ライフサイエンスコーパス: oligonucleotide probe

1 n vitro-translated proteins and radiolabeled oligonucleotide probe.

2 polymerase chain reaction-sequence-specific oligonucleotide probe.

3 V8 proteolytic-digest fragment to design an oligonucleotide probe.

4 dization with a set of fluorescently labeled oligonucleotide probes.

5 saturating fluorescent DNA dye and unlabeled oligonucleotide probes.

6 to gold surface-attached single-stranded DNA oligonucleotide probes.

7 n differences in hybridization to individual oligonucleotide probes.

8 all three criteria for selection of optimal oligonucleotide probes.

9 systematic problems associated with specific oligonucleotide probes.

10 aces to serve as stencils for patterning the oligonucleotide probes.

11 , near the steric-saturation limit for short oligonucleotide probes.

12 was then hybridized successively to pairs of oligonucleotide probes.

13 directly functionalized with amino-modified oligonucleotide probes.

14 and subtype-specific covalently immobilized oligonucleotide probes.

15 products to membrane-bound, highly specific oligonucleotide probes.

16 hundreds of human precursor and mature miRNA oligonucleotide probes.

17 ely fails to bind the same site within short oligonucleotide probes.

18 nd enhanced specificity compared with linear oligonucleotide probes.

19 orophores or functional groups conjugated to oligonucleotide probes.

20 nce of exogenous dNTPs by annealing specific oligonucleotide probes.

21 nd enhanced specificity compared with linear oligonucleotide probes.

22 ferent fluorescently labeled allele-specific oligonucleotide probes.

23 chip is measured by 20 pairs of independent oligonucleotide probes.

24 t it obviates gel electrophoresis or labeled oligonucleotide probes.

25 ied by the hybridization of species-specific oligonucleotide probes.

26 xes were inserted at various positions along oligonucleotide probes.

27 destabilised to assist its interaction with oligonucleotide probes.

28 ntly labeled query sequence to surface-bound oligonucleotide probes.

29 Diagnosis of ETEC infection was done with oligonucleotide probes.

30 by their abilities to specifically bind DNA oligonucleotide probes.

31 n reaction (PCR) using fluorescently labeled oligonucleotide probes.

32 in plants by using locked nucleic acid (LNA) oligonucleotide probes.

33 e to facilitate the design of DNA microarray oligonucleotide probes.

34 onstruct a PPBE model prior to designing new oligonucleotide probes.

35 mer sensing element with covalently attached oligonucleotide probes.

36 sting ways in which to improve the design of oligonucleotide probes.

37 tern, which can be differentially altered by oligonucleotide probes.

38 lls using locked nucleic acid (LNA)-modified oligonucleotide probes.

39 rray hybridisation intensities even for long oligonucleotide probes.

40 , this approach has not been used for longer oligonucleotide probes.

41 pecies with 48 or more short, singly labeled oligonucleotide probes.

42 similarity with target sequences (within the oligonucleotide probe 50 base target region) will contri

43 tion between p50 and C/EBP proteins using an oligonucleotide probe (-63/-41) derived from the CRP pro

44 g by hybridization to high-density arrays of oligonucleotide probes, 97.4% were concordant by both me

45 tu hybridization with a T. whipplei-specific oligonucleotide probe, a broad-range bacterial probe, an

46 ase mutants was analyzed using a 5'-proximal oligonucleotide probe and a series of oligonucleotide pr

47 , duplex formation between a single-stranded oligonucleotide probe and a structured region of a targe

48 by a competitive EMSA using a consensus E2F oligonucleotide probe and by demonstrating a supershift

49 Upon hybridization of the oligonucleotide probe and helper probe to their compleme

50 nal for various spacer molecules between the oligonucleotide probe and the gold surface revealed that

51 on and immunohistochemistry, using antisense oligonucleotide probes and a PIP4Kgamma-specific antibod

52 archers to download a complete repository of oligonucleotide probes and design customized capture ass

53 nt proteins to illuminate mRNAs, use labeled oligonucleotide probes and exploit aptamers that render

54 pression measurements made with spotted long oligonucleotide probes and in situ-synthesized 25-mer pr

55 ance site-specific DNA binding on both short oligonucleotide probes and long DNA fragments.

56 ontitis adults was performed with the use of oligonucleotide probes and PCR.

57 ueness score, U, a novel quality measure for oligonucleotide probes and present a method to quickly c

58 A targets should facilitate the use of short oligonucleotide probes and promote development of generi

59 Understanding the interaction between oligonucleotide probes and RNA targets in living cells i

60 s that occur in an ungapped alignment of the oligonucleotide (probe) and a longer sequence (target).

61 or dot blot hybridization with (32)P-labeled oligonucleotide probes, and we compared these methods to

62 onstructed for this region using overlapping oligonucleotides probes, and BAC-end sequences (BES) wer

63 "D-loop." Sequentially, chemically modified oligonucleotide probes anneal to the displaced DNA stran

64 Specificity studies showed that for a given oligonucleotide probe any 'non-target' transcripts (cDNA

65 These double-stranded oligonucleotide probes are activated for recognition of

66 surface of the islands, and allele-specific oligonucleotide probes are attached to discrete spots on

67 These oligonucleotide probes are conjugated to enzymes that ef

68 cyanine-dye labeled 2'-deoxy and 2'-O-methyl oligonucleotide probes are inside living cells for >5 h,

69 However, when oligonucleotide probes are introduced into cells, they a

70 When oligonucleotide probes are microinjected into cells to i

71 The oligonucleotide probes are renewable, highly efficient,

72 Slides where oligonucleotide probes are spotted in 6-fold redundancy

73 fragment, a 16 to 23S rRNA spacer region, to oligonucleotide probes arranged in lines on a membrane s

74 of a high-density Arabidopsis'whole genome' oligonucleotide probe array for expression analysis (the

75 ing method was determined using high density oligonucleotide probe arrays as a read-out methodology a

76 Oligonucleotide probe arrays have enabled massively para

77 ation kinetics of oligonucleotide targets to oligonucleotide probe arrays synthesized using photolith

78 ysis of transcripts detected by high-density oligonucleotide probe arrays, to predict the presence of

79 of label position and secondary structure in oligonucleotide probes as a function of hybridization bu

80 nt work using quenched fluorescently labeled oligonucleotide probes as sensors for RNA in bacterial a

81 ng the polymerase chain reaction (PCR)-based oligonucleotide probe assay.

82 found that the non-specific accumulation of oligonucleotide probes at mitochondria was driven by mit

83 s described that employs the sequence of the oligonucleotide probe attached to each microsphere as po

84 frequency and voltage for target binding to oligonucleotide probes attached to the sensor array surf

85 From a cDNA library and synthetic oligonucleotide probes based on a partial amino acid seq

86 DNA library was screened by using degenerate oligonucleotide probes based on the amino acid sequence

87 c hybridization (aCGH) platform with 385 000 oligonucleotide probes based on the reference genome seq

88 The study indicates that oligonucleotide probe-based DNA chip assays provide a po

89 rane-based cDNA macroarrays and high-density oligonucleotide probe-based microarrays identified induc

90 In this work, we report on oligonucleotide probes bearing metallacarborane [3-iron

91 crocantilever biosensors functionalized with oligonucleotide probes, before and after hybridization w

92 drolase whose homology was restricted to the oligonucleotide probe (BestFit quality=215 versus 100 fo

93 Only a small fraction of short oligonucleotide probes bind efficiently to complementary

94 en Ref-1/Ape was immunoprecipitated from the oligonucleotide probe, both HIF-1 and p300 remained prob

95 By gel-shift analysis, the corresponding oligonucleotide probe bound endogenous FKHRL1 in an LPS/

96 HIA utilizes a pair of sequence-specific oligonucleotide probes bound to magnetic microbeads.

97 large majority of all genes using 1 million oligonucleotide probes built on 1.2-cm2 glass substrates

98 These genes are targets for only 22% of the oligonucleotide probes but account for 69% of the polymo

99 Fluorescein-labeled oligonucleotide probes can be used to continuously monit

100 tantly, our data indicate that intracellular oligonucleotide probing can be a powerful complement to

101 wells, each specifically functionalized with oligonucleotide probes capable of capturing biotinylated

102 Molecular beacons are oligonucleotide probes capable of forming a stem-loop ha

103 We have prepared a [32P]-labled oligonucleotide probe carrying a free primary amine at i

104 Binding of an analyte to the oligonucleotide probe changes its structure and dynamics

105 genomic DNA of E. coli O157:H7 by a specific oligonucleotide probe coated onto the transistor array r

106 344 genes that were represented in both long oligonucleotide probe collections and the in situ-synthe

107 Although oligonucleotide probes complementary to single nucleotid

108 idize with good specificity and stability to oligonucleotide probes composed of the standard bases.

109 (i) hybridization of a target DNA to a Ramp-oligonucleotide probe conjugate, followed by (ii) specif

110 The oligonucleotide probes consist on anabolic androgenic st

111 e performed using the whole-cell extract and oligonucleotide probes consisting of the two conserved E

112 BP that contains the CXXC domain binds to an oligonucleotide probe containing a single CpG site, and

113 The oligonucleotide probes containing 5'-terminal NH2 group

114 Readily synthesized bifunctional oligonucleotide probes containing a modified pyrimidine

115 Using double-stranded oligonucleotide probes containing a single ribose, we de

116 Gel shift studies reveal that oligonucleotide probes containing an IRS from the IGFBP-

117 n HMG-domain proteins and a series of 16-mer oligonucleotide probes containing both a 1,2-intrastrand

118 owed that constitutive factors could bind to oligonucleotide probes containing each element.

119 e inducible complexes could be detected with oligonucleotide probes containing either the proximal or

120 Oligonucleotide probes containing locked nucleic acid (L

121 s) detection using digoxigenin (DIG)-labeled oligonucleotide probes containing locked nucleic acids (

122 -down assays revealed that GATA-3 could bind oligonucleotide probes containing the wild type but not

123 The oligonucleotide probe contains a non-fluorescent quenche

124 ed to decreased retardation of a labeled DNA oligonucleotide probe corresponding to the -88/-66 regio

125 The method was evaluated using an array of oligonucleotide probes corresponding to IS6110 insertion

126 Short oligonucleotide probes currently synthesized on microarr

127 Electrophoretic mobility shift assays using oligonucleotide probes demonstrated that TGF-beta rapidl

128 Most current microarray oligonucleotide probe design strategies are based on pro

129 Our original interest was motivated by oligonucleotide probe design, and we describe a general

130 By arraying oligonucleotide probes designed from the human genome se

131 Molecular beacons are single-stranded oligonucleotide probes designed to report the presence o

132 Short oligonucleotide probes designed to specifically target s

133 43 animal) were tested with three individual oligonucleotide probes directed against an Asp-87-to-Asn

134 Oligonucleotide probes, directed to the internal transcr

135 These spots with mixed oligonucleotide probes display cooperative hybridization

136 e first time a "click" chemistry approach to oligonucleotide probe elongation as a novel approach to

137 analysis with sense RNA and strand-specific oligonucleotide probes followed by 5' rapid amplificatio

138 y deposition (or 'spotting')of a single long oligonucleotide probe for each gene may be an attractive

139 ray predicated on the use of non-polymorphic oligonucleotide probes for CNV detection.

140 SNP arrays, e.g. use multiple sets of short oligonucleotide probes for each known SNP, and require e

141 situ hybridization histochemistry with (35)S-oligonucleotide probes for GAT-1 mRNA.

142 a web server that facilitates design of DNA oligonucleotide probes for high-density tiling arrays, w

143 An important consideration in the design of oligonucleotide probes for homogeneous hybridization ass

144 RNA sample, is required to design successful oligonucleotide probes for quality microarray results.

145 , synthesis and application of pyrene binary oligonucleotide probes for selective detection of cellul

146 e in situ hybridization technique using rRNA oligonucleotide probes for the identification of M. tube

147 Selecting oligonucleotide probes for use in microarray design, and

148 gle-step, 2 min assay, using only one set of oligonucleotide probes, for a total analysis time of les

149 We show that such adsorbed oligonucleotide probes form a densely packed monolayer,

150 Using gene expression data covering 39,296 oligonucleotide probes from 1109 human liver samples, we

151 raction with RY elements present in 40-42 bp oligonucleotide probes has been shown in vitro for Arabi

152 Large arrays of oligonucleotide probes have become popular tools for ana

153 Short oligonucleotide probes have been linked to a solid suppo

154 A sequence-specific oligonucleotide probe hybridization assay was developed

155 l format, where an immobilized complementary oligonucleotide probe hybridized with the biotinylated t

156 d nucleotides were differentiated for 50-mer oligonucleotide probes hybridized at 50, 45 and 42 degre

157 aptured, purified, and preconcentrated by an oligonucleotide probe immobilized in an in situ polymeri

158 tion of the PCR product to a fungus-specific oligonucleotide probe immobilized on a nylon membrane.

159 e duo-genosensor consisting of two different oligonucleotide probes immobilized covalently on the sur

160 d hybridized to a series of species-specific oligonucleotide probes immobilized on a microchip.

161 antibody binding to the corresponding hapten-oligonucleotide probes immobilized on the nanostructured

162 ver, mGBP-2 inhibits p65 binding to a kappaB oligonucleotide probe in gel shift assays and to the MMP

163 from 206 isolates was characterized by using oligonucleotide probes in a checkerboard hybridization a

164 Allele-discriminating oligonucleotide probes in conjunction with RCA also were

165 am) and motif finding algorithms to identify oligonucleotide probes in conserved amino acid regions a

166 eins inhibit the ability of ESE-1 to bind to oligonucleotide probes in gel mobility shift assays.

167 ribe the use of modified fluorescent-labeled oligonucleotide probes in the sequence-specific detectio

168 strand-DNA-specific nuclease and overlapping oligonucleotide-probes interrogating WT-DNA targets and

169 Fluorescence of the oligonucleotide probe is efficiently quenched by the int

170 The intensity of fluorescence bound to each oligonucleotide probe is intended to reveal which sequen

171 rget oligonucleotide to magnetic bead-linked oligonucleotide probes is followed by binding of the str

172 A set of fluorescently labeled oligonucleotide probes is hybridized to the target mRNA,

173 Molecular beacons are stem-loop hairpin oligonucleotide probes labeled with a fluorescent dye at

174 Molecular beacons are stem-loop hairpin oligonucleotide probes labeled with a fluorescent dye at

175 Oligonucleotide probes labeled with pyrene pairs that fo

176 Interestingly, oligonucleotides probes labeled respectively with Alexa

177 ignals among different tissues at individual oligonucleotide probe level.

178 s, which are based on RNA template-dependent oligonucleotide probe ligation, have been developed to m

179 rious obstacle to the practical use of short oligonucleotide probes (<20-mers).

180 A few strain-specific oligonucleotide probes matching each of the eight segmen

181 y viruses in susceptible hosts, high-density oligonucleotide probe microarray technology was used.

182 the gravitropic response using high-density oligonucleotide probe microarrays.

183 ty and performance of 50mer oligonucleotide (oligonucleotide probe) microarrays, gene-specific oligon

184 aptamer-based) sensors, are comprised of an oligonucleotide probe modified with a redox reporter (in

185 Two new classes of quenched oligonucleotide probes, molecular beacons and quenched a

186 ient heuristics for minimizing the number of oligonucleotide probes needed for analyzing populations

187 Gene-specific oligonucleotide probing of multiple-tissue Northern blot

188 tudy and show that these disulphide-modified oligonucleotide probes offer significant improvements in

189 The microarray included 71 pairs of oligonucleotide probes (oligoprobes) immobilized on glas

190 rticles (AuNPS) followed by coating of ZAP70 oligonucleotide probe on the surface to detect specific

191 on of labeled mRNA molecules to short length oligonucleotide probes on a glass surface.

192 Using an extensive set of 18mer oligonucleotide probes on an in situ synthesized biochip

193 Here, we demonstrate in situ synthesis of oligonucleotide probes on carbon-based substrates using

194 perties, so we adapted it to handle the long-oligonucleotide probes on our arrays (hence LO-BaFL).

195 s paper, we demonstrate in situ synthesis of oligonucleotide probes on poly(dimethylsiloxane) (PDMS)

196 ives rise to a heterogeneous distribution of oligonucleotide probes on the surface, negatively affect

197 cle amplification of circularizable, linear, oligonucleotide probes (padlock probes) was developed.

198 terial 16S rRNA target sequences with 35-mer oligonucleotide probe pairs at 65 degrees C.

199 In conclusion, we have developed short oligonucleotide probe pairs for the species-specific ide

200 A panel of oligonucleotide probe pairs ranging from 11 to 23 nucleo

201 polymerase chain reaction-sequence specific oligonucleotide probes (PCR-SSOP) to HLA-DR.

202 itu hybridization using fluorescence-labeled oligonucleotide probes, PCR amplification of species-spe

203 Sequence-specific oligonucleotide probes play a crucial role in hybridizat

204 it is essential to design microarrays whose oligonucleotide probes produce hybridization intensities

205 protocol that utilizes multiple radioactive oligonucleotide probes, providing for increased sensitiv

206 Using a set of 21,807 60-mer oligonucleotide probes representing >98% of the Unigene

207 atform containing in situ-synthesized 60-mer oligonucleotide probes representing approximately 22,000

208 We also demonstrate that oligonucleotide probe response depends significantly on

209 Experiments with specific oligonucleotide probes revealed signal for preU2 RNA wit

210 region accessibility using complementary RNA oligonucleotide probes revealed significant changes in g

211 DNA positive specimens with species-specific oligonucleotide probes revealed that 44% of the 50 ather

212 hybridization with DNA microchips containing oligonucleotide probes selected for identification of 16

213 hwestern blot analyses indicate that the IUR oligonucleotide probe selectively binds a 115-kDa protei

214 racterized by single-stranded DNA target, an oligonucleotide probe, separated from a helper oligonucl

215 kemia (CML) by immobilizing amine terminated oligonucleotide probe sequence containing 22 base pairs,

216 covalently immobilizing the thiol-terminated oligonucleotide probe sequence via a displacement reacti

217 irs using a combination of sequence-specific oligonucleotide probes, sequence-specific priming, and s

218 Oligonucleotide probe sequences placed on a custom 44 K

219 Allele-specific oligonucleotide probe sequences targeting each of these

220 rophoresis was used to decorate the QDs with oligonucleotide probe sequences.

221 Two hundred twenty-two of 62,839 oligonucleotide probe sets detected expression of genes

222 Of the 56,475 oligonucleotide probe sets interrogated, 415 were statis

223 freely fed and 48-h fasted rats using 26,379 oligonucleotide probe sets.

224 lyzed by hybridization to over 12,000 unique oligonucleotide probe sets.

225 (most commonly methylene blue or ferrocene) oligonucleotide probes site-specifically attached to an

226 ce the specificity of hybridization, such as oligonucleotide probe size, spacer length, surface densi

227 on of DNA or RNA targets to surface-tethered oligonucleotide probes (solid-phase hybridization) and h

228 Finally, CLE with fluorescence labelled oligonucleotide probe specific for C. difficile was perf

229 gels by Southern hybridization with a 20-mer oligonucleotide probe specific for the Salmonella invA g

230 cence in situ hybridization using a 16S rRNA oligonucleotide probe specific to strain 299R.

231 PCR products by microchip hybridization with oligonucleotide probes specific for each ent gene.

232 and hybridization to the multiple individual oligonucleotide probes specific for each Listeria specie

233 DNA microarray using microsphere-immobilized oligonucleotide probes specific for the Salmonella invA

234 An amino-modified single stranded DNA oligonucleotide probe synthesised based on complementary

235 The MitoChip contains oligonucleotide probes synthesized using standard photol

236 mmonly achieved with a two-color fluorescent oligonucleotide probe (TaqMan) design.

237 We designed a microarray of 50-mer oligonucleotide probes targeted to a unique region of th

238 Oligonucleotide probes targeting unmethylated sequences

239 uence-specific primers and sequence-specific oligonucleotide probing techniques.

240 ed, in a strand displacement reaction, by an oligonucleotide probe that becomes covalently attached t

241 should lead to an ideal target for use with oligonucleotide probes that are <25 nt in length.

242 sure that the target DNA binds reliably, the oligonucleotide probes that are attached to the chip arr

243 uspension hybridization format with specific oligonucleotide probes that are covalently bound to the

244 Many genomics assays use profluorescent oligonucleotide probes that are covalently labeled at th

245 Conventional oligonucleotide probes that are perfectly matched to tar

246 amplicons are then hybridized to immobilized oligonucleotide probes that are specific for known IS611

247 Molecular beacons are oligonucleotide probes that become fluorescent upon hybr

248 measurements should facilitate the design of oligonucleotide probes that contain interactive fluoroph

249 Molecular beacons (MBs) are oligonucleotide probes that fluoresce upon hybridization

250 The assay consists of two oligonucleotide probes that hybridise to a specific targ

251 We describe a set of rRNA-based oligonucleotide probes that specifically detect either M

252 oximal oligonucleotide probe and a series of oligonucleotide probes that were complementary to overla

253 The technique utilizes oligonucleotide-probes that direct DSN activity to multi

254 Oligonucleotide probes (the perfect match [PM] probe of

255 By using appropriate oligonucleotide probes, the method can be tailored to an

256 el method for direct QD labeling of modified oligonucleotide probes through streptavidin and biotin i

257 The sensor, which uses a programmable oligonucleotide probe to generate a target-specific sign

258 Oligonucleotide probes to 5 VRs of each class were used

259 er of base pairs formed upon the addition of oligonucleotide probes to a solution containing the vira

260 nt of the sequence-dependent response of the oligonucleotide probes to achieve quantitative comparabi

261 Targeted RNA sequencing (CaptureSeq) uses oligonucleotide probes to capture RNAs for sequencing, p

262 MEC, RT-PCR and hybridization using specific oligonucleotide probes to CIITA promoter sequences ident

263 eleost Fundulus heteroclitus with degenerate oligonucleotide probes to conserved alpha-helical region

264 Targeted genome capture (TGC) utilizes oligonucleotide probes to enrich specific nucleic acids

265 parameters that influence the attachment of oligonucleotide probes to GAPSII slides, shedding light

266 Specific oligonucleotide probes to identify these fungi, as well

267 checkerboard hybridizations performed using oligonucleotide probes to regions encoding 5 variable lo

268 le fluorescent locked nucleic acid (LNA)-DNA oligonucleotide probes to the miRNA of interest, and the

269 2) carbodiimide coupling of amine-terminated oligonucleotide probes to the surface (via an amide bond

270 llow covalent attachment of amine-terminated oligonucleotide probes to these surface groups through c

271 PROBER generates Tiling Oligonucleotide Probes (TOPs) by masking repetitive geno

272 Sequence-specific oligonucleotide probe typing was used to determine DQA1,

273 get duplex allows the use of extremely short oligonucleotide probes, up to tetranucleotides in length

274 d conjugated to various amino-functionalized oligonucleotide probes via cyanuric chloride.

275 The specificity of oligonucleotide probes was studied using target RNAs tha

276 arget sequences and 7693 short perfect match oligonucleotide probes, we have assessed current approac

277 paper, and then biotinylated single-stranded oligonucleotide probes were conjugated onto the UCPs via

278 Eighteen-base oligonucleotide probes were covalently attached to the m

279 atarrhalis DNA microarrays containing 70-mer oligonucleotide probes were designed from the genome-der

280 Specific oligonucleotide probes were developed to identify medica

281 m has been reported in which single-stranded oligonucleotide probes were doubly labeled with adjacent

282 ing-based photolithography technique, 36-mer oligonucleotide probes were found to be more useful in i

283 el RNA target to which fluorescently labeled oligonucleotide probes were hybridized in a complex back

284 We further demonstrated that the dye-labeled oligonucleotide probes were likely on/near the surface o

285 e but did not identify nine isolates because oligonucleotide probes were not available in the current

286 nucleotide probe) microarrays, gene-specific oligonucleotide probes were spotted along with PCR probe

287 Oligonucleotide probes were used to measure bacterial ge

288 C533G mutation of the RET gene, biotinylated oligonucleotide probes were used.

289 ging inside live cells based on programmable oligonucleotide probes, which self-assemble through the

290 red with the common approach that employs an oligonucleotide probe with a covalently linked fluoropho

291 A molecular beacon, an oligonucleotide probe with inherent signal transduction

292 Molecular beacons are dual-labeled, hairpin oligonucleotide probes with a reporter fluorophore at on

293 by band-shift assays to bind double-stranded oligonucleotide probes with at least two internal tandem

294 has been developed that uses biotin-labeled oligonucleotide probes with chemiluminescence detection

295 ridization can suffer from the drawback that oligonucleotide probes with different nucleotide composi

296 The combination of lanthanide-tagged oligonucleotide probes with inductively coupled plasma m

297 soenergetic pentamer and hexamer 2'-O-methyl oligonucleotide probes with LNA (locked nucleic acid) an

298 re a series of 5'TIAM(Tb)/3'BHQ dual-labeled oligonucleotide probes with no secondary structure.

299 Analysis of oligonucleotide probes with reference and clinical isola

300 using molecular beacons (MBs) - fluorogenic oligonucleotide probes - with minimal target engineering