ライフサイエンスコーパス: fluorescence labeling

1 microscope upon isothermal amplification and fluorescence labeling.

2 membrane topology generated by site-directed fluorescence labeling.

3 e mainly limited to indirect observation via fluorescence labeling.

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

5 and excellent molecular specificity through fluorescence labeling.

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

7 or beta4 nAChR subunits and visualized with fluorescence labeling.

8 ting approach permits specific intracellular fluorescence labeling.

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

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

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

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

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

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

15 Recent developments of fluorescence labeling and highly advanced microscopy tec

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

17 Advances in fluorescence labeling and imaging have made it possible

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

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

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

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

22 Using fluorescence labeling and radiolabeling, we show that ch

23 Using site-directed fluorescence labeling and several independent fluorescen

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

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

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

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

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

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

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

31 However, fluorescence labeling data implied that FepA was active

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

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

34 Fluorescence labeling demonstrates the immobilization of

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

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

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

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

39 Furthermore, fluorescence labeling is significantly more compatible w

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

41 Fluorescence labeling of adenoviral particles is one new

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

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

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

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

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

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

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

49 Fluorescence labeling of proteins has become increasingl

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

51 Fluorescence labeling of rat lung slices and in vivo mou

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

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

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

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

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

57 Fluorescence labeling of the two ends of the molecule en

58 A strategy for fluorescence labeling of three autoligating energy trans

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

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

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

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

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

64 Double-fluorescence labeling showed that two clusters of melano

65 Fluorescence labeling shows that compact states of yeast

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

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

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

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

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

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

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

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

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

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

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

77 Fluorescence labeling using a pH-sensitive dye confirmed

78 ANTS fluorescence labeling was not biased by oligomannoside l

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

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

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

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

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

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