CRISPR-Cas Methods
Humana (Verlag)
978-1-0716-4357-0 (ISBN)
Authoritative and cutting-edge, CRISPR-Cas Methods, Volume 3 aims to be a useful and practical guide for researches to help further their study in this field.
Targeted base editing in rice using Target-AID.- Accelerated laboratory evolution of conjugative plasmids for CRISPR delivery in bacteria.- A SERS-signalled, CRISPR-Cas-powered bioassay for amplification-free and anti-interference detection of SARS-CoV-2 in foods and environmental samples using a single tube-in-tube vessel.- Genetic Engineering of Bacteriophage Using CRISPR-Cas12a.- CRISPR-Cas12a-powered dual-mode biosensor for ultrasensitive and cross-validating detection of pathogenic bacteria.- Intronization of coding sequences for optimization of gene expression.- Sensitive small molecule aptasensing-based on hybridization chain reaction and CRISPR-Cas12a using a portable 3D-printed visualizer.- Highly efficient genome editing in plants with the LbCas12a-RRV variant.- CRISPR-Cas13a-based bacterial detection platform: Sensing pathogen Staphylococcus aureus in food samples.- High efficiency Cas12a mediated A-to-G base editing in rice.- A smartphone-based visual biosensor for CRISPR-Cas powered SARS-CoV-2 diagnostics.- Efficient single-cell cloning of genome-edited cultured human cells.- Ultrasensitive pathogenic bacteria detection by a smartphone-read G-quadruplex-based CRISPR-Cas12a bioassay.- A ratiometric fluorescent biosensing platform for ultrasensitive detection of Salmonella typhimurium via CRISPR-Cas12a and silver nanoclusters.- CRISPR-Cas12a-based aptasensor for sensitive and selective ATP detection.- A portable, visual and dual-mode biosensor for ultrasensitive and self-validating detection of foodborne pathogenic bacteria based on CRISPR-Cas9 system.- CRISPR-Cas12-based PCV2 viral detection.- Surface-enhanced Raman scattering -based CRISPR-Cas assay on microfluidic paper analytical devices for supersensitive detection of pathogenic bacteria in foods.- CRISPR-Cas in woody perennial plants: methods, efficiency, applications, and challenges to creating commercial varieties with high ecological and economic value.- A Unified Protocol for Genome Editing in Monocot and Dicot Plants Using a Transposon-Associated TnpB System.- CRISPR-Cas12a-Based DNA Detection for Rapid Diagnosis of Wheat Blast Disease.
| Erscheinungsdatum | 10.04.2025 |
|---|---|
| Reihe/Serie | Springer Protocols Handbooks |
| Zusatzinfo | 61 Illustrations, color; 6 Illustrations, black and white |
| Sprache | englisch |
| Maße | 178 x 254 mm |
| Themenwelt | Naturwissenschaften ► Biologie |
| Schlagworte | Chromosome engineering • CRISPR-Cas associated transposes • De-novo crop domestication • Gene Drive • Organellar base editing |
| ISBN-10 | 1-0716-4357-6 / 1071643576 |
| ISBN-13 | 978-1-0716-4357-0 / 9781071643570 |
| Zustand | Neuware |
| Informationen gemäß Produktsicherheitsverordnung (GPSR) | |
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