PCR Cloning Protocols

Detalles Bibliográficos
Autor Corporativo: SpringerLink (Online service)
Otros Autores: Chen, Bing-Yuan. (Editor ), Janes, Harry W. (Editor )
Formato: eBook
Lenguaje:English
Publicado: Totowa, NJ : Humana Press : Imprint: Humana, 2002.
Edición:2nd ed. 2002.
Colección:Methods in Molecular Biology, 192
Materias:
Acceso en línea:https://doi.org/10.1385/1592591779
Tabla de Contenidos:
  • Performing and Optimizing PCR
  • Polymerase Chain Reaction
  • Computer Programs for PCR Primer Design and Analysis
  • Single-Step PCR Optimization Using Touchdown and Stepdown PCR Programming
  • XL PCR Amplification of Long Targets from Genomic DNA
  • Coupled One-Step Reverse Transcription and Polymerase Chain Reaction Procedure for Cloning Large cDNA Fragments
  • Long Distance Reverse-Transcription PCR
  • Increasing PCR Sensitivity for Amplification from Paraffin-Embedded Tissues
  • GC-Rich Template Amplification by Inverse PCR
  • PCR Procedure for the Isolation of Trinucleotide Repeats
  • Methylation-Specific PCR
  • Direct Cloning of Full-Length Cell Differentially Expressed Genes by Multiple Rounds of Subtractive Hybridization Based on Long-Distance PCR and Magnetic Beads
  • Cloning PCR Products
  • Cloning PCR Products
  • Using T4 DNA Polymerase to Generate Clonable PCR Products
  • Enzyme-Free Cloning of PCR Products and Fusion Protein Expression
  • Directional Restriction Site-Free Insertion of PCR Products into Vectors
  • Autosticky PCR
  • A Rapid and Simple Procedure for Direct Cloning of PCR Products into Baculoviruses
  • Mutagenesis and Recombination
  • PCR Approaches to DNA Mutagenesis and Recombination
  • In-Frame Cloning of Synthetic Genes Using PCR Inserts
  • Megaprimer PCR
  • PCR-Mediated Recombination
  • PCR Method for Generating Multiple Mutations at Adjacent Sites
  • A Fast Polymerase Chain Reaction-Mediated Strategy for Introducing Repeat Expansions into CAG-Repeat Containing Genes
  • PCR Screening in Signature-Tagged Mutagenesis of Essential Genes
  • Staggered Extension Process (StEP) In Vitro Recombination
  • Random Mutagenesis by Whole-Plasmid PCR Amplification
  • Cloning Unknown Neighboring DNA
  • PCR-Based Strategies to Clone Unknown DNA Regions from Known Foreign Integrants
  • Long Distance Vectorette PCR (LDV PCR)
  • Nonspecific, Nested Suppression PCR Method for Isolation of Unknown Flanking DNA (“Cold-Start Method”)
  • Inverse PCR
  • 31 Inverse PCR
  • Gene Cloning and Expression Profiling by Rapid Amplification of Gene Inserts with Universal Vector Primers
  • The Isolation of DNA Sequences Flanking Tn5 Transposon Insertions by Inverse PCR
  • Rapid Amplification of Genomic DNA Sequences Tagged by Insertional Mutagenesis
  • Isolation of Large-Terminal Sequences of BAC Inserts Based on Double-Restriction-Enzyme Digestion Followed by Anchored PCR
  • A #x201C;Step Down#x201D; PCR-Based Technique for Walking Into and the Subsequent Direct-Sequence Analysis of Flanking Genomic DNA
  • Library Construction and Screening
  • Use of PCR in Library Screening
  • Cloning of Homologous Genes by Gene-Capture PCR
  • Rapid and Nonradioactive Screening of Recombinant Libraries by PCR
  • Rapid cDNA Cloning by PCR Screening (RC-PCR)
  • Generation and PCR Screening of Bacteriophage ? Sublibraries Enriched for Rare Clones (the “Sublibrary Method ”)
  • PCR-Based Screening for Bacterial Artificial Chromosome Libraries
  • A 384-Well Microtiter-Plate-Based Template Preparation and Sequencing Method
  • A Microtiter-Plate-Based High Throughput PCR Product Purification Method.