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ÌýÎÅHigh-Efficiency gRNA-Cas9-Puro Plasmid (linear) Assembly Kit¿ÉÒÔ¿ìËÙ¼ì²âÇóýÑùÆ·£¬¾ÍÏëÎÊÎÊÓÐûÓÐÓùý£¿Ð§¹ûÈçºÎ

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CRISPR/Cas9 mediated genome editing is a powerful technique that allows you to create knock-in, knock-out, gene up-regulation/repression, and mutations of any gene, in any cell, in a highly targeted manner.

The CRISPR/Cas system mainly consists of two major components: the Cas nuclease Cas9 and the specific guide RNA (gRNA). They can form a very stable ribonucleoprotein (RNP) complex. Once a specific DNA region is matched by the gRNA carrying Cas9, the target DNA can be cleaved into double strand break. Cas9 RNP complex can be introduced into cells directly and act immediately after it enters the cell without transcription and translation. By fusion with different functional domain, CRISPR/Cas9 and its mutants have been used in a broad gene editing fields (knock-out, knock-in, gene up/down, genome purification and visualization et. al.).
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