ライフサイエンスコーパス: amplified product

1 t 407bp on gel electrophoresis confirmed the amplified product.

2 iction enzyme digestion or sequencing of the amplified product.

3 tored by using the dissociation curve of the amplified product.

4 h polymorphism analysis or sequencing of the amplified product.

5 ic for IS1549 were positive for the expected amplified product.

6 s, whereas three normal marrows contained no amplified product.

7 by size fractionation and sequencing of the amplified product.

8 fluorescent label to allow detection of the amplified product.

9 least 7263 human genes, as mini-pools of PCR-amplified products.

10 genes and restriction enzyme analysis of the amplified products.

11 HIV-2-specific probes are hybridized to the amplified products.

12 scent microwell assay was used to detect the amplified products.

13 Restriction digests of amplified products allowed the identification and differ

14 d for the region carrying the differentially amplified product and a corresponding region from an adj

15 resentation of the template molecules in the amplified product and introduces random errors.

16 facts present in PCR or in the sequencing of amplified products, and it requires no chemical labels a

17 Allelic nucleotides in the amplified product are then typed by a colorimetric imple

18 Amplified products are detected by probes arrayed on a m

19 rom the targeted gene family and many of the amplified products are novel sequences.

20 ctratyping, and nucleotide sequencing of the amplified products at different times following adoptive

21 y a set of universal primers and to type the amplified products by serotype-specific capture probes.

22 ecific primers followed by sequencing of the amplified products, by Northern blot analysis using a Ca

23 Amplified products can also be used for in vitro cloning

24 The amplified products can be sequenced directly, thus elimi

25 Following a cHDA reaction, the amplified products can be used directly for sequencing a

26 5 deletions in the 129-nucleotide segment of amplified products, compared with the corresponding port

27 Sequencing of 21 amplified products confirmed the melting peak results, w

28 Sequencing of a subset of amplified products confirmed the presence of DNA sequenc

29 strate that the fluorescent intensity of the amplified product correlates with the amount of incorpor

30 Nucleotide sequence analysis of the amplified product demonstrated that the detected virus w

31 Electrophoretic analysis of amplified products demonstrated simultaneous detection o

32 RT-PCR and sequencing of the amplified products demonstrated that the retinal canine

33 r turnaround time and the need to manipulate amplified product during the protocol, increasing the po

34 Restriction digestion of the amplified products followed by fragment size analysis on

35 ion of the DNA by PCR, and collection of the amplified product for delivery to an integral CE chip.

36 e amplified product was identical to that of amplified product from deli ham and students' stool spec

37 ed by contrasting expression profiles of the amplified products from inputs of 500, 50 and 5 ng total

38 Size differences in UBQ3 and UBQ11 amplified products from several ecotypes were observed,

39 RP families, by direct sequencing of the PCR-amplified products from the genomic DNA.

40 Lethality of the amplified products in the presence of tetracycline is a

41 rinting gel that contains the differentially amplified product is cut out, reamplified and the correc

42 However, after a differentially amplified product is detected the next steps are labor-i

43 e new isoforms, the predominant, full-length amplified product is encoded by exons 1-5, exon 13 (v8),

44 e relative abundance of RNA templates in the amplified product is frequently biased.

45 standard, and colorimetric detection of the amplified product is performed with microwell plates.

46 e directly cloned because the differentially amplified product is relatively pure, (ii) those that ne

47 The ratio of alleles in the amplified product is then determined by a single nucleot

48 The amplified product, labeled with an intercalating fluores

49 ting from the viral 5' noncoding region, the amplified product mixture was treated with genotype-spec

50 For easy visualization of the amplified product, molecular-beacon was designed and amp

51 Both were the same size as the amplified product obtained from liver mRNA.

52 tely 680 bp in length and corresponds to the amplified product of a previously reported splice varian

53 enomovar III and B. stabilis internal to the amplified product of G1-G2.

54 Amplified product of the correct size was obtained from

55 tely 643 bp in length and corresponds to the amplified product of the native hK2 mRNA.

56 und a limit of detection of 10 fg/mL for PCR amplified products of 122 bp.

57 etinas showed an absence of the Y chromosome-amplified product on day 10, but the presence of this pr

58 Sequencing verified that the amplified products originated from B. burgdorferi templa

59 and subsequent nucleotide sequencing of the amplified product revealed no extra adenosine residues a

60 tored at different temperatures, the type of amplified product(s) (RNA and/or DNA), and the similarit

61 "Complexity analysis" of the sequence of the amplified product strongly suggests that local DNA motif

62 Multiple PCR primers designed to this region amplified products that differentiate between the seroty

63 ditions, glmM-specific primers generated PCR-amplified products that were specific for H. pylori and

64 ene coupled with very deep sequencing of the amplified products, the microbes on 20 human vaginal epi

65 The amplified product, therefore, may contain a pool of DNA

66 can be used for directional ligation of the amplified product to other preselected DNA molecules.

67 ent sizes from different genes, and allowing amplified products to be resolved electrophoretically.

68 gel image was used for quantification of the amplified product using ImageJ software.

69 The amplified product was detected by a probe-hybridization

70 The resulting amplified product was digoxigeninlabeled at its 3'-end a

71 e for NLV by RT-PCR, and the sequence of the amplified product was identical to that of amplified pro

72 rse-transcriptase PCR (RT-PCR), and a single amplified product was obtained from alveolar macrophages

73 Detection of the amplified product was performed with an oligonucleotide

74 the amount of retinal RNA and the amount of amplified product was used to quantify transcripts from

75 Yeast DNA in amplified products was identified using electrospray ion

76 Direct sequencing of PCR-amplified products was performed for all nine exons of P

77 and HhaI restriction enzyme analyses of the amplified product were able to differentiate among the m

78 escued by reverse transcription-PCR, and the amplified products were cloned and used in differential

79 Amplified products were cloned into an expression plasmi

80 enomic DNAs were amplified with PCR, and the amplified products were covalently attached to chip well

81 Amplified products were reproducibly obtained for seven

82 The amplified products were sequenced and analyzed by phylog

83 Amplified products were sequenced by using a commercial

84 cells were amplified by nested PCR, and the amplified products were sequenced directly without cloni

85 In each case, amplified products were sufficiently pure to be cloned w

86 The amplified products were then reacted separately with ITS

87 00 genomic copies or 25 to 250 PFU) when the amplified products were visualized by ethidium bromide f

88 Amplified products were visualized by staining with ethi

89 site polymorphisms were found in five of the amplified products when they were subjected to digestion

90 er 70 PCR cycles, nearly all samples yielded amplified products which were homologous to various bact

91 gnostic assay with easy visualization of the amplified product will be profitable.

92 Large quantities of amplified product, with a high frequency of nearly indis

93 The amplified product yielded restriction enzyme fragments o