
Molecular Biology Techniques : A Classroom Laboratory Manual.
Title:
Molecular Biology Techniques : A Classroom Laboratory Manual.
Author:
Miller, Heather.
ISBN:
9780123855459
Personal Author:
Edition:
3rd ed.
Physical Description:
1 online resource (227 pages)
Contents:
Front Cover -- Molecular Biology Techniques: A Classroom Laboratory Manual -- Copyright Page -- Contents -- Preface -- About the Authors -- Acknowledgements -- Note to Instructors -- Instrumentation -- Nomenclature -- Introduction -- Conceptual Outline for Experiments -- Experimental Procedures -- Laboratory Safety -- General Operating Procedures -- 1 - Manipulation of DNA -- Reference -- Lab Session 1. Getting Oriented: Practicing with Micropipettes -- Station Checklist -- Micropipetting -- Micropipetting Self-Test -- Laboratory Exercise: BSA Serial Dilutions and Nitrocellulose Spot Test -- Preparing BSA Dilutions -- Performing a Nitrocellulose Spot Test -- Discussion Questions -- Lab Session 2. Purification and Digestion of Plasmid (Vector) DNA -- Introduction to Plasmid Purification -- Alkaline Lysis -- Silica Adsorption -- DNA Quantification -- Introduction to Expression Vectors -- Principles of Gene Expression -- Expression Vectors -- Orientation and Reading Frame -- Orientation -- Reading Frame -- Laboratory Exercises -- Alkaline Lysis and Silica Adsorption Protocol -- DNA Quantification -- Restriction Digestion of Expression Vector DNA pET-41a, a GST Fusion Protein Vector -- Discussion Questions -- Reference -- Lab Session 3. PCR Amplification of egfp and Completion of Vector Preparation -- Introduction -- What is the Polymerase Chain Reaction (PCR)? -- Why Clone by PCR? -- TA Cloning -- PCR Cloning by Incorporation of Restriction Sites -- Cloning Synthetic Genes -- Laboratory Exercises -- PCR Amplification of egfp from the pEGFP-N1 Plasmid -- PCR Protocol -- Clean-up of Digested pET-41a Vector -- Agarose Gel Electrophoresis -- Discussion Questions -- References -- Lab Session 4. Preparation of Insert DNA (egfp) PCR Product -- Check PCR Reactions on an Agarose Gel -- Spin Column Cleanup of PCR Product -- Quantification of egfp PCR Product.
Restriction Digestion of egfp PCR Product -- Removing Enzymes and Cleaning Digested DNA Using a Spin Column -- Discussion Questions -- Lab Session 5. DNA Ligation and Transformation of Escherichia coli -- Introduction -- Ligation -- Transformation -- Laboratory Exercises -- Ligations and Ligation Controls -- Divalent Cation-Mediated Transformation -- Electrophoresis of Ligation Reactions -- Discussion Questions -- Reference -- 2 - Screening Transformants -- Lab Session 6. Colony Hybridization -- Lab Session 6A. Interim Laboratory Session -- Introduction -- Laboratory Exercises -- Counting Transformants and Replica Plating -- Replica Plating -- Lab Session 6B. Colony Hybridization: Monoclonal Antibody Probe -- Introduction -- Laboratory Exercises -- Colony Hybridization with an α-EGFP Monoclonal Antibody Probe: Part 1 -- Lab Session 6. Discussion Questions -- Lab Session 7. Characterization of Recombinant Clones: Part 1 -- Lab Session 7A. Completion of Colony Hybridization with a Monoclonal Antibody Probe -- Introduction -- Laboratory Exercise -- Colony Hybridization with an α-EGFP Monoclonal Antibody Probe: Part 2 -- Lab Session 7B. PCR Screening -- Introduction -- Laboratory Exercise -- Polymerase Chain Reaction Screen for Recombinant Clones -- Lab Session 7C. Prepare Fresh Replica Plate -- Lab Session 7. Discussion Questions -- Lab Session 8. Characterization of Recombinant Clones: Part 2 -- Lab Session 8A. Interim Laboratory Session -- Laboratory Exercise -- Inoculate Cultures for Minipreps -- Lab Session 8B. Analysis of PCR Screen Results -- Introduction -- Laboratory Exercise -- Gel Electrophoresis and Analysis of PCR Samples from Last Week -- Lab Session 8C. Isolation of Miniprep DNA from Potential Transformants -- Introduction -- Laboratory Exercise -- Isolation of Miniprep DNA from Potential Transformants.
Plasmid DNA Purification Using the QIAprep Spin Miniprep Kit and a Microcentrifuge -- Lab Session 8D. Visualization of Green Fluorescent Protein: Part 1 -- Introduction -- Laboratory Exercise -- Green Fluorescence Assay and Preparation of a Fresh Master Plate -- Lab Session 8. Discussion Questions -- Lab Session 9. Characterization of Recombinant Clones: Part 3 -- Lab Session 9A. Characterization of Miniprep DNA from Potential Transformants (Restriction Enzyme Analysis of Putative Transformants) -- Introduction -- Laboratory Exercise -- Restriction Enzyme Analysis of Miniprep DNA -- Lab Session 9B. Visualization of Green Fluorescent Protein: Part 2 -- Introduction -- Laboratory Exercise -- Visualization of Clones Expressing the Enhanced Green Fluorescent Protein on IPTG Plates -- Lab Session 9C. Computational Analysis of DNA Sequence from a Positive Clone: Part 1 -- Introduction -- Laboratory Exercise -- References -- Lab Session 9. Discussion Questions -- Lab Session 10. Computational Analysis of DNA Sequence from a Positive Clone: Part 2 -- Introduction -- Laboratory Exercise -- Discussion Questions -- Reference -- 3 - Expression, Detection and Purification of Recombinant Proteins from Bacteria -- Lab Session 11. Expression of Fusion Protein from Positive Clones, SDS-PAGE and Western Blot: Part 1 -- Lab Session 11A. Interim Laboratory Session -- Laboratory Exercise -- Inoculate Cultures for SDS-PAGE -- Lab Session 11B. Expression of Fusion Protein from Positive Clones, SDS-PAGE and Western Blot -- Introduction -- Laboratory Exercise -- SDS-PAGE and Western Blot: Part 1 -- Reference -- Lab Session 11. Discussion Questions -- Lab Session 12. Expression of Fusion Protein from Positive Clones, SDS-PAGE and Western Blot: Part 2 -- Introduction -- Laboratory Exercises -- SDS-PAGE and Western Blot: Part 2 -- Replica Plate Positive Clone.
Discussion Questions -- Lab Session 13. Extraction of Recombinant Protein from Escherichia coli Using a Glutathione Affinity Column -- Lab Session 13A. Interim Laboratory Session -- Laboratory Exercise -- Inoculate Cultures for Protein Purification -- Lab Session 13B. Extraction of Recombinant Protein from Escherichia coli and Purification Using a Glutathione Affinity Column -- Introduction -- Laboratory Exercises -- Growing Bacterial Suspension Cultures for Fusion Protein Purification -- Harvesting IPTG-Induced Cultures -- Breaking Open Bacterial Cells -- Removing Insoluble Debris from the Crude Homogenate -- Purifying Protein by Affinity Chromatography -- Lab Session 13. Discussion Questions -- Lab Session 14. Analysis of Purification Fractions -- Lab Session 14A. Analysis of Purification Fractions -- Introduction -- Laboratory Exercises -- SDS-PAGE of Purified Fusion Protein -- Fluorescence Analysis of Affinity Purification -- Lab Session 14B. Replica Plate Positive Clone -- Lab Session 14. Discussion Questions -- 4 - Analysis of mRNA Levels -- Challenges of Working with RNA -- References -- Lab Session 15. Total RNA Purification -- Lab Session 15A. Interim Laboratory Session -- Laboratory Exercise -- Inoculate Cultures for RNA Purification -- Lab Session 15B. Total RNA Purification -- Introduction -- Laboratory Exercises -- Purification of Total RNA -- DNase Digestion -- Quantification of RNA -- References -- Lab Session 15. Discussion Questions -- Lab Session 16. Analysis of gst::egfp mRNA Levels by RT-qPCR: Part 1 -- Introduction -- Reverse Transcription -- Quantitative PCR -- Laboratory Exercises -- Reverse Transcription -- Quantitative PCR (qPCR) -- Discussion Questions -- Reference -- Lab Session 17. Analysis of gst::egfp mRNA Levels by RT-qPCR: Part 2 -- Introduction -- Laboratory Exercise -- Relative Quantification of gst::egfp Levels.
References -- Discussion Questions -- Lab Session 18. Analysis of gst::egfp mRNA Levels by Semi-Quantitative RT-PCR: Part 1 -- Introduction -- Laboratory Exercises -- Reverse Transcription (RT) -- Semi-Quantitative PCR -- Discussion Questions -- Lab Session 19. Analysis of gst::egfp mRNA Levels by Semi-Quantitative RT-PCR: Part 2 -- Introduction -- Laboratory Exercises -- Agarose Gel Electrophoresis -- Quantification -- Discussion Questions -- Reference -- Appendix 1: Equipment -- Shared Equipment -- Appendix 2: Prep List -- Notes to Prep Staff -- Plasmids and E. coli Host Strains -- Antibiotics -- Aliquots -- Bacterial Waste -- Autoclaving -- General Lab Preparation -- Students -- Supplies and Reagents -- Supplies and Reagents for General Use -- Recipes for General Use -- LAB SESSION 1 -- BSA Serial Dilutions and Nitrocellulose Spot Test -- Recipes -- LAB SESSION 2 -- Purification and Digestion of Plasmid (Vector) DNA -- LAB SESSION 3 -- PCR Amplification of egfp from pEGFP-N1 -- Clean-up and Visualization of Digested pET-41a Vector -- Recipes -- LAB SESSION 4 -- Preparation of Insert DNA (egfp) PCR Product -- LAB SESSION 5 -- DNA Ligation and Transformation of Escherichia coli -- LAB SESSION 6 -- Interim Lab -- LAB SESSION 6 -- Colony Hybridization: Monoclonal Antibody Probe -- Recipes -- LAB SESSION 7 -- Characterization of Recombinant Clones -- Recipes -- Chloronaphthol Stock Solution -- Peroxide Stain -- LAB SESSION 8 -- Interim Lab -- LAB SESSION 8 -- Characterization of Recombinant Clones: Part 2 -- LAB SESSION 9 -- Characterization of Recombinant Clones: Part 3 -- LAB SESSION 10 -- Computational Analysis of DNA Sequence from a Positive Clone: Part 2 -- LAB SESSION 11 -- Interim Lab -- LAB SESSION 11 -- Expression of Fusion Protein from Positive Clones, SDS-PAGE and Western Blot: Part 1 -- Recipes -- LAB SESSION 12.
Expression of Fusion Protein from Positive Clones, SDS-PAGE and Western Blot: Part 2.
Abstract:
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 third 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.
Local Note:
Electronic reproduction. Ann Arbor, Michigan : ProQuest Ebook Central, 2017. Available via World Wide Web. Access may be limited to ProQuest Ebook Central affiliated libraries.
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