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Multiplexed GuideRNA-expression to Efficiently Mutagenize Multiple Loci in Arabidopsis by CRISPR-Cas9.

Plant Methods.. 2017-03; 
J Schumacher,K Kaufmann, W Yan.
Products/Services Used Details Operation
... Genotyping (bacteria) a. Green Taq DNA polymerase (GenScript, catalog number: E00043) b. 10x Taq buffer (GenScript, catalog number: B0005, supplied with the enzyme) c. 10 mM dNTPs (Carl Roth, catalog number: K039) …

摘要

Since the discovery of the CRISPR (clustered regularly interspaced short palindromic repeats)-associated protein (Cas) as an efficient tool for genome editing in plants (Li et al., 2013; Shan et al., 2013; Nekrasov et al., 2013), a large variety of applications, such as gene knock-out, knock-in or transcriptional regulation, has been published. So far, the generation of multiple mutants in plants involved tedious crossing or mutagenesis followed by time-consuming screening of huge populations and the use of the Cas9-system appeared a promising method to overcome these issues. We designed a binary vector that combines both the coding sequence of the codon optimized Streptococcus pyogenes Cas9 nuclease under the ... More

关键词

CRISPR-Cas9, Multiplexing, gRNA, Gene editing, Arabidopsis