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1 heY3-P in vitro and eluted as a homodimer in gel filtration chromatography.
2 to be a homotrimeric protein as assessed by gel filtration chromatography.
3 omere restriction fragments were purified by gel filtration chromatography.
4 onuclease 1 (APE1) over phosphocellulose and gel filtration chromatography.
5 ring IF-cobalamin affinity and nondenaturing 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 apientum (MSP) were isolated and purified by gel filtration chromatography.
11 ative polyacrylamide gel electrophoresis and gel filtration chromatography.
12 was estimated to be approximately 125 kDa by 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 exchange chromatography, ultrafiltration and gel filtration chromatography.
18 uilibrium analytical ultracentrifugation and gel filtration chromatography.
19 ely 270-300 and 400-450 kDa as determined by gel filtration chromatography.
20 e that can be purified by anion-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 native enzyme was estimated to be 160 kDa by gel filtration chromatography.
25 eneity in two steps by DEAE ion exchange and gel filtration chromatography.
26 fied using ultrafiltration, ion exchange and gel filtration chromatography.
27 decamer in solution has been demonstrated by gel filtration chromatography.
28 nd activity measurements in combination with gel filtration chromatography.
29 ing agents, and anomalous retardation during gel filtration chromatography.
30 sequences, and analyzing the products by P2 gel filtration chromatography.
31 ntibody complexes which could be isolated by gel filtration chromatography.
32 The hydrolysate was further purified by gel filtration chromatography.
33 homogeneity by sequential metal-chelate and gel filtration chromatography.
34 y hydrophobic interaction, ion exchange, and gel filtration chromatography.
35 pitation with ammonium sulphate, followed by 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 ein still elutes in the void upon analytical gel filtration chromatography.
41 eneity from strain DNT by anion exchange and gel filtration chromatography.
42 ss (32 kDa) forms that could be separated by gel filtration chromatography.
43 kd for the binding complex was determined by gel filtration chromatography.
44 ow density lipoprotein particles observed by gel filtration chromatography.
45 eneity using ion-exchange, DNA-affinity, and gel filtration chromatography.
46 -cell line MLA 144 by ionic, hydrophobic and gel filtration chromatography.
47 tion from HeLa cell extracts fractionated by gel filtration chromatography.
48 f the YABP was determined to be 74 300 using gel filtration chromatography.
49 d from partially constructed basal bodies by gel filtration chromatography.
50 measurements below the polymer's LCST using gel filtration chromatography.
51 metal affinity, hydrophobic interaction, and gel filtration chromatography.
52 ueous hydrogen fluoride (HF) and purified by gel filtration chromatography.
53 roteins were purified by Ni-NTA affinity and gel filtration chromatography.
54 was stable during affinity purification 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 ies, neither of which could be restored upon gel-filtration chromatography.
60 hexamers were purified by anion-exchange and gel-filtration chromatography.
61 olumn and from elution steps in conventional gel-filtration chromatography.
62 s by a combination of hydrophobic column and gel-filtration chromatography.
63 ivum L. cv Alaska) epicotyls was examined by gel-filtration chromatography.
64 eity using a combination of ion-exchange and gel-filtration chromatography.
65 alpha-synuclein by sedimentation followed by gel-filtration chromatography.
66 orresponding to approximately 170-180 kDa by gel-filtration chromatography.
67 d by both analytical ultracentrifugation and gel-filtration chromatography.
68 nant protein purified by heparin-agarose and gel-filtration chromatography.
69 from pigments and larger protein material by gel-filtration chromatography.
70 ve molecular mass of approximately 18 kDa by gel-filtration chromatography.
71 ricted to oligomer-containing fractions from gel-filtration chromatography.
72 dentical subunits) that the complex survives gel-filtration chromatography.
73 pharose, Source 15Q, DEAE2, and Superdex 200 gel filtration chromatographies.
74 5 kD fraction (Ara h 2/6; 20 kD fraction) on gel filtration chromatography, account for the majority
75 sonance spectroscopy, titration calorimetry, gel-filtration chromatography, affinity chromatography,
76 or, AmiC, immobilized on a solid support and gel filtration chromatography, an AmiC-AmiR complex has
79 inary approach, including live cell imaging, gel filtration chromatography analysis, split ubiquitin
81 ta-Pol-gapped DNA complex were determined by gel filtration chromatography and a gel mobility shift a
82 urified to near homogeneity then analyzed by gel filtration chromatography and analytical ultracentri
87 brium in the absence of DNA when examined by gel filtration chromatography and atomic force microscop
88 recursor cleaving activity by Sephacryl S200 gel filtration chromatography and by a single band of 35
92 trary to previous findings, a combination of gel filtration chromatography and co-purification studie
93 pper form of the heterodimer was isolated by gel filtration chromatography and contains one copper an
94 mbination of ion-exchange chromatography and gel filtration chromatography and demonstrated for the f
95 with alpha and theta was investigated using gel filtration chromatography and exonuclease stimulatio
96 ed to consist of six nucleotides, GGTTAC, by gel filtration chromatography and filter-binding assay (
100 Both enzymes were found to be homodimeric by gel filtration chromatography and homotetrameric by dyna
106 monomer with an Mr of 21,814 +/- 20 based on gel filtration chromatography and mass spectrometric res
107 ve molecular mass of approximately 68 kDa by gel filtration chromatography and migrated as a single b
108 dimer to a monomeric protein on the basis of gel filtration chromatography and multiple-angle laser l
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
115 on procedures including membrane filtration, gel filtration chromatography and reversed-phase high-pe
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
131 Disaggregation of AgLDL was verified by gel-filtration chromatography and electron microscopy th
134 of monomer-dimer equilibrium as assessed by gel-filtration chromatography and ultracentrifugation st
135 eraction, Sephadex G-100 and Sephacryl S-200 gel filtration chromatographies, and sodium dodecyl sulf
136 3.5 A) in the Stokes radius as determined by gel filtration chromatography, and (iii) a similar decre
137 N. americanus homogenate was fractionated by gel filtration chromatography, and a FACS-based bioassay
138 ad a molecular mass of 320 kDa, estimated by gel filtration chromatography, and a subunit size of 90.
139 wn to be trimeric by chemical cross-linking, gel filtration chromatography, and analytical ultracentr
140 , we used a combination of NMR spectroscopy, gel filtration chromatography, and analytical ultracentr
142 interaction in the yeast two-hybrid system, gel filtration chromatography, and equilibrium sedimenta
143 action of MDH2 with PCK1 using Hummel-Dreyer gel filtration chromatography, and for interactions of M
145 agment was purified as an 800-kDa complex by gel filtration chromatography, and the associating prote
146 the enzyme was estimated to be 65 000 using gel filtration chromatography, and the pH optimum was 4.
148 nd the methods of gel mobility shift assays, gel filtration chromatography, and UV-cross-linking, we
150 rm agglutinin chromatography, Sephacryl S300 gel filtration chromatography, anti-FLAG immunoaffinity
151 The native molecular mass, as determined by gel filtration chromatography, appeared to be approximat
153 ferric siderophores with high affinity: in a gel filtration chromatography assay the K(d) of the ferr
155 ion with proteinase K and after dissociative gel filtration chromatography, but was completely abolis
157 ) of S100P using equilibrium centrifugation, gel-filtration chromatography, circular dichroism and fl
158 mbined approaches of chemical cross-linking, gel filtration chromatography, co-immunoprecipitation, c
163 of PDE3A2 by PKC led to shifts in elution on gel-filtration chromatography consistent with increased
165 ulldown assays of a Orai1-CMBD(W76E) mutant, gel filtration chromatography data, and NOE signals indi
169 enzymatic activity similar to HGPRT-II, and gel filtration chromatography demonstrates that its size
178 ith the results of coimmunoprecipitation and gel filtration chromatography experiments reported here,
182 mitochondria by sequential ion-exchange and gel filtration chromatography, followed by glycerol grad
183 molecular mass around 140 kDa determined by gel filtration chromatography for each of the enzymes.
184 was purified to homogeneity by affinity and gel-filtration chromatography for antibody production an
185 RA from cell extracts by nickel affinity and gel-filtration chromatography found a multicomponent com
186 se peptides were purified after affinity and gel filtration chromatography from a chickpea protein hy
187 led under aprotic conditions and purified by gel-filtration chromatography (GFC) using high-specific-
188 om brush border membrane vesicles (BBMVs) by gel filtration chromatography hinders the cleavage of BT
189 ) leaves and purified using ion exchange and gel filtration chromatography in combination with yeast
190 0 Da, relative to globular standards, during gel filtration chromatography in the absence of polyanio
191 from the 28-kDa fragment (residues 1-257) by gel filtration chromatography in the presence of 4 M ure
192 l misfolding of the enzyme as it eluted from gel filtration chromatography in the same fraction as th
193 revealed a single band at 36 kDa, and native gel filtration chromatography indicated a molecular mass
198 ined 0.92 +/- 0.11 apoE molecules/apoB after gel filtration chromatography, indicating stable complex
199 t molecular mass of 110 kDa as determined by gel-filtration chromatography, indicating that the prote
200 med structural studies of this protein using gel filtration chromatography, intrinsic tryptophan fluo
201 interaction of EIIA with HPr was detected by gel-filtration chromatography, intrinsic tryptophanyl re
203 of R120G alphaB-crystallin, as determined by gel filtration chromatography, is 1.4 MDa, which is more
204 ion bodies, but when subjected to analytical gel filtration chromatography, it elutes in the void vol
207 rial lysate from HeLa cells was submitted to gel filtration chromatography, mTERF was eluted in two p
213 r mass of about 70 to 80 kDa was detected by gel filtration chromatography of extracts from wild-type
217 micellar complex is 5 nm as determined from gel filtration chromatography of SKC1 in dodecyl maltosi
220 resis, N-terminal amino acid sequencing, and gel filtration chromatography of the purified lectin sho
222 The hOAT1 oligomer was also detected in gel filtration chromatography of total membranes from hO
225 lypeptide cofractionated with V-ATPases upon gel-filtration chromatography of detergent-solubilized t
226 ith an apparent molecular mass, estimated by gel filtration chromatography, of greater than 2 million
228 isolation and purification of native MG1 by gel filtration chromatography on Sepharose CL-2B which d
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
236 Chemical cross-linking and high pressure gel filtration chromatography provided little evidence f
238 from an M9 salts medium and fractionation by gel filtration chromatography resulted in fractions with
240 electrophoresis, Western-blot analysis, and gel filtration chromatography revealed that P-8 antigen
243 olysis, circular dichroism spectroscopy, and gel filtration chromatography revealed that the N-termin
246 Electrophoretic mobility shift assays and gel-filtration chromatography revealed a native molecula
250 determined using a combination of analytical gel filtration chromatography, SDS-polyacrylamide gel el
257 mical assays using chemical crosslinking and gel filtration chromatography showed that TraM forms hom
259 However, examination of P-TEFb complexes by gel-filtration chromatography showed that TCR signaling
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
267 crylamide gel electrophoresis and analytical gel filtration chromatography suggested that the native
268 lecular mass of approximately 500 kDa during gel filtration chromatography, suggesting the existence
269 ry activity was analysed using Sephadex G-75 gel filtration chromatography, Superdex peptide 10/300 G
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-
275 scence resonance energy transfer (FRET), and gel filtration chromatography to examine the structure o
277 variant, we used chemical cross-linking and gel filtration chromatography to show that each exists a
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
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
291 tics, nondenaturing gel electrophoresis, and gel filtration chromatography we show that the receptor
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
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