ライフサイエンスコーパス: RNA probe

1 ridization using a CYP2J2-specific antisense RNA probe.

2 ry using an intron-specific VP heteronuclear RNA probe.

3 t DNA to liberate and hybridize with another RNA probe.

4 und to bind strongly and specifically to the RNA probe.

5 lity of the fusion protein to stably bind an RNA probe.

6 chemistry using a 35S-labelled complementary RNA probe.

7 tive miRNA detection is achieved using 2'OMe-RNA probes.

8 ine pyrene as a fluorescent label for DNA or RNA probes.

9 75 mRNA using digoxigenin-labeled anti-sense RNA probes.

10 tinas after labeling with cell type-specific RNA probes.

11 situ hybridization with digoxigenin-labeled RNA probes.

12 d it does not bind to single-stranded DNA or RNA probes.

13 sections of chick scleras using 33P-labeled RNA probes.

14 e by in situ hybridization using 35S-labeled RNA probes.

15 In situ hybridization with an RNA probe against vascular endothelial growth factor rec

16 eptible to RNAse H enzymatic cleavage of the RNA probe, allowing the target DNA to liberate and hybri

17 RNA probing analyses outlined a specific UTR1 conformati

18 hybridization using a specific 16S ribosomal RNA probe and genomic DNA probe.

19 ation assay using chemiluminescence with HPV RNA probes and by polymerase chain reaction using SPF10

20 -linking with synthetic diazirine-containing RNA probes and quantitative proteomics to profile RNA-pr

21 ection of five differently labeled antisense RNA probes and up to seven differ-ent transcripts in a s

22 Using RNA probing and mutagenesis, we demonstrate that the HIV

23 luorescein-urease conjugate with the labeled RNA probe, and quantitative detection of the membrane-bo

24 pecific sequences, pathogen-specific DNA and RNA probes, and identification of pathogen-specific ions

25 We used messenger RNA probes, antibodies, a LacZ reporter mouse model, and

26 Next, the short DNA sequence and the RNA probe are linked using a T4 DNA ligase.

27 This continuously happens until all of the RNA probes are cleaved, leaving the nanoparticles unprot

28 ular genetic strategy in which two different RNA probes are hybridized to adjacent positions on a tar

29 RNA probes are hybridized to fixed, mixed-staged Drosoph

30 DNA and RNA probes are important analytical reagents in molecula

31 Digoxygenin (dig)-labeled antisense RNA probes are in vitro transcribed from a template synt

32 ) and light (NF-L) NF mRNAs when radioactive RNA probes are incubated with high-speed supernatants (S

33 Aptamers, single-stranded DNA/RNA probes, are poised to become a chemist's antibody an

34 TP potentiated TTP binding to ARE-containing RNA probes, as determined by RNA gel shift assays; AUF1p

35 lished with the target miRNA for a thiolated RNA probe assembled onto a gold nanoparticles (AuNPs) mo

36 itu hybridization, by employing an antisense RNA probe; BDNF protein was detected by employing a sens

37 bes are an attractive alternative to DNA and RNA probes because they are chemically and biologically

38 onucleotides are incorporated into antisense RNA probes by in vitro transcription.

39 hybridization of the cDNA PCR product to an RNA probe, capture of the RNA-DNA hybrid on a solid phas

40 RNA probes carrying the sequence GCGC in place of the ce

41 nd monkeys, using in situ hybridization with RNA probes complementary to Cad6, Dlx1, Dlx2, Dlx5, Gbx2

42 With this approach, RNA probes complementary to mRNA targets trigger chain r

43 A Northern blot assay using single-stranded RNA probes complementary to the spliced in vivo 8.4-kb l

44 Proteins in cell extracts bind to an RNA probe containing six copies of the cycling sequence.

45 A Gtx RNA probe containing this complementarity could be photo

46 e screened a cDNA expression library with an RNA probe containing this sequence.

47 As high-quality RNA probing data become widely available, structurally-i

48 l-principled framework, which in turn allows RNA probing data to be easily integrated into a wide ran

49 Biotinylated RNA probes deleted of the conserved CAGA motif in the te

50 RNA probing demonstrated that the drug protects a specif

51 The 526 base pair antisense, but not sense, RNA probe derived from exons 10-13 stained cystic fibros

52 tic mobility-shift assays using radiolabeled RNA probes derived from different regions of cyclin D1 m

53 In situ hybridization using RNA probes derived from this clone revealed that alveola

54 method takes advantage of inexpensive, long RNA probes detected with antibodies, and we present nove

55 RNA probes encoding the APP IRE stem loop exhibited the

56 obility gel shift analyses using a series of RNA probes encompassing the entire GROalpha transcript.

57 e reaction via the formation of single probe-RNA-probe (enzyme) complex on magnetic beads.

58 RNA probing experiments demonstrated that the fourU elem

59 lection from the lysate using a biotinylated-RNA probe followed by mass spectrometry identified methy

60 We used the cDNA to make an RNA probe for a ribonuclease protection assay (RPA).

61 We then used the RNA probe for in situ hybridization (ISH) experiments.

62 Subsequently, a biotinylated RNA probe for the HIC was transcribed from a nested sequ

63 A similar fraction hybridize with RNA probes for GAD65 and GAD67.

64 was cloned and used to synthesize antisense RNA probes for in situ hybridization analyses of zebrafi

65 We have developed RNA probes for the direct identification of wild poliovi

66 Using RNA probes from SR30 intron 10, whose splicing is altere

67 RNA probes from wild-type and Brn3b(-/-) E14.5, E16.5 an

68 olarization assay that works well, even with RNA probes >90 nucleotides long.

69 Also, RNA probe hybridization confirmed their belonging to the

70 Single-stranded U16 and U17 gene-specific RNA probes hybridized with at least five RNA species fro

71 his system utilizes capture of the protected RNA probe hybrids to streptavidin-coated membranes attac

72 esults from Northwestern analysis using a PU-RNA probe identified the regions within Puralpha that ar

73 ic protein to more than 240 000 unstructured RNA probes in one experiment.

74 situ hybridization with digoxigenin-labeled RNA probes in tissue sections of human jejunum.

75 situ hybridization using digoxigenin-labeled RNA probes in wholemounts and tissue sections.

76 he electroporation-based delivery of DNA and RNA probes into mammalian cells.

77 e used antisense, sense, and double-stranded RNA probes made from the Marsilea centrin cDNA, MvCen1,

78 1 open cores were incubated with 32P-labeled RNA probes of viral and nonviral origin and the reaction

79 ve antigens for protein detection and enable RNA probe penetration for IF/FISH, we perform IF before

80 Unlike conventional sequence-specific DNA or RNA probes, polyamides can recognize their target sequen

81 With the use of RNA probes progressively upstream of the translational s

82 By RNA probe protection we found that transcripts of SpRunt

83 f each probe is evaluated before ISH using a RNA probe quantification (dot blot) assay.

84 In situ hybridization using a radioactive RNA probe resulted in distinct signals in the developing

85 orthern analysis using a VMAT2 complementary RNA probe revealed a single 4 kb mRNA species in corpus

86 In situ hybridization with an RNA probe revealed that the gene is widely expressed; ho

87 ort, biotinylated DNA oligonucleotide and an RNA probe sequence to DNA templates spotted onto a maste

88 er average in a moving window around a given RNA probe set, biologically relevant information can be

89 tu hybridization using a digoxigenin-labeled RNA probe showed that the tissue distribution of amelobl

90 pen) virion-derived cores and virus-specific RNA probes showed that VP3 has affinity for single-stran

91 studies using EBV Epstein-Barr viral-encoded RNA probes showed viral RNA expression in both CD8(+) T-

92 platform involves immobilization of a 40-mer RNA probe specific for a characteristic fragment of the

93 o assess PIC gene expression using antisense RNA probes specific for bovine interleukin-1alpha (IL-1a

94 Finally, using RNA probes specific for RSV genomic RNA, we found that v

95 mRNAs in the adult gut with single-stranded RNA probes specific for trkA, trkB, and trkC.

96 We designed radiolabeled antisense RNA probes, specific for the "adult" Na(V)1.4 and "fetal

97 ER-Library; and a DNA capture approach using RNA probes targeting both DNA strands, termed DEEPER-Cap

98 DNA Input with Probe-based DNA Enrichment by RNA probes targeting DNA duplex (DEEPER-Seq).

99 tracts bound less well to an AU-rich element RNA probe than did the same amount of TTP following deph

100 exhibit a similar increase in binding to the RNA probe that contains the direct repeat of the pH-RE.

101 protection assays using a 710 bp anti-sense RNA probe that spanned the alternatively spliced and nat

102 sults were obtained with a small interfering RNA probe that specifically inhibited PP2A expression.

103 d a nonisotopic RNase protection assay using RNA probes that are dual-labeled with biotin and fluores

104 The assay uses RNA probes that hybridize to ACT1 intron RNA.

105 sing digoxigenin-labeled sense and antisense RNA probes that recognize chicken Pax-6 and Prox 1 (whos

106 sample sequences are hybridized to the same RNA probe, the hybrids are partially digested with RNAse

107 RNA probe titrations and RT-PCR demonstrated that BRCA1

108 we have used an antibody and a complementary RNA probe to explore the distribution of neurons that ex

109 In situ hybridization, using RNA probes to 20 of these sequences, demonstrates differ

110 was directly correlated with the ability of RNA probes to bind to ribosomes.

111 Furthermore, we use RNA probes to show that selective inhibition of E2F3, no

112 scribes ISH of digoxigenin-labeled antisense RNA probes to whole-mount zebrafish embryos.

113 s based on hybridization of complex (cDNA or RNA) probes to cDNA microarrays, either on glass slides

114 el shift assays; AUF1p45 did not bind to the RNA probes under these conditions.

115 zation (ISH) using digoxigenin (DIG)-labeled RNA probes was used to localize mRNA for IL-6 and TNF al

116 Using a single-strand RNA probe, we demonstrated that FSHR mRNA expression is

117 In hindbrain, AptCB1R RNA probe weakly labeled inhibitory interneurons in the

118 In diencephalon, AptCB1R RNA probe weakly stained the central-posterior (CP) and

119 ellular localization, Y2 sense and antisense RNA probes were hybridized to female mouse lacrimal glan

120 Biotinylated RNA probes were used to isolate additional proteins that

121 a template for the synthesis of an antisense RNA probe, which is labeled with digoxigenin-linked nucl

122 sizes, on Northern blots of Caco-2 poly(A)+ RNA probed with a 630 bp 5' hPepT1 cDNA probe, correspon

123 We hybridized ovule RNA probes with Affymetrix ATH1 genome arrays and valida

124 nsfer interactions yield fluorescent DNA and RNA probes with dual emission color readout.

125 RNA probes with perfect complementarity to 18S or 28S rR