Titlebook: Lab-on-Chips for Cellomics; Micro and Nanotechno Helene Andersson,Albert van den Berg Book 2004 Springer Science+Business Media B.V. 2004 B

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Anal-Canal

978-1-4020-6562-0Springer Science+Business Media B.V. 2004

枫树

Helene Andersson,Albert van den BergProvides readers with a quick introduction to the field as well as with a variety of specific examples of such Lab-on-Chip systems for cellomics applications

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Microfluidic Cell-Culture Devices,d microfluidic cell-culture devices and experimental attempts towards in vitro liver tissue reconstitution are presented for further discussion on the possible developments in the field of lab-on-a-chip for cellomics.

失望未来

e this potential with this book focusing on microfluidics technologies for “cellomics”, research on or with cells. In our view, the field is still too immature to comp978-1-4020-6562-0978-1-4020-2975-2

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Basilar-Artery

Helene Andersson,Albert van den Bergriods. Data on diploid, tetraploid, and hyperploid species for which no quantitative DNA values are available are also given. The durations of G1, S, G2, M, and CT at different temperatures are listed in Table 2, and those of cells in different histological loci are shown in Table 3. Unless noted ot

不适当

Jerome P. Ferrance,James P. Landersriods. Data on diploid, tetraploid, and hyperploid species for which no quantitative DNA values are available are also given. The durations of G1, S, G2, M, and CT at different temperatures are listed in Table 2, and those of cells in different histological loci are shown in Table 3. Unless noted ot

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Laurie E. Locascio,Wyatt N. Vreeland,Andreas Jahn,Michael Gaitanriods. Data on diploid, tetraploid, and hyperploid species for which no quantitative DNA values are available are also given. The durations of G1, S, G2, M, and CT at different temperatures are listed in Table 2, and those of cells in different histological loci are shown in Table 3. Unless noted ot