ライフサイエンスコーパス: Western immunoblotting

1 ase-polymerase chain reactions (RT-PCR), and Western immunoblotting.

2 atient serum, and polyclonal rabbit serum by Western immunoblotting.

3 nd nutrient-starved bacteria by quantitative Western immunoblotting.

4 ed cardioprotective proteins was analyzed by Western immunoblotting.

5 TGF-beta1, and caspase-3 were determined by Western immunoblotting.

6 zyme from the cytosol to membrane as seen by Western immunoblotting.

7 tically activated forms of these caspases by Western immunoblotting.

8 GAD(65) protein levels were quantified using western immunoblotting.

9 PDH for standardizing protein samples during western immunoblotting.

10 d detection of virus in cell supernatants by Western immunoblotting.

11 resenting gag, pol, and env gene products by Western immunoblotting.

12 we analyzed histone H3 and H4 acetylation by Western immunoblotting.

13 keletal muscle, Kell protein was detected by Western immunoblotting.

14 ile specific collagenases were identified by Western immunoblotting.

15 anced serology consisting of two-dimensional Western-immunoblotting.

16 e analysis, confocal immunolocalization, and Western immunoblotting after 24 and 48 hours.

17 By Western immunoblotting all defined terminal organelle pr

18 wing proteins were confirmed by conventional western immunoblotting: all-trans-retinoic acid increase

19 desorption ionization-mass spectrometry and Western immunoblotting analysis identified this co-purif

20 Western immunoblotting analysis verified that the altere

21 Quantitative RT-PCR, Western immunoblotting and an HA ELISA assay were used t

22 frontal cortex, amygdala and pituitary using Western immunoblotting and ELISA, respectively.

23 HUVECs were also analyzed by Western immunoblotting and enzyme activity assays for NA

24 Western immunoblotting and enzyme-linked immunosorbent a

25 Western immunoblotting and flow cytometry revealed highe

26 ing an enzyme-linked immunosorbent assay and Western immunoblotting and found that PAO almost complet

27 Western immunoblotting and immunocytochemistry determine

28 Western immunoblotting and immunofluorescence imaging al

29 Western immunoblotting and immunohistochemistry were use

30 tron), 2 additional techniques consisting of Western immunoblotting and infrared spectroscopy, and 4

31 uction, flow cytometry, quantitative RT-PCR, Western immunoblotting and intracellular recordings.

32 Oxtr localization was conclusively shown by Western immunoblotting and MS of nuclear lysate proteins

33 Using Western immunoblotting and quantitative polymerase chain

34 , laser scanning confocal microscopy (LSCM), Western immunoblotting and RT-PCR to investigate the exp

35 nd beta1 integrin expression was detected by Western immunoblotting and the ability of alpha-melanocy

36 when the two EIA strategies were followed by Western immunoblotting and when used in an MTTT, respect

37 otein was detected at approximately 60kDa by Western immunoblotting and, in the isolated extracts, we

38 Western immunoblotting and/or immunofluorescent microsco

39 ire epitope-bearing P29 product (detected by Western immunoblotting) and contrasts with phase variati

40 by a marked increase in p65 content (+164%; Western immunoblotting) and NF-kappaB DNA binding activi

41 cription-polymerase chain reaction (RT-PCR), Western immunoblotting, and ELISA to evaluate NGF expres

42 ed by electrophoretic mobility shift assays, Western immunoblotting, and enzyme-linked immunoassays,

43 using electrophoretic mobility shift assay, Western immunoblotting, and immunofluorescence imaging.

44 ice was studies by core and envelope ELISAs, Western immunoblotting, and immunofluorescence.

45 Enzyme-linked immunosorbent assay, Western immunoblotting, and immunohistochemistry were us

46 arated, and assessed by Stains-All staining, Western immunoblotting, and mass spectrometry.

47 Binding assays, Western immunoblotting, and reverse transcription-PCR an

48 etermined by indirect immunofluorescence and Western immunoblotting, and the distribution and quantit

49 that if positive or equivocal is reflexed to Western immunoblotting as the second tier.

50 Enzyme-linked immunosorbent assay and Western immunoblotting assays of the IVIG revealed high

51 on GluR1 phosphorylation using quantitative Western immunoblotting assays.

52 ged caspase-specific substrate peptides, and Western immunoblotting confirmed the involvement of prim

53 Western immunoblotting confirmed the presence of ER beta

54 Western immunoblotting confirmed the production of: LFN-

55 Western immunoblotting demonstrated ABGA reactivity to t

56 In VSMC treated with aldosterone, Western immunoblotting detected evidence of GC beta(1)-s

57 ed by protein N-glycosidase F digestions and Western immunoblotting, did not enable it to function as

58 rtin (POMC) was analyzed by means of RT-PCR, Western immunoblotting, fluorescence-activated cell sort

59 examined both by enzyme immunoassays and by Western immunoblotting for autoantibodies to MAP-2.

60 ng phospholipase A(2) (PLA(2)) activity, and Western immunoblotting for protein expression.

61 infected, drug-treated cells and examined by Western immunoblotting for the presence of two packaging

62 qPCR, Western immunoblotting, immunocytochemistry, and ELISA i

63 Western immunoblotting, immunoprecipitation, and immunod

64 hBH was also detected by Western immunoblotting in a high-speed particulate fract

65 C/EBPdelta was detected by Western immunoblotting in osteoblast nuclear extracts af

66 he level of p50 in COS-1 cells determined by Western immunoblotting is 0.10% of total protein, which

67 Using Western immunoblotting, it was demonstrated that the acu

68 Western immunoblotting, liquid chromatography, and mass

69 Neither the level (as revealed by Western immunoblotting) nor the cellular distribution (a

70 Oryza sativa L. leaves was characterized by Western immunoblotting, Northern blotting, and electron

71 These findings were corroborated by Western immunoblotting of mitochondrial membrane isolate

72 Western immunoblotting of patient sera demonstrated an e

73 Western immunoblotting of polysome fractions showed that

74 ron fusion were corroborated by quantitative Western immunoblotting of SerC (PdxF), which was present

75 performed a comprehensive evaluation (using Western immunoblotting) of the expression and subcellula

76 e quantitative polymerase chain reaction and Western immunoblotting, respectively.

77 Western immunoblotting revealed a 56 +/- 6% decrease in

78 Analysis by Western immunoblotting revealed a truncated HMW1 (HMW1')

79 nd vir-phoA translational fusions as well as Western immunoblotting revealed that the expression of V

80 Western immunoblotting revealed that these catalytic pro

81 c analysis of IL-1R2 RNA message levels with Western immunoblotting revealed tight coupling of de nov

82 Finally, results of western immunoblotting show that yohimbine does not sign

83 In genipin-treated TM cells, Western immunoblotting showed a reduction of active MMP2

84 Quantitative RT-PCR and Western immunoblotting showed a reduction of each HAS in

85 ere purified using streptavidin-agarose, and Western immunoblotting showed HSP27 was present.

86 Western immunoblotting showed increases of the iron stor

87 Furthermore, western immunoblotting showed that 95% of EL patients ha

88 Quantitative Western immunoblotting showed that MiaA is an abundant p

89 Western immunoblotting showed that platelet ERbeta migra

90 Results of Western immunoblotting showed that the HMW gelatinase wa

91 Western immunoblotting showed that the UL25 protein was

92 Western immunoblotting showed that transformants produce

93 Western immunoblotting shows enrichment of both isoforms

94 tent of dopamine (DA) terminal changes using Western immunoblotting [striatal dopamine transporter (D

95 spreading, growth, and differentiation using Western immunoblotting techniques, image analysis, flow

96 owed an E. ewingii infection-like profile by Western immunoblotting, the results of Western and dot b

97 e TIMP-1 gene into INS-1 cells and performed Western immunoblotting to demonstrate expression of TIMP

98 Using Western immunoblotting to examine the cytosolic and memb

99 ectron microscopy, immunohistochemistry, and Western immunoblotting to examine the morphology and mic

100 ificantly elevated antibody were examined by Western immunoblotting to outer membrane antigens from A

101 xpression in renal cortex were determined by Western immunoblotting; urine sFlt-1, urine free VEGF-A,

102 from SEC-enriched fractions were examined by Western immunoblotting, urokinase plasminogen activator

103 Western immunoblotting using an antibody directed agains

104 The antigen was clearly identified by Western immunoblotting using antihistidine antibody and

105 The antigen was clearly identified by Western immunoblotting using antihistidine antibody.

106 Western immunoblotting using purified E. chaffeensis and

107 d chromatin modifications were determined by Western immunoblotting using specific antibodies.

108 period, MAP kinase content as determined by Western immunoblotting was constant.

109 Western immunoblotting was performed to analyze the anti

110 Western immunoblotting was performed to identify various

111 Western immunoblotting was used to detect Fas, FasL, sFa

112 Western immunoblotting was used to detect FN fragments i

113 Western immunoblotting was used to evaluate alphaA cryst

114 and subjected to quantitative PCR (qPCR) and Western immunoblotting (WB) for BMP1.

115 e disease (LD), with EIA testing followed by Western immunoblotting (WB) of EIA-equivocal and -positi

116 e assay (IFA), enzyme immunoassay (EIA), and Western immunoblotting (WB) using HL-60 cell culture-der

117 aging, fluorescent immunohistochemistry, and Western immunoblotting, we investigated (1) the expressi

118 els of catalytic subunit protein revealed by Western immunoblotting were consistent with the measured

119 Quantitative real-time PCR and Western immunoblotting were used to examine the mRNA and

120 Quantitative RT-PCR and Western immunoblotting were used to study the effect of

121 oximately 90,000-120,000), were confirmed by Western immunoblotting, when compared with Caco-2 cell c

122 ) for 24 h before 2D gel electrophoresis and Western immunoblotting with antiphosphotyrosine monoclon

123 ransgenic mice, and samples were analyzed by Western immunoblotting with antisera specific for the CO

124 Western immunoblotting with hamster antisera against inf

125 ntities of all three bands were confirmed by Western immunoblotting with specific antibodies.

126 ells and was detected in nuclear extracts by Western immunoblotting with TRP120-specific antibody.