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1 circular dichroism and differential scanning fluorimetry.
2 nt inhibitor missed by differential scanning fluorimetry.
3 by mass spectrometry, spectrophotometry and fluorimetry.
4 cted by EMSA, steady-state, and stopped-flow fluorimetry.
5 s of H/D exchange) and differential scanning fluorimetry.
6 em and BODIPY-diacylglycerol was detected by fluorimetry.
7 fusion of dyes was assessed by microscopy or fluorimetry.
8 lular Ca2+ level were monitored using Fura-2 fluorimetry.
9 .3, and 92 microm, pH 10.0) were measured by fluorimetry.
10 by measuring their affinities for m(7)GDP by fluorimetry.
11 lcium, using multifrequency phase-modulation fluorimetry.
12 in fura-2-loaded cells using dual wavelength fluorimetry.
13 nerves at 20 Hz and were monitored by fura-2 fluorimetry.
14 mpared with those from differential scanning fluorimetry, a commonly used primary screening technique
15 ociation were determined by a combination of fluorimetry and 2D NMR exchange spectroscopy (EXSY).
18 doxorubicin accumulation was determined with fluorimetry and correlated with the imaging and tissue-c
19 -induced aggregation of FcepsilonRI, we used fluorimetry and flow cytometry to quantitatively monitor
21 To this end, using differential scanning fluorimetry and hydrogen-deuterium exchange mass spectro
22 gment-based screen via differential scanning fluorimetry and in silico structure-based screening, eac
24 BLG-LA complex formation was monitored by fluorimetry and it was observed that a moderate heat tre
25 have used Forster resonance energy transfer fluorimetry and kinetic modeling to characterize the lig
26 of the biosynthetic reaction was followed by fluorimetry and reverse-phase, paired-ion high pressure
30 es and lengths of mismatches were assayed by fluorimetry, and in many instances, our MismatCHA design
31 ngle light scattering, differential scanning fluorimetry, and isothermal calorimetry, to characterize
32 have used protein engineering, stopped-flow fluorimetry, and rapid acid quenching techniques to eluc
34 fluorescence microscopy and automated plate fluorimetry (APF) are coupled with facile husbandry to f
36 amics simulations, and differential scanning fluorimetry assays and describe for the first time a str
39 e, NAD hydrolysis, and differential scanning fluorimetry data, contribute to a comprehensive characte
40 s, monitored in real time using stopped flow fluorimetry, demonstrate simultaneous binding and bendin
41 olid-phase microsphere assay coupled to flow-fluorimetry detection, based on the Luminex xMap technol
42 ity measurements using differential scanning fluorimetry, differential scanning calorimetry, and elec
43 calorimetry (ITC) and differential scanning fluorimetry (DSF) analyses demonstrate that the recombin
44 Microbalance (QCM) and Differential Scanning Fluorimetry (DSF) are consistent with our single molecul
45 of measurements using Differential Scanning Fluorimetry (DSF) as an inexpensive, high throughput scr
46 iety of proteins, that differential scanning fluorimetry (DSF) can be used to determine and optimize
48 tency, suggesting that differential scanning fluorimetry (DSF) is a useful orthogonal measure of inhi
49 minary screening using differential scanning fluorimetry (DSF), (ii) validation by NMR spectroscopy a
50 tures derived from the differential scanning fluorimetry experiments indicated a significant differen
52 Equilibrium constants were determined by fluorimetry from 10 to 20 degrees C by nonlinear curve f
53 Fragment screening by differential scanning fluorimetry has been performed to discover new chemical
56 meabilities were measured using stopped-flow fluorimetry in SM vesicles with entrapped carboxyfluores
57 recordings in COS-7 cells, and voltage-clamp fluorimetry in Xenopus oocytes, both heterologously expr
58 imited proteolysis and differential scanning fluorimetry indicate that RIG-I is in an extended and fl
60 were observed with 4-s time resolution using fluorimetry of TorA-green fluorescent protein mutant 3*
63 ured peptide scaffold, GGG, we have employed fluorimetry, potentiometry, and calorimetry to determine
65 s, gel filtration, and differential scanning fluorimetry revealed that polyphosphate binds to and des
67 raterminal Ca2+ stores either because fura-2 fluorimetry showed extremely low Ca2+ elevation (approxi
71 by various techniques (differential scanning fluorimetry, surface plasmon resonance, and microscale t
74 nuclear in origin and suggested by in vitro fluorimetry to have been caused by K3 thiol arylation.
75 were next evaluated by differential scanning fluorimetry to identify compounds that must bind to NC o
77 d bending reaction steps, using stopped-flow fluorimetry to observe changes in resonance energy trans
78 gs, cysteine accessibility and voltage clamp fluorimetry to probe the relationships between voltage s
85 mass spectrometry, and differential scanning fluorimetry, we showed that zinc binds to this TDP-43 do
86 24 hours at 5 degrees C and quantified with fluorimetry) were measured 48 hours after treatment and
87 ) have now been investigated by stopped-flow fluorimetry, which allowed a pre-steady-state analysis t
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