ライフサイエンスコーパス: calcium green

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1 The fluorescent Ca2+ dye indicators Calcium Green 1 and Oregon Green 488 BAPTA-2 were inject

2 n-labeled high molecular weight dextran, and Calcium Green 1, we provide evidence that lysosomes resp

3 using the fluorescent calcium-sensitive dye, Calcium Green-1 3000 mw dextran conjugate (CG-1), which

4 Using Calcium Green-1 and rhod-2 as optical measures of cytopl

5 s were loaded with the calcium-sensitive dye Calcium Green-1 and the responses of the astrocytes to e

6 nts from retinal axon terminals labeled with Calcium Green-1 dextran revealed that 5HT1 and GABA(B) r

7 The fluorescent dye employed, calcium green-1 dextran, is a selective chelator for Ca2

8 racellular [Ca2+] ([Ca2+]i) was estimated by calcium green-1 fluorescence.

9 Zn2+ is the primary source of the increasing Calcium Green-1 fluorescence.

10 Popular indicators such as Calcium Green-1 or Fluo-3 fulfill these conditions.

11 Ca2+ imaging using the fluorescent indicator Calcium Green-1 revealed about twice as many hotspots of

12 , primary cortical neurons were labeled with Calcium Green-1 which was then cross-linked with EDAC, p

13 Using confocal fluorescent microscopy of Calcium Green-1, a widely used Ca2+ indicator, we detect

14 ices was monitored by confocal microscopy of calcium green-1.

15 undle fluorescence in cells loaded with 1 mm Calcium Green-1.

16 y striatal neurons with two Ca2+ indicators, calcium green 1N and rhod-2, and visualized the fluoresc

17 d with the acetoxymethyl esters of Fluo-3 or Calcium Green-2, or with Fluo-3 and Fura Red, and change

18 bules in Ringer's solution, determined using Calcium Green-2, was 3.6+/-0.7 microM (n = 23).

19 using the calcium-sensitive fluorescent dye, calcium green 5N, confirmed that calcium bound to the te

20 cope in hair cells filled with the indicator Calcium Green-5N introduced via the patch pipette.

21 The fluorescent dyes Fluo-3 and Calcium Green-5N were used to monitor local Ca2+ elevati

22 es loaded with the lower affinity indicator, Calcium Green-5N, caused almost complete emptying of the

23 tal with Fura 2 and largely non-quantal with Calcium Green-5N; the discrepancy is not, therefore, a d

24 late indicators (BTC, calcium-orange-5N, and calcium-green-5N) and one tricarboxylate indicator (magn

25 were preloaded with the calcium reporter dye Calcium Green, and astrocytes were selectively stained b

26 isualization of the membrane bound indicator Calcium Green C18, revealed internalization of the surfa

27 as provided by the membrane-bound Ca2+ probe Calcium Green C18.

28 e calcium uptake, using cells preloaded with calcium green (CaGr), and membrane permeability, using F

29 lls of rat foliate papillae were loaded with calcium green dextran (CaGD).

30 njected with the calcium-sensitive indicator calcium green dextran and/or the ER-specific probe "DiI.

31 Quin-2, chlortetracycline, calcium green dextran, Indo-1, and Fura-2 all show tempe

32 from populations of motoneurons labeled with calcium-green dextran.

33 urrent recording and fluorescence imaging of Calcium Green-dextran were used to measure the longitudi

34 esting Cac reported by the probes indo-1 and Calcium Green, or its dextran conjugate in the cytoplasm

35 In kinetic data analysis, only calcium green signals from predefined cytosolic areas an

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