Manipulation and expression of recombinant DNA : a laboratory manual /

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Bibliographic Details
Author / Creator:Carson, Sue (Susan)
Edition:2nd ed.
Imprint:Burlington, MA : Elsevier Academic Press, ©2006.
Description:1 online resource (xvi, 151 pages) : illustrations (some color)
Language:English
Subject:
Format: E-Resource Book
URL for this record:http://pi.lib.uchicago.edu/1001/cat/bib/11148737
Hidden Bibliographic Details
Other authors / contributors:Robertson, Dominique, 1951-
ISBN:0080456545
9780080456546
0120884186
Notes:Includes bibliographical references and index.
Print version record.
Summary: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,
Other form:Print version: Carson, Sue, Dr. Manipulation and expression of recombinant DNA. 2nd ed. Burlington, MA : Elsevier Academic Press, ©2006 0120884186

MARC

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245 1 0 |a Manipulation and expression of recombinant DNA :  |b a laboratory manual /  |c Susan Carson, Dominique Robertson. 
250 |a 2nd ed. 
260 |a Burlington, MA :  |b Elsevier Academic Press,  |c ©2006. 
300 |a 1 online resource (xvi, 151 pages) :  |b illustrations (some color) 
336 |a text  |b txt  |2 rdacontent 
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588 0 |a Print version record. 
505 0 |a Cover; Contents; Preface; Acknowledgments; Note to Instructors; Instrumentation; Nomenclature; Introduction; Conceptual Outline for Experiments; Experimental Procedures; Laboratory Safety; General Operating Procedures; Emergency Contact Information; Part I; Manipulation of DNA; Lab Session 1; Getting Oriented; Practicing with Micropipettes; Station Checklist; Micropipetting; Laboratory Exercise; Preparing BSA Dilutions; Performing a Nitrocellulose Spot Test; Lab Session 2; Large-Scale Purification of Plasmid DNA; Introduction; Laboratory Exercises 
505 8 |a Alkaline Lysis and Anion Exchange ChromatograhyDNA Quantification; Lab Session 3; Preparation of Expression Vector DNA (pET-41a(+), a GST Fusion Protein Vector); Introduction; Laboratory Exercises; Restriction Digestion of Vector (pET41a) Restriction Enzyme Digestions; Agarose Gel Electrophoresis; Cleaning DNA Using a Spin Column; Lab Session 4; Preparation of Insert DNA (egfp); Introduction; Laboratory Exercises; Restriction Digestion of pEGFP-N1; Isolation of egfp DNA from Agarose; Lab Session 5; Preparation of Transformation-Competent Cells and Control Transformation; Introduction 
505 8 |a Laboratory Exercises Preparation of Chemically Competent Cells by Calcium Chloride Treatment; Transformation Control; Lab Session 6; DNA Ligation and Transformation of Escherichia coli; Introduction; Laboratory Exercises; Ligations and Ligation Controls; Divalent Cation-Mediated Transformation; Electrophoresis of Ligation Reactions; Part II; Screening Transformants; Lab Session 7; Colony Hybridizations; Lab Session 7A; Interim Laboratory Session; Introduction; Laboratory Exercises; Counting Transformants; Replica Plating; Lab Session 7B; Colony Hybridization: DNA Probe; Introduction 
505 8 |a Laboratory Exercises Colony Hybridization with an egfp DNA Probe: Part 1; Labeling of DNA Probe by PCR Using Digoxigenin-11-dUTP; Lab Session 7C; Colony Hybridization: Monoclonal Antibody Probe; Introduction; Laboratory Exercise; Colony Hybridization with an a-GFP Monoclonal Antibody Probe: Part 1; Lab Session 8; Completion of Colony Hybridization with DNA Probe; Introduction; Laboratory Exercise; Colony Hybridization with an egfp DNA Probe: Part 2; Lab Session 9; Characterization of Recombinant Clones; Lab Session 9A; Completion of Colony Hybridization with mAB Probe; Introduction 
505 8 |a Laboratory Exercise Colony Hybridization with an a-GFP monoclonal Antibody Probe: Part 2; Lab Session 9B; PCR Screening; Introduction; Polymerase Chain Reaction; Laboratory Exercise; Polymerase Chain Reaction Screen for Recombinant Clones: Part 1; Lab Session 9C; Visualization of Green Fluorescent Protein: Part 1; Introduction; Laboratory Exercise; Green Fluorescence Assay and Preparation of a Fresh Master Plate; Lab Session 10; Further Characterization of Recombinant Clones; Lab Session 10A:; Interim Laboratory Session; Laboratory Exercise; Inoculate Cultures for Minipreps; Lab Session 10B 
520 |a 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, 
650 0 |a Recombinant DNA  |v Laboratory manuals. 
650 1 2 |a DNA, Recombinant  |x analysis  |v Laboratory Manuals. 
650 1 2 |a DNA, Recombinant  |x isolation and purification  |v Laboratory Manuals. 
650 2 2 |a Recombinant Proteins  |x analysis  |v Laboratory Manuals. 
650 2 2 |a Recombinant Proteins  |x isolation & purification  |v Laboratory Manuals. 
650 2 2 |a Genetic Techniques  |v Laboratory Manuals. 
650 7 |a SCIENCE  |x Biotechnology.  |2 bisacsh 
650 7 |a Recombinant DNA.  |2 fast  |0 (OCoLC)fst01091466 
655 0 |a Electronic books. 
655 2 |a Laboratory Manual. 
655 4 |a Electronic books. 
655 7 |a Laboratory manuals.  |2 fast  |0 (OCoLC)fst01920776 
700 1 |a Robertson, Dominique,  |d 1951-  |0 http://id.loc.gov/authorities/names/n90605676 
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