ライフサイエンスコーパス: complementary DNA

1 be strands display very high affinity toward complementary DNA.

2 sity of the ssDNA probe, and hybridized with complementary DNA.

3 hich genomic RNA is reverse transcribed into complementary DNA.

4 7A) variants were generated in the mouse VWF complementary DNA.

5 ing specificity between the PNA used and the complementary DNA.

6 ce at neutral pH that repels the hybridizing complementary DNA.

7 nterfering with efficient synthesis of viral complementary DNA.

8 ons was compared with the reference Na(v)1.7 complementary DNA.

9 rRNAs) that guide Cas12a cleavage of foreign complementary DNA.

10 lver nanoparticles (AgNPs) in the absence of complementary DNA.

11 single base pair mismatch between probe and complementary DNA.

12 lysis led to the identification of eight TPS complementary DNAs.

13 d be rescued by both human and zebrafish at3 complementary DNAs.

14 er and human TLR4 were transfected with CFTR complementary DNAs.

15 erized the enzymes encoded by three of these complementary DNAs: a monoterpene synthase that belongs

16 tified duplications 55 kilobases upstream of complementary DNA AK123120 (P = 3.6 x 10(-6)).

17 imens were processed by sequence-independent complementary DNA amplification and next-generation sequ

18 sequent translational frameshift as shown by complementary DNA analysis.

19 to aptamer molecules pre-hybridized to their complementary DNA anchor molecules immobilized on the gr

20 50% change in fluorescence intensity between complementary DNA and 1 base mismatch DNA which shows th

21 uctures consisting of mRNA hybridized to the complementary DNA and a single-stranded DNA loop, are fo

22 high sensitivity (0.7859 m(0)pM(-1)) towards complementary DNA and can be used to detect it in the co

23 Subsequently, we analyzed complementary DNA and evaluated the methylation status o

24 Furthermore, sequence analyses of ZmYuc1 complementary DNA and genomic clones revealed many chang

25 These formed duplexes with complementary DNA and RNA as shown by UV and circular di

26 entrations by investigating the annealing of complementary DNA and RNA hairpins derived from the tran

27 te relevant biological interactions based on complementary DNA and RNA oligonucleotides that could be

28 TtAgo cleaves specifically guide-complementary DNA and RNA with single nucleotide precisi

29 n is moderately stabilizing when paired with complementary DNA and RNA, but less stabilizing than bot

30 te that it is destabilizing when paired with complementary DNA and RNA.

31 Variations were reproduced in the ABCB4 complementary DNA and the mutants, thus obtained, expres

32 itivities for a series of concentrations for complementary DNA and wild type versus mutant DNA hybrid

33 irus 2/2 (rAAV2/2) vector carrying the RPE65 complementary DNA, and measured visual function over the

34 Two squalene synthase (SS)-like complementary DNAs are identified in race L with one enc

35 n that becomes linear via hybridization to a complementary DNA) are described.

36 and exchange that requires two base pairs of complementary DNA at the site of cleavage; a sequence id

37 n of the subjects' lymphocytes with KINDLIN3 complementary DNA but not CALDAGGEF1 cDNA reverses the L

38 es are not only restricted to protein-coding complementary DNAs but also include short hairpin RNAs a

39 netic microbeads (Strep-MBs) modified with a complementary DNA capture probe.

40 ies specific tmRNA molecules are targeted by complementary DNA capture probes that are covalently att

41 ncing (FISSEQ), in which stably cross-linked complementary DNA (cDNA) amplicons are sequenced within

42 mplicon sequencing of genomic DNA (gDNA) and complementary DNA (cDNA) and metatranscriptomics to inve

43 ods typically require RNA to be converted to complementary DNA (cDNA) before measurements, even thoug

44 and functional cloning, we have identified a complementary DNA (cDNA) encoding a bona fide FcmuR in h

45 ing polyA capture, 3' rapid amplification of complementary DNA (cDNA) ends, full-length cDNAs, and RN

46 In this study, we isolated a 1,520-bp complementary DNA (cDNA) for mimosinase from L. leucocep

47 d the murine phenylalanine hydroxylase (Pah) complementary DNA (cDNA) from a liver-specific promoter

48 cBROCA analysis is undertaken by deriving complementary DNA (cDNA) from puromycin-treated patient

49 With probe complementary DNA (cDNA) immobilized on the PEPS surface

50 When the complementary DNA (cDNA) is added, the thickness of the

51 Using a subtracted complementary DNA (cDNA) library and sequence informatio

52 diated polymerase chain reaction (LMPCR) and complementary DNA (cDNA) library construction.

53 rther advance its utility in high-throughput complementary DNA (cDNA) library screening, we report th

54 h we named AmeloD, by screening a tooth germ complementary DNA (cDNA) library using a yeast 2-hybrid

55 teracting protein by screening a human liver complementary DNA (cDNA) library using mammalian two-hyb

56 a cells with a pooled lentivirus-based human complementary DNA (cDNA) library, transfected the cells

57 combined laser capture microdissection with complementary DNA (cDNA) microarray analysis.

58 human HCC gene expression data obtained from complementary DNA (cDNA) microarrays and corresponding D

59 ly primed second-strand synthesis to recover complementary DNA (cDNA) molecules that were successfull

60 ndividuals and 756 additional sequences from complementary DNA (cDNA) of seven of those individuals.

61 Aptamer-complementary DNA (cDNA) oligonucleotides were tested to

62 of Polymerase chain reaction (PCR)-amplified complementary DNA (cDNA) on the GMR for the reference ge

63 Compared with complementary DNA (cDNA) or messenger RNA (mRNA) microar

64 Analysis of allelic imbalance in complementary DNA (cDNA) samples from human liver (n = 2

65 the sea floor, represented by over 1 billion complementary DNA (cDNA) sequence reads.

66 Single-molecule full-length complementary DNA (cDNA) sequencing can aid genome annot

67 Several procedures for RNA extraction and complementary DNA (cDNA) synthesis were compared for the

68 s inhibiting reverse transcription and viral complementary DNA (cDNA) synthesis.

69 ine brain endothelial cells (ECs) with MMP-9 complementary DNA (cDNA) using pc DNA3.1 (+)/Myc-His A e

70 struct containing full-length mouse fetuin-A complementary DNA (cDNA), linked to a His-tag, to the li

71 As previously noted, the positions of complementary DNA (cDNA)-starts depend on cDNA length in

72 orescence enhancement in the presence of its complementary DNA (cDNA).

73 e nucleotide polymorphisms (SNPs) in SLC22A1 complementary DNA (cDNA).

74 cells by supplementation with wild-type K14 complementary DNA (cDNA).

75 copper-transporting beta polypeptide (ATP7B) complementary DNA (cDNA; AAV8-ATP7B) is able to provide

76 was replaced with a lacZ (beta-gal) reporter complementary DNA (cDNA; IkappaB alpha(+/lacZ)) suggests

77 Multiple mutations were found in CD247 complementary DNAs (cDNAs) cloned from the patient as we

78 functionally characterized three strawberry complementary DNAs (cDNAs) that encode proteins with hig

79 Here we report the complementary DNA cloning and systematic analysis of all

80 Based on transcriptome analysis, full-length complementary DNA cloning, and characterization of expre

81 ated SPR chip has been used to detect target complementary DNA concentration by monitoring the change

82 The expression of a complementary DNA containing only the coding region of M

83 We cloned a full-length complementary DNA (cotton PHYTOCYANIN-LIKE ARABINOGALACT

84 able, ultraviolet light-based method to bond complementary DNA covalently.

85 In the presence of complementary DNAs dA(8) and dG(6) at neutral pH, bm-Cal

86 Restriction factors, such as the retroviral complementary DNA deaminase APOBEC3G, are cellular prote

87 of crystal structures of cLNA modified self-complementary DNA decamer duplexes revealed that the met

88 the wild-type complementary DNA, the mutant complementary DNA depressed VWF secretion, although mult

89 Ectopic expression of a HAB1 complementary DNA derived from wild-type mRNAs partially

90 Upon hybridization with its complementary DNA, desorption of the nanostructures take

91 For this purpose we chose a non-self-complementary DNA duplex containing the biologically-rel

92 ic-oligonucleotide monomers, and a series of complementary DNA-duplex-based multivalent ligands, also

93 material for nanoscale construction because complementary DNA duplexes are programmable and structur

94 encoding genes were isolated and cloned from complementary DNA (EcNHX1-EcNHX4).

95 A complementary DNA encoding either Cre recombinase or a t

96 eno-associated virus serotype 9 carrying SMN complementary DNA encoding the missing SMN protein.

97 tion of C4 photosynthesis in this group, the complementary DNAs encoding four distinct beta-carbonic

98 ne reporter analysis, rapid amplification of complementary DNA ends (RACE), chemical inhibition exper

99 Using 5' Rapid amplification of complementary DNA ends (RACE), two transcriptional start

100 ethods, including six rapid amplification of complementary DNA ends (RACE)-polymerase chain reaction

101 RNA ligase-mediated rapid amplification of complementary DNA ends analysis validated SQUAMOSA PROMO

102 ' RNA ligase-mediated rapid amplification of complementary DNA ends identified 2 novel ERBB4-truncate

103 Using rapid amplification of 5' complementary DNA ends in human brain, we identified a p

104 Here we combined 5' rapid amplification of complementary DNA ends PCR with deep sequencing to quant

105 dentified by 5' RACE (rapid amplification of complementary DNA ends).

106 ction, polyA tail, 3' rapid amplification of complementary DNA ends, Southern blot, immunoblot, histo

107 as then assayed by 5' rapid amplification of complementary DNA ends.

108 polymorphism, markers, QTL and alignments to complementary DNAs, ESTs and protein homologs.

109 LX2 cells transfected with AZIN1 full-length complementary DNA expressed 35% less collagen I mRNA (P

110 hereas the control reporter is an intronless complementary DNA expression cassette.

111 We employed a designed complementary DNA featuring a guanine-rich section in it

112 four output files: a gene prediction file, a complementary DNA file, an alignment file, and a gene fe

113 peptide encompassing the H3.3K27M mutation, complementary DNA for T cell receptor (TCR) alpha- and b

114 In this study, complementary DNAs for each gene were overexpressed to d

115 eq for mapping transcribed regions, in which complementary DNA fragments are subjected to high-throug

116 In this study, we sequenced complementary DNA fragments of cultured human B-cells an

117 The biosensor has the ability to detect complementary DNA fragments with a detection limit down

118 found in 4 of 5 patients, and sequencing of complementary DNA from affected patients confirmed that

119 Sequence analysis of aggrecan complementary DNA from an affected individual revealed h

120 in reaction on the affected exon junction in complementary DNA from blood total RNA.

121 We sequenced complementary DNA from bone marrow of 47 refractory anem

122 reverse transcriptases (RTs) to synthesize a complementary DNA from natural RNA and a range of unnatu

123 ptome variation across mammals, we sequenced complementary DNA from nine tissues from four mammals an

124 amplified by polymerase chain reaction using complementary DNA from renal tissue and cloned in frame

125 Coexpression of Fah complementary DNA from the transposon vector allowed for

126 We sequenced polyadenylated RNA-derived complementary DNAs from 92 psoriatic and 82 normal punch

127 When complementary DNAs from barley MTs were expressed in Cu-

128 newly identified brain SGR produces genomic complementary DNAs (gencDNAs) lacking introns, which int

129 erse genetics based on a tandem minus-strand complementary DNA genome copy under the control of a cyt

130 e probes which have been hybridized to their complementary DNA, GNPs and MNPs, via the hydrogen, elec

131 kinetics for different DNA sequences, where complementary DNA homopolymers are adsorbed faster than

132 Here, we show by expression of the des complementary DNA in Escherichia coli that DES has the c

133 d virus vector (AAV) expressing a normal ND4 complementary DNA in patients with a G to A mutation at

134 expression of a Brassica napus ACBP (BnACBP) complementary DNA in the developing seeds of Arabidopsis

135 l DNA guides for endonucleolytic cleavage of complementary DNA in vitro.

136 pecificity for different matching degrees of complementary DNA, indicating the potential use of such

137 by adenoviral expression of a CaR antisense complementary DNA inhibited Ca(2+)(o)-induced activation

138 pod super green fluorescent protein (copGFP) complementary DNA, inserted at the Kit locus, were gener

139 ribonucleases, DSB repair proceeds through a complementary DNA intermediate, whereas in their absence

140 Transient transfection of AZIN1 SV2 complementary DNA into LX2 cells reduced collagen I gene

141 tion of Gp1ba promoter-driven human alphaIIb complementary DNA into the AAVS1 locus of iPSCs led to h

142 al of our strategy by targeting a corrective complementary DNA into the IL2RG gene of HSCs from healt

143 Sequence analysis was performed on viral complementary DNA isolated from serum specimens collecte

144 n reaction and direct RNA sequencing without complementary DNA isolation.

145 xtracellular coding region of a maize zmbri1 complementary DNA knocked down the expression of all fiv

146 assembled 277,224,180 Illumina reads from 12 complementary DNA libraries to build what is to our know

147 Complementary DNA libraries were sequenced by Solexa.

148 yzed from GT:CD46 and GTKO porcine aortic EC complementary DNA libraries, respectively.

149 rstand the PA pathway in tea, we generated a complementary DNA library from leaf tissue of the bliste

150 Using a complementary DNA library screen, we identified the tran

151 Here we show, using an iterative complementary DNA library screening approach, that human

152 In this study, we used a phage display complementary DNA library screening strategy to identify

153 cising floral organs, and used to generate a complementary DNA library.

154 ture, and self-complementary versus non-self-complementary DNA linker strands (1- versus 2-component

155 and fusion are mediated by hybridization of complementary DNA-lipid conjugates inserted into the two

156 We previously showed that complementary DNA-lipids, inserted into small unilamella

157 Examination of complementary DNA methylation data in a subset of surviv

158 lls were similarly analyzed and also used in complementary DNA microarray analyses.

159 Laser capture microdissection-coupled complementary DNA microarray analysis is a powerful tool

160 Complementary DNA microarray analysis was performed on I

161 the hippocampus was analyzed by genome-wide complementary DNA microarray analysis.

162 rom 9 obese subjects was analyzed by using a complementary DNA microarray at baseline after weight lo

163 New molecular technologies such as complementary-DNA microarray have the potential to incre

164 cluded hepatic gene expression profile using complementary DNA microarrays, genotype at the IL28B SNP

165 core diameters ranging from 5 to 40 nm) with complementary DNA-modified 2 nm gold nanoparticles (~15

166 Although a wide variety of complementary DNA-modified nanoparticles, differentiated

167 cooling, over several days, of solutions of complementary-DNA-modified nanoparticles through the mel

168 s with perfect-matched and single-mismatched complementary DNA molecules were examined by using circu

169 was applied for the detection of a synthetic complementary DNA of SARS-CoV-2 (severe acute respirator

170 s of the long-range stem interaction using a complementary DNA oligomer, which effectively shifts the

171 proach, linear copolymers were prepared from complementary DNA oligomers containing covalently attach

172 reduced through hybridization with a set of complementary DNA oligomers labeled with a fluorescence

173 er to a specific protein selectively or to a complementary DNA oligonucleotide reversibly using toeho

174 achieved by annealing two partly-overlapping complementary DNA oligonucleotides for insertion into an

175 bit the nucleocapsid-chaperoned annealing of complementary DNA oligonucleotides to the TAR and RRE-II

176 uble duplexes by simultaneous binding to two complementary DNAs, one to the base sequence on t-amide

177 mixed samples, SC probes covalently capture complementary DNA or RNA oligo targets and reject two-nu

178 oorthogonal cycloaddition in the presence of complementary DNA or RNA templates.

179 They bind complementary DNA or RNA with sequence specificity to fo

180 ave a higher melting temperature with either complementary DNA or RNA, whereas the remaining PMO anal

181 ere engineered to express an inducible Mist1 complementary DNA or to express a short hairpin RNA that

182 hieved by grafting either molecular beacons, complementary DNA, or proteins to a DNA molecular carrie

183 es were validated using individual sgRNA and complementary DNA overexpression.

184 Here we use pyrosequencing of complementary DNA-PCR amplicons as a general approach to

185 m tests and overexpression of wild-type RGP2 complementary DNA placed under the control of the 35S pr

186 2-aminoethylglycyl (aeg)-PNA is better with complementary DNA (PNA:DNA) than with complementary RNA

187 hybridized with excess fluorescently labeled complementary DNA probes.

188 ominent increases in thermal affinity toward complementary DNA relative to reference strands (average

189 ric selectivity: Hybridization kinetics with complementary DNA remains nearly unaffected, but interac

190 Overexpression of complementary DNA represents the most commonly used gain

191 Sequencing of complementary DNA revealed heterozygous transcripts lack

192 applied direct high-throughput sequencing of complementary DNAs (RNA-Seq), supplemented with data fro

193 between the lower portion of DNA S1 and its complementary DNA S2 formed an identical double-stranded

194 er portion of DNA S1 was hybridized with its complementary DNA S3 modified on AuNPs to bring the DNA

195 ingle-stranded DNA (ssDNA), or dimeric, self-complementary DNA (scDNA) genomes.

196 h a retroviral vector encoding the human ADA complementary DNA sequence (GSK2696273) as part of singl

197 These results suggest that annealing of self-complementary DNA sequence engages an alternative telome

198 inant products (derived from the full-length complementary DNA sequence of human factor VIII), second

199 eaks in DNA upon RNA-guided recognition of a complementary DNA sequence, which strictly requires the

200 ology search and engages in pairing with the complementary DNA sequence.

201 fied samples were also tested for binding of complementary DNA sequences and the results were less st

202 driven by native regulatory regions and from complementary DNA sequences driven by the constitutive m

203 tis carinii, and Pneumocystis jirovecii bgl2 complementary DNA sequences encode proteins of 437, 447,

204 he reversibility of the interactions between complementary DNA sequences is an advantage.

205 nscriptomic' studies have reported that many complementary DNA sequences shared no significant homolo

206 gated to proteins of interest, contain short complementary DNA sequences that provide additional bind

207 to form pcPNA-pcPNA duplexes but can bind to complementary DNA sequences via double duplex-invasion c

208 No-complementary and complementary DNA sequences were clearly discriminated a

209 on containing PcGs binding sites and miR-223 complementary DNA sequences, evolutionarily conserved in

210 Moreover, upon comparison of DNA and complementary DNA sequences, we discovered cytidine-to-u

211 cell adhesion to other surfaces coated with complementary DNA sequences.

212 ng or other techniques based on annealing of complementary DNA sequences.

213 ive to the presence of a large excess of non-complementary DNA sequences.

214 h relies on the inherent interaction between complementary DNA sequences.

215 anding of psoriasis, we used high-throughput complementary DNA sequencing (RNA-seq) to assay the tran

216 equencing but a homozygous L526S mutation in complementary DNA sequencing in our independently genera

217 High-throughput complementary DNA sequencing technologies have advanced

218 polymerase chain reaction with cloning, and complementary DNA sequencing were used to confirm pathog

219 tance of performing simultaneous genomic and complementary DNA sequencing when attributing mutational

220 ree multigene cassettes containing up to six complementary DNAs/short hairpin RNAs.

221 on of the synthesis and properties of pseudo-complementary DNA should lead to an ideal target for use

222 atched that encoded by a recently identified complementary DNA (SlGOMT1) from a white campion flower

223 double stranded DNA (dsDNA, hybridized), non-complementary DNA (ssDNA, un-hybridized) and single nucl

224 and microscale self-assembly processes, with complementary DNA "sticky ends" as one of the most notab

225 electrode (GE) surface that hybridizes to a complementary DNA strand (cDNA) to form a double-strande

226 erature induced melting transition of a self-complementary DNA strand covalently attached at the 5' e

227 d in a surface-tethered vesicle encounters a complementary DNA strand from another vesicle indicates

228 y hRad52 occurred most efficiently when each complementary DNA strand or each ssDNA-hRPA complex was

229 We then site-selectively attached the complementary DNA strand to the N-terminus of a protein.

230 a heterogeneous competitive exchange with a complementary DNA strand which breaks PSA-aptamer intera

231 hich unwinds this intermediate to reveal the complementary DNA strand with a 5'-end that is degraded

232 viral RNA that is hybridized at one end to a complementary DNA strand.

233 A hybridized to RNA, as well as the expelled complementary DNA strand.

234 cent bases, most of which are purines of the complementary DNA strand.

235 erparamagnetic Fe(3) O(4) nanoparticles with complementary DNA strands assemble into crystalline, pse

236 The chemical bond between the two complementary DNA strands can be reversibly broken upon

237 LGA alone shows minimal DNA loading, and non-complementary DNA strands do not get encapsulated within

238 y inhibiting the hybridization of conjugated complementary DNA strands to electrode-bound DNA strands

239 model system that uses the hybridization of complementary DNA strands to model the formation of the

240 (5' to 3' translocase), that operate on the complementary DNA strands to unwind duplex DNA.

241 terstrand cross-links (ICLs) covalently link complementary DNA strands, block DNA replication, and tr

242 Transcription requires unwinding complementary DNA strands, generating torsional stress,

243 small interfering DNAs guide TtAgo to cleave complementary DNA strands.

244 es are prepared through the self-assembly of complementary DNA strands.

245 RNAs (miRNAs) can be produced from the fully complementary DNA strands.

246 thesized, and hybridize efficiently with the complementary DNA strands.

247 cripts, and protein-binding sites on the two complementary DNA strands.

248 o those of bimolecular association of small, complementary DNA strands.

249 interleukin-2 receptor gamma-chain (gammac) complementary DNA successfully restored immunity in most

250 d by zinc finger nuclease editing of a human complementary DNA superexon, spanning exon 2-27, with a

251 and chromosomal integration of nascent viral complementary DNA suppressed.

252 eled DNA oligonucleotides to bind and unbind complementary DNA suspended between two trapped beads.

253 directed evolution of RNA RTs with very high complementary DNA synthesis fidelities, even in the abse

254 ously perform proximity extension assays and complementary DNA synthesis in the same reaction.

255 ermore, we demonstrate that the amount of L1 complementary DNA synthesized by L1 reverse transcriptas

256 PNAs were found to be specific toward their complementary DNA target as seen from their significantl

257 B. melitensis) based on the screening of its complementary DNA target by using two different newly de

258 hybridization between a given probe and the complementary DNA target induced a large decrease in the

259 ates of individual probes in the presence of complementary DNA target influences the electrode potent

260 analyte (Bmax) values for the interaction of complementary DNA target with the immobilized DNA probes

261 wing a high degree of specificity toward the complementary DNA target, as well as single-base mismatc

262 uctance of the nanotube in the presence of a complementary DNA target.

263 to form an "E-DNA" sensor responsive to its complementary DNA target.

264 tal data showed that the interaction between complementary DNA targets and probe 1 is more effective

265 ense) uses CRISPR RNA (crRNA) guides to bind complementary DNA targets at sites adjacent to a trinucl

266 acids) display extraordinary affinity toward complementary DNA targets due to favorable preorganizati

267 oligonucleotides (ITOs) that hybridize with complementary DNA targets for subsequent capture using a

268 ) enabled sensitive detection and capture of complementary DNA targets in the presence of complex med

269 zed MO or DNA "probe" strands hybridize with complementary DNA "targets" from solution, both the MO-D

270 d in a predetermined linear arrangement to a complementary DNA template that was chemoselectively mod

271 d R-loops that form when RNA hybridizes with complementary DNA templates behind RNA polymerases.

272 e-DNA (P-DNA) molecules on a surface through complementary DNA tethers directing cells to adhere and

273 A detection without reverse transcription to complementary DNA that is faster, simpler, and less pron

274 ected in equal quantities with the wild-type complementary DNA, the mutant complementary DNA depresse

275 biotinylated DNA probes with mutant DNA and complementary DNA, the resulting duplex DNA helixes were

276 ately stable parallel stranded duplexes with complementary DNA, they do not form stable hybrids with

277 udy of a lentiviral vector to transfer IL2RG complementary DNA to bone marrow stem cells after low-ex

278 , was used in combination with a fluorescent complementary DNA to create dense clusters of fluorescen

279 onstrated to concurrently bind two different complementary DNAs, to form duplexes from both tert-amid

280 rrection of ribosomal protein deficiency via complementary DNA transfer into the "safe harbor" AAVS1

281 e model expressing a full-length ATXN2(Q127)-complementary DNA under control of the Pcp2 promoter (a

282 notype of eda9 was complemented with an EDA9 complementary DNA under the control of a 35S promoter (P

283 discriminated between non-complementary and complementary DNA using fluorophore-tagged DNA as a mode

284 mRNA expression by targeted resequencing of complementary DNA using single-molecule molecular invers

285 rom all samples and reverse transcribed into complementary DNA; V1-V2 regions of 16S ribosomal RNA ge

286 everse transcriptases, produce virus-derived complementary DNAs (vDNA).

287 replications of DPV measurement of 0.2microM complementary DNA was 4.88%.

288 Norovirus complementary DNA was amplified by overlapping polymeras

289 Hg(2+) leads to DNA hybridization, in which complementary DNA was captured onto the biosensor surfac

290 equence of the 5'-flanking region of mVGLUT2 complementary DNA was cloned.

291 METHODS AND Complementary DNA was prepared from C57BL/6-mice subject

292 The porcine complementary DNA was recovered by polymerase chain reac

293 4A, E562A, and E564A mutants containing self-complementary DNA were compared with virus containing si

294 Transporter complementary DNAs were also expressed in the companion

295 Complementary DNAs were transfected into HEK293 cells.

296 his mutation creates a new exon in the STAT3 complementary DNA, which, when overexpressed, generates

297 acid (Fc-PNA) and a Fc-PNA hybridized with a complementary DNA, while the DNA polymerase-assisted tar

298 detection limit of approximately 500 aM for complementary DNA with a linear dynamic range up to 10(-

299 ence of a DNA toehold in a similar manner to complementary DNA, with kinetic details specific to the

300 f Me10, we developed a tomato immune induced complementary DNA yeast two-hybrid library and screened