ライフサイエンスコーパス: amplification product

1 and 10(7) to 10(8) molecules of biotinylated amplification product.

2 of energy transfer-labeled primers into the amplification product.

3 ly when the primers are incorporated into an amplification product.

4 account for signals arising from nonspecific amplification products.

5 ilies, and (iii) redundant sequencing of the amplification products.

6 mer selection, and formation of chimeric 16S amplification products.

7 by automated Web-based sequence analysis of amplification products.

8 CR and was confirmed by direct sequencing of amplification products.

9 by automated web-based sequence analysis of amplification products.

10 y (MS) analysis of base-specifically cleaved amplification products.

11 y preparation and sequence analyses of these amplification products.

12 identified based on the presence/absence of amplification products.

13 ired and in improving the yield of desirable amplification products.

14 priming ability without yielding exponential amplification products.

15 which is due to the accumulation of spurious amplification products.

16 erase chain reaction and sequencing of viral amplification products.

17 direct sequencing and genotyping of desalted amplification products.

18 By gel detection of amplification products, 12 of 181 culture-negative sampl

19 nin-specific polymerase chain-reaction (PCR) amplification products, 5' and 3' rapid amplification of

20 chain reactions (PCR), pooling the resulting amplification products and hybridizing the mixture to a

21 Amplification products are detected with leuco crystal v

22 Second, the amplification products are used as templates in single b

23 Taq DNA polymerase by up to 150% and yielded amplification products at sample dilutions at which Taq

24 Detection of amplification products based on labeled probe primers wa

25 CR methodology, followed by detection of the amplification product by the hybridization protection as

26 specific PCR with the discrimination between amplification products by their melting temperatures (Tm

27 rget nucleic acid, captures the biotinylated amplification products by using magnetic particles coate

28 Genotyping was conducted from HIV-amplification products, by automated sequencing.

29 ESI-MS) and base composition analysis of PCR amplification products can quickly and accurately identi

30 on by standard PCR and DNA sequencing of the amplification product confirmed all real-time PCR tox-po

31 DNA sequence characterization of an RT-PCR amplification product confirmed expression of tuftelin i

32 se-polymerase chain reaction, which revealed amplification products derived from PAF receptor mRNA co

33 amplified with eubacterial primers, and the amplification products derived from the fecal sample DNA

34 The other four samples failed to yield any amplification product even with a control set of primers

35 Specifically identified were amplification products for the following NTs: NGF, BDNF,

36 Amplification products for the full-length Trk A and Trk

37 the conditions under which such recombinant amplification products form we monitored the exchange of

38 (STS)-PCR assay yielded the appropriate size amplification product from both total human DNA and hybr

39 e-specific primers to increase the Tm of the amplification product from the corresponding allele.

40 The pattern of amplification products from all of the reactions, visual

41 d by gel electrophoresis, and representative amplification products from each patient were sequenced.

42 The amplification products from eight air samples were clone

43 labeled PCR primers are used to produce PCR amplification products from eight VNTR regions in the B.

44 Sequence comparisons of the amplification products from four cna negative and four c

45 rometry and base composition analysis of PCR amplification products from highly conserved genomic reg

46 and high throughput, such as the checking of amplification products from many loci, from many clones,

47 escent probe hybridized to Southern blots of amplification products from Neospora DNA but not to Sout

48 or was available from 1 patient, and the IgH amplification products from plasma and tumor were sequen

49 A meiotic breakpoint strategy employing PCR amplification products from recombinant sperm was then u

50 1,000-fold difference in the quantity of the amplification products from the specific and nonspecific

51 The amplification is very sensitive; amplification products generated from as few as three ba

52 Screening of over 2,000 cDNA amplification products identified 42 cDNAs that were pre

53 Cloning and sequencing of the purified amplification products identified a cytosine deletion in

54 AA40 allowed the generation of mixed RNA-DNA amplification products in PCR demonstrating DNA polymera

55 Amplification products increase when degraded genomic DN

56 Sequencing and cross-hybridization of amplification products indicated that at least 12 classe

57 Sequencing of amplification products indicated that at least nine clas

58 be used to transduce isothermal nucleic acid amplification products into signals that can be readable

59 most common methods to detect the different amplification products is the use of fluorogenic probes

60 ctivity of HDA, which makes the detection of amplification products more reliable, we have developed

61 Two amplification products, named IL-2delta2 and IL-2delta3,

62 rimers was verified, since there were no PCR amplification products observed from heterologous nocard

63 Whole genome amplification products obtained by DOP-PCR proved to be

64 Amplification products obtained from the HCV-positive ca

65 82 degrees C product was identical with the amplification product of CEA-cDNA and cDNA from differen

66 positive staphylococci produced a single PCR amplification product of either 875, 660, 603, or 547 bp

67 oduct that was easily distinguished from the amplification product of viral RNA by agarose gel electr

68 esults obtained from unpurified COBAS TaqMan amplification products of 111 retrospectively selected c

69 Random sequencing of the PCR amplification products of CD4+ peripheral blood T cells

70 PCR amplification products of ITS-1 display a approximately

71 Amplification products of the expected size for 15 growt

72 Amplification products of the expected size for HGF and

73 Amplification products of the expected size for NTs were

74 Amplification products of the expected size for the grow

75 he sequence-specific detection of unpurified amplification products of the gyrB gene of Salmonella ty

76 nd Macaca fascicularis yielded three TRIMCyp amplification products, one of which is predicted to enc

77 ers for the mur-2(ed) gene gave the expected amplification product only with E. durans strains.

78 After cloning and sequencing of the amplification products, patient-specific ABL primers wer

79 analyze up to 44 kb of diploid, color-coded amplification product per gel lane.

80 sion of the linear DNA molecules so that the amplification products remain localized near their respe

81 riction endonuclease digestions of the cpDNA amplification products resolved diagnostic restriction s

82 says, producing the expected 108- and 125-bp amplification products, respectively.

83 Stools and water samples yielded identical amplification product sequences.

84 m capillary electrophoresis for the expected amplification products showed that amplification in micr

85 However, failure to recover amplification products spanning the nad4L-msh1 gene junc

86 ynucleotide detector probe hybridizes to the amplification product that rises in concentration during

87 m this population appears to yield two ITS-1 amplification products that match both C. bilineata and

88 Both approaches yielded PCR amplification products that served as probes for screeni

89 on of perfect nucleic acid duplexes with the amplification products, these are enzyme-labeled and ele

90 alized because most laboratories subject the amplification products to lengthy probe hybridization pr

91 However, the size of the amplification products used in these mRNA assays (approx

92 rmed by cloning and random sequencing of PCR amplification products using TCRBV region family-specifi

93 hain reaction; a 144 base-pair region of the amplification product was sequenced; and phylogenetic an

94 me quantitative PCR revealed that 96% of the amplification products were all within 4-fold of the ave

95 Amplification products were also obtained from isolates

96 f RNA from ischemic and control retinas, and amplification products were analyzed by agarose gel elec

97 uclear small-subunit rRNA gene sequence, and amplification products were confirmed by hybridization w

98 cterization of the polymerase chain reaction amplification products were determined by nucleic acid s

99 polymerase chain reaction, and the purified amplification products were directly sequenced with [35S

100 Amplification products were generated only from the DNAs

101 No cross-amplification products were observed when primers design

102 No amplification products were observed with template DNA f

103 Amplification products were obtained from 118 HCV-seropo

104 No amplification products were obtained from DNA extracted

105 P. carinii-specific amplification products were obtained from samples from e

106 Amplification products were obtained that were similar i

107 Different patterns of amplification products were obtained with DNA from desic

108 Amplification products were probed with nested oligonucl

109 results, I found that products from Mtb rRNA amplification products were processed with fluorescent r

110 No amplification products were produced for the full-length

111 The amplification products were resolved and quantified by t

112 The resultant amplification products were used to isolate cDNAs, conta

113 First, PCQ-PCR provided amplification products with an accurate proportion of mu

114 These markers produce amplification products with genomic DNA from allotetrapl

115 Similarly, PCR yielded GCC-specific amplification products with specimens from normal intest