ライフサイエンスコーパス: Northern hybridization

1 ffs, and alpha-tmRNA) was next confirmed by Northern hybridization.

2 appeared to be full length, as determined by Northern hybridization.

3 and hyphal forms of C. albicans as judged by Northern hybridization.

4 nohistochemistry, in situ hybridization, and Northern hybridization.

5 th Moa1 isoforms were detected in the eye by Northern hybridization.

6 confirmed by transcriptomic data, RT-PCR and Northern hybridization.

7 -9 expression by semiquantitative RT-PCR and Northern hybridization.

8 was subjected to semiquantitative RT-PCR and Northern hybridization.

9 e and infected tissue culture cells by using Northern hybridization.

10 stry and a 3-kb transcript was identified by Northern hybridization.

11 ental stages and in various adult tissues by Northern hybridization.

12 electrophoretic mobility shift analysis and Northern hybridization.

13 solateral Na(+)-K(+)-ATPase were measured by Northern hybridization.

14 ion of GAP-43 expression was corroborated by Northern hybridization.

15 he tissue distribution of gene expression by Northern hybridization.

16 d transfected-cell cultures was confirmed by Northern hybridization.

17 own to be a single copy gene by Southern and Northern hybridization.

18 own to be a single copy gene by Southern and Northern hybridizations.

19 By Northern hybridization, a factor XI mRNA transcript of a

20 Northern hybridization analyses demonstrated that e subu

21 Using Northern hybridization analyses of RNA isolated from tra

22 that of tad secretion complex genes, we used Northern hybridization analysis and a lacZ reporter assa

23 Northern hybridization analysis demonstrated that Pt4CL1

24 transcription polymerase chain reaction and Northern hybridization analysis did not show significant

25 Northern hybridization analysis indicated that AtPRP1 an

26 Northern hybridization analysis indicated that overexpre

27 Northern hybridization analysis of 460 surveillance samp

28 Northern hybridization analysis of HUVECs revealed that

29 Northern hybridization analysis of mRNA levels and enzym

30 Northern hybridization analysis of the cbl locus identif

31 Northern hybridization analysis revealed that an intact

32 Northern hybridization analysis revealed that arp1 is de

33 Northern hybridization analysis revealed that in fetal t

34 Northern hybridization analysis reveals a peak of TIP60

35 Northern hybridization analysis showed high level arfoph

36 expression is restricted to embryogenesis, a Northern hybridization analysis showed low-level express

37 Northern hybridization analysis showed strong expression

38 Northern hybridization analysis showed that high level e

39 Northern hybridization analysis suggested that hisCl1 an

40 iption-polymerase chain reaction (RT-PCR) or Northern hybridization analysis to quantify TTase mRNA.

41 procollagen messenger RNA were evaluated by Northern hybridization analysis, and the transcriptional

42 ntation, gene replacement, DNA sequence, and Northern hybridization analysis.

43 ted sid2 transcript of 11 kb was detected by Northern hybridization analysis.

44 induction in WEHI7.2 cells, detected by both Northern hybridization and a grp78 promoter-luciferase r

45 ved a single mRNA ( approximately 7.5 kb) by Northern hybridization and a major approximately 130 kDa

46 Using Northern hybridization and beta-galactosidase assays of

47 Northern hybridization and immunoblotting of tissue extr

48 Northern hybridization and immunoblotting studies indica

49 Northern hybridization and in situ hybridization indicat

50 transcription in WEHI7.2 cells, measured by Northern hybridization and nuclear run-on assays, even i

51 Northern hybridization and primer extension experiments

52 nd other putative promoters was performed by Northern hybridization and primer extension experiments.

53 Analysis of HRV-5 expression by Northern hybridization and reverse transcriptase PCR ind

54 Intriguingly, Northern hybridization and reverse transcriptase-polymer

55 Northern hybridization and reverse transcription-PCR ana

56 Now, using Northern hybridization and RNase protection assay, we pr

57 Northern hybridization and RT-PCR demonstrated that the

58 a1 RNA was detected in both skin and eyes by Northern hybridization and was not affected by the absen

59 Northern hybridization and Western blot analysis demonst

60 The results of Northern hybridization and/or real-time reverse transcri

61 Northern hybridizations and RT-PCR indicate that d4-662

62 ) collagens and fibronectin were assessed by Northern hybridization, and the transcription of the alp

63 mRNA levels, and stability were assessed by Northern hybridizations, and COL1A1 transcription by in

64 DNA microarrays, Northern hybridizations, and RNA slot blot analyses were

65 The results of Northern hybridization confirmed that SOWgp expression i

66 Northern hybridization confirmed the production of HaCHI

67 Northern hybridization confirms that the expression of N

68 Southern and northern hybridization data indicate that A. thaliana ex

69 Analysis of RNA by Northern hybridization demonstrated that the emml, hasA

70 Northern hybridizations demonstrated that in the outer m

71 Northern hybridizations demonstrated that the E1-b varia

72 Northern hybridizations demonstrated that TSP-1 expressi

73 Northern hybridization detects the expression of three s

74 9, TIMP-1, TIMP-2, and uPA was determined by Northern hybridization, ELISA, and Western blotting, res

75 nctivochalasis fibroblasts was determined by Northern hybridization, enzyme-linked immunosorbent assa

76 nctivochalasis fibroblasts was determined by Northern hybridization, enzyme-linked immunosorbent assa

77 Further, Northern hybridization experiments defined the tissue di

78 The analysis of total RNA by Northern hybridization experiments reveals the presence

79 Northern hybridization experiments with several differen

80 A cDNA was obtained which, in Northern hybridization experiments, revealed a character

81 examined the expression of human Id mRNAs by Northern hybridization in 11 human myeloid cell lines, s

82 ifferential display pattern was confirmed by Northern hybridization in both prostate tissue and cell

83 UT-A3b mRNA was easily detected by Northern hybridization in the inner medulla.

84 ecrosis factor-alpha mRNA levels, assayed by Northern hybridization, increased in the order +/+ < fa/

85 Northern hybridization indicated that pepO is transcribe

86 Mapping of these transcripts by Northern hybridization indicated that the 1.4- and 2.0-k

87 Based on Northern hybridization, mRNA for GC-G was predominantly

88 Northern hybridization of RNA isolated from transfected

89 Northern hybridization of the transcript expression of t

90 Northern hybridization of tissue RNA indicated that epil

91 Northern hybridizations of mutant leaf, root, tassel, en

92 DNA fragments were used as probes to perform Northern hybridization on RNA from P. carinii-infected a

93 ther monitor one gene at a time, for example northern hybridization or RT-PCR methods, or are designe

94 decreases in levels of Thy-1 mRNA assayed by Northern hybridization or T2 nuclease protection.

95 Northern hybridization, quantitative RT-PCR, and splinte

96 Northern hybridization revealed that gamma-FBG mRNA incr

97 Northern hybridization revealed that mRNA levels for the

98 Northern hybridization revealed that the expression of R

99 Semiquantitative RT-PCR and Northern hybridization revealed that the mRNAs of MMP-1,

100 Northern hybridization revealed that vimentin was expres

101 Northern hybridizations revealed that the cellulosomal c

102 Northern hybridizations revealed that the engO gene is t

103 Northern hybridizations revealed that xynB is transcribe

104 Northern hybridization reveals that the dFKBP59 mRNA is

105 As assessed by northern hybridization, RNase protection assay, and reve

106 only 1 of 34 tested clones showed a band in Northern hybridization, RT-PCR demonstrated that at leas

107 Northern hybridization showed differential distribution

108 immunoblot, indirect immunofluorescence, and Northern hybridization showed dramatically reduced expre

109 Northern hybridization studies revealed that mibp1 is ex

110 Northern-hybridization studies performed on developing s

111 In Northern hybridizations, the C mu 4 probe detected two t

112 rveillance samples were analyzed by dot-blot Northern hybridization to detect RotaTeq vaccine-derived

113 nce of bisabolene synthase mRNA was shown by Northern hybridization to lag behind that of mRNAs respo

114 measurement of [3H]ouabain binding and (ii) Northern hybridization to measure expression of alpha-1

115 -oncogene in adult Syrian hamster tissues by northern hybridization using cph-specific genomic probes

116 normal lymphoid cells were characterized by Northern hybridization using DNA probes from various reg

117 However, by Northern hybridization using either the entire cap8 gene

118 By Northern hybridization using the entire gene cluster as

119 Northern hybridization was performed on 15 of the most a

120 Northern hybridization was used to show that clusterin i

121 ot hybridization, and for gene expression by Northern hybridization, Western immunoblot, or immunohis

122 d during TAM treatment, and was confirmed by Northern hybridization, which showed a 2.7-kb band in bo

123 epitope-specific anti-keratin 12 antibodies, Northern hybridization with 32P-labeled keratin 12 cDNA,

124 Primer extension analysis and Northern hybridization with 5'-untranslated region probe

125 Northern hybridization with the maize cDNA clone shows a