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1 Brilliant Blue R-250 for 16 to 24 h and then destained.
2 ed using capacitance measurements and FM-dye destaining.
3 ed fainter staining and significantly faster destaining.
4 stimulation at 0.5 Hz evoked about 66 +/- 5% destaining.
5 ostriatal kinetics with depression of FM1-43 destaining.
6 differences in the rate or extent of FM1-43 destaining.
7 tly smaller effect on stimulus-evoked FM1-43 destaining.
8 fold more rapidly than restoration of FM2-10 destaining.
9 ally released into the bathing medium during destaining.
12 alcium ionophore calcimycin stimulate FM1-43 destaining and quantal release in csp mutants at 32 degr
13 und a fixed proportionality between staining/destaining and summed endplate potentials (EPPs) represe
15 BDNF was absent during dye loading, imaging, destaining and whole-cell recordings, these results demo
16 for their size range, stained with ethidium, destained, and a quantitative electronic image obtained.
18 ue is relatively slow and requires staining, destaining, and scanning before the data can be processe
19 iminating the need for fixing, staining, and destaining as required for the conventional procedures.
20 f csp mutant neuromuscular junctions fail to destain at 32 degrees C after K+ depolarization, and tha
21 Moreover, quantitative analysis of FM1-43 destaining at these orphan release sites reveals similar
22 xin (type A, C, or D) blocked exocytosis and destaining, but intense nerve stimulation still did not
29 tion model, indicates that the small, slowly destaining events may be mediated by a narrow approximat
30 nerve stimulation in the absence of dye; the destaining evidently reflects escape of dye into the bat
32 n the evoked and spontaneous rates of FM1-43 destaining from terminals in CA1 stratum radiatum, mostl
34 Finding neurotransmission in the absence of destaining implied that rapidly endocytosed RRP vesicles
35 additional dye-loaded vesicles showed rapid destaining in response to strong stimulation and were al
41 aded with kinetics substantially slower than destaining of FM dye, indicating that full-collapse fusi
42 -89; 10 microm), then washed for 60 min, the destaining of FM1-43 fluorescence evoked by the same sti
43 Observations of the dynamic staining and destaining of FM1-43 in frog motor nerve terminals sugge
47 here was no direct dependence of staining or destaining on stimulus frequency, as would be expected i
50 In contrast, SDS-CGE requires no staining or destaining procedures and the peak quantitation is super
52 orders of magnitude faster than the overall destaining rate (timescale of seconds) of these dyes fro
53 TrkB-IgG prevented the enhancement of FM1-43 destaining rate caused by induction of long-term potenti
54 lation of the RRP, BDNF increased the evoked destaining rate of FM4-64 only during the initial phase
55 gel slices, the procedure combines washing, destaining, reduction and alkylation into a single step.
59 ing of postsynaptic responses and styryl dye destaining showed that after an initial round of exocyto
65 (10 Hz/2 min) elicited a frequency-dependent destaining that peaked at 20% reduction in fluorescence.
66 Cooling also reduced the terminal FM1-43 destaining that was induced by direct depolarization wit
67 r staining with Coomassie brilliant blue and destaining, the gels were analyzed with a video area den
68 reserpine-treated mice, quinpirole decreased destaining to a greater extent, and at a lower dose, con
69 tain removal with Kimwipes helps in reducing destain use and in reducing organic liquid waste, and it
71 ations loaded with the optical probe FM1-43, destaining was reduced by latrunculin treatment, suggest
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