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Titlebook: Genetic Library Construction and Screening; Advanced Techniques R. Curtis Bird,Bruce F. Smith Book 2002 Springer-Verlag Berlin Heidelberg

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樓主: estrange
21#
發(fā)表于 2025-3-25 03:57:55 | 只看該作者
R. Curtis Bird,Bruce F. SmithA comprehensive, up-to-date guide on all aspects of synthesis and screening of genetic libraries.Detailed step-by-step protocols and extensive hands-on advice gleaned from the authors‘ experience.Perf
22#
發(fā)表于 2025-3-25 10:00:13 | 只看該作者
Das Problem der theoretischen TermeThe study of molecular interactions is becoming more and more important in all fields of biomedical and biological research. During the past decade, independent systems for large scale studying of such interactions have been developed and made commercially available.
23#
發(fā)表于 2025-3-25 12:14:09 | 只看該作者
24#
發(fā)表于 2025-3-25 18:43:23 | 只看該作者
Two Hybrid cDNA CloningThe study of molecular interactions is becoming more and more important in all fields of biomedical and biological research. During the past decade, independent systems for large scale studying of such interactions have been developed and made commercially available.
25#
發(fā)表于 2025-3-25 20:07:05 | 只看該作者
26#
發(fā)表于 2025-3-26 01:03:07 | 只看該作者
https://doi.org/10.1007/978-3-642-56408-62-Hybrid; DNA; Gene Cloning; Gene Library; Molecular Biology; PCR; Polymerase Chain Reaction; RNA; cDNA; clon
27#
發(fā)表于 2025-3-26 08:07:38 | 只看該作者
28#
發(fā)表于 2025-3-26 09:20:31 | 只看該作者
29#
發(fā)表于 2025-3-26 14:30:04 | 只看該作者
Die Stellengliederung des Produkt-Managementnal detection on high density filters that allows us to routinely screen about 50 probes per day on membranes each carrying 55,000 individual clones. This fast and cost-effective alternative to massive parallel PCR protocols requires little specialized equipment and can be operational within a few days.
30#
發(fā)表于 2025-3-26 20:20:30 | 只看該作者
High-Throughput Library Screening by Fluorescent Hybridizations on Gridded Membranesnal detection on high density filters that allows us to routinely screen about 50 probes per day on membranes each carrying 55,000 individual clones. This fast and cost-effective alternative to massive parallel PCR protocols requires little specialized equipment and can be operational within a few days.
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