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The PRESAT-vector: Asymmetric T-vector for high-throughput screening of soluble protein domains for structural proteomics

A rapid unidirectional method for cloning PCR-amplified cDNA fragments into virtually any fusion protein expression vector is described. The method, termed PRESAT-vector cloning, is based on a T-vector technique that does not require restriction endonuclease digestion of the PCR product. Subsequentl...

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Autori principali: Goda, Natsuko, Tenno, Takeshi, Takasu, Hirotoshi, Hiroaki, Hidekazu, Shirakawa, Masahiro
Natura: Artigo
Lingua:Inglês
Pubblicazione: Cold Spring Harbor Laboratory Press 2004
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2286733/
https://ncbi.nlm.nih.gov/pubmed/14978305
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1110/ps.03439004
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