A single-copy galK promoter cloning vector suitable for cloning strong promoters
Research output: Contribution to journal › Journal article › Research › peer-review
We report the construction of lambda galK promoter cloning vectors for cloning and characterization of strong promoters. This phage, which contains a unique HindIII cloning site, was applied to the cloning and analysis of transcription initiations of the regulatory region of the deo-operon of Escherichia coli and the PL promoter of bacteriophage lambda.
Original language | English |
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Journal | Gene Analysis Techniques |
Volume | 3 |
Issue number | 6 |
Pages (from-to) | 102-111 |
ISSN | 0735-0651 |
Publication status | Published - 1986 |
ID: 2107068