Buch, Englisch, Band 2967, 254 Seiten, Format (B × H): 178 mm x 254 mm, Gewicht: 511 g
Reihe: Methods in Molecular Biology
Methods and Protocols
Buch, Englisch, Band 2967, 254 Seiten, Format (B × H): 178 mm x 254 mm, Gewicht: 511 g
Reihe: Methods in Molecular Biology
ISBN: 978-1-0716-3360-1
Verlag: Springer US
This second volume focuses on PCR methods and PCR application specificities to the biotechnology and bioengineering field. New and updated chapters detail real-time PCR protocols, synthetic biology applications, pathogen detection, microfluidics, digital, multiplex detection recent advances. Written in the highly successful Methods in Molecular Biology series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and key tips on troubleshooting and avoiding known pitfalls.
Authoritative and cutting-edge, PCR: Methods and Protocols, Second Editionaims to be a useful and practical guide to new researchers and experts looking to expand their knowledge.
Zielgruppe
Professional/practitioner
Autoren/Hrsg.
Fachgebiete
Weitere Infos & Material
Digital PCR: A partitioning-based application for detection and surveillance of SARS-CoV-2 from sewage samples.- Digital PCR: A tool to authenticate herbal products and spice.- Emulsion Polymerase Chain Reaction coupled with Denaturant Gradient Gel Electrophoresis for microbial diversity studies.- Real-Time PCR High-Resolution Melting Assays for the Detection of Foodborne Pathogens.- High-Throughput real-time qPCR and High-Resolution Melting (HRM) assay for fungal detection in plant matrices.- Multiplex real-time PCR for the detection of Shiga Toxin-producing Escherichia coli in foods.- DNA isolation from cocoa-derived products and cocoa authentication by TaqMan real-time PCR.- Quantitative real-time PCR for the detection of allergenic species in foods.- Accurate absolute quantification of bacterial populations in mixed cultures by qPCR.- Real-time PCR method for assessment of ParA-mediated recombination efficiency in minicircle production.- Gene expression quantification from pathogenic bacterial biofilms by quantitative PCR.- A real-time quantitative PCR protocol for the quantification of plasmid copy number in Lactococcus lactis.- Improved PCR by the use of disruptors, a new class of oligonucleotide reagents.- Mitochondrial DNA D-loop amplification and sequencing for species differentiation in milk.- Long-range Polymerase Chain Reaction.- Megaprimer-based PCR to synthesise fusion genes for cloning.- Bacteria and Yeast ColonyPCR.- Inverse PCR for site-directed mutagenesis.- Optimized design of degenerate primers for PCR based on DNA or protein sequence comparisons.
