This manual is an indispensable tool for introducing advanced undergraduates and beginning graduate students to the techniques of recombinant DNA technology, or gene cloning and expression. The techniques used in basic research and biotechnology laboratories are covered in detail. Students gain hands-on experience from start to finish in subcloning a gene into an expression vector, through purification of the recombinant protein. The second edition has been completely re-written, with new laboratory exercises and all new illustrations and text, designed for a typical 15-week semester, rather than a 4-week intensive course. The 'project' approach to experiments was maintained: students still follow a cloning project through to completion, culminating in the purification of recombinant protein. It takes advantage of the enhanced green fluorescent protein - students can actually visualize positive clones following IPTG induction. It covers basic concepts and techniques used in molecular biology research labs. Student-tested labs proven successful in a real classroom laboratories. It includes exercises that simulate a cloning project that would be performed in a real research lab. Its 'project' approach to experiments gives students an overview of the entire process. Its prep-list appendix contains necessary recipes and catalog numbers, providing staff with detailed instructions.