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Titlebook: Confocal Microscopy; Methods and Protocol Stephen W. Paddock Book 19991st edition Humana Press 1999

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發(fā)表于 2025-3-21 18:37:27 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Confocal Microscopy
副標(biāo)題Methods and Protocol
編輯Stephen W. Paddock
視頻videohttp://file.papertrans.cn/236/235401/235401.mp4
叢書名稱Methods in Molecular Biology
圖書封面Titlebook: Confocal Microscopy; Methods and Protocol Stephen W. Paddock Book 19991st edition Humana Press 1999
描述In Confocal Microscopy Methods and Protocols, Stephen Paddock and a highly skilled panel ofexperts lead the researcher using confocal techniques from the bench top, through the imaging process, to the journal page. They concisely describe all the key stages of confocal imaging-from tissue sampling methods, through the staining process, to the manipulation, presentation, and publication of the realized image. Written in a user-friendly, nontechnical style, the methods specifically cover most of the commonly used model organisms: worms, sea urchins, flies, plants, yeast, frogs, and zebrafish. ..Centered in the many biological applications of the confocal microscope, the book makes possible the successful imaging of both fixed and living specimens using primarily the laser scanning confocal microscope. The powerful hands-on methods collected in Confocal Microscopy Methods and Protocols will help even the novice to produce first-class cover-quality confocal images.......
出版日期Book 19991st edition
版次1
doihttps://doi.org/10.1385/159259722X
isbn_softcover978-1-61737-062-5
isbn_ebook978-1-59259-722-2Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightHumana Press 1999
The information of publication is updating

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沙發(fā)
發(fā)表于 2025-3-21 21:52:37 | 只看該作者
Preparation of Yeast Cells for Confocal Microscopy,copy has been used to examine the distribution of actin in fixed cells prepared from reverting protoplasts, and to show that a monoclonal antibody raised to rat liver nuclear proteins recognized two protein components of the yeast nuclear pore complex, p95 and p110 (.,.).
板凳
發(fā)表于 2025-3-22 02:34:16 | 只看該作者
Confocal Microscopy on , Oocytes and Embryos,opy. Optical sectioning eliminates the need for manual sectioning and makes background fluorescence and autofluorescence negligible. It is still difficult to image the deep structures within the embryo, but thick wax sections can be cut and confocal microscopy again applied.
地板
發(fā)表于 2025-3-22 06:03:27 | 只看該作者
5#
發(fā)表于 2025-3-22 09:59:39 | 只看該作者
Live Imaging with Green Fluorescent Protein,mit each stage of development to be studied in a single, intact embryo. Third, it would function in all cell types and would reveal their morphology, making it simple to identify different cells without compromising their viability.
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發(fā)表于 2025-3-22 23:29:07 | 只看該作者
copy has been used to examine the distribution of actin in fixed cells prepared from reverting protoplasts, and to show that a monoclonal antibody raised to rat liver nuclear proteins recognized two protein components of the yeast nuclear pore complex, p95 and p110 (.,.).
9#
發(fā)表于 2025-3-23 04:10:29 | 只看該作者
opy. Optical sectioning eliminates the need for manual sectioning and makes background fluorescence and autofluorescence negligible. It is still difficult to image the deep structures within the embryo, but thick wax sections can be cut and confocal microscopy again applied.
10#
發(fā)表于 2025-3-23 08:18:28 | 只看該作者
1064-3745 ques from the bench top, through the imaging process, to the journal page. They concisely describe all the key stages of confocal imaging-from tissue sampling methods, through the staining process, to the manipulation, presentation, and publication of the realized image. Written in a user-friendly,
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