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Titlebook: Maple and Mathematica; A Problem Solving Ap Inna Shingareva,Carlos Lizàrraga-Celaya Textbook 20071st edition Springer-Verlag Vienna 2007 Al

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11#
發(fā)表于 2025-3-23 13:17:53 | 只看該作者
hoton is emitted. In its active form, the protein includes a covalently bound prosthetic group (coelenterazine) that is released in the Ca. triggered reaction. In the 60s and 70s aequorin was, together with metallochromic indicators, the most widely employed probe for intracellular Ca. (Ridgway and
12#
發(fā)表于 2025-3-23 14:29:58 | 只看該作者
13#
發(fā)表于 2025-3-23 18:22:38 | 只看該作者
r studies. For each habitat, in which beetles live, we included active and passive collecting methods. We present 30 types of collecting methods that the collector can employ in beetle surveys. Furthermore, we provided information about the habit and habitat of 79 Coleoptera families. Therefore, we
14#
發(fā)表于 2025-3-23 23:52:56 | 只看該作者
15#
發(fā)表于 2025-3-24 02:48:57 | 只看該作者
16#
發(fā)表于 2025-3-24 06:42:26 | 只看該作者
This chapter will summarize the general principles of impedimetric cell monitoring, introduce the available assay formats, and show how these have been applied to unravel the biological response of nanoscale particles on different levels of cell physiology. The description and interpretation of imp
17#
發(fā)表于 2025-3-24 12:09:10 | 只看該作者
18#
發(fā)表于 2025-3-24 17:15:26 | 只看該作者
ien (Tsien et al. 1982; Grynkiewicz et al., 1985), is that the protein does not permeate across cell membranes and thus needs to be microinjected. The technique was thus limited to large, sessile cells. The isolation of the aequorin cDNA (Inouye et al., 1985) completely changed this perspective. Ind
19#
發(fā)表于 2025-3-24 22:07:11 | 只看該作者
ien (Tsien et al. 1982; Grynkiewicz et al., 1985), is that the protein does not permeate across cell membranes and thus needs to be microinjected. The technique was thus limited to large, sessile cells. The isolation of the aequorin cDNA (Inouye et al., 1985) completely changed this perspective. Ind
20#
發(fā)表于 2025-3-25 02:08:23 | 只看該作者
ien (Tsien et al. 1982; Grynkiewicz et al., 1985), is that the protein does not permeate across cell membranes and thus needs to be microinjected. The technique was thus limited to large, sessile cells. The isolation of the aequorin cDNA (Inouye et al., 1985) completely changed this perspective. Ind
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