Madison 发表于 2025-3-21 17:21:32
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Chr. Gutenbrunner,G. Hildebrandtew crop variety. This chapter briefly describes the methods of CRISPR-Cas9 vector construction with single and multiple gene targets in rice. The protocol covers all important steps of target sequence selection, single/multiple-target vector construction, mutation detection, and selection of T-DNA free mutant lines.乐意 发表于 2025-3-22 00:36:35
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In Vitro Cas9 Cleavage Assay to Check Guide RNA Efficiency,ro method to screen multiple sgRNAs to identify the most suitable one that can efficiently introduce a double-stranded break at a particular genomic target site. This screening method allows a researcher to choose the best one among several online predicted sgRNAs prior to deliver genome editing reagents into live plant or animal cells.墙壁 发表于 2025-3-22 18:34:18
Generation of Knockout and Fragment Deletion Mutants in Soybean by CRISPR-Cas9,o the CRISPR-Cas9-mediated targeted mutagenesis or large fragment deletions in soybean. Detailed procedures will guide through the essential steps including the design of sgRNAs, construction of CRISPR-Cas9 vectors, .-mediated soybean transformation, and identification of mutant lines.minimal 发表于 2025-3-23 00:39:44
1949-2448 ation advice from the experts.This second volume provides new and updated methods detailing advancements in CRISPR-Cas technical protocols. Chapters guide readers through protocols on prime editing, base editing, multiplex editing, editing in cell-free extract, in silico analysis of gRNA secondary s不透气 发表于 2025-3-23 02:38:36
https://doi.org/10.1007/978-3-662-25284-0e, wheat, maize, and tomato, which substantially expands the scope and capabilities of precision plant breeding. Here, we describe a fast and efficient method for construction of prime editing vectors based on Gateway assembly and efficiency assessment of prime editors through transient expression analyses in rice protoplasts.engrave 发表于 2025-3-23 07:41:14
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