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1 cellular HSPG enriched from cell lysates by ion exchange chromatography.
2 idated proteins were purified by affinity or ion exchange chromatography.
3 d from conditioned medium using affinity and ion exchange chromatography.
4 solved by gel electrophoresis or purified by ion exchange chromatography.
5 E. coli, and purified using Ni2+-agarose and ion exchange chromatography.
6 using heparin-agarose, phosphocellulose, and ion exchange chromatography.
7 atase activity cofractionates with PP1 after ion exchange chromatography.
8 arose column, followed by gel filtration and ion exchange chromatography.
9 ted from cyclic inositol phosphohydrolase on ion exchange chromatography.
10 g Ni-NTA affinity chromatography followed by ion exchange chromatography.
11 ccessive 32-48% glycerol gradients, and DE52 ion exchange chromatography.
12 y ethanol precipitation, gel filtration, and ion exchange chromatography.
13 are usually carried out using extraction or ion exchange chromatography.
14 re Fgr through subsequent size-exclusion and ion exchange chromatography.
15 tested: (i) ion-pair chromatography and (ii) ion exchange chromatography.
16 m sulphate precipitation, gel filtration and ion exchange chromatography.
17 0-80%), Sephadex G-100, and Mono Q-Sepharose ion exchange chromatography.
18 romatography, but resolved from met-tRNAi by ion exchange chromatography.
19 g these two conformations to be separated by ion exchange chromatography.
20 e displacers for a binary protein mixture in ion exchange chromatography.
21 , counting the thialysine product, following ion exchange chromatography.
22 GC-activating effect was further purified by ion exchange chromatography.
23 n-Plus, and purified by nickel chelation and ion exchange chromatography.
24 ride in flagellin preparation was removed by ion exchange chromatography.
25 es hybrid tetramers that can be separated by ion exchange chromatography.
26 nsect cells and purified the two proteins by ion exchange chromatography.
27 ivers using a combination of hydrophobic and ion-exchange chromatography.
28 utant was purified by protein A affinity and ion-exchange chromatography.
29 xtractable antigens of virulent shigellae by ion-exchange chromatography.
30 r buds was purified using concanavalin A and ion-exchange chromatography.
31 monium sulfate precipitation and heparin and ion-exchange chromatography.
32 high performance liquid chromatography, and ion-exchange chromatography.
33 membrane with nonionic detergent followed by ion-exchange chromatography.
34 olecule isolated by four successive steps of ion-exchange chromatography.
35 ee distinct enzymes that were isolated using ion-exchange chromatography.
36 acid precipitation, reverse-phase HPLC, and ion-exchange chromatography.
37 h were purified from periplasmic extracts by ion-exchange chromatography.
38 o LPS by using a combination of affinity and ion-exchange chromatography.
39 line monitoring of proteins from preparative ion-exchange chromatography.
40 s separated into isoenzymes S1A1 and S1A2 by ion-exchange chromatography.
41 in surface diffusion in protein transport in ion-exchange chromatography.
42 altoside, and the RC complex was purified by ion-exchange chromatography.
43 ignificantly different from that obtained by ion-exchange chromatography.
44 c orientation toward the stationary phase in ion-exchange chromatography.
45 into L1-L5, increasingly electronegative, by ion-exchange chromatography.
46 (diameter = 1.03 nm) from HiPco tubes using ion-exchange chromatography.
47 spectra of DNA-wrapped SWNT fractionated by ion-exchange chromatography.
48 proteins and purified by metal-affinity and ion-exchange chromatography.
49 tive Aging Study were assayed for sulfate by ion-exchange chromatography.
50 chia coli and purified by gel-filtration and ion-exchange chromatography.
51 xpression under osmotic shock conditions and ion-exchange chromatography.
52 ions with different electronic structures by ion-exchange chromatography.
53 m inclusion bodies and partially purified by ion-exchange chromatography.
54 led human tear samples by size exclusion and ion exchange chromatographies.
55 ocker-binding protein by lectin-affinity and ion-exchange chromatographies.
56 tion of acid extraction, gel permeation, and ion-exchange chromatographies.
57 lubilized with 6 M urea and then purified by ion-exchange chromatography, a procedure that produced s
58 ploys weak anion and strong cation mixed-bed ion exchange chromatography (ACE) in the first separatio
59 interfacing of size-exclusion and mixed-bed ion-exchange chromatography achieves high coverage of en
60 new fractions separated from Acacia gums by Ion Exchange Chromatography affected foamability of spar
62 partially purified from membrane extracts by ion-exchange chromatography, an oligohistidine tag was a
65 rough time by separating U(VI) from U(IV) by ion exchange chromatography and characterize the reactio
66 two-step chromatographic procedure, avoiding ion exchange chromatography and high salt conditions to
67 stone-activated PDE6 peaks were separated by ion exchange chromatography and identified by mass spect
68 ectrophoresis for identifying fragmentation, ion exchange chromatography and isoelectric focusing for
69 olved overexpression of the plcHR1,2 operon, ion exchange chromatography and native preparative polya
71 y improved compatibility between (salt-free) ion exchange chromatography and reversed phase chromatog
73 n human skeletal muscle was determined using ion-exchange chromatography and a highly sensitive high-
75 an oocyte extract by using a combination of ion-exchange chromatography and gel filtration chromatog
78 ave now purified the native minor fimbria by ion-exchange chromatography and sequenced the fimbria by
79 ormed by fractionation of charge variants by ion-exchange chromatography and subsequent online LC-MS
80 olive oil matrix (via EDTA complexation and ion-exchange chromatography) and to determine its isotop
81 stem, purified with Ni-NTA affinity and DEAE-ion exchange chromatographies, and characterized by SDS-
82 e derivatized with acetylated serum albumin, ion exchange chromatography, and gel permeation chromato
83 three steps: dye-ligand binding and elution, ion exchange chromatography, and high performance liquid
84 N product generated in vitro was purified by ion exchange chromatography, and its structure was confi
86 lated mitochondria, 200-fold purification by ion exchange chromatography, and reconstitution into lip
87 of proteins, isolation of 3-nitrotyrosine by ion exchange chromatography, and reduction of 3-nitrotyr
88 ionation steps, including gel filtration and ion exchange chromatography, and sucrose gradient ultrac
89 mbination of ammonium sulfate fractionation, ion-exchange chromatography, and adsorption chromatograp
90 ins were purified by sequential affinity and ion-exchange chromatography, and at 30 nM concentration
91 oimmunoassay, IP3 production was measured by ion-exchange chromatography, and changes in tension were
92 oimmunoassay, IP3 production was measured by ion-exchange chromatography, and changes in tension were
93 hyl methanethiosulfonate, fractionated using ion-exchange chromatography, and digested with trypsin a
94 nositol phosphate production was measured by ion-exchange chromatography, and phospholipase C (PLC)-b
95 by sedimentation velocity, high-performance ion-exchange chromatography, and reversed-phase and SDS-
96 radient centrifugation, molecular sieve, and ion exchange chromatography; and then characterized.
99 pture and polishing steps using affinity and ion-exchange chromatography before characterization can
100 mistry, such as liquid-liquid extraction and ion-exchange chromatography, can be adapted for such min
101 Charge sensitive separation methods such as ion exchange chromatography (CEX) and capillary electrop
102 tion of analysed compounds were performed by ion-exchange chromatography coupled with ICP-MS in one c
104 cryl-S 300 gel filtration and DEAE-Sepharose ion exchange chromatography demonstrated that AKR1B10 ex
105 lipolytic activity using gel filtration and ion-exchange chromatography demonstrates that a protein
106 cribe for the first time the use of nanoflow ion-exchange chromatography directly coupled with native
107 Filtration, size-exclusion chromatography, ion-exchange chromatography, electrophoresis, and centri
108 Partial purification of a p38 MAP kinase by ion exchange chromatography established it as distinct f
109 and then purified with DEAE-Sepharose CL-6B ion exchange chromatography followed by Sephacryl S-300
110 ted XBP was purified from human macula using ion-exchange chromatography followed by gel-exclusion ch
111 each species was purified to homogeneity by ion-exchange chromatography followed by hydrophobic inte
112 purified from human peripheral retina using ion-exchange chromatography followed by size-exclusion c
113 protein activator were determined using DEAE ion exchange chromatography, gel filtration, and a lecti
114 y of 13% by adsorbent column chromatography, ion-exchange chromatography, gel filtration, and prepara
115 uence of steps that included heat treatment, ion-exchange chromatography, hydrophobic interaction chr
116 ch that uses lectin affinity chromatography, ion-exchange chromatography, hydrophobic-interaction chr
118 sections of chromatograms, demonstrated for ion-exchange chromatography (IC) and hydrophilic interac
119 dominated by liquid chromatography (LC) and ion-exchange chromatography (IC), with sub/supercritical
120 d a novel 3DLC strategy by coupling HIC with ion exchange chromatography (IEC) and reverse phase chro
121 growth combined with chemical separation by ion exchange chromatography (IEC) greatly facilitates ac
123 Diagnosis of cystinuria is made typically by ion-exchange chromatography (IEC) detection and quantita
124 hotometric detector and applied in capillary ion-exchange chromatography (IEC) for the detection of c
126 tionary phase interactions that occur during ion-exchange chromatography (IEX) can provide critical i
127 auses (i) an electronegative charge shift on ion exchange chromatography, (ii) a similar increase ( a
128 ectronegative charge shift of each enzyme on ion exchange chromatography, (ii) an increase in the Sto
129 ed membranes, followed by gel filtration and ion-exchange chromatography in a chloroform/methanol/H(2
130 erythrocyte samples by either extraction and ion-exchange chromatography in preparation for mass spec
131 o isotopes of approximately 1.5%o/amu during ion-exchange chromatography in the laboratory and a shif
132 influence of protein structure on binding in ion-exchange chromatography, in which electrostatic inte
135 2+)-independent peak III kinase, obtained by ion-exchange chromatography, is confirmed to be the pred
137 (LAC-M), selective precipitation (LAC-P) and ion-exchange chromatography (LAC-IE), were fortified wit
138 hy separation with a flash oxidation system [ion exchange chromatography liquid chromatography-flash
142 iously implicated in various disease states, ion-exchange chromatography, microfluidic capillary elec
143 omplexes were isolated by gel filtration and ion exchange chromatographies, monitored with absorption
144 urification by affinity, gel filtration, and ion exchange chromatography, NR3A S1S2 behaves as a mono
145 Bromine is extracted from the samples by ion exchange chromatography on anion exchange resin AG 1
146 ed from media conditioned by AtT-20 cells by ion exchange chromatography on DEAE-Sephacel, molecular
147 llowing fractionation of cellular lysates by ion exchange chromatography on HiTrap Q and Mono Q resin
148 t homogeneity (>90% purity) in 5.7% yield by ion exchange chromatography on SP-Sepharose, affinity ch
151 fied by a combination of salt fractionation, ion-exchange chromatography on DEAE-Sephacel, and gel fi
155 n concentrated by ultracentrifugation and/or ion exchange chromatography, or by precipitation using p
157 take of the protein lysozyme into individual ion exchange chromatography particles in a packed bed in
159 cular contributions to protein adsorption in ion-exchange chromatography, protein-adsorbent electrost
160 rison and validation on real wine samples by ion-exchange chromatography prove that this procedure yi
161 sodium in liquid ammonia and purification by ion exchange chromatography provided 4ab in 60% yield.
162 n the present work a fast, reliable and safe Ion Exchange Chromatography-Pulsed Amperometry Detection
163 ifferential solubility, failure to adsorb to ion-exchange chromatography resins, and retention time o
164 n of PKI activities from mouse heart by DEAE ion exchange chromatography resolved two major inhibitor
166 onium sulfate precipitation followed by DEAE ion-exchange chromatography, resulting in 10 to 15 mg of
167 ifactorial combination in reversed phase and ion exchange chromatography (RPLC and IEC) modes are gen
168 esults from immunoprecipitation analysis and ion-exchange chromatography showed that the differential
170 ied from unstripped membranes using a single ion-exchange chromatography step (MonoS) in the non-ioni
172 , requires only the adjustment of pH between ion exchange chromatography steps, does not require buff
173 e aqueous extracts obtained were purified by ion exchange chromatography techniques and membrane sepa
175 rified P450 enzyme was isolated by multistep ion exchange chromatography to electrophoretic homogenei
177 from HeLa cells and then further purified by ion-exchange chromatography to resolve by net charge and
178 gs, refolded a mixture of monomers, and used ion-exchange chromatography to resolve tetramers accordi
179 Lunasin was purified using a combination of ion-exchange chromatography, ultrafiltration and gel fil
180 ose binding activities after purification by ion exchange chromatography under denaturing conditions
181 btained upon ammonium sulfate fractionation, ion exchange chromatography using DEAE-Toyopearl 650 M a
182 Scandium radionuclides were purified via ion-exchange chromatography using branched N,N,N',N'-tet
183 lso compared with conventional NaCl gradient ion-exchange chromatography using the same Mono P column
186 ng a stirred fluidized bed adsorption system ion exchange chromatography where STREAMLINE SP and SP-X
187 tes with cyclic inositol phosphohydrolase on ion exchange chromatography, while guinea pig kidney ann
191 termed CAX-PAGE/RPLC-MSMS, combines biphasic ion-exchange chromatography with polyacrylamide gel elec
193 ood categories, by means of high-performance ion-exchange chromatography with suppressed conductometr