ライフサイエンスコーパス: fluorescence analysis

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1 intained) and B2 (epithelium removed for the fluorescence analysis).

2 pheral EGF features, as quantified by radial fluorescence analysis.

3 y the Griess method and intracellular ROS by fluorescence analysis.

4 ial expression was evaluated by quantitative fluorescence analysis.

5 enylenediamine to form a product amenable to fluorescence analysis.

6 formation as determined by CD and tryptophan fluorescence analysis.

7 fferences in hybridization are determined by fluorescence analysis.

8 Our multiparameter fluorescence analysis allowed us to gain new insights in

9 shows that under the conditions used for the fluorescence analysis, alpha-synuclein is predominantly

10 Leaf chlorophyll fluorescence analysis and thylakoid membrane composition

11 Functional studies, fluorescence analysis, and citrullination experiments re

12 Fluorescence analysis by pulse-amplitude modulation fluo

13 In vivo fluorescence analysis demonstrates that the proteins are

14 the combined method grazing incidence X-ray fluorescence analysis (GIXRF) and near edge X-ray absorp

15 confers tolerance to lower salt levels, and fluorescence analysis in 30% sucrose reveals instability

16 o using the purified proteins and in vivo by fluorescence analysis in human cells, using the split-EG

17 Atomic force microscopy and fluorescence analysis in solution and on surfaces at the

18 te of O(2) evolution measured by chlorophyll fluorescence analysis in the PEPC mutant; this increase

19 of approximately 2:1 was found by Kalphabeta fluorescence analysis, indicating 2 Ni per [Fe(4)S(4)].

20 n affinity similar to that of TnI(96-131) by fluorescence analysis (K(d)=380nM), its binding was not

21 This fluorescence analysis of collagen-like peptides lays a f

22 d here via an unprecedented super-resolution fluorescence analysis of ex vivo tissue slices confirmin

23 Importantly, fluorescence analysis of fibroblast growth factor 2 and

24 ace AMPA receptors in isolated synaptosomes: fluorescence analysis of single-synapse long-term potent

25 Fluorescence analysis of TcsL with 2-(p-toluidinyl) naph

26 's blood and milk samples was determined via fluorescence analysis of the functionalized QDs.

27 mbrane and their subsequent elution prior to fluorescence analysis of the quenching effect produced o

28 Fluorescence analysis of the subcellular localization of

29 Steady-state fluorescence analysis of these hybrids reveals that the

30 Double-label fluorescence analysis of these membranes indicated that

31 We used quantitative fluorescence analysis of tissues to measure two fluoresc

32 Fluorescence analysis of wild-type, crd1, and sct1 strai

33 kage, "PyMca", primarily developed for X-ray fluorescence analysis offers an easy-to-use interface fo

34 Gamma-ray spectrometry and X-ray fluorescence analysis on a collected Pu particle indicat

35 Using single-molecule fluorescence analysis on a prototypical superfamily 1 he

36 Using fluorescence analysis over concentration based analysis

37 Protein fluorescence analysis provided evidence for conformation

38 Single-molecule fluorescence analysis revealed that instead of unwinding

39 Fluorescence analysis revealed that two native Trp resid

40 Optical micrographs and fluorescence analysis show the successful topographic an

41 Tryptophan fluorescence analysis showed that all of the tested muta

42 CD and fluorescence analysis showed that it contained ordered t

43 Chlorophyll fluorescence analysis shows that in vivo the Ndh complex

44 llowing for a direct linking of quantitative fluorescence analysis to XPS quantification.

45 In a complementary approach, site-directed fluorescence analysis using an environmentally sensitive

46 pase activity and by performing quantitative fluorescence analysis using fluorescence-activated cell

47 Using single-molecule fluorescence analysis, we showed that NS3 unwinds DNA in

48 absolute brightness values and quantitative fluorescence analysis with particle systems that can be

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