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標(biāo)題: Titlebook: Biophysical and Biochemical Aspects of Fluorescence Spectroscopy; T. Gregory Dewey Book 1991 Springer Science+Business Media New York 1991 [打印本頁]

作者: 浮標(biāo)    時間: 2025-3-21 17:05
書目名稱Biophysical and Biochemical Aspects of Fluorescence Spectroscopy影響因子(影響力)




書目名稱Biophysical and Biochemical Aspects of Fluorescence Spectroscopy影響因子(影響力)學(xué)科排名




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書目名稱Biophysical and Biochemical Aspects of Fluorescence Spectroscopy被引頻次




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書目名稱Biophysical and Biochemical Aspects of Fluorescence Spectroscopy讀者反饋




書目名稱Biophysical and Biochemical Aspects of Fluorescence Spectroscopy讀者反饋學(xué)科排名





作者: 假設(shè)    時間: 2025-3-22 00:02

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https://doi.org/10.1007/978-3-030-20511-9e the fundamental considerations and to provide the reader with a feeling for the practical aspects that must be apprehended before time-resolved methods can be profitably applied to complex biological systems.
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作者: MOCK    時間: 2025-3-22 13:30
lly occurring fluorescent biomolecules, fluorescence spectroscopy offers a combination of great specificity and sensitivity. Historically, these features have been ex- ploited with great success utilizing both intrinsic and extrinsic probes. Re- cent applications have built upon these traditional st
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Luminescent Trivalent Lanthanides in Studies of Cation Binding Sites, radius and, as such, are useful as steric probes of systems such as ion channels. Second, their paramagnetic and luminescent properties make them versatile spectroscopic probes of cation binding sites.
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Time-Resolved Fluorescence in Biology and Biochemistry,e the fundamental considerations and to provide the reader with a feeling for the practical aspects that must be apprehended before time-resolved methods can be profitably applied to complex biological systems.
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Fluorescence Quenching Reactions,ormational changes in the biomacromolecule can then be monitored in terms of changes in the accessibility to the quencher of the fluorophore. In addition to such topographical information, in some cases information about the conformational dynamics of globular proteins has been obtained with solute quenching reactions.
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https://doi.org/10.1007/978-1-4757-1887-4eavis, 1989; Lakowicz, 1983; Eftink and Ghiron, 1981; Eftink, 1991). Such quenching reactions have been used primarily to obtain topographical information about proteins, nucleic acids, and membrane systems. The accessibility of intrinsic or extrinsic fluorescence probes (e.g., the amino acid, trypt
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https://doi.org/10.1057/9780230240773echnique for measuring distances in biological systems. Early studies usually measured distances between a single donor and a single acceptor each at a specific location. The extension to transfer between multiple donors and multiple acceptors has proven quite useful for the study of multienzyme com
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978-1-4757-9515-8Springer Science+Business Media New York 1991
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Continuous, On-Line, Real Time DNA Sequencing Using Multifluorescently Tagged Primers,DNA sequencing is a relatively new technique, just over a decade old. Scientifically, it is a very important technique because the DNA sequence gives us the ultimate resolution of the genetic material to the single base level and thus its complete information.
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作者: 向外才掩飾    時間: 2025-3-26 02:40
Time-Resolved Fluorescence in Biology and Biochemistry,ctroscopy in the chemical and biological sciences (Badea and Brand, 1979; Demas, 1983; Lakowicz, 1983; Cundall and Dale, 1983; Gratton ., 1984a; Jameson ., 1984; Taylor ., 1987; Jameson and Reinhart, 1989). Our goal in this chapter is thus not to treat the subject exhaustively but rather to reiterat
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Analysis of Ligand Binding and Cross-Linking of Receptors in Solution and on Cell Surfaces,of this method is that nanomolar concentrations of fluorophores can be detected in the presence of a high level of background noise provided by the cells. An ideal fluorescent probe absorbs and emits at wavelengths not in common with the cellular components, has a high quantum yield, and can be plac
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作者: triptans    時間: 2025-3-26 19:58
Imaging Membrane Organization and Dynamics,ry after photobleaching (FRAP) can be extended, by coupling these techniques to low-light-level video microscopy and digital image processing, to provide an additional dimension of information. That is, what new information can be gained when, rather than integrating the fluorescence signal over a p
作者: arcane    時間: 2025-3-26 22:26
The Dynamic Parameter,rocesses are elaborated upon as a hierarchy of interdependence established between cells and tissues. Through the ebb and flow of signaling and metabolic molecules, dynamic linkages may be maintained between cells for the coordination, synchronization, and initiation of cellular cycles (Fig. 1). In
作者: 合唱團(tuán)    時間: 2025-3-27 02:17
https://doi.org/10.1057/9780230240773s, 1983; Wallace and Fain, 1985; Bokoch and Gilman, 1984; Smith ., 1986), arachidonic acid release (Burch ., 1986; Jelsema and Axelrod, 1987), activation of Ca. channels found in excitatory cells (Hescheler ., 1987; Yatani ., 1987), and cardiac K. channels (Codina ., 1987; Logothetis ., 1987). Vario
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https://doi.org/10.1057/9780230240773and specific monoclonal antibodies that can be fluorescently modified are valuable reagents. In this chapter we describe our use of quantitative fluorescence measurements to investigate the binding properties of cell surface receptors.
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Panayiota Vassilopoulou,Stephen R. L. Clark flow are generally classified as channels or pores that serve either as passive transport routes for low-molecular-weight molecules (Loewenstein, 1979; Nikaido and Nakae, 1979; Gunning and Overall, 1983) or as ion pumps or transporters requiring some type of coupled gradient dissipation or energy.s
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Fluorescence Investigations of Receptor-Mediated Processes,s, 1983; Wallace and Fain, 1985; Bokoch and Gilman, 1984; Smith ., 1986), arachidonic acid release (Burch ., 1986; Jelsema and Axelrod, 1987), activation of Ca. channels found in excitatory cells (Hescheler ., 1987; Yatani ., 1987), and cardiac K. channels (Codina ., 1987; Logothetis ., 1987). Vario
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Analysis of Ligand Binding and Cross-Linking of Receptors in Solution and on Cell Surfaces,and specific monoclonal antibodies that can be fluorescently modified are valuable reagents. In this chapter we describe our use of quantitative fluorescence measurements to investigate the binding properties of cell surface receptors.
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Fluorescence Energy Transfer in Membrane Biochemistry,s and multiple donors in three dimensions (Foerster, 1949) and derived the appropriate expression for two dimensions. Unfortunately, these results went unnoticed and identical expressions have been derived in several subsequent works. The first studies on lipid bilayer systems were aimed at determin
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Book 1991ther areas. The goal of this book is to provide detailed monographs on the use of fluorescence to investigate problems at the forefront of biochemistry and cell biology. This book is not meant to be a comprehensive survey but rather to highlight areas of recent developments. It is designed to be rea
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erest in other areas. The goal of this book is to provide detailed monographs on the use of fluorescence to investigate problems at the forefront of biochemistry and cell biology. This book is not meant to be a comprehensive survey but rather to highlight areas of recent developments. It is designed to be rea978-1-4757-9515-8978-1-4757-9513-4
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https://doi.org/10.1007/978-3-642-92345-6y devoid of polymers. The implantation of polymers into concrete has taken effect in the form of Concrete Polymer Composite [C-PC?=?PMC?+?PCC?+?PIC?+?PC]. Several milestones are recognised in the development of C-PC. They are discussed here with particular emphasis on the innovative milestones that




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