ライフサイエンスコーパス: density gradient centrifugation

1 Mucins were separated by cesium chloride density gradient centrifugation.

2 riched membrane fractions as seen by sucrose density gradient centrifugation.

3 and size fractionation were purified by CsCl density gradient centrifugation.

4 nate without detergent), followed by sucrose density gradient centrifugation.

5 preparation was purified by cesium chloride density gradient centrifugation.

6 reitol (DTT)-mediated reduction, and buoyant density gradient centrifugation.

7 erol were incubated and subjected to sucrose density gradient centrifugation.

8 papain and DNase digestion, trituration, and density gradient centrifugation.

9 ed from cells and from membrane fragments by density gradient centrifugation.

10 Oocysts were initially isolated by sucrose density gradient centrifugation.

11 nts with lysosomal enzyme markers by Percoll density gradient centrifugation.

12 y applying serial filtration steps and using density gradient centrifugation.

13 Macrophages were isolated after Ficoll density gradient centrifugation.

14 enriched symbionts according to cell size by density gradient centrifugation.

15 PHB-containing bacteria were concentrated by density gradient centrifugation.

16 iltration column but were made visible after density gradient centrifugation.

17 suspension-cultured cells following sucrose density gradient centrifugation.

18 consistent with previous measurements using density gradient centrifugation.

19 olated by collagenase-pronase-perfusion, and density gradient centrifugation.

20 ith centrosome fractions isolated by sucrose density gradient centrifugation.

21 psin population was isolated and purified by density gradient centrifugation.

22 hromatographic matrices followed by glycerol density gradient centrifugation.

23 to be an outer membrane protein by isopycnic density gradient centrifugation.

24 fferent fractions by detergent treatment and density gradient centrifugation.

25 liac crest and cells were enriched by Ficoll density gradient centrifugation.

26 llagenase digestion of the liver followed by density gradient centrifugation.

27 additional separation using cesium chloride density gradient centrifugation.

28 te, and in particulate fractions obtained by density gradient centrifugation.

29 lubilized oligomers was confirmed by sucrose density gradient centrifugation.

30 and/or membrane fractionation using OptiPrep density gradient centrifugation.

31 of detergent extraction and differential and density gradient centrifugation.

32 to insulin binding as determined by sucrose density gradient centrifugation.

33 ble membranes then were separated by sucrose density gradient centrifugation.

34 heir light buoyant densities through sucrose density gradient centrifugation.

35 s and luminal contents were subjected to KBr density gradient centrifugation.

36 disruption and initial separation by sucrose density gradient centrifugation.

37 ticks by velocity centrifugation and Percoll density gradient centrifugation.

38 of gel filtration chromatography and sucrose density gradient centrifugation.

39 g low- and high-salt extractions followed by density gradient centrifugation.

40 Mouse BMCs were isolated by density-gradient centrifugation.

41 genase perfusion of the liver and subsequent density-gradient centrifugation.

42 determined by immunoprecipitation or sucrose density-gradient centrifugation.

43 from stationary-phase (SP) yeast cultures by density-gradient centrifugation.

44 rbon source, can be resolved from 12C-DNA by density-gradient centrifugation.

45 gated these species by Blue Native PAGE, Suc density gradient centrifugation, 77K fluorescence, circu

46 Using density gradient centrifugation, a subcellular compartme

47 heat gave only two fractions on equilibrium density gradient centrifugation: a fraction comprised of

48 Density gradient centrifugation, affinity purification,

49 ffectively separated from each other by CsCl density gradient centrifugation alone.

50 partitioned to the cytoplasmic fraction, and density gradient centrifugation analysis demonstrated th

51 Using a combination of density gradient centrifugation and agarose gel electrop

52 ated through multiple rounds of differential density gradient centrifugation and analyzed by immunoel

53 Using sucrose density gradient centrifugation and antibody pulldowns,

54 Triton X-100 extraction followed by OptiPrep density gradient centrifugation and cholera toxin beta-s

55 Instead, sucrose density gradient centrifugation and electron microscopy

56 Together with the results from density gradient centrifugation and fluorescence correla

57 l-enriched LRs were isolated from Giardia by density gradient centrifugation and found to be sensitiv

58 outer membranes were fractionated by sucrose density gradient centrifugation and identified by appear

59 h ATP-sensitive microtubule affinity/sucrose density gradient centrifugation and immunoprecipitation

60 cogen selection/screening regimen of buoyant density gradient centrifugation and iodine vapor colony

61 ance of hydrodynamically large structures in density gradient centrifugation and native gel electroph

62 -purify with high density lipoprotein during density gradient centrifugation and subsequent gel filtr

63 re isolated from adult mice via Ficoll-Paque density-gradient centrifugation and cultured in the pres

64 e wild-type helper virus by CsCl equilibrium density-gradient centrifugation and used to superinfect

65 homogeneity by a combination of elutriation, density gradient centrifugation, and 48-hour culture.

66 from normal human subjects with Ficoll-Paque density gradient centrifugation, and adherent cells were

67 llular granules were fractionated by Percoll density gradient centrifugation, and N- and O-glycans pr

68 volunteers (n=7) were isolated using Ficoll density gradient centrifugation, and plated on fibronect

69 were purified by negative viscosity-positive density gradient centrifugation, and their component pro

70 analyzed purified MUC2-N by gel filtration, density gradient centrifugation, and transmission electr

71 n by aqueous two-phase partitioning, sucrose density-gradient centrifugation, and immunoelectron micr

72 " into the light vesicle fraction in sucrose density gradient centrifugation assays, as did the wild-

73 ion, native gel electrophoresis, and sucrose density gradient centrifugation assays.

74 ected in outer membranes produced by sucrose density gradient centrifugation, but it is sarcosyl solu

75 We compare our device against a density gradient centrifugation by processing 0.5 mL por

76 Moreover, chemical cross-linking and density gradient centrifugation demonstrate that there i

77 Cross-linking sucrose density gradient centrifugation demonstrated an associat

78 Cesium chloride density gradient centrifugation demonstrated banding of

79 Immunoblotting of rafts isolated by sucrose density gradient centrifugation demonstrated recruitment

80 r, pulse-chase studies employing metrizamide density gradient centrifugation demonstrated that the gl

81 le reduction of non-vascular cells following density gradient centrifugation (DGC) and subsequent fil

82 Physical partitioning by density gradient centrifugation did not separate phyllos

83 le proteins from the melanosome fractions by density gradient centrifugation does not diminish organe

84 centrifugation (DC) and equilibrium buoyant density gradient centrifugation (EBDC).

85 away from mosquito salivary gland debris by density gradient centrifugation eliminated salivary glan

86 Continuous density gradient centrifugation enriched NEP activity in

87 On the other hand, density gradient centrifugation experiments suggested a

88 l stromal cells with their nuclei removed by density-gradient centrifugation following the genetic mo

89 A comparison of proteins in CsCl density gradient centrifugation fractions from supernata

90 A cell fraction separated by density gradient centrifugation from blood had TSC2 LOH

91 d mononuclear cells (PBMCs) were isolated by density gradient centrifugation from the blood of patien

92 ents from infected cells by differential and density gradient centrifugation further indicated that P

93 Mutant viral particles, purified by sucrose density gradient centrifugation, had low infectivity and

94 Sucrose density gradient centrifugation, immunoblot, and immunoh

95 Enzymatic assays, sucrose density gradient centrifugation, immunoprecipitation, do

96 ed gel filtration chromatography and sucrose density gradient centrifugations in H(2)O and D(2)O, and

97 subjected to size-exclusion HPLC and sucrose density gradient centrifugation, in the presence of DodG

98 CsCl density gradient centrifugation indicated that almost al

99 Density gradient centrifugation indicated that, unlike s

100 the native enzyme when subjected to glycerol density gradient centrifugation, indicating that they fo

101 ocrine tissue and are difficult to purify by density gradient centrifugation, leading to poor islet r

102 to known proteoglycans; purified using CsCl density gradient centrifugation, molecular sieve, and io

103 Sucrose density gradient centrifugation of a maize mitochondrial

104 After density gradient centrifugation of a microsomal fraction

105 Sucrose density gradient centrifugation of A6 cell detergent ext

106 enes 100S ribosomes were observed by sucrose density gradient centrifugation of bacterial extracts du

107 core-like complexes were isolated by sucrose density gradient centrifugation of detergent-treated vir

108 In agreement, density gradient centrifugation of heated and nonheated

109 in subcellular fractions obtained by sucrose density gradient centrifugation of human umbilical vein

110 Density gradient centrifugation of IgG1 molecules indica

111 Density gradient centrifugation of isolated exosomes rev

112 Density gradient centrifugation of L1 ribonucleoprotein

113 Sucrose density gradient centrifugation of large ribosomal subun

114 By sucrose density gradient centrifugation of membranes, however, m

115 oluble membrane fraction prepared by sucrose density gradient centrifugation of postnuclear fraction

116 Sucrose density gradient centrifugation of postnuclear supernata

117 Similarly, sucrose density gradient centrifugation of purified MAO B exhibi

118 Density gradient centrifugation of subcellular organelle

119 Sucrose density gradient centrifugation of the culture medium re

120 Sucrose density gradient centrifugation of the ribosomal fractio

121 Density gradient centrifugation of Triton X-100 lysates

122 fractionated into two subpopulations by Suc density gradient centrifugation: one subpopulation of bu

123 o exclude nonviable cells require the use of density gradient centrifugation or antibody-based cell s

124 solated from peripheral blood by a series of density-gradient centrifugations or magnetic bead separa

125 Density gradient centrifugation procedures reduce the le

126 veolin-containing lipid-rich fraction during density gradient centrifugation, properties that are con

127 approaches including gel filtration, sucrose density gradient centrifugation, pull-down of differenti

128 When yeast cell lysates are fractionated by density gradient centrifugation, Qsr1p separates from or

129 In 25 min of operating time, density gradient centrifugation recovers an average of 3

130 Discontinuous sucrose density gradient centrifugation revealed NET in the lipi

131 Density gradient centrifugation revealed that in the ini

132 rization of the circulating mRNAs by sucrose density gradient centrifugation revealed that the liver-

133 by size exclusion chromatography and sucrose-density gradient centrifugation revealed that the phosph

134 tion of organelles in the pellet fraction by density gradient centrifugation revealed that VLCS activ

135 amination of lipid rafts isolated by sucrose density gradient centrifugation revealed the constitutiv

136 Sucrose density gradient centrifugation reveals two major forms

137 tems, were calculated from isopycnic banding density gradient centrifugation runs.

138 ver, the splitting was observed with sucrose density gradient centrifugation (SDGC) without IF3 if RR

139 od mononuclear cells were isolated by Ficoll density gradient centrifugation, separated into cellular

140 f the Golgi complex into two fractions using density gradient centrifugation showed effects of aged A

141 ternal ribosome entry mechanisms and sucrose density gradient centrifugation showed that BC1-mediated

142 Sucrose density gradient centrifugation showed that exposure of

143 Density gradient centrifugation showed that secreted apo

144 eparation of purified E1 proteins by sucrose density gradient centrifugation showed that the wild-typ

145 Sucrose density-gradient centrifugation showed that the oleosins

146 he transducing particles by equilibrium CsCl density-gradient centrifugation showed that the particle

147 llular fractionation analysis using OptiPrep density gradient centrifugation shows an increase of fun

148 Correspondingly, glycerol density gradient centrifugation shows that at neutral pH

149 Density gradient centrifugation studies reveal that thes

150 e HbE/beta thalassemia; this is confirmed by density-gradient centrifugation studies that show no dec

151 e show by chemical cross-linking and sucrose density-gradient centrifugation that in the absence of b

152 ated from unreplicated LL-DNA by equilibrium density gradient centrifugation, then both fractions are

153 Using sucrose density gradient centrifugation, this study evaluated wh

154 Using sucrose density gradient centrifugation to analyze ribosome comp

155 we have combined pulse-chase techniques with density gradient centrifugation to identify, isolate, an

156 Triton X-100 at 4 degrees C and subjected to density gradient centrifugation to isolate DRMs from the

157 We used density gradient centrifugation to isolate LDL in plasma

158 One branch utilizes discontinuous density gradient centrifugation to isolate semipure mito

159 ed onto WBC isolation media and subjected to density gradient centrifugation to measure WBC-associate

160 Livers were removed and fractionated by density gradient centrifugation to obtain endosomal and

161 Using alkaline density-gradient centrifugation to separate repaired DNA

162 uorescent labeling, ultracentrifugation, and density gradient centrifugation, virtually all CD46 was

163 Isopycnic banding by density gradient centrifugation was used to measure dens

164 ernal reflection fluorescence microscopy and density gradient centrifugation we found that mouse TRPA

165 sting and osmotic lysis, followed by sucrose density gradient centrifugation, which separated OMs fro

166 As shown by sucrose density gradient centrifugation, WT gamma-PAK, S490A, an

167 membranes with DodGlc2, followed by sucrose density gradient centrifugation, yielded a super complex