ライフサイエンスコーパス: agarose gel electrophoresis

1 size distributions using denaturing glyoxal-agarose gel electrophoresis.

2 dUTP terminal nick-end labeling assay and by agarose gel electrophoresis.

3 nt length polymorphisms (RFLPs) generated by agarose gel electrophoresis.

4 nick end labeling (TUNEL) histochemistry and agarose gel electrophoresis.

5 as associated with DNA laddering as shown by agarose gel electrophoresis.

6 mplicons with sizes easily differentiated by agarose gel electrophoresis.

7 onfirmed by restriction enzyme digestion and agarose gel electrophoresis.

8 viability and the fragmentation of DNA using agarose gel electrophoresis.

9 ved with HindIII and HaeIII and subjected to agarose gel electrophoresis.

10 idence of DNA fragmentation when analyzed by agarose gel electrophoresis.

11 opoisomerase I (Topo I), and two-dimensional agarose gel electrophoresis.

12 ation was investigated in tissue extracts by agarose gel electrophoresis.

13 enzymes HhaI, MboI, and AluI and analyzed by agarose gel electrophoresis.

14 termediates were examined by two-dimensional agarose gel electrophoresis.

15 ncatemers which migrated as a single band in agarose gel electrophoresis.

16 ls and reveals more polymorphic markers than agarose gel electrophoresis.

17 osslinking of resolvase subunits followed by agarose gel electrophoresis.

18 time that DNA fragmentation was apparent by agarose gel electrophoresis.

19 nternucleosomal cleavage of DNA, assessed by agarose gel electrophoresis.

20 renaturation, as measured by Tris-phosphate agarose gel electrophoresis.

21 y, circular dichroism (CD) spectroscopy, and agarose gel electrophoresis.

22 (apo(a)) polymorphs by SDS polyacrylamide or agarose gel electrophoresis.

23 amined using changes in plasmid migration on agarose gel electrophoresis.

24 ]heparan sulfate subpopulations separated by agarose gel electrophoresis.

25 ragments are separated and directly sized by agarose gel electrophoresis.

26 on a specially prepared surface, followed by agarose gel electrophoresis.

27 and the same preparation gave two bands upon agarose gel electrophoresis.

28 as few as three bacteria can be detected by agarose gel electrophoresis.

29 gher sensitivity as compared to conventional agarose gel electrophoresis.

30 rometry, and sodium dodecyl sulfate-vertical agarose gel electrophoresis.

31 ng transmission electron microscopy and 1.2% agarose gel electrophoresis.

32 ugation, and retarded mobility during native agarose gel electrophoresis.

33 when positive, and results were verified by agarose gel electrophoresis.

34 gut cells and DNA fragmentation analyses by agarose gel electrophoresis.

35 ed, as revealed by semi-denaturing detergent agarose gel electrophoresis.

36 d transfer complex can be isolated by native agarose gel electrophoresis.

37 generate monovalent quantum dots (QDs) using agarose gel electrophoresis.

38 is beyond the resolution capacity of regular agarose gel electrophoresis.

39 blot and DNA fragmentation was determined by agarose gel electrophoresis.

40 ry, terminal dUTP nick-end labeling, and DNA agarose gel electrophoresis.

41 SA and apo(a) size by Western blot after SDS-agarose gel electrophoresis.

42 light of new data using two-dimensional (2D) agarose gel electrophoresis.

43 e last annealing cycle are separated by 4-6% agarose gel electrophoresis.

44 rphisms were detected at 9 of the 11 loci by agarose gel electrophoresis.

45 ells was analyzed by native, two-dimensional agarose gel electrophoresis.

46 om the amplification product of viral RNA by agarose gel electrophoresis.

47 nd the restriction fragments are resolved by agarose gel electrophoresis.

48 wed by amplifications with ISSR and SCoT and agarose gel electrophoresis.

49 cies-specific fingerprints for comparison by agarose gel electrophoresis.

50 SA and apo(a) size by Western blot after SDS-agarose gel electrophoresis.

51 hese DNA fragments are typically analyzed by agarose gel electrophoresis.

52 leosomal DNA degradation was assessed by DNA agarose gel electrophoresis.

53 osomal fragmentation (ladder pattern) by DNA agarose gel electrophoresis.

54 quirement of 2 days to examine 96 samples by agarose gel electrophoresis.

55 rmed by "deoxyribonucleic acid laddering" on agarose-gel electrophoresis.

56 e-specific PCR qualitative assay followed by agarose-gel electrophoresis.

57 Using two-dimensional agarose gel electrophoresis (2D-gels) and electron micro

58 describe the development of 2D intact mtDNA agarose gel electrophoresis (2D-IMAGE) for the separatio

59 As analyzed by two-dimensional agarose gel electrophoresis, a plasmid containing 151 bp

60 eosomal arrays were determined by analytical agarose gel electrophoresis (AAGE) and single molecules

61 Product analysis by renaturing agarose gel electrophoresis after cross-linking with 250

62 d be resolved by size in the same lane using agarose gel electrophoresis after simultaneous amplifica

63 HPLC analysis was validated in parallel with agarose gel electrophoresis (AGE), enzyme digestion, and

64 rformance liquid chromatography (AEC) and an agarose gel electrophoresis (AGE)-based method developed

65 purifying DNA-origami nanostructures rely on agarose-gel electrophoresis (AGE) for separation.

66 cts from all of the reactions, visualized by agarose gel electrophoresis, allowed immediate identific

67 ts of 0.95, 1.3, and 1.8 kb were detected by agarose gel electrophoresis, although the transcripts hy

68 d tissue was measured using a combination of agarose gel electrophoresis and a radiometric assay.

69 block architectures were characterized by 1% agarose gel electrophoresis and atomic force microscope

70 d tubules and 20 glomeruli were separated by agarose gel electrophoresis and by isoelectric focusing,

71 Apoptosis was determined using agarose gel electrophoresis and by measuring the cytopla

72 tively to single-stranded DNA as measured by agarose gel electrophoresis and confirmed by steady-stat

73 We used two-dimensional agarose gel electrophoresis and electron microscopy to a

74 With alkaline agarose gel electrophoresis and filter blot hybridizatio

75 , involving circular dichroism spectroscopy, agarose gel electrophoresis and fluorescence quenching,

76 NE increased DNA laddering on agarose gel electrophoresis and increased the percentage

77 ling, aggregation, loss of resolution during agarose gel electrophoresis and loss of transformation a

78 lation, RNA was subjected to high-resolution agarose gel electrophoresis and Northern (RNA) analysis,

79 n comparing MIRU-VNTR profiles obtained from agarose gel electrophoresis and PCRs analyzed on a WAVE

80 The quantity and quality were confirmed by agarose gel electrophoresis and polymerase chain reactio

81 DNA fragmentation determined by agarose gel electrophoresis and quantitation of [3H]thym

82 y a dye-doped silica shell were separated by agarose gel electrophoresis and scanned by a conventiona

83 urse of infection by one and two-dimensional agarose gel electrophoresis and Southern hybridization.

84 t method, the DNA segments were separated by agarose gel electrophoresis and stained with ethidium br

85 ucts (e.g., open circle and linear forms) by agarose gel electrophoresis and subsequently quantified

86 dation, and DNA degradation as determined by agarose gel electrophoresis and the terminal deoxynucleo

87 csL was also examined at pH 8.0 by using SDS-agarose gel electrophoresis and transmission electron mi

88 Agarose gel electrophoresis and ultraviolet spectrophoto

89 splenic lymphocytes by DNA fragmentation in agarose gel electrophoresis and was confined to the CD4+

90 as DNA polymerase pausings, two-dimensional agarose gel electrophoresis, and chemical probe analyses

91 nd enzymatic probe analyses, two-dimensional agarose gel electrophoresis, and immunological studies.

92 ed cells, using two-dimensional (2D) neutral agarose gel electrophoresis, and in a cell-free SV40 DNA

93 PCR amplification, agarose gel electrophoresis, and sequencing methods were

94 reaction (PCR) are exploited using on-column agarose gel electrophoresis as separation and inductivel

95 ed with DNA fragmentation when determined by agarose gel electrophoresis, as seen in the case of THP-

96 By adopting a native agarose gel electrophoresis assay that can specifically

97 and ultrasonic waves was confirmed using an agarose gel electrophoresis assay.

98 used to detect apoptosis, including: a) DNA agarose gel electrophoresis; b) terminal deoxynucleotidy

99 ide gel electrophoresis-band mobility shift, agarose gel electrophoresis-band mobility shift, and nit

100 ic internucleosomal ladder of genomic DNA by agarose gel electrophoresis, by finding nuclear fragment

101 Agarose gel electrophoresis, circular dichroism and diff

102 Native agarose gel electrophoresis confirmed that FliH and FliI

103 ation of density gradient centrifugation and agarose gel electrophoresis coupled with probes specific

104 face of toroid-shaped Pdots was confirmed by agarose gel electrophoresis, cryogenic transmission elec

105 in BPAEC treated with 2-ME was identified by agarose gel electrophoresis (DNA ladder) as well as in s

106 analytical ultracentrifugation, quantitative agarose gel electrophoresis, electron cryomicroscopy, an

107 are based on two-dimensional, non-denaturing agarose gel electrophoresis, followed by structure deter

108 Examination of the hepatocellular DNA by agarose gel electrophoresis following treatment with BPQ

109 A direct comparison of SSDS with agarose gel electrophoresis for +/- screening shows that

110 were examined by electron microscopy and DNA agarose gel electrophoresis for characteristic features

111 capsids that migrated more slowly in native agarose gel electrophoresis from A36V mutant than from t

112 e liver using atomic force microscopy and 2D agarose gel electrophoresis in order to resolve this iss

113 SSRs are robust (with basic PCR methods and agarose gel electrophoresis), informative, and applicabl

114 the SDS-treated full-length particles during agarose gel electrophoresis is most likely caused by dis

115 d in vitro using a low-temperature EDTA-free agarose gel electrophoresis (LTEAGE) procedure.

116 In the current work, an improved agarose gel electrophoresis method for analysis of high

117 The widely used agarose gel electrophoresis method for assessing radiati

118 In SDS capillary agarose gel electrophoresis mode, addition of gamma-cycl

119 However, when analyzed by agarose gel electrophoresis, most RAPD-PCR markers segre

120 However, here, non-denaturing agarose gel electrophoresis of bacteriophage T7 reveals

121 Agarose gel electrophoresis of DNA and RNA is routinely

122 over, DNA laddering was shown in myocytes by agarose gel electrophoresis of DNA fragments.

123 their retinas were evaluated by morphology, agarose gel electrophoresis of DNA, in situ terminal deo

124 onucleosomal DNA degradation was assessed by agarose gel electrophoresis of DNA, which showed DNA fra

125 inhibitor, lovastatin, and was evaluated by agarose gel electrophoresis of genomic DNA, morphologica

126 d using classical morphological features and agarose gel electrophoresis of genomic DNA.

127 6-diamidino-2-phenylindole staining, and (3) agarose gel electrophoresis of low molecular weight cell

128 minimize errors and is broadly applicable to agarose gel electrophoresis of RNA samples and their sub

129 loci was determined by PCR amplification and agarose gel electrophoresis of the amplicons.

130 The introns were sized by agarose gel electrophoresis of the PCR products.

131 ically by in situ end-labeling as well as by agarose-gel electrophoresis of end-labeled DNA.

132 d-UTP nick-end labeling (TUNEL) staining and agarose-gel electrophoresis of extracted slice DNA.

133 articles, were stable during purification by agarose gel electrophoresis or sucrose density gradient

134 chromatin condensation, DNA fragmentation by agarose gel electrophoresis, or terminal deoxynucleotidy

135 luated PCR product detection by using either agarose gel electrophoresis (PCR-gel) or dot blot hybrid

136 An agarose gel electrophoresis pre-screening strategy ident

137 cles successfully separated by using a novel agarose gel electrophoresis procedure.

138 Agarose gel electrophoresis provided further biochemical

139 -screening non-sequence verified clones with agarose gel electrophoresis provides an inexpensive and

140 In addition, agarose gel electrophoresis revealed a 49% increase (P <

141 Marker validation by PCR and low-cost agarose gel electrophoresis revealed that 92.5% were pol

142 ild-type and mutant plants by single-nucleus agarose gel electrophoresis revealed that bleomycin-indu

143 Agarose gel electrophoresis revealed that both NMDA and

144 Agarose gel electrophoresis revealed that KA (2.5 nmol)

145 Two-dimensional agarose gel electrophoresis revealed that ORC2 depletion

146 alysis of mammalian mtDNA by two-dimensional agarose gel electrophoresis revealed two classes of repl

147 se digestion with Asel and Fspl, followed by agarose gel electrophoresis, revealed the predicted abno

148 nnector or the procapsid, as investigated by agarose gel electrophoresis, SDS-PAGE, sucrose gradient

149 We verified these AFM results by agarose gel electrophoresis separation of UV-irradiated

150 itro replication products by two-dimensional agarose gel electrophoresis showed simple Y patterns for

151 Agarose gel electrophoresis showed that high molecular w

152 were isolated from the gel and reanalyzed by agarose-gel electrophoresis, single-nanoparticle-upconve

153 and amplification products were analyzed by agarose gel electrophoresis, Southern blot, and nucleoti

154 Two-dimensional agarose gel electrophoresis studies on fully methylated

155 nation of TUNEL staining and pulse-field and agarose gel electrophoresis, suggesting a predominantly

156 d sequences were used in conjunction with an agarose gel electrophoresis system incorporating an AT-b

157 ple criteria, including DNA fragmentation by agarose gel electrophoresis, terminal deoxynucleotidyltr

158 We show by two-dimensional (2D) agarose gel electrophoresis that replication forks natur

159 Upon agarose gel electrophoresis, the VLDL and IDL from both

160 degrees C and 37 degrees C and shown by SDS-agarose gel electrophoresis to be comprised of a large,

161 mplified, and the amplicons were analyzed by agarose gel electrophoresis to determine the copy number

162 We used plasmid pBR322 and two-dimensional agarose gel electrophoresis to examine the collision of

163 genetics and high resolution two-dimensional agarose gel electrophoresis to examine the torsional ten

164 A screening with custom TTN reporter assays, agarose gel electrophoresis to quantify TTN protein leve

165 We apply agarose gel electrophoresis to sensitively evaluate prot

166 ation forks recover, we used two-dimensional agarose gel electrophoresis to show that replication-blo

167 We have exploited the separation power of agarose-gel electrophoresis to purify milligram amounts

168 The amplified DNA was separated by agarose gel electrophoresis, transferred to nylon membra

169 Here, by native agarose gel electrophoresis, using recombinant IN with a

170 this study, neutral/neutral two-dimensional agarose gel electrophoresis was employed to analyze simi

171 Two-dimensional agarose gel electrophoresis was performed on the product

172 it against DNaseI and ultrasonic waves using agarose gel electrophoresis was studied.

173 Agarose gel electrophoresis was subsequently used to sep

174 Agarose-gel electrophoresis was performed on all serum s

175 Using two-dimensional agarose gel electrophoresis we also show that UvsW acts

176 ragment length polymorphism (RFLP) typing by agarose gel electrophoresis, we compared the analyzer wi

177 Using two-dimensional agarose gel electrophoresis, we examined DNA replication

178 Using two-dimensional agarose gel electrophoresis, we show that mitochondrial

179 Using one- and two-dimensional agarose gel electrophoresis, we show that the linear mtD

180 Using 2D agarose gel electrophoresis, we show that the six o'cloc

181 Using two-dimensional agarose-gel electrophoresis, we show that there is no sp

182 om the present method and those derived from agarose gel electrophoresis were compared.

183 polymerase chain reaction amplification and agarose gel electrophoresis were related to a potato cul

184 ported by analysis of mtDNA molecules by 2-D agarose gel electrophoresis, which indicated the presenc

185 was more sensitive than conventional PCR and agarose gel electrophoresis with ultraviolet transillumi