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Color Atlas of Veterinary Anatomy, Volume 2: The Horse (2nd by Stanley H. Done, Raymond R. Ashdown

By Stanley H. Done, Raymond R. Ashdown

The colour Atlas of Veterinary Anatomy quantity 2 provides a different photographic checklist of dissections displaying the topographical anatomy of the pony. With this publication it is possible for you to to work out the placement and relationships of the bones, muscle groups, nerves, blood vessels and viscera that visit make up every one quarter of the physique and every organ procedure. each one booklet during this three quantity sequence is choked with full-color images and drawings of dissections ready in particular for those texts.

Key features

• Accessibly and systematically dependent with each one bankruptcy dedicated to a particular physique region

• vital good points of local and topographical anatomy offered utilizing complete colour photographs of designated dissections

• Dissections awarded within the status position

• specified colour line drawings make clear the relationships of suitable structures

• offers anatomy in a medical context

This re-creation moment variation deals very important new positive aspects, including:

• Accompanying site offers over a hundred interactive quizzes and self-assessment questions

• Many extra radiographs throughout

• extra CT and MRI images

• medical notes spotlight components of specific medical significance

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Extra resources for Color Atlas of Veterinary Anatomy, Volume 2: The Horse (2nd Edition)

Sample text

Margoliash, this series, Vol. 53 [18]. 4o U. Bilge, Dissertation, Fachbereich Chemie, Philipps-Universit~t, Marburg 0985). m = 12 m M i cm-~ [G. von Jagow and M. Klingenberg, FEBS Lett. 24, 278 (1972)]. Protein was determined by the L o w r y m e t h o d . 38 b T h e activity was calculated as turnover n u m b e r (mol c y t o c h r o m e c/sec × tool cytoc h r o m e aa3). 25 m M laurylmaltoside, 40/xM reduced c y t o c h r o m e c, and 2 n M c y t o c h r o m e - c oxidase. 7 m M T M P D , 1 m M laurylmaltoside, 20 n M c y t o c h r o m e - c oxidase, and was calculated for infinite c y t o c h r o m e c concentration.

E. Jacobs, Biochim. Biophys. Acta 153, 804 (1968). l0 E. E. Jacobs, E. C. Andrews, W. Cunningham, and F. L. Crane, Biochem. Biophys. Res. Commun. 25, 87 (1966). METHODS IN ENZYMOLOGY, VOL. 126 Copyright © 1986 by Academic Press, Inc. All rights of reproduction in any form reserved. [3] S T R U C T U R E OF CYTOCHROME-C O X I D A S E 23 dimensional crystals follows closely the isolation procedure described by Sun et al. 8. 2 M and the solution allowed to incubate on ice. The pellet, recovered by centrifugation at 78,000 g for 20 min, is resolubilized in Triton X-100 (1 mg/mg protein) in the same buffer.

144, 359 (1982). 13] STRUCTURE OF CYTOCHROME-C OXIDASE 31 FIG. 4. Schematic depiction of the high-affinity binding site for cytochrome c in the cytochrome-c oxidase dimer based on cross-linking studies. the low-resolution structure is between monomers in the cytochrome-c oxidase dimer 12,13 (Fig. 4). Conclusions and Prospects This brief review shows a picture of mammalian cytochrome-c oxidase built up by combining the data of biochemical studies with a low-resolution structure provided by electron microscopy and image reconstruction.

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