Isbn: 9780896037663 - kinesin protocols (methods in molecular biology, band 164) (19 Ergebnisse)

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Zustand: New. Presents techniques for the identification, purification, and characterization of the kinesin superfamily of microtubule-dependent motors. This book includes methods to express and purify kinesins in different systems, to characterize microtubule-enhanced ATPase activity and motility properties, and to test microtubule destabilizing activity. Editor(s): Vernos, Isabelle. Series: Methods in Molecular Biology. Num Pages: 258 pages, biography. BIC Classification: PDN; PSAK; PSD; PSF. Category: (P) Professional & Vocational; (UP) Postgraduate, Research & Scholarly; (UU) Undergraduate. Dimension: 235 x 155 x 15. Weight in Grams: 559. . 2000. Hardback. . . . .…

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Hardcover. Zustand: Brand New. 258 pages. 9.50x6.50x1.00 inches. In Stock.

Zustand: New. Presents techniques for the identification, purification, and characterization of the kinesin superfamily of microtubule-dependent motors. This book includes methods to express and purify kinesins in different systems, to characterize microtubule-enhanced ATPase activity and motility properties, and to test microtubule destabilizing activity. Editor(s): Vernos, Isabelle. Series: Methods in Molecular Biology. Num Pages: 258 pages, biography. BIC Classification: PDN; PSAK; PSD; PSF. Category: (P) Professional & Vocational; (UP) Postgraduate, Research & Scholarly; (UU) Undergraduate. Dimension: 235 x 155 x 15. Weight in Grams: 559. . 2000. Hardback. . . . . Books ship from the US and Ireland.…

Gebunden. Zustand: New. By the end of the 1980s only two microtubule-dependent motors, the plus end-directed kinesin and the minus end-directed cytoplasmic dynein, had been identified. At the time, these two motors seemed almost sufficient to explain directional motility events on.

Buch. Zustand: Neu. Neuware - By the end of the 1980s only two microtubule-dependent motors, the plus end-directed kinesin and the minus end-directed cytoplasmic dynein, had been identified. At the time, these two motors seemed almost sufficient to explain directional motility events on polar microtubule tracks in the cell. No- theless, shortly after, the tip of the iceberg began to emerge with the identi- cation of proteins containing in their sequences a domain found in kinesin. This domain, called the 'motor domain,' conferred on these proteins the essential property of moving on microtubules, using the energy derived from ATP hydro- sis. Since then, the identification of new proteins belonging to the kinesin superfamily of microtubule-dependent motors has gone at such a pace that nowadays more than 200 entries with motor domain sequences are deposited in the database. Kinesin family members are found in all eukaryotic org- isms tested. They present a wide range of domain organizations with a motor domain located at different positions in the molecule. Their motility prop- ties are also variable in directionality, velocity, and such other characteristics as bundling activity and processivity. Finally, and most important, they p- ticipate in a multitude of cellular functions. Our understanding of many cel- lar events, such as mitotic spindle assembly and neuronal transport, to cite only two, has progressed substantially in the last few years thanks to the id- tification of these motors.…