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Efficient Generation of hiPSC Neural Lineage Specific Knockin Reporters Using the CRISPR/Cas9 and Cas9 Double Nickase System - a 2 minute Preview of the Experimental Protocol
Shenglan Li, Haipeng Xue, Bo Long, Li Sun, Tai Truong, Ying Liu
The University of Texas Health Science Center at Houston, Department of Neurosurgery; The University of Texas Health Science Center at Houston, Center for Stem Cell and Regenerative Medicine, Brown Foundation Institute of Molecular Medicine; The University of Texas Health Science Center at Houston, The Senator Lloyd & B. A. Bentsen Center for Stroke Research, Brown Foundation Institute of Molecular Medicine; The University of Texas Health Science Center at Houston, Summer Research Program, Office of Educational Programs; Shengjing Hospital, China Medical University, Department of Anesthesiology; Shanghai Jiaotong University School of Medicine, Department of Oncology, Renji Hospital; University of West Georgia, Biology Department;
Genome editing tools such as the CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats)/Cas (CRISPR-associated) system have greatly improved gene targeting efficiency in human induced pluripotent stem cells (hiPSCs). This manuscript describes a protocol for generating lineage specific hiPSC reporter using CRISPR/Cas system assisted homologous recombination.
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