Manipulation and Expression of Recombinant DNA
- 2nd Edition - December 6, 2005
- Authors: Sue Carson, Dominique Robertson
- Language: English
- Paperback ISBN:9 7 8 - 0 - 1 2 - 0 8 8 4 1 8 - 6
- eBook ISBN:9 7 8 - 0 - 0 8 - 0 4 5 6 5 4 - 6
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… Read more
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.
*Cover basic concepts and techniques used in molecular biology research labs*Student-tested labs proven successful in a real classroom laboratories*Exercises simulate a cloning project that would be performed in a real research lab*"Project" approach to experiments gives students an overview of the entire process*Prep-list appendix contains necessary recipes and catalog numbers, providing staff with detailed instructions
Graduate and undergraduate students studying biochemistry, molecular biology, biotechnology, and cell biology
CONTENTSForewordAcknowledgementsNote to InstructorsInstrumentationNomenclatureINTRODUCTION: Conceptual outline for experimentsPART I MANIPULATION OF DNALab session 1: Getting oriented; Practicing with pipetmenLab session 2: Large scale purification of plasmid DNA Lab session 3: Preparation of expression vector DNA (pET-41a(+), a GST fusion protein vector)Lab session 4: Preparation of insert DNA (egfp)Lab session 5: Preparation of transformation-competent cells and control transformationLab session 6: DNA ligation and transformation of Escherichia coli PART II SCREENING TRANSFORMANTSLab session 7: Colony hybridizationsLab session 7a: Interim laboratory session:Lab session 7b: Colony hybridization: DNA probeLab session 7c: Colony hybridization: Monoclonal antibody probeLab session 8: Completion of colony hybridization with DNA probeLab session 9: Characterization of recombinant clones Lab session 9a: Completion of colony hybridization with mAB probeLab session 9b: PCR screenLab session 9c: Visualization of green fluorescent protein: Part 1 Lab session 10: Further characterization of recombinant clonesLab session 10a: Interim laboratory session:Lab session 10b: Analysis of PCR screen resultsLab session 10c: Isolation and characterization of miniprep DNA from potential transformants (Restriction analysis of putative transformants)Lab session 10d: Visualization of green fluorescent protein: Part 2 PART III EXPRESSION, DETECTION, AND PURIFICATION OF RECOMBINANT PROTEINS FROM BACTERIALab session 11: Expression of fusion protein from positive clones and sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and Immunological analysis (Western blot): Part 1Lab session 12: Expression of fusion protein from positive clones and sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and Immunological analysis (Western blot): Part 2Lab session 13: Extraction of recombinant protein from Escherichia coli using a glutathione affinity columnInterim laboratory session: I. Laboratory exercise: Inoculate cultures for protein purificationLab session 14: Analysis of purification fractionsAppendices: Equipment, Prep list, Making sense of orientation
- Edition: 2
- Published: December 6, 2005
- Language: English
SC
Sue Carson
Dr. Carson’s area of scientific expertise is in molecular mechanisms of bacterial pathogenesis. She currently serves as the Director of the Master of Microbial Biotechnology Program and as a Fellow in the Office of Faculty Excellence. Prior to this appointment, she led the NC State Quality Enhancement Plan (QEP), focused on faculty development to cultivate students’ critical and creative thinking skills across disciplines. During that period, she also acted as Executive Director of Academic Enrichment Programs, overseeing the Office of Undergraduate Research, Fellowship Advising, and the University Honors and Scholars Programs. Dr. Carson spent over ten years leading curriculum development for the NC State Biotechnology Program. She has received multiple awards for teaching excellence and innovation and was a member of the Howard Hughes Science Education Alliance, promoting and implementing inquiry-guided learning and authentic research in undergraduate curricula. She authored three molecular biology lab manuals and has published numerous peer-reviewed papers in the area of course and curriculum development. She has mentored over 100 undergraduate students in research projects and was the PI and Director of the National Science Foundation (NSF)-funded Integrative Plant and Microbial Systems Research Experience for Undergraduates (REU) Program for over a decade. Most recently, she completed a 2-year rotation at the National Science Foundation in the Directorate for Education and Human Resources. Within the Triangle community, she has served on the Board of Directors of the Wake County Beekeeping Association and the Triangle Swing Dance Society.
Affiliations and expertise
Department of Plant and Microbial Biology, North Carolina State University, Raleigh, USADR
Dominique Robertson
Affiliations and expertise
North Carolina State University, Raleigh, U.S.A.