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

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

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

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

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

5 gher sensitivity as compared to conventional 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 ng transmission electron microscopy and 1.2% agarose gel electrophoresis.

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

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

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

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

19 osslinking of resolvase subunits followed by agarose gel electrophoresis.

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

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

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

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

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

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

26 ]heparan sulfate subpopulations separated by agarose gel electrophoresis.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

49 size distributions using denaturing glyoxal-agarose gel electrophoresis.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

69 With alkaline agarose gel electrophoresis and filter blot hybridizatio

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

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

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

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

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

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

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

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

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

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

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

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

82 Agarose gel electrophoresis and ultraviolet spectrophoto

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

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

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

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

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

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

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

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

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

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

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

94 Agarose gel electrophoresis, circular dichroism and diff

95 Native agarose gel electrophoresis confirmed that FliH and FliI

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

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

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

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

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

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

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

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

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

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

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

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

108 The widely used agarose gel electrophoresis method for assessing radiati

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

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

111 Agarose gel electrophoresis of DNA and RNA is routinely

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

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

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

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

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

117 6-diamidino-2-phenylindole staining, and (3) agarose gel electrophoresis of low molecular weight cell

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

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

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

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

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

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

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

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

126 An agarose gel electrophoresis pre-screening strategy ident

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

128 Agarose gel electrophoresis provided further biochemical

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

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

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

132 Agarose gel electrophoresis revealed that both NMDA and

133 Agarose gel electrophoresis revealed that KA (2.5 nmol)

134 Two-dimensional agarose gel electrophoresis revealed that ORC2 depletion

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

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

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

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

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

140 Agarose gel electrophoresis showed that high molecular w

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

142 Two-dimensional agarose gel electrophoresis studies on fully methylated

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

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

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

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

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

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

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

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

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

152 We apply agarose gel electrophoresis to sensitively evaluate prot

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

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

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

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

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

158 Agarose gel electrophoresis was subsequently used to sep

159 Agarose-gel electrophoresis was performed on all serum s

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

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

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

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

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

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

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

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

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

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

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