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Titlebook: Chromosomal Mutagenesis; Shondra M. Pruett-Miller Book 2015Latest edition Springer Science+Business Media New York 2015 Genome editing too

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21#
發(fā)表于 2025-3-25 04:22:10 | 只看該作者
Key Concepts in Chinese Thought and Cultureoaches that efficiently reduce the expression of these transcripts. Here, I describe a method that allows a specific and efficient targeting of the highly abundant lncRNA . in human (lung) cancer cells. The method relies on the site-specific integration of RNA-destabilizing elements mediated by Zinc Finger Nucleases (ZFNs).
22#
發(fā)表于 2025-3-25 08:52:27 | 只看該作者
Redefining Chinese Literature and Art enrich for genome-edited cells such that they can be more easily identified. This chapter discusses several different approaches including the use of cold-shock, exonucleases, surrogate markers, specialized donor vectors, and oligonucleotides to enhance the frequency of genome editing or to facilitate the identification of genome-edited cells.
23#
發(fā)表于 2025-3-25 12:44:35 | 只看該作者
https://doi.org/10.1007/978-1-4899-0961-9aced short palindromic repeats (CRISPR)-Cas9. These endonucleases are useful for simple and rapid production of gene knockout/knockin animals without using embryonic stem (ES) cells. This chapter introduces the latest protocols for producing genetically modified rodents using ZFN, TALEN, and CRISPR/Cas9.
24#
發(fā)表于 2025-3-25 16:42:26 | 只看該作者
25#
發(fā)表于 2025-3-25 21:53:28 | 只看該作者
Strategies to Increase Genome Editing Frequencies and to Facilitate the Identification of Edited Ce enrich for genome-edited cells such that they can be more easily identified. This chapter discusses several different approaches including the use of cold-shock, exonucleases, surrogate markers, specialized donor vectors, and oligonucleotides to enhance the frequency of genome editing or to facilitate the identification of genome-edited cells.
26#
發(fā)表于 2025-3-26 02:37:36 | 只看該作者
27#
發(fā)表于 2025-3-26 08:06:51 | 只看該作者
28#
發(fā)表于 2025-3-26 11:37:06 | 只看該作者
Introduction: Political Cultures,g tools that are amenable to multiplexing and compatible with multiple cellular delivery methods. In this chapter, we describe the process of assembling a megaTAL from a meganuclease, as well as a method for characterization of nuclease cleavage activity in vivo using a fluorescence reporter assay.
29#
發(fā)表于 2025-3-26 15:21:30 | 只看該作者
30#
發(fā)表于 2025-3-26 19:13:04 | 只看該作者
Adele Eskeles Gottfried,Allen W. Gottfriedsing liquid nitrogen. This chapter introduces our latest protocols for freeze-drying of mouse and rat spermatozoa, and the anticipated results of the fertilizing ability of these gametes following long-term preservation or transportation.
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