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This genetic construct features various fluorescent proteins including GFP, YFP, and RFP linked to different regulatory elements such as RBS (Ribosome Binding Sites) and promoters like PLac and PBAD. The design includes multiple degradation tags to control protein stability and expression levels. Restriction enzyme sites are also incorporated for convenient cloning, including EcoRI, SpeI, XbaI, and PstI. This versatile construct allows for controlled expression of fluorescent proteins in bacterial systems, facilitating studies in protein localization, dynamics, and interactions.
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