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DNA Cloning: A Hands-on Approach

This book offers step-by-step instruction on DNA cloning, defined as moving genes around plasmids, mutating genes, or mining new genes. The aim is to provide those new to the field with reliable and up-to-date practical guidance while at the same time conveying the scope for creativity. After a brie...

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Main Authors: Choi, Seok-Yong. (Author, http://id.loc.gov/vocabulary/relators/aut), Ro, Hyunju. (http://id.loc.gov/vocabulary/relators/aut), Yi, Hankuil. (http://id.loc.gov/vocabulary/relators/aut)
Corporate Author: SpringerLink (Online service)
Language:English
Published: Dordrecht : Springer Netherlands : Imprint: Springer, 2019.
Edition:1st ed. 2019.
Subjects:
Gene expression.
Genetic engineering.
Plant genetics.
Animal genetics.
Gene Expression.
Genetic Engineering.
Plant Genetics and Genomics.
Animal Genetics and Genomics.
Online Access:https://doi.org/10.1007/978-94-024-1662-6
Table of Contents:
  • Part I. What is cloning?
  • Chapter 1.1 Definition of cloning
  • Chapter 1.2 Discovering a new gene
  • Chapter 1.3 Cloning in the past
  • Chapter 1.4 Cloning in the present
  • Part II. A prerequisite for cloning
  • Chapter 2.1 Software useful for cloning design
  • Chapter 2.2 Vector, plasmid, construct and the Kozak consensus sequence
  • Chapter 2.3 Multiple cloning sites (MCS)
  • Chapter 2.4 Restriction endonucleases and star activity
  • Chapter 2.5 Agarose gel electrophoresis
  • Chapter 2.6 Pouring LB agar plates
  • Chapter 2.7 Competent cells
  • Chapter 2.8 The conversion of DNA mass into molar concentration
  • Chapter 2.9 Upon receiving new plasmids
  • Chapter 2.10 cDNA library
  • Part III. The first step in cloning
  • Chapter 3.1 Cut & paste
  • Chapter 3.2 DNA sequencing and direct sequencing
  • Chapter 3.3 PCR and nested PCR
  • Chapter 3.4 Fill-in (Full & Partial)
  • Chapter 3.5 Compatible cohesive ends
  • Chapter 3.6 Methylation
  • Chapter 3.7 Three-piece ligation
  • Chapter 3.8 Site-directed mutagenesis
  • Chapter 3.9 Structure of plant transformation vectors
  • Chapter 3.10 Transformation of R. radiobacter
  • Part IV. The next step of cloning
  • Chapter 4.1 How to insert a DNA fragment into a gene
  • Chapter 4.2 How to delete an internal region of a gene
  • Chapter 4.3 How to insert an epitope tag into a gene
  • Chapter 4.4 Translational fusion vs. transcriptional fusion
  • Part V. The last steps of cloning
  • Chapter 5.1 Method for cloning similar genes in different species
  • Chapter 5.2 RACE (rapid amplification of cDNA ends)
  • Chapter 5.3 BAC recombineering
  • Chapter 5.4 Old trick: partial digestion
  • Chapter 5.5 Modification of a vector
  • Chapter 5.6 When you notice a frame shift mutation upon cloning
  • Chapter 5.7 Reality of cloning: an extremely unlucky case
  • Part VI. Methods that make your cloning life easier
  • Chapter 6.1 TA cloning and production of a T-vector
  • Chapter 6.2 TOPO TA cloning
  • Chapter 6.3 Gateway cloning
  • Chapter 6.4 Golden Gate Assembly for a modular cloning
  • Chapter 6.5 In-Fusion Sequence and Ligation-Independent Cloning (In-Fusion SLIC)
  • Chapter 6.6 T4 DNA Polymerase Sequence-and Ligation-Independent Cloning (T4 DNA Pol SLIC)
  • Chapter 6.7 Non-template PCR cloning
  • Part VII. Advice to cloners
  • Chapter 7.1 When cloning is not going well
  • Chapter 7.2 Keep your cloning data organized
  • Appendix 1. Further readings
  • Appendix 2. Abbreviations
  • Appendix 3. Index.

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