl S200 gel filtration chromatography and by a single band of 35
90                                              Gel filtration chromatography and chemical cross-linking
91                                              Gel filtration chromatography and co-immunoprecipitation
92                                              Gel filtration chromatography and co-immunoprecipitation
93 trary to previous findings, a combination of gel filtration chromatography and co-purification studie
94 pper form of the heterodimer was isolated by gel filtration chromatography and contains one copper an
95 mbination of ion-exchange chromatography and gel filtration chromatography and demonstrated for the f
96  with alpha and theta was investigated using gel filtration chromatography and exonuclease stimulatio
97 ed to consist of six nucleotides, GGTTAC, by gel filtration chromatography and filter-binding assay (
98                            Supplemented with gel filtration chromatography and fluorescence-adapted s
99        The inhibited protein was isolated by gel filtration chromatography and found to be an AlF4-AD
100                                              Gel filtration chromatography and glycerol gradient sedi
101 Both enzymes were found to be homodimeric by gel filtration chromatography and homotetrameric by dyna
102                                     By using gel filtration chromatography and immunoprecipitation as
103                                      Second, gel filtration chromatography and immunoprecipitation in
104         Such a complex can be isolated using gel filtration chromatography and is by itself sufficien
105                                        Using gel filtration chromatography and isothermal titration c
106                                         Both gel filtration chromatography and mass analysis from two
107 monomer with an Mr of 21,814 +/- 20 based on gel filtration chromatography and mass spectrometric res
108 ve molecular mass of approximately 68 kDa by gel filtration chromatography and migrated as a single b
109 dimer to a monomeric protein on the basis of gel filtration chromatography and multiple-angle laser l
110                                              Gel filtration chromatography and native gel electrophor
111                                              Gel filtration chromatography and native polyacrylamide
112 ses for the THT oxygenase estimated by using gel filtration chromatography and nondenaturing gel elec
113 rm of Prt1p (His-Prt1p) by Ni2+ affinity and gel filtration chromatography and obtained a complex of
114                                 In addition, gel filtration chromatography and protein cross-linking
115 on procedures including membrane filtration, gel filtration chromatography and reversed-phase high-pe
116                                              Gel filtration chromatography and SDS-PAGE revealed that
117                                              Gel filtration chromatography and sedimentation equilibr
118                                   Analytical gel filtration chromatography and sedimentation velocity
119 7 cofractionated through successive steps of gel filtration chromatography and sucrose density gradie
120 lammonio]-1-propanesulfonic acid), performed gel filtration chromatography and sucrose density gradie
121 otein was isolated together with lysozyme by gel filtration chromatography and then separated from ly
122 tration membranes was further purified using gel filtration chromatography and two steps of reverse-p
123 nuclein was quantified by the combination of Gel filtration chromatography and Western blot, respecti
124                                              Gel-filtration chromatography and analytical ultracentri
125                                              Gel-filtration chromatography and analytical ultracentri
126                   We also show by analytical gel-filtration chromatography and analytical ultracentri
127                                   Analytical gel-filtration chromatography and chemical cross-linking
128                                              Gel-filtration chromatography and chemical cross-linking
129                             A combination of gel-filtration chromatography and circular dichroism spe
130      Disaggregation of AgLDL was verified by gel-filtration chromatography and electron microscopy th
131          We have purified this complex using gel-filtration chromatography and have found that it is
132                             A combination of gel-filtration chromatography and protein overlay assays
133  of monomer-dimer equilibrium as assessed by gel-filtration chromatography and ultracentrifugation st
134 eraction, Sephadex G-100 and Sephacryl S-200 gel filtration chromatographies, and sodium dodecyl sulf
135 3.5 A) in the Stokes radius as determined by gel filtration chromatography, and (iii) a similar decre
136 N. americanus homogenate was fractionated by gel filtration chromatography, and a FACS-based bioassay
137 ad a molecular mass of 320 kDa, estimated by gel filtration chromatography, and a subunit size of 90.
138 wn to be trimeric by chemical cross-linking, gel filtration chromatography, and analytical ultracentr
139 , we used a combination of NMR spectroscopy, gel filtration chromatography, and analytical ultracentr
140                 Using the prenylation assay, gel filtration chromatography, and density ultracentrifu
141  interaction in the yeast two-hybrid system, gel filtration chromatography, and equilibrium sedimenta
142 action of MDH2 with PCK1 using Hummel-Dreyer gel filtration chromatography, and for interactions of M
143            Using native gel electrophoresis, gel filtration chromatography, and surface plasmon reson
144 agment was purified as an 800-kDa complex by gel filtration chromatography, and the associating prote
145  the enzyme was estimated to be 65 000 using gel filtration chromatography, and the pH optimum was 4.
146        Sera were subjected to Sephadex G-200 gel filtration chromatography, and the structure and bio
147 nd the methods of gel mobility shift assays, gel filtration chromatography, and UV-cross-linking, we
148                Plasma was fractionated using gel-filtration chromatography, and lipid-associated prot
149 rm agglutinin chromatography, Sephacryl S300 gel filtration chromatography, anti-FLAG immunoaffinity
150  The native molecular mass, as determined by gel filtration chromatography, appeared to be approximat
151                             It migrated upon gel filtration chromatography as a monomer with an appar
152 ferric siderophores with high affinity: in a gel filtration chromatography assay the K(d) of the ferr
153                                              Gel filtration chromatography at high and low temperatur
154 ion with proteinase K and after dissociative gel filtration chromatography, but was completely abolis
155                             As determined by gel filtration chromatography, cGMP binding caused elong
156 ) of S100P using equilibrium centrifugation, gel-filtration chromatography, circular dichroism and fl
157 mbined approaches of chemical cross-linking, gel filtration chromatography, co-immunoprecipitation, c
158          Circular dichroism spectroscopy and gel filtration chromatography conducted on wild-type and
159                         Purification through gel filtration chromatography confirmed the formation of
160                                              Gel filtration chromatography confirms the differentiati
161                                   Analytical gel-filtration chromatography confirms that the OMP.OPRT
162 of PDE3A2 by PKC led to shifts in elution on gel-filtration chromatography consistent with increased
163                                              Gel filtration chromatography data show that the MoFe pr
164 ulldown assays of a Orai1-CMBD(W76E) mutant, gel filtration chromatography data, and NOE signals indi
165                                  Analysis by gel filtration chromatography demonstrated that each of
166                                              Gel-filtration chromatography demonstrated an interactio
167                                              Gel-filtration chromatography demonstrated that ASRT for
168  enzymatic activity similar to HGPRT-II, and gel filtration chromatography demonstrates that its size
169                                   Analytical gel filtration chromatography demonstrates that Slit D2
170                                              Gel filtration chromatography demonstrates that upon bin
171                       Using a combination of gel filtration chromatography, differential scanning cal
172                               In this study, gel filtration chromatography, dynamic light scattering,
173                                              Gel filtration chromatography, dynamic light scattering,
174                                 According to gel filtration chromatography, dynamic light scattering,
175                Here, we use a combination of gel filtration chromatography, dynamic light-scattering,
176                    Protein cross-linking and gel filtration chromatography experiments established th
177 ith the results of coimmunoprecipitation and gel filtration chromatography experiments reported here,
178                              With the use of gel filtration chromatography followed by affinity purif
179                   Fractionation of plasma by gel filtration chromatography followed by bioassays indi
180       The resolving exudate was subjected to gel filtration chromatography followed by proteomics, id
181  mitochondria by sequential ion-exchange and gel filtration chromatography, followed by glycerol grad
182  molecular mass around 140 kDa determined by gel filtration chromatography for each of the enzymes.
183  was purified to homogeneity by affinity and gel-filtration chromatography for antibody production an
184 RA from cell extracts by nickel affinity and gel-filtration chromatography found a multicomponent com
185 se peptides were purified after affinity and gel filtration chromatography from a chickpea protein hy
186 led under aprotic conditions and purified by gel-filtration chromatography (GFC) using high-specific-
187 om brush border membrane vesicles (BBMVs) by gel filtration chromatography hinders the cleavage of BT
188 ) leaves and purified using ion exchange and gel filtration chromatography in combination with yeast
189 0 Da, relative to globular standards, during gel filtration chromatography in the absence of polyanio
190 from the 28-kDa fragment (residues 1-257) by gel filtration chromatography in the presence of 4 M ure
191 l misfolding of the enzyme as it eluted from gel filtration chromatography in the same fraction as th
192 revealed a single band at 36 kDa, and native gel filtration chromatography indicated a molecular mass
193                                              Gel filtration chromatography indicated that the protein
194                                              Gel-filtration chromatography indicated that HSP16.5 is
195                                              Gel filtration chromatography indicates CofE is a dimer.
196                                              Gel filtration chromatography indicates that the E1A- an
197 ined 0.92 +/- 0.11 apoE molecules/apoB after gel filtration chromatography, indicating stable complex
198 t molecular mass of 110 kDa as determined by gel-filtration chromatography, indicating that the prote
199 med structural studies of this protein using gel filtration chromatography, intrinsic tryptophan fluo
200 interaction of EIIA with HPr was detected by gel-filtration chromatography, intrinsic tryptophanyl re
201 olecular mass of native DmPBP as measured by gel-filtration chromatography is 375 kDa.
202 of R120G alphaB-crystallin, as determined by gel filtration chromatography, is 1.4 MDa, which is more
203 ion bodies, but when subjected to analytical gel filtration chromatography, it elutes in the void vol
204                    Fractionation of serum by gel filtration chromatography led to the identification
205                                        After gel-filtration chromatography, macrophage-derived protei
206 rial lysate from HeLa cells was submitted to gel filtration chromatography, mTERF was eluted in two p
207                                              Gel filtration chromatography, native gel electrophoresi
208                    We characterized NABBs by gel-filtration chromatography, native polyacrylamide gra
209                                              Gel filtration chromatography of a sonicate of M. avium
210                                              Gel filtration chromatography of conditioned medium from
211                                              Gel filtration chromatography of COS7 cell cytosol showe
212 r mass of about 70 to 80 kDa was detected by gel filtration chromatography of extracts from wild-type
213                                              Gel filtration chromatography of leukocyte cytosol revea
214                      In the present studies, gel filtration chromatography of liver cytosol from LFAB
215                                              Gel filtration chromatography of Salmonella conditioned
216  micellar complex is 5 nm as determined from gel filtration chromatography of SKC1 in dodecyl maltosi
217                                       During gel filtration chromatography of solubilized SR membrane
218                                              Gel filtration chromatography of the full-length fusion
219 resis, N-terminal amino acid sequencing, and gel filtration chromatography of the purified lectin sho
220                                              Gel filtration chromatography of the purified protein re
221      The hOAT1 oligomer was also detected in gel filtration chromatography of total membranes from hO
222                                              Gel filtration chromatography of wild-type S. typhimuriu
223         Protein cross-linking and calibrated gel filtration chromatography of yNAP1 indicate the prot
224 lypeptide cofractionated with V-ATPases upon gel-filtration chromatography of detergent-solubilized t
225 ith an apparent molecular mass, estimated by gel filtration chromatography, of greater than 2 million
226                                    Following gel filtration chromatography on Sephacryl S-200 in the
227 ed by the various serotypes were obtained by gel filtration chromatography on Sephadex G-200.
228  isolation and purification of native MG1 by gel filtration chromatography on Sepharose CL-2B which d
229 ilized asialo-bovine submaxillary mucin, and gel filtration chromatography on Superose 12.
230                                           By gel filtration chromatography, one of the mutant Cdc28 p
231 c and dimeric forms of TrfA are separated by gel filtration chromatography, only the protein in the c
232 id not comigrate with the TAFs during either gel filtration chromatography or rate-zonal sedimentatio
233 ntibody complexes which could be isolated by gel-filtration chromatography, precipitated sHer2 during
234 rophoresis, western blot analysis as well as gel filtration chromatography predicted the molecular ma
235                                              Gel filtration chromatography predicts mtODE's molecular
236     Chemical cross-linking and high pressure gel filtration chromatography provided little evidence f
237 lfate-polyacrylamide gel electrophoresis and gel filtration chromatography, respectively.
238 from an M9 salts medium and fractionation by gel filtration chromatography resulted in fractions with
239                                 Furthermore, gel filtration chromatography revealed normal elution pa
240  electrophoresis, Western-blot analysis, and gel filtration chromatography revealed that P-8 antigen
241                                              Gel filtration chromatography revealed that recombinant
242                                              Gel filtration chromatography revealed that SC in CF was
243 olysis, circular dichroism spectroscopy, and gel filtration chromatography revealed that the N-termin
244              Circular dichroism analysis and gel filtration chromatography revealed that the rational
245                                              Gel filtration chromatography revealed these Gag protein
246    Electrophoretic mobility shift assays and gel-filtration chromatography revealed a native molecula
247                                              Gel-filtration chromatography revealed two populations o
248                                           As gel-filtration chromatography reveals a range of molecul
249                                              Gel filtration chromatography, SDS-polyacrylamide gel el
250 determined using a combination of analytical gel filtration chromatography, SDS-polyacrylamide gel el
251                                  Here, using gel filtration chromatography, sedimentation, fluorescen
252                                 In addition, gel filtration chromatography separated multimeric and m
253                                              Gel filtration chromatography showed a native molecular
254                   Initial purification using gel filtration chromatography showed that the activity w
255                                     However, gel filtration chromatography showed that the bulk of SC
256                                              Gel filtration chromatography showed that the recombinan
257 mical assays using chemical crosslinking and gel filtration chromatography showed that TraM forms hom
258                                              Gel filtration chromatography showed the native mass of
259  However, examination of P-TEFb complexes by gel-filtration chromatography showed that TCR signaling
260               Bioactive peptide separated by gel-filtration chromatography, showed the higher antioxi
261                                              Gel filtration chromatography shows that all five of the
262                                   Similarly, gel filtration chromatography shows that Coq1p, Coq3p, C
263                                 We have used gel filtration chromatography, site-directed mutagenesis
264 determined using a combination of analytical gel filtration chromatography, sodium dodecyl sulfate-po
265 he results of solid-phase binding assays and gel filtration chromatography suggest that the N-termina
266 ults from denaturing gel electrophoresis and gel-filtration chromatography suggest that six 70-kD sub
267                                      Whereas gel filtration chromatography suggested that purified bo
268 crylamide gel electrophoresis and analytical gel filtration chromatography suggested that the native
269 lecular mass of approximately 500 kDa during gel filtration chromatography, suggesting the existence
270 ecombinant protein expression and analytical gel filtration chromatography, surface plasmon resonance
271 tion followed by fluorescence, far-UV CD and gel-filtration chromatography techniques indicated a co-
272                                           By gel filtration chromatography, the complex between gD-1(
273                                           On gel filtration chromatography, the crystallin was recove
274                                         Upon gel filtration chromatography, the Pol I holoenzyme elut
275 scence resonance energy transfer (FRET), and gel filtration chromatography to examine the structure o
276                                      We used gel filtration chromatography to gain insight into the m
277  variant, we used chemical cross-linking and gel filtration chromatography to show that each exists a
278                 In this study, we first used gel filtration chromatography to show that OccR is dimer
279 ass spectrometry, co-immunoprecipitation and gel-filtration chromatography to define higher-order pro
280 uble inclusion bodies by Ni(2+) affinity and gel filtration chromatography under denaturing condition
281  C5 was demonstrated by Western blotting and gel filtration chromatography using 125I-labeled protein
282 s resolved from the excision activity during gel filtration chromatography using Sephacryl S-300.
283 hromatography using DEAE-Toyopearl 650 M and gel filtration chromatography using Sephadex G-100.
284 lecular mass of XPA determined by the native gel filtration chromatography was about 71 kDa, suggesti
285 olate and identify BV2 microglial particles, gel filtration chromatography was employed to fractionat
286 n-dodecyl beta-D-maltoside (DDM) examined by gel filtration chromatography was generally modest, and
287                                              Gel filtration chromatography was used to isolate both p
288 rate the potential for real-time monitoring, gel filtration chromatography was used to separate diffe
289 mass of the native protein, as determined by gel-filtration chromatography, was estimated to be 195 k
290                                           By gel filtration chromatography we observed at least three
291 tics, nondenaturing gel electrophoresis, and gel filtration chromatography we show that the receptor
292                                        Using gel filtration chromatography, we assessed the effects o
293 s, PCNA-coupled affinity beads pull-down and gel filtration chromatography, we show that the same reg
294 ated with high density lipoproteins (HDL) by gel-filtration chromatography, we found no evidence that
295                          By using Superose-6 gel-filtration chromatography, we have discovered that t
296          Using sequential size-exclusion and gel-filtration chromatography, we identified a condition
297   Sucrose density gradient fractionation and gel filtration chromatography were performed to determin
298 crylamide gel electrophoresis and analytical gel filtration chromatography were used to detect the di
299       Comparison of the migration of NrpR in gel-filtration chromatography with its subunit molecular
300       Separation of cytosolic proteins using gel filtration chromatography yields a high molecular we

WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。
 
Page Top