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The pIEx™-7 Ek/LIC Vector is a ligation-independent cloning-prepared derivative of the pIEx-6 vector designed to allow rapid, high-level protein expression in insect cells without the time-consuming process of creating a recombinant baculovirus. This vector features the hr5 enhancer and the IE1 (immediate early) promoter to direct expression in insect cells and a minimal N-terminal His•Tag® coding sequence. This promoter/enhancer combination recruits endogenous insect cell transcription machinery, thereby avoiding baculovirus infection and the associated cytotoxic effects. The Ek/LIC cloning site is designed to allow the generation of fusion proteins with minimal vector-encoded sequence. An optional S•Tag™ coding sequence is present at the 3′ end of the MCS for generating a carboxy-terminal tag compatible with purification, detection and quantification (1).
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Product information
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Components
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| • | 1 µg | Ek/LIC Vector
| | • | 25 units | T4 DNA Polymerase, LIC-qualified
| | • | 50 µl | 25 mM EDTA
| | • | 40 µl | 25 mM dATP
| | • | 8 µl | Ek/LIC β-gal Control Insert
| | • | 100 µl | 100 mM DTT
| | • | 50 µl | 10X T4 DNA Polymerase Buffer
| | • | 1.5 ml | Nuclease-free Water
| | • | 5 × 2 ml | SOC Medium
| | • | 10 µl | Test Plasmid
| | • | 22 × 50 µl | NovaBlue GigaSingles™ Competent Cells
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Store and ship information
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Storage
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≤ -70°C
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Ship
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Dry Ice Only
Multiple Toxicity Values, refer to MSDS
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