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Titlebook: Genetic Engineering in Eukaryotes; Paul F. Lurquin,Andris Kleinhofs Book 1983 Springer Science+Business Media New York 1983 ethics.food.ge

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61#
發(fā)表于 2025-4-1 04:47:02 | 只看該作者
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發(fā)表于 2025-4-1 09:30:49 | 只看該作者
63#
發(fā)表于 2025-4-1 11:45:26 | 只看該作者
Use of Transformation and Meiotic Gene Conversion to Construct a Yeast Strain Containing a Deletionome of the features of the yeast system, we describe the construction of a yeast strain which contains a deletion of the 5′ end of the alcohol dehydrogenase I (ADHI) gene (.) of yeast. Deletions are, in general, rare events in yeast so the ability to introduce . created deletions into the yeast genome is quite useful.
64#
發(fā)表于 2025-4-1 18:13:52 | 只看該作者
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發(fā)表于 2025-4-1 22:08:48 | 只看該作者
https://doi.org/10.1007/978-3-662-39798-5olyhedrin gene with passenger DNA was previously suggested as an approach to using baculoviruses as recombinant DNA vectors (Miller, 1981a). The initial experimental advances our laboratory has made in developing the baculovirus . nuclear polyhedrosis virus (AcNPV) as a vector in insect cells are described herein.
66#
發(fā)表于 2025-4-2 01:42:28 | 只看該作者
An Insect Virus for Genetic Engineering: Developing Baculovirus Polyhedrin Substitution Vectors,olyhedrin gene with passenger DNA was previously suggested as an approach to using baculoviruses as recombinant DNA vectors (Miller, 1981a). The initial experimental advances our laboratory has made in developing the baculovirus . nuclear polyhedrosis virus (AcNPV) as a vector in insect cells are described herein.
67#
發(fā)表于 2025-4-2 05:10:29 | 只看該作者
Book 1983st 6, 1982. Although genetic engineering in eukaryotes is best developed in yeast and mammalian cells, the reader will find that some emphasis has been put on plant systems. Indeed, it was our position that the development of plant cell genetic transformation would benefit from the interactions betw
68#
發(fā)表于 2025-4-2 09:19:35 | 只看該作者
Aktueller Stand der Forschung (Literatur),time required for the detection of transformants is dramatically reduced. We have adapted this procedure to allow the storage of competent yeast cells for up to 2 weeks at -70°C without significant loss of transformation efficiency.
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