Titlebook: Bacterial Artificial Chromosomes; Kumaran Narayanan Book 2015Latest edition Springer Science+Business Media New York 2015 BAC construction

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书目名称Bacterial Artificial Chromosomes影响因子(影响力)




书目名称Bacterial Artificial Chromosomes影响因子(影响力)学科排名




书目名称Bacterial Artificial Chromosomes网络公开度




书目名称Bacterial Artificial Chromosomes网络公开度学科排名




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书目名称Bacterial Artificial Chromosomes被引频次学科排名




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书目名称Bacterial Artificial Chromosomes年度引用学科排名




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书目名称Bacterial Artificial Chromosomes读者反馈学科排名

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forecast

Retinal Vascular Characteristicslleles by conventional methods like Southern Blotting. Recently, we introduced a novel BAC targeting strategy, in which Restriction Fragment Length Polymorphisms (RFLPs) are targeted in polymorphic mouse ES cells, enabling an efficient and easy PCR-based readout to identify properly targeted alleles

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MacIntyre’s Influence on Business Ethicsnome. (2) Introduction of the transfer plasmid sequences into the alphaherpesvirus genome via homologous recombination in mammalian cells. (3) Isolation of recombinant virus genomes containing the BAC backbone sequences from infected mammalian cells and electroporation into .. (4) Preparation of inf

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meretricious

https://doi.org/10.1007/978-94-007-6729-4 be applied on large inborn or acquired derivative chromosomes. The main feature of this set is that the probes are applied in a chromosome-specific manner and they align along the chromosome in average intervals of ten megabasepairs. Hence PCL-FISH provides denser coverage and a more precise anchor

mechanical

Recombineering Linear BACsere structures. Linear BACs may be useful for functional expression of genomic loci in cells, maintenance of linear viral genomes in their natural conformation, and for constructing innovative artificial chromosome structures for applications in mammalian and plant cells.

Fretful

Making BAC Transgene Constructs with Lambda-Red Recombineering System for Transgenic Animals or Cellnotyping, BAC coverage and integrity as well as quality of BAC DNA will be addressed. Not only does this approach provide a practical and effective way to modify large DNA constructs, the same recombineering principles can apply to smaller high copy plasmids as well as to chromosome engineering.

antiquated

Directing Enhancer-Traps and iTol2 End-Sequences to Deleted BAC Ends with loxP- and lox511-Tn10 Tranis procedure are suitable for numerous mapping studies. Because DNA in front of the loxP (or lox511) arrowheads in the Tn10 transposon is retained at the newly created BAC end, exogenous DNA cassettes such as enhancer-traps and iTol2 ends can be efficiently introduced into BAC ends for germline expr