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Binding of the IS903 transposase to its inverted repeat in vitro.

We have purified the transposase of IS903 in three different ways. We find that transposase expressed as a fusion protein with either glutathione-S-transferase or maltose-binding protein is soluble and can be purified rapidly using affinity chromatography. The third purification requires extracting...

詳細記述

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書誌詳細
主要な著者: Derbyshire, K M, Grindley, N D
フォーマット: Artigo
言語:Inglês
出版事項: 1992
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC556880/
https://ncbi.nlm.nih.gov/pubmed/1324175
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