ライフサイエンスコーパス: primer extension assay

1 xonuclease to remove mispaired 3' bases in a primer extension assay.

2 rapid amplification of cDNA ends (RACE) and primer extension assay.

3 ficial array could be quantified by a simple primer extension assay.

4 avage and to highly visible stop points in a primer extension assay.

5 site was identified by RNase protection and primer extension assay.

6 cific ligation assay and a single nucleotide primer extension assay.

7 cleavage were detected and analyzed using a primer-extension assay.

8 at least in the context of reporter gene and primer extension assays.

9 of the fxbA promoter that was identified in primer extension assays.

10 substrate for nucleic acid hybridization and primer extension assays.

11 -dependent toxT transcription by time course primer extension assays.

12 sults were compared with those of individual primer extension assays.

13 In primer extension assays, afRFC stimulated the processivi

14 Using RPA, primer extension assay and 5' rapid amplification of cDN

15 iptional start point (tsp) was identified by primer extension assay and a rapid amplification of cDNA

16 t of rRNA depurination in vivo using a novel primer extension assay and show that the temporal patter

17 We established a new automated primer extension assay and successfully validated it for

18 Using an in vitro primer extension assay and the mammalian DNA polymerase

19 osition 249, exhibits a mutator phenotype in primer extension assays and in the herpes simplex virus-

20 eir interactions using primase, helicase and primer extension assays, and a 'stripped down' reconstit

21 te that the purified O-ribosomes are pure by primer extension assays, and structurally homogenous by

22 By primer extension assays, cadBA expression was detected w

23 A primer extension assay demonstrated that the appropriate

24 e structure and function of mt-tRNA(Asp) The primer extension assay demonstrated that the m.7551A > G

25 of plasmid pIJ101 and, employing an in vitro primer extension assay, determined that the modification

26 ive allele-specific RT-PCR single nucleotide primer extension assays developed for two imprinted gene

27 chromatography (RP-HPLC) and quantified in a primer extension assay from cord blood.

28 Nucleotide-sequencing and multiplexed primer-extension assays have been used to quantitate the

29 ition, promoter consensus binding search and primer extension assay helped us to identify a new sigma

30 Primer extension assays identified multiple transcriptio

31 We carried out primer extension assays in conjunction with molecular mo

32 Using primer extension assays in vitro, we found that a single

33 strong pause sites in reverse transcriptase primer extension assays in vitro.

34 These enzymes were characterized in primer extension assays in which the template DNA was ad

35 itatively, a strand bias was observed in the primer extension assay, in that polymerase synthesis ter

36 Ribonuclease protection and primer extension assays indicate that alpha1aAR gene tra

37 Primer extension assays indicate two major transcription

38 Biochemical, reporter-based and primer-extension assays indicate that BCX4430 inhibits v

39 The results of ribonuclease protection and primer extension assays indicated that Bmp2 transcriptio

40 In vitro DNA primer extension assays indicated that Cl-F-ara-ATP comp

41 prtF and rofA transcripts by S1 nuclease and primer extension assays indicated that the same promoter

42 Primer extension assay indicates that the transcription

43 ensitive and highly reproducible multiplexed primer extension assay is described for quantitative mut

44 A primer extension assay is used to perform highly multipl

45 Primer extension assay localized the transcription initi

46 cipitated with HBV core antibody; and (iv) a primer extension assay maps the 5' end of the minus stra

47 on of Western blotting and a novel multiplex primer extension assay (MPEA), we showed that, although

48 Using RNase protection and primer extension assays, multiple transcription initiati

49 Specific primer extension assays on total RNA from HeLa cells sho

50 Primer extension assays performed in the presence of hig

51 In primer extension assays, pol eta and pol kappa replicate

52 A simple poisoned primer extension assay readily quantified editing extent

53 Primer extension assay results demonstrated that both di

54 Polymerase-mediated primer-extension assays reveal that tCfTP is efficiently

55 Primer extension assay revealed a transcription initiati

56 Moreover, primer extension assay revealed that N(4)-CMdC was a str

57 Primer extension assays ruled out an increase in abortiv

58 Ribonuclease protection and primer extension assays show that each promoter is activ

59 (selective 2'-hydroxyl acylation analysed by primer extension) assays show that part of the regulated

60 In vitro standing-start primer-extension assays show that the preferential inser

61 varying the order of reagent addition in the primer extension assay showed no distinct differences in

62 Primer extension assays showed that both polymerases sto

63 ng site was near dsbG, Northern blotting and primer extension assays showed that OxyR binding to the

64 Both beta-galactosidase assays and primer extension assays showed that these regions functi

65 on mutants of LAP1 by in vitro transcription-primer extension assays showed that upstream elements in

66 ata from mRNA decay studies and quantitative primer extension assays support a model in which bound C

67 nt inhibitors of human telomerase by using a primer extension assay that does not use PCR-based ampli

68 A primer-extension assay that allowed determination of DNA

69 We also developed a primer-extension assay that can monitor the methylation

70 By employing the primer extension assay, the transcription start site of

71 We used an in vitro primer extension assay to examine the progression of DNA

72 y (ZIBS assay); (ii) an S1 nuclease cleavage-primer extension assay to map B-Z junctions; and (iii) a

73 We used S1 nuclease protection and primer extension assays to define nucleolar dominance at

74 e seven nucleotides were analyzed by a novel primer extension assay using a mixture of one dNTP compl

75 Primer extension assays using recombinant templates cons

76 Primer extension assays using substrates possessing sing

77 native substrate and RNA-chain terminator in primer-extension assays using a surrogate respiratory sy

78 etous yeast species, and the allele-specific primer extension assay was designed to identify a total

79 A primer extension assay was developed to assess HIV-1 RT

80 A primer extension assay was used for the detection of uri

81 A primer extension assay was used to monitor quantitativel

82 Using an in vitro primer extension assay, we observed sequence-specific sy

83 In a missing base primer extension assay, we observed that the mutant enzy

84 Using RNA primer extension assays, we determined that the mdm-2 mR

85 Using primer extension assays, we mapped the transcriptional s

86 omatin immunoprecipitation-single-nucleotide primer extension assays, we measured the chromatin compo

87 Using transcriptional fusions and primer extension assays, we show here that tolC has two

88 Primer extension assays were used to determine the trans

89 Primer extension assays were used to show that individua

90 nged this notion by presenting evidence from primer extension assays which appeared to indicate that

91 y of copying both DNA and RNA templates in a primer extension assay with biased dNTP pools.

92 eloped an SNP genotyping method based on the primer extension assay with fluorescence quenching as th

93 This procedure combines the versatility of a primer extension assay with nucleotide-level resolution,

94 However, a primer extension assay with three dNTPs showed that F227

95 Primer extension assays with purified BALB/cJ and A/J pr

96 Primer extension assays with RNA isolated from Escherich