High-throughput cloning for proteomics research.

Sharon A Doyle

doi:10.1007/978-1-59259-948-6_7

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High-throughput cloning for proteomics research.

Sharon A Doyle

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Abstract

Ligation-independent cloning (LIC) is a simple, rapid, and efficient method for high-throughput cloning. In this system, linear plasmid vector and insert DNA are treated to generate complementary single-stranded overhangs that anneal during a short incubation. The LIC system is adaptable for use with any vector following an alteration of the vector sequence. This chapter describes the creation of an LIC-compatible vector, with tips on how to make any vector LIC-enabled. It also includes a protocol for generating high-quality linearized vector template for the LIC reaction. Lastly, a step-by-step protocol of the LIC reaction is outlined, with useful tips and tricks for optimization and screening.

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Amino Acid Sequence Base Sequence Cloning, Molecular DNA, Complementary Genetic Vectors Molecular Sequence Data Plasmids Proteomics Journal Article Research Support, U.S. Gov't, Non-P.H.S.

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Sharon A Doyle. 2005. High-throughput cloning for proteomics research.. https://doi.org/10.1007/978-1-59259-948-6_7

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