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Construction of a High Efficiency PCR Products Cloning T Vector Using pGEM-5zf (+)

A highly efficient cloning vector was constructed for cloning PCR products by inserting an 80 bp DNA fragment into pGEM-5zf (+) vector. The Xcm I digestion of this vector gave rise to a 3′ overhanging deoxythymidine offering the possibility of cloning PCR products with 3′ adenosine overhang created...

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Autors principals: Zhao, Yaofeng, Liu, Zhancai, Yu, Shuyang, Wen, Sicheng, Hammarstrom, Lennart, Rabbani, Hodjattallah
Format: Artigo
Idioma:Inglês
Publicat: Avicenna Research Institute 2009
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3558116/
https://ncbi.nlm.nih.gov/pubmed/23407719
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