ライフサイエンスコーパス: fluorescence labeling

1 a Cys-lite variant needed for site-specific fluorescence labeling.

2 QUAD opsins, with or without a SNAP tag for fluorescence labeling.

3 single prostate cancer cells with post-click fluorescence labeling.

4 bacteria in roots and soil matrices without fluorescence labeling.

5 membrane topology generated by site-directed fluorescence labeling.

6 e mainly limited to indirect observation via fluorescence labeling.

7 ty, measured as loss of ATP-activated FM1-43 fluorescence labeling.

8 ations without the need for amplification or fluorescence labeling.

9 or beta4 nAChR subunits and visualized with fluorescence labeling.

10 For the first time, it was reached without fluorescence labeling.

11 microscope upon isothermal amplification and fluorescence labeling.

12 ting approach permits specific intracellular fluorescence labeling.

13 and excellent molecular specificity through fluorescence labeling.

14 Using a novel saturation fluorescence labeling 2-DE analysis, we showed that 15 u

15 nsducer HtrI, we identified by site-directed fluorescence labeling a site (Ser(155)) on SRI that is c

16 formigenes, was established by site-directed fluorescence labeling, a simple strategy that generates

17 rom an analytical point of view, since smart fluorescence labeling allows profiting from the excellen

18 RD1 in cell proliferation is confirmed using fluorescence labeling analysis of cell division.

19 Through the use of triple-fluorescence labeling and confocal laser microscopy, ter

20 tic protein-RNA-DNA complex was confirmed by fluorescence labeling and cryo-electron microscopy studi

21 Flow cytometry commonly utilizes fluorescence labeling and extensive sample preparation t

22 sayed on the yeast cell surface using immuno-fluorescence labeling and flow cytometry, time-consuming

23 Recent developments of fluorescence labeling and highly advanced microscopy tec

24 detecting and subtyping viruses but require fluorescence labeling and imaging equipment.

25 Advances in fluorescence labeling and imaging have made it possible

26 ues such as selective chemical modification, fluorescence labeling and mutations are cumbersome for t

27 selected by using (deliberately) inefficient fluorescence labeling and observing fluorescent molecule

28 We have used a site-directed fluorescence labeling and quenching strategy to determin

29 We have used a site-directed fluorescence labeling and quenching strategy to investig

30 Using fluorescence labeling and radiolabeling, we show that ch

31 Using site-directed fluorescence labeling and several independent fluorescen

32 lmonella based on immunomagnetic separation, fluorescence labeling and smartphone video processing.

33 been probed using site-directed mutagenesis, fluorescence labeling, and chemical cross-linking, with

34 Radioisotope, fluorescence labeling, and heme analog studies suggest t

35 rom aggregation, liposome rupture, extensive fluorescence labeling, and light scattering.

36 cluding enzymatic reactions, chromatography, fluorescence labeling, and mass spectrometry.

37 orthogonal click chemistry for site-specific fluorescence labeling, and transition metal FLIM-FRET.

38 behind this behavior, using a site-directed fluorescence labeling approach.

39 However, conventional extrinsic fluorescence labeling approaches are not readily applied

40 Using site-directed fluorescence labeling combined with our novel helical pe

41 ng methods (such as mass spectrometry-based, fluorescence labeling, conventional optical imaging) can

42 netic, mutagenesis, structural modeling, and fluorescence labeling data highlight allosteric features

43 However, fluorescence labeling data implied that FepA was active

44 The site-directed fluorescence labeling data indicate opsin is constrained

45 Active site-specific fluorescence labeling demonstrated directly that the act

46 Fluorescence labeling demonstrates the immobilization of

47 beads underwent serial quality controls via fluorescence labeling, e.g., reproducibility (R square =

48 ed stable sieve element (SE) plasma membrane fluorescence labeling, even after plastic (methacrylate)

49 luorescent protein/cyan fluorescent protein) fluorescence labeling experiments showed that mutational

50 ion is based on time-resolved, site-directed fluorescence labeling experiments that show a small, but

51 nic and postnatal mouse cortex by retrograde fluorescence labeling, followed by fluorescence-activate

52 Near-infrared (NIR) fluorescence labeling/imaging of tumor in the NIR-I (800

53 ate for applications in oxoanion binding and fluorescence labeling in biological (e.g., the delivery

54 ost widely used method for intracellular RNA fluorescence labeling is MS2 labeling, which generally r

55 Furthermore, fluorescence labeling is significantly more compatible w

56 nt fibers are actin-based using conventional fluorescence-labeling methods.

57 Fluorescence labeling of adenoviral particles is one new

58 Fluorescence labeling of biomolecules and fluorescence d

59 CXCR5 and CXCR3 receptors and enabled rapid fluorescence labeling of CXCR5+ CXCR3+ resistant B cells

60 of high sensitivity and specificity based on fluorescence labeling of DNA adducts combined with high-

61 Fluorescence labeling of DNAs is broadly useful, but met

62 convenient and versatile method for general fluorescence labeling of DNAs.

63 However, a main disadvantage of fluorescence labeling of drugs is that the introduction

64 zed the capillary tufts by combining in vivo fluorescence labeling of endothelial cells, a novel tiss

65 We used fluorescence labeling of epitope-tagged AML-1B (CBFA2) t

66 Here, we introduce exchangeable ligands for fluorescence labeling of HaloTag (xHTLs) that reversibly

67 Using site-specific fluorescence labeling of individual residues along a str

68 -controllable permeability, and non-invasive fluorescence labeling of living cells.

69 ssreactivity with related subunits, specific fluorescence labeling of nerve terminals and cell bodies

70 It is based on fluorescence labeling of newly formed reducing ends of B

71 Here we describe a general method for fluorescence labeling of oligonucleotides readily and co

72 ed and cost-effective approach to saturation fluorescence labeling of protein thiols for proteomic an

73 Fluorescence labeling of proteins has become increasingl

74 We utilized this chemistry for site-specific fluorescence labeling of proteins on the cell surface an

75 Fluorescence labeling of rat lung slices and in vivo mou

76 highly efficient procedure for site-specific fluorescence labeling of Rep and a bio-friendly immobili

77 Site-specific fluorescence labeling of single cysteine-containing apoE

78 We here report a novel strategy for specific fluorescence labeling of such motifs.

79 Allergen uptake was studied after fluorescence labeling of the major birch pollen allergen

80 As shown by fluorescence labeling of the nuclei of membrane-damaged

81 hy of polymers extracted from the cells, and fluorescence labeling of the polymer directly inside the

82 ul detection but requires pre- or postcolumn fluorescence labeling of the proteins.

83 Fluorescence labeling of the two ends of the molecule en

84 A strategy for fluorescence labeling of three autoligating energy trans

85 Two-photon microscopy in combination with fluorescence labeling offers a powerful tool to peek int

86 ovel flow cytometry technique involving dual fluorescence labeling, remains unaltered.

87 Our approach used site-directed fluorescence labeling (SDFL) spectroscopy to compare ops

88 tion could be obtained using a site-directed fluorescence labeling (SDFL) strategy.

89 We present a site-directed fluorescence labeling (SDFL) study of 25 different T4 ly

90 Double-fluorescence labeling showed that two clusters of melano

91 Fluorescence labeling shows that compact states of yeast

92 netic approaches permit mosaic and inducible fluorescence-labeling strategies, whereas intrinsic cont

93 Here, we present a nanoparticle-based fluorescence labeling strategy for the multicolor labeli

94 Furthermore, immunohistochemical and double fluorescence labeling studies reveal that SOD1 forms pro

95 Finally, site-directed fluorescence labeling studies show the CB1 structure sta

96 l heterogeneity, we developed the MoonTag, a fluorescence labeling system to visualize translation of

97 ng 34 single-cysteine mutants and a modified fluorescence labeling technique designated multiplex lab

98 We therefore adapted a site-directed fluorescence labeling technique to permit topology mappi

99 licin E1 was investigated by a site-directed fluorescence labeling technique.

100 multispecies biofilm in vitro using a novel fluorescence labeling technique.

101 Lineage tracing using global fluorescence labeling techniques is complicated by incre

102 these nanoparticles successfully in various fluorescence labeling techniques, including fluorescent-

103 We have used site-directed spin and fluorescence labeling to test molecular models of the ac

104 Prior work has demonstrated that fluorescence labeling tools and radiographic imaging are

105 imaging studies of polymer transport involve fluorescence labeling uniformly along the chain, which s

106 Fluorescence labeling using a pH-sensitive dye confirmed

107 ANTS fluorescence labeling was not biased by oligomannoside l

108 Using site-directed fluorescence labeling we show a voltage-dependent fluore

109 Using site-directed fluorescence labeling, we probe ClC-ec1, a prokaryotic C

110 proteins is the lack of a general method for fluorescence labeling with high efficiency, specificity

111 errogate single molecules, it often requires fluorescence labeling with lasers and microscopes.

112 In this study, we employ site-specific fluorescence labeling with pyrene maleimide to gain insi

113 used biocytin backfills of CBCs followed by fluorescence labeling with streptavidin-lissamine rhodam

114 heria toxin was studied using site-selective fluorescence labeling with subsequent application of sev