ライフサイエンスコーパス: nucleic acid probe

1 n of citrate AuNPs decorated with a specific nucleic acid probe.

2 as they must be detected with a single short nucleic acid probe.

3 flow-FISH with a fluorescein-labeled peptide nucleic acid probe.

4 denaturing dsDNA and hybridizing fluorescent nucleic acid probes.

5 chieved by in situ hybridization with locked nucleic acid probes.

6 by hybridization with labeled complementary nucleic acid probes.

7 ative to traditional fluorophore labeling in nucleic acid probes.

8 rane by molecular hybridization with labeled nucleic acid probes.

9 , mycolic acid analysis, and narrow-spectrum nucleic acid probes.

10 tly from positive ESP-Myco bottles by use of nucleic acid probes.

11 iously identified by biochemical test and/or nucleic acid probes.

12 dies with fluorogenic protease substrates or nucleic acids probes.

13 n-embedded tissues were hybridized to locked nucleic acid probes against 752 human miRNAs (representi

14 paper with BioPen using "ink" consisting of nucleic acid probes and nucleic acid-modified gold nanop

15 In silico-designed nucleic acid probes and primers often do not achieve fav

16 cal isolates that test negative with the MAC nucleic acid probes and suggest that standard methods us

17 SELEX) to identify glioblastoma TIC-specific nucleic acid probes-aptamers-that specifically bind TICs

18 Nucleic acid probes are used for diverse applications in

19 1% to 6.0%) when the clinics switched from a nucleic acid probe assay to a ligase chain reaction test

20 ternative method uses a signal-amplification nucleic acid probe assay, which measures RNA directly by

21 Meanwhile, nucleic acid probes based on Watson-Crick base-pairing r

22 ent T790M resistance mutation with a peptide nucleic acid probe-based real-time PCR.

23 l in a number of assay procedures, including nucleic acid probe-based systems.

24 A commercially available, nonamplified, nucleic acid probe-based test system (BD Affirm VPIII) w

25 detected in live cells employing appropriate nucleic acid probes bearing a tetrazine-reactive NIR flu

26 ve a significant advantage over conventional nucleic acid probes because they exhibit a higher degree

27 Fluorescently labeled nucleic acid probe binding and subsequent denaturation f

28 detection of M. tuberculosis in culture and nucleic acid probes, but biochemicals are preferred for

29 imal hybridization parameters for 130 locked nucleic acid probes by recording nucleic acid melting te

30 With this approach, nucleic acid probes complementary to RNA targets trigger

31 The isolates were initially hybridized with nucleic acid probes complementary to the rRNA of the res

32 r-beacons are single-stranded hairpin shaped nucleic acid probes composed of a stem, with fluorophore

33 electrophoretically mobilized bead-(peptide nucleic acid probe) conjugates upon hybridization with t

34 A new concept for nucleic acid probe design is reported.

35 i protein farnesyltransferase (TB-PFT) using nucleic acid probes designed from partial amino acid seq

36 Carbohydrate antigen detection, nucleic acid probe detection, and bacterial culture are

37 ic acid sensors based on fluorogenic peptide nucleic acid probes embedded in permeable, physically cr

38 cleotide-templated reactions between peptide nucleic acid probes embedded within permeable agarose an

39 hat l-DNA is useful for designing functional nucleic acid probes especially for biological applicatio

40 We used locked nucleic acid probes for in situ hybridization analysis o

41 to obtain the complete primary structure or nucleic acid probes for the alpha3(V) chain or its biosy

42 Hairpin nucleic acid probes have been highly useful in many area

43 re (29%); rapid (radiometric methods, use of nucleic acid probes, high-performance liquid chromatogra

44 s, several did intratypic differentiation by nucleic acid probe hybridization, and 2 sequenced wild p

45 making these modified PNAs ideal for use as nucleic acid probes in genomic analysis.

46 We used locked nucleic acid probes in in situ hybridisation reactions t

47 situ hybridization (flow-FISH) using locked-nucleic acid probes is combined with rolling circle ampl

48 e derivatives have been covalently linked to nucleic acid probe molecules and have been further chara

49 The design of modified nucleic acid probes, primers, and therapeutics is improv

50 miologic markers nor molecular analysis with nucleic acid probes reliably distinguishes between virus

51 ated with Raman probes and carrying specific nucleic acid probe sequences can be uptaken by the proto

52 ch case, fluorescence intensity of a peptide nucleic acid probe specific for telomeric sequence was e

53 Commercially available nucleic-acid probes specific for the Mycobacterium avium

54 are both necessary and sufficient to design nucleic acid probe systems with consistently high specif

55 aluated in three clinical settings against a nucleic acid probe test method according to the personne

56 The structural features of nucleic acid probes tethered to a solid support and the

57 n (QUAL) probes are a class of self-reacting nucleic acid probes that give strong fluorescence signal

58 identify interactions and characteristics of nucleic acid probes that maximize BSI signal upon bindin

59 We have developed novel nucleic acid probes that recognize and report the presen

60 The nucleic acid probe tiles have been used to study positio

61 by short staple segments, was used to create nucleic acid probe tiles that are molecular analogs of m

62 PICh uses a specific nucleic acid probe to isolate genomic DNA with its assoc

63 These then were used as unique nucleic-acid probes to isolate a 12-kb RPS24 gene fragme

64 Using hybridization with locked nucleic acid probes, we directly detected abortive trans

65 rs are conjugated to high-affinity antisense nucleic acid probes, which show highly selective fluorog

66 se-long RNA target to an immobilized peptide nucleic acid probe, while fragmented mRNA targets from t

67 Molecular beacons are self-reporting, nucleic acid probes whose structure includes complementa

68 from this polypeptide was used to generate a nucleic acid probe with which the corresponding cDNA was

69 , hybridization of cellular DNA with peptide nucleic acid probes with cells intact, and analysis by f

70 the unique recognition properties of locked nucleic acid probes with enzyme-labeled fluorescence.