ライフサイエンスコーパス: DEAE

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 ugation and ion-exchange chromatography on a DEAE-5PW column.

8 Intrinsic adsorption rates for Ad5-DEAE interaction are 16 times faster than intrinsic adso

9 Additionally, DEAE-dextran and liposome-mediated transfection resulted

10 s protein size decrease was confirmed, after DEAE column purification, by dynamic light scattering (D

11 sequential chromatography on Ni-NTA-agarose, DEAE-Toyopearl, and heparin-Sepharose.

12 ng glutathione-agarose, Sephacryl S-200, and DEAE-cellulose chromatography.

13 uential chromatography on Bio-Gel A-1.5m and DEAE-Sepharose.

14 aliphatic compounds as compared to XAD-8 and DEAE-isolates.

15 us system, purified with Ni-NTA affinity and DEAE-ion exchange chromatographies, and characterized by

16 of LEF-1 and LEF-2 from ssDNA-cellulose and DEAE resin suggested that LEF-2 may bind to both DNA and

17 quential heparin affinity chromatography and DEAE anion exchange chromatography.

18 ned after purification by gel filtration and DEAE liquid chromatography.

19 -3 cells, Sephacryl-S 300 gel filtration and DEAE-Sepharose ion exchange chromatography demonstrated

20 estramustine as detected by fluorescence and DEAE filter assays.

21 Two-dimensional PAGE and DEAE purification of ACCase protein demonstrated that th

22 ial chromatographies on phosphocellulose and DEAE-Sephadex.

23 fraction was purified by Sephacryl S100 and DEAE Sephacel.

24 he presence of additional compounds, such as DEAE-dextran, that appeared to alter the nature of the c

25 e reduced GTPase activity is not enhanced by DEAE-dextran-induced assembly, indicating it has a defec

26 These N-acyl-PS species were enriched by DEAE-cellulose column chromatography, and they were then

27 scription system was purified extensively by DEAE-Sepharose, Biorex 70, Sephacryl S300, and Mono Q ch

28 ere isolated by beta-elimination followed by DEAE chromatography.

29 , ammonium sulfate precipitation followed by DEAE ion-exchange chromatography, resulting in 10 to 15

30 chloroform/methanol extraction, followed by DEAE-cellulose chromatography, mild alkaline hydrolysis,

31 ase in the presence of 1 M urea, followed by DEAE-Sepharose CL-6B column chromatography under anaerob

32 EJ was fractionated by DEAE chromatography in 6 M urea/4% beta-mercaptoethanol.

33 reticulocyte lysate into three fractions by DEAE chromatography and then reconstitute the GR.hsp90 h

34 non-ionic detergent and purified further by DEAE-Sepharose chromatography.

35 cation of PKI activities from mouse heart by DEAE ion exchange chromatography resolved two major inhi

36 has been purified to apparent homogeneity by DEAE-cellulose, heparin-agarose, and DNA-specific affini

37 been purified 6,000-fold from rat livers by DEAE-Sepharose, heparin-Sepharose, and DNA affinity chro

38 p60 from a heat-treated neutrophil lysate by DEAE-cellulose chromatography and SDS-polyacrylamide gel

39 MTF was separated from uncross-linked MTF by DEAE-cellulose chromatography, and the tRNA in the cross

40 The separation of PD, by DEAE-cellulose column chromatography, yielded two pectic

41 ted a persistent, autonomously active PKC by DEAE-cellulose column chromatography from hippocampal sl

42 separated from MBP and factor Xa protease by DEAE-Sephacel chromatography.

43 The HbRC core was purified by DEAE ion-exchange chromatography and resolved by SDS-PAG

44 the parent cell extract that was purified by DEAE Sephacel column chromatography and by a wheat germ

45 to mild base hydrolysis and was purified by DEAE-cellulose column chromatography.

46 ne hydrochloride, renatured, and purified by DEAE-Sephacel and Sephadex G-75 chromatography.

47 cross-linked peptide was further purified by DEAE-Sepharose and C18 column chromatography and subject

48 lyoxyethylene-9-lauryl ether and purified by DEAE-Sepharose CL-6B column chromatography.

49 th PP6R1 and PP6R3 subunits were resolved by DEAE chromatography and eluted together with Ankrd28 at

50 lubilized with taurochlorate and resolved by DEAE--Cibacron Blue--Sepharose column chromatography int

51 clear neutrophils is shown to be resolved by DEAE-Sepharose chromatography into two fractions: an NAD

52 extracts of acetone-grown R. rhodochrous by DEAE-Sepharose chromatography.

53 then purified to homogeneity in two steps by DEAE ion exchange and gel filtration chromatography.

54 pha1 subunit by diethylaminoethyl cellulose (DEAE)-purified amyotrophic lateral sclerosis IgG was not

55 as subjected to anion column chromatography (DEAE-8HR), and the fractions collected were screened by

56 n, affinity and ion exchange chromatography (DEAE-Sepharose).

57 nvective interaction media diethylamine (CIM DEAE) monolithic chromatographic column and quantified b

58 purification using three different columns (DEAE-Sepharose, Econo S, and heparin-agarose), LRP was p

59 y sequential chromatography on five columns: DEAE-Sepharose, Biorex 70, Sephacryl S300, Mono Q, and D

60 virus type 5 (Ad5) onto a diethylaminoethyl (DEAE) anion exchange surface are measured for the first

61 es fluorescein-casein, by diethylaminoethyl (DEAE) gel column chromatography.

62 ere partially purified by diethylaminoethyl (DEAE) gel column chromatography.

63 ne anion exchanging resin-diethylaminoethyl (DEAE) -cellulose.

64 enzyme was further purified by ion exchange (DEAE-Bio-Gel) and lentil-lectin-Sepharose 4B chromatogra

65 ion procedure involved detergent extraction, DEAE-Sepharose ion exchange, Phenyl-Sepharose hydrophobi

66 s, including ammonium sulfate fractionation, DEAE-Sephacel, phenyl-Sepharose, S-Sepharose, Sephadex G

67 Connectors isolated as single peaks from DEAE-Sepharose and phosphocellulose chromatography gave

68 idase (pl 4.6) on DEAE-Trisacryl and TSK-gel DEAE-5PW columns.

69 ns, hydroxyapatite HPLC, reverse-phase HPLC, DEAE ion exchange, and affinity chromatography with a Be

70 -dependent Cdk2/Cdk6 phosphatase activity in DEAE-Sepharose, Superdex-200, and Mono Q chromatographie

71 ve reconstituted SIC1 multiubiquitination in DEAE-fractionated yeast extract.

72 and several chromatographic steps, including DEAE-Sepharose CL-6B, hydroxyapatite, strong anionic and

73 ort here an improved chromatographic method (DEAE-cellulose, calcium hydroxylapatite, and Sephadex G-

74 the absence of agonist is also seen for N,N-DEAE and N,N-diethylaminopropyl esters, both binding wit

75 ubstrates was measured by the nitrocellulose-DEAE double filter binding assay, binding affinity at bo

76 In the absence of DEAE-dextran, FtsZ2 fails to assemble unless supplemente

77 In contrast, in the absence of DEAE-dextran, virion infectivity increases monotonically

78 tent retention of nucleotides in the case of DEAE cellulose filter papers.

79 aximum GalNAc kinase activity on a column of DEAE-Cibacron blue.

80 apparent homogeneity using a combination of DEAE-cellulose column chromatography, ammonium sulfate p

81 fied by a three-step procedure consisting of DEAE, heparin, and Sephacryl S-200 chromatography.

82 In the presence of DEAE-dextran, the polycation known to enhance HIV-1 infe

83 y of anionic extensin peroxidase (pl 4.6) on DEAE-Trisacryl and TSK-gel DEAE-5PW columns.

84 /or in organ culture were chromatographed on DEAE Sephadex to isolate gangliosides.

85 ted to sequential column chromatographies on DEAE-Sepharose, hydroxyapatite, phenyl-Sepharose, and ch

86 protein precipitation and chromatography on DEAE Sepharose CL-6B.

87 nt extraction, followed by chromatography on DEAE-cellulose, C18 reverse phase resin, and silicic aci

88 fold) from insect cells by chromatography on DEAE-cellulose, phosphocellulose, heparin-agarose, and s

89 fibrinogen by ion-exchange chromatography on DEAE-cellulose.

90 edure and then by stepwise chromatography on DEAE-cellulose.

91 was partially purified by chromatography on DEAE-Sephacel and Cibacron Blue 3GA-1000 agarose.

92 ractionation, ion-exchange chromatography on DEAE-Sephacel, and gel filtration on Sephadex G-200.

93 After chromatography on DEAE-Sephacel, hydroxylapatite, and Mono Q and precipita

94 T-20 cells by ion exchange chromatography on DEAE-Sephacel, molecular sieve chromatography on Sephacr

95 l-Synsorb and ion-exchange chromatography on DEAE-Sephacel.

96 er, followed by sequential chromatography on DEAE-Sepharose and butyl-agarose.

97 fied from liver cytosol by chromatography on DEAE-Sepharose which had characteristics of the [3Fe-4S]

98 utes independently from peak 2 fibrinogen on DEAE-cellulose chromatography.

99 eins from lactating bovine mammary glands on DEAE-Sepharose, reactive green 19-agarose, and Superose

100 by co-chromatography of the two proteins on DEAE-5PW following fractionation of a rat liver extract

101 ased on absorption of the acidic proteins on DEAE-cellulose and gel filtration through agarose.

102 bining VSV with ruxolitinib and Polybrene or DEAE-dextran successfully broke the resistance of HPAF-I

103 improved by treating cells with Polybrene or DEAE-dextran.

104 a single component during purification over DEAE-, phenyl-, Reactive Blue-4-, GDP-adipate-, GDP-hexa

105 mplex I and observed that it segregates over DEAE-Sepharose into two subcomplexes (termed I-L and I-U

106 Assembly in GDP plus DEAE dextran produces tubular polymers that are related

107 sed by a facilitator, for example polybrene, DEAE-dextran or a liposome.

108 purified by ammonium sulfate precipitation, DEAE chromatography, and size exclusion chromatography.

109 Factor XIII alone applied to the same DEAE column elutes at a position between peak 1 and peak

110 hies, including diethylaminoethyl sepharose (DEAE) and Sephadex G-75 size exclusion columns.

111 med using Con-A Sepharose, Phenyl Sepharose, DEAE Sephacel, and Superdex 75 FPLC.

112 Sequential DEAE, wheat germ lectin affinity, and hydroxyapatite chr

113 teracting protein was purified by sequential DEAE and size exclusion chromatography, and subsequent m

114 The separation included sequential DEAE-Sephacel, phenyl-Sepharose FF, heparin-Sepharose CL

115 Similarly, DEAE-cellulose chromatography showed slightly stronger b

116 an be isolated from human plasma by a simple DEAE microspin column technique and can be quantified us

117 n TLC of the acidic fraction eluted from the DEAE column, only two radiolabeled glycolipids (GL1 and

118 a parallel increase of radioactivity in the DEAE filter.

119 en demonstrated that the introduction of the DEAE filter increases the assay sensitivity and eliminat

120 o near homogeneity by chromatography through DEAE Sepharose, Heparin Sepharose, and phosphocellulose

121 ate precipitation and chromatography through DEAE-Sepharose and gel filtration columns.

122 in cheese whey and further purified through DEAE-Sepharose XK26.

123 2 fibrinogen plus factor XIII are applied to DEAE columns, the peak 1/factor XIII mixture elutes in t

124 ms, monomers (approximately 40 kDa) bound to DEAE-Sepharose column and protein complexes (approximate

125 , and the resulting extract was subjected to DEAE-cellulose column chromatography.

126 A rapid bioassay of the pheromone uses DEAE-Toyopearl 650M beads to which the pheromone adsorbs

127 tionation, ion exchange chromatography using DEAE-Toyopearl 650 M and gel filtration chromatography u

128 he G-protein activator were determined using DEAE ion exchange chromatography, gel filtration, and a

129 ed to either CEL or PTL were separated using DEAE-chromatography.

130 ease in autonomous PKC activity isolated via DEAE column chromatography also was associated with LTP.

131 mous PKC activity that could be isolated via DEAE column chromatography.

132 Both strong (Q) and weak (DEAE) anion exchange resins were found to adsorb surpris

133 her filter, which is positively charged with DEAE active groups, traps low-molecular-weight DNA fragm

134 S. pneumoniae by serial chromatography with DEAE-Sepharose and Sephacryl S-200.

135 d from the basidioma, and then purified with DEAE-Sepharose CL-6B ion exchange chromatography followe

136 ain membrane were purified sequentially with DEAE-Sephacel, heparin-Sepharose, ceramic hydroxyapatite