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1                                              DEAE chromatography of GC agar extracts and sodium dodec
2                                              DEAE-cellulose chromatography and gel mobility shift ass
3                                              DEAE-cellulose chromatography performed in a boric acid-
4                                              DEAE-Toyopearl column chromatography of aorta extracts s
5 ation and chromatography on Ultrogel AcA 34, DEAE-Sephacel, heparin-Sepharose, hydroxylapatite, and U
6  a scintillation proximity assay (SPA) and a DEAE membrane-based assay for [(3)H]AAG binding to Hsp90
7 atography method (NaCl gradient elution on a DEAE Sepharose(TM) Fast Flow gel column) was developed t
8 ugation and ion-exchange chromatography on a DEAE-5PW column.
9 rnatant was then efficiently adsorbed over a DEAE cellulose-treated paper wick assembled in the syrin
10           Intrinsic adsorption rates for Ad5-DEAE interaction are 16 times faster than intrinsic adso
11                                Additionally, DEAE-dextran and liposome-mediated transfection resulted
12 s protein size decrease was confirmed, after DEAE column purification, by dynamic light scattering (D
13 sequential chromatography on Ni-NTA-agarose, DEAE-Toyopearl, and heparin-Sepharose.
14 ng glutathione-agarose, Sephacryl S-200, and DEAE-cellulose chromatography.
15 uential chromatography on Bio-Gel A-1.5m and DEAE-Sepharose.
16 aliphatic compounds as compared to XAD-8 and DEAE-isolates.
17 us system, purified with Ni-NTA affinity and DEAE-ion exchange chromatographies, and characterized by
18  of LEF-1 and LEF-2 from ssDNA-cellulose and DEAE resin suggested that LEF-2 may bind to both DNA and
19 quential heparin affinity chromatography and DEAE anion exchange chromatography.
20 ned after purification by gel filtration and DEAE liquid chromatography.
21 -3 cells, Sephacryl-S 300 gel filtration and DEAE-Sepharose ion exchange chromatography demonstrated
22 estramustine as detected by fluorescence and DEAE filter assays.
23                     Two-dimensional PAGE and DEAE purification of ACCase protein demonstrated that th
24 ial chromatographies on phosphocellulose and DEAE-Sephadex.
25  fraction was purified by Sephacryl S100 and DEAE Sephacel.
26 he presence of additional compounds, such as DEAE-dextran, that appeared to alter the nature of the c
27 e reduced GTPase activity is not enhanced by DEAE-dextran-induced assembly, indicating it has a defec
28     These N-acyl-PS species were enriched by DEAE-cellulose column chromatography, and they were then
29 scription system was purified extensively by DEAE-Sepharose, Biorex 70, Sephacryl S300, and Mono Q ch
30 ere isolated by beta-elimination followed by DEAE chromatography.
31 , ammonium sulfate precipitation followed by DEAE ion-exchange chromatography, resulting in 10 to 15
32  chloroform/methanol extraction, followed by DEAE-cellulose chromatography, mild alkaline hydrolysis,
33 ase in the presence of 1 M urea, followed by DEAE-Sepharose CL-6B column chromatography under anaerob
34                       EJ was fractionated by DEAE chromatography in 6 M urea/4% beta-mercaptoethanol.
35  reticulocyte lysate into three fractions by DEAE chromatography and then reconstitute the GR.hsp90 h
36  non-ionic detergent and purified further by DEAE-Sepharose chromatography.
37 cation of PKI activities from mouse heart by DEAE ion exchange chromatography resolved two major inhi
38 has been purified to apparent homogeneity by DEAE-cellulose, heparin-agarose, and DNA-specific affini
39  been purified 6,000-fold from rat livers by DEAE-Sepharose, heparin-Sepharose, and DNA affinity chro
40 p60 from a heat-treated neutrophil lysate by DEAE-cellulose chromatography and SDS-polyacrylamide gel
41 MTF was separated from uncross-linked MTF by DEAE-cellulose chromatography, and the tRNA in the cross
42                     The separation of PD, by DEAE-cellulose column chromatography, yielded two pectic
43 ted a persistent, autonomously active PKC by DEAE-cellulose column chromatography from hippocampal sl
44 separated from MBP and factor Xa protease by DEAE-Sephacel chromatography.
45                capsulatus LH1-RC purified by DEAE chromatography.
46                The HbRC core was purified by DEAE ion-exchange chromatography and resolved by SDS-PAG
47 the parent cell extract that was purified by DEAE Sephacel column chromatography and by a wheat germ
48  to mild base hydrolysis and was purified by DEAE-cellulose column chromatography.
49 ne hydrochloride, renatured, and purified by DEAE-Sephacel and Sephadex G-75 chromatography.
50 cross-linked peptide was further purified by DEAE-Sepharose and C18 column chromatography and subject
51 lyoxyethylene-9-lauryl ether and purified by DEAE-Sepharose CL-6B column chromatography.
52 th PP6R1 and PP6R3 subunits were resolved by DEAE chromatography and eluted together with Ankrd28 at
53 lubilized with taurochlorate and resolved by DEAE--Cibacron Blue--Sepharose column chromatography int
54 clear neutrophils is shown to be resolved by DEAE-Sepharose chromatography into two fractions: an NAD
55  extracts of acetone-grown R. rhodochrous by DEAE-Sepharose chromatography.
56 then purified to homogeneity in two steps by DEAE ion exchange and gel filtration chromatography.
57 pha1 subunit by diethylaminoethyl cellulose (DEAE)-purified amyotrophic lateral sclerosis IgG was not
58 as subjected to anion column chromatography (DEAE-8HR), and the fractions collected were screened by
59 n, affinity and ion exchange chromatography (DEAE-Sepharose).
60 nvective interaction media diethylamine (CIM DEAE) monolithic chromatographic column and quantified b
61  purification using three different columns (DEAE-Sepharose, Econo S, and heparin-agarose), LRP was p
62 y sequential chromatography on five columns: DEAE-Sepharose, Biorex 70, Sephacryl S300, Mono Q, and D
63     Thus, with rationally chosen conditions, DEAE was demonstrated ideal for CCMC.
64 virus type 5 (Ad5) onto a diethylaminoethyl (DEAE) anion exchange surface are measured for the first
65 es fluorescein-casein, by diethylaminoethyl (DEAE) gel column chromatography.
66 ere partially purified by diethylaminoethyl (DEAE) gel column chromatography.
67 ne anion exchanging resin-diethylaminoethyl (DEAE) -cellulose.
68 rmining DNA loading using diethylaminoethyl (DEAE)-functionalized beads.
69 amine, DIPA), tertiary (diethylethanolamine, DEAE), and triamine (diethylenetriamine, DETA), respecti
70 enzyme was further purified by ion exchange (DEAE-Bio-Gel) and lentil-lectin-Sepharose 4B chromatogra
71 ion procedure involved detergent extraction, DEAE-Sepharose ion exchange, Phenyl-Sepharose hydrophobi
72 s, including ammonium sulfate fractionation, DEAE-Sephacel, phenyl-Sepharose, S-Sepharose, Sephadex G
73     Connectors isolated as single peaks from DEAE-Sepharose and phosphocellulose chromatography gave
74 idase (pl 4.6) on DEAE-Trisacryl and TSK-gel DEAE-5PW columns.
75 ns, hydroxyapatite HPLC, reverse-phase HPLC, DEAE ion exchange, and affinity chromatography with a Be
76 -dependent Cdk2/Cdk6 phosphatase activity in DEAE-Sepharose, Superdex-200, and Mono Q chromatographie
77 ve reconstituted SIC1 multiubiquitination in DEAE-fractionated yeast extract.
78 and several chromatographic steps, including DEAE-Sepharose CL-6B, hydroxyapatite, strong anionic and
79 ort here an improved chromatographic method (DEAE-cellulose, calcium hydroxylapatite, and Sephadex G-
80  the absence of agonist is also seen for N,N-DEAE and N,N-diethylaminopropyl esters, both binding wit
81 ubstrates was measured by the nitrocellulose-DEAE double filter binding assay, binding affinity at bo
82                            In the absence of DEAE-dextran, FtsZ2 fails to assemble unless supplemente
83               In contrast, in the absence of DEAE-dextran, virion infectivity increases monotonically
84                           The carbonation of DEAE demonstrated the least sensitivity to temperature.
85 tent retention of nucleotides in the case of DEAE cellulose filter papers.
86 aximum GalNAc kinase activity on a column of DEAE-Cibacron blue.
87  apparent homogeneity using a combination of DEAE-cellulose column chromatography, ammonium sulfate p
88 fied by a three-step procedure consisting of DEAE, heparin, and Sephacryl S-200 chromatography.
89 2 mol/L reduced the absorption efficiency of DEAE due to the hydration mechanism, motivating a ration
90                           In the presence of DEAE-dextran, the polycation known to enhance HIV-1 infe
91 y of anionic extensin peroxidase (pl 4.6) on DEAE-Trisacryl and TSK-gel DEAE-5PW columns.
92 /or in organ culture were chromatographed on DEAE Sephadex to isolate gangliosides.
93 ted to sequential column chromatographies on DEAE-Sepharose, hydroxyapatite, phenyl-Sepharose, and ch
94  protein precipitation and chromatography on DEAE Sepharose CL-6B.
95 nt extraction, followed by chromatography on DEAE-cellulose, C18 reverse phase resin, and silicic aci
96 fold) from insect cells by chromatography on DEAE-cellulose, phosphocellulose, heparin-agarose, and s
97 fibrinogen by ion-exchange chromatography on DEAE-cellulose.
98 edure and then by stepwise chromatography on DEAE-cellulose.
99  was partially purified by chromatography on DEAE-Sephacel and Cibacron Blue 3GA-1000 agarose.
100 ractionation, ion-exchange chromatography on DEAE-Sephacel, and gel filtration on Sephadex G-200.
101                      After chromatography on DEAE-Sephacel, hydroxylapatite, and Mono Q and precipita
102 T-20 cells by ion exchange chromatography on DEAE-Sephacel, molecular sieve chromatography on Sephacr
103 l-Synsorb and ion-exchange chromatography on DEAE-Sephacel.
104 er, followed by sequential chromatography on DEAE-Sepharose and butyl-agarose.
105 fied from liver cytosol by chromatography on DEAE-Sepharose which had characteristics of the [3Fe-4S]
106 utes independently from peak 2 fibrinogen on DEAE-cellulose chromatography.
107 ygalacturonase, followed by fractionation on DEAE-cellulose.
108 eins from lactating bovine mammary glands on DEAE-Sepharose, reactive green 19-agarose, and Superose
109  by co-chromatography of the two proteins on DEAE-5PW following fractionation of a rat liver extract
110 ased on absorption of the acidic proteins on DEAE-cellulose and gel filtration through agarose.
111 when the amine concentration increased, only DEAE exhibited an increased carbonation efficiency of up
112 bining VSV with ruxolitinib and Polybrene or DEAE-dextran successfully broke the resistance of HPAF-I
113 improved by treating cells with Polybrene or DEAE-dextran.
114  a single component during purification over DEAE-, phenyl-, Reactive Blue-4-, GDP-adipate-, GDP-hexa
115 mplex I and observed that it segregates over DEAE-Sepharose into two subcomplexes (termed I-L and I-U
116                         Assembly in GDP plus DEAE dextran produces tubular polymers that are related
117 sed by a facilitator, for example polybrene, DEAE-dextran or a liposome.
118  purified by ammonium sulfate precipitation, DEAE chromatography, and size exclusion chromatography.
119        Factor XIII alone applied to the same DEAE column elutes at a position between peak 1 and peak
120 hies, including diethylaminoethyl sepharose (DEAE) and Sephadex G-75 size exclusion columns.
121 med using Con-A Sepharose, Phenyl Sepharose, DEAE Sephacel, and Superdex 75 FPLC.
122                                   Sequential DEAE, wheat germ lectin affinity, and hydroxyapatite chr
123 teracting protein was purified by sequential DEAE and size exclusion chromatography, and subsequent m
124           The separation included sequential DEAE-Sephacel, phenyl-Sepharose FF, heparin-Sepharose CL
125                                   Similarly, DEAE-cellulose chromatography showed slightly stronger b
126 an be isolated from human plasma by a simple DEAE microspin column technique and can be quantified us
127 n TLC of the acidic fraction eluted from the DEAE column, only two radiolabeled glycolipids (GL1 and
128  a parallel increase of radioactivity in the DEAE filter.
129 en demonstrated that the introduction of the DEAE filter increases the assay sensitivity and eliminat
130 o near homogeneity by chromatography through DEAE Sepharose, Heparin Sepharose, and phosphocellulose
131 ate precipitation and chromatography through DEAE-Sepharose and gel filtration columns.
132  in cheese whey and further purified through DEAE-Sepharose XK26.
133 2 fibrinogen plus factor XIII are applied to DEAE columns, the peak 1/factor XIII mixture elutes in t
134 ms, monomers (approximately 40 kDa) bound to DEAE-Sepharose column and protein complexes (approximate
135 engths of free and nanoparticle-bound DNA to DEAE, allowing the selective elution of free DNA by adju
136 , and the resulting extract was subjected to DEAE-cellulose column chromatography.
137       A rapid bioassay of the pheromone uses DEAE-Toyopearl 650M beads to which the pheromone adsorbs
138 tionation, ion exchange chromatography using DEAE-Toyopearl 650 M and gel filtration chromatography u
139 he G-protein activator were determined using DEAE ion exchange chromatography, gel filtration, and a
140 ed to either CEL or PTL were separated using DEAE-chromatography.
141 ease in autonomous PKC activity isolated via DEAE column chromatography also was associated with LTP.
142 mous PKC activity that could be isolated via DEAE column chromatography.
143                    Both strong (Q) and weak (DEAE) anion exchange resins were found to adsorb surpris
144       Vaccination with VPEAR adjuvanted with DEAE-dextran induced antibody titers in 5 out of 6 vacci
145 her filter, which is positively charged with DEAE active groups, traps low-molecular-weight DNA fragm
146  S. pneumoniae by serial chromatography with DEAE-Sepharose and Sephacryl S-200.
147 d from the basidioma, and then purified with DEAE-Sepharose CL-6B ion exchange chromatography followe
148 ain membrane were purified sequentially with DEAE-Sephacel, heparin-Sepharose, ceramic hydroxyapatite

 
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