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Molecular Biology Techniques An Intensive Laboratory Course [Paperback]

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  • Category: Books (Science)
  • Author:  Walt Ream, Katharine G. Field
  • Author:  Walt Ream, Katharine G. Field
  • ISBN-10:  0125839901
  • ISBN-10:  0125839901
  • ISBN-13:  9780125839907
  • ISBN-13:  9780125839907
  • Publisher:  Academic Press
  • Publisher:  Academic Press
  • Pages:  234
  • Pages:  234
  • Binding:  Paperback
  • Binding:  Paperback
  • Pub Date:  01-Apr-1998
  • Pub Date:  01-Apr-1998
  • SKU:  0125839901-11-MPOD
  • SKU:  0125839901-11-MPOD
  • Item ID: 100835809
  • Seller: ShopSpell
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  • Delivery by: Dec 19 to Dec 21
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This manual is designed as an intensive introduction to the various tools of molecular biology. It introduces all the basic methods of molecular biology including cloning, PCR, Southern (DNA) blotting, Northern (RNA) blotting, Western blotting, DNA sequencing, oligo-directed mutagenesis, and protein expression.

  • Provides well-tested experimental protocols for each technique
  • Lists the reagents and preparation of each experiment separately
  • Contains a complete schedule of experiments and the preparation required
  • Includes study questions at the end of each chapter
Preface.
Course Synopsis:
Introduction.
Safety Precautions.
Daily Schedule.
Acknowledgements.
Exercises: I. DNA Preparation, Polymerase Chain Reaction, and Molecular Cloning:
Cesium chloride-ethidium bromide density gradient centrifugation.
PCR to synthesize virD2 flanked with restriction sites.
Restriction digests of plasmid pGEX2 and PCR products.
Purification of DNA fragments from agarose.
Ligation of PCR product to pGEX2 vector.
Transformation of E. coli with the ligated plasmid.
Small-scale preparation of plasmid DNA by the alkaline lysis method.
Restriction analysis.
Study questions.
Protein Expression, Purification, and Analysis:
Expression and purification of a fusion protein.
SDS-polyacrylamide gel electrophoresis.
Silver stain detection of proteins.
Study questions.
Oligonucleotide-Directed Mutagenesis:
Restriction digests of virD2 (in pCS64) and pUC119.
Purification of DNA fragments from agarose.
Ligatation of restriction fragment and vectló›
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