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Titlebook: Biotechnology Applications of Microinjection, Microscopic Imaging, and Fluorescence; Peter H. Bach (Faculty of Science),C. Hugh Reynold Bo

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發(fā)表于 2025-3-21 17:31:52 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
期刊全稱Biotechnology Applications of Microinjection, Microscopic Imaging, and Fluorescence
影響因子2023Peter H. Bach (Faculty of Science),C. Hugh Reynold
視頻videohttp://file.papertrans.cn/189/188695/188695.mp4
圖書(shū)封面Titlebook: Biotechnology Applications of Microinjection, Microscopic Imaging, and Fluorescence;  Peter H. Bach (Faculty of Science),C. Hugh Reynold Bo
影響因子Individual cells behave in surpnsmg ways that cannot be deduced from the averaged results of an organ as assessed by the use of conventional biochemical methods. Thus multicellular plant and animals systems are being investigated by an increasing array of histochemical and cytochemical techniques based on general chemical or specific immunological interactions to identify structural materials and to assess biological activities. In recent years there has been an increasing range of fluorescent probes, along with advanced computerised imaging and analysis techniques, which allows the behaviour of individual living cells to be followed in considerable detail. The parallel use of microinjection, microelectrodes and patch-clamping provides additional information about cells and their responses. Recombinant DNA technology has highlighted the desirability and the power of microinjecting defined materials into specific cells and so manipulating their fundamental biochemistry. New hypotheses are being tested which will form the cornerstone of future developments across the whole spectrum of biotechnology. The First European Workshop on Biotechnology Applications of Microinjection, Microsco
Pindex Book 1993
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Lebenslanges Lernen in der Universit?t isolated sperm cells into synergids of ., using micromanipulation (Keijzer ., 1988a; Keijzer, 1992). The rate of successful sperm cell transfers in these studies was, however, low (Keijzer, 1992) but serve to illustrate the potential usefulness of the technique to be described below.
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How to Make Glass Microtools for the Injection of Isolated Plant Sperm Cells into Embryo SAC Cells isolated sperm cells into synergids of ., using micromanipulation (Keijzer ., 1988a; Keijzer, 1992). The rate of successful sperm cell transfers in these studies was, however, low (Keijzer, 1992) but serve to illustrate the potential usefulness of the technique to be described below.
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Application of the Firefly Luciferase Reporter Gene to Microinjection Experiments in , Oocytes,open reading frames that encode various regulatory proteins making it one of the most complex retroviruses that has been described (Varmus ., 1984). The regulation of gene expression in HIV-1 has been shown to be critically dependent on the virally-encoded TAT protein (Dayton ., 1986).
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,Fluorescent Probes — Where Do they Go in Cells, and Why?,ent probes, are excluded by this definition. Thus, macromolecular probes (e.g., fluorescent antibodies and lectins; nucleic acid probes) are not considered here. Neither are histochemical fluorochromes applied to fixed (i.e. dead) cells and tissues.
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Selection of Fluorescent Golgi Complex Probes Using Structure-Activity Relationship Models,0). It was thought that such Golgi staining was due to the dyes dissolving in the lipid constituents of membranes. More recently, the fluorescent compound NBD-ceramide (i.e. N-(E-7-nitrobenz-2-oxa-l,3-di-azol-4-yl-aminocaproyl)-D-erythrosphingosine) is widely used as a Golgi complex stain (Pagano ., 1989).
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