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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
9 rnatant was then efficiently adsorbed over a DEAE cellulose-treated paper wick assembled in the syrin
12 s protein size decrease was confirmed, after DEAE column purification, by dynamic light scattering (D
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
21 -3 cells, Sephacryl-S 300 gel filtration and DEAE-Sepharose ion exchange chromatography demonstrated
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
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
35 reticulocyte lysate into three fractions by DEAE chromatography and then reconstitute the GR.hsp90 h
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
43 ted a persistent, autonomously active PKC by DEAE-cellulose column chromatography from hippocampal sl
47 the parent cell extract that was purified by DEAE Sephacel column chromatography and by a wheat germ
50 cross-linked peptide was further purified by DEAE-Sepharose and C18 column chromatography and subject
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
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
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
64 virus type 5 (Ad5) onto a diethylaminoethyl (DEAE) anion exchange surface are measured for the first
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
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
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
87 apparent homogeneity using a combination of DEAE-cellulose column chromatography, ammonium sulfate p
89 2 mol/L reduced the absorption efficiency of DEAE due to the hydration mechanism, motivating a ration
93 ted to sequential column chromatographies on DEAE-Sepharose, hydroxyapatite, phenyl-Sepharose, and ch
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
100 ractionation, ion-exchange chromatography on DEAE-Sephacel, and gel filtration on Sephadex G-200.
102 T-20 cells by ion exchange chromatography on DEAE-Sephacel, molecular sieve chromatography on Sephacr
105 fied from liver cytosol by chromatography on DEAE-Sepharose which had characteristics of the [3Fe-4S]
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
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
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
118 purified by ammonium sulfate precipitation, DEAE chromatography, and size exclusion chromatography.
123 teracting protein was purified by sequential DEAE and size exclusion chromatography, and subsequent m
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
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
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
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
141 ease in autonomous PKC activity isolated via DEAE column chromatography also was associated with LTP.
145 her filter, which is positively charged with DEAE active groups, traps low-molecular-weight DNA fragm
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