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knockout cells .pdf



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Knockout Cell Line
CRISPR/Cas9 system consists of a “guide” RNA (gRNA) and a bacterial
CRISPR-associated endonuclease (Cas9). The gRNA is a short synthetic RNA
composed of a Cas9-binding “scaffold” sequence and ∼ 20 nucleotide
“targeting” sequence that defines the target genomic site to be modified.
Cas9 contains two nuclease domains to induce site-specific DNA cleavage. It’s
a scalable genome-wide editing technology for its ease of generating gRNAs.
The simplicity and high-efficiency of CRISPR/Cas9 system make it a preferable
genomic knockout method to the traditional ZFN and TALEN system. Our
scientists are experts at performing gene knockout with CRISPR/Cas9, from
designing gRNA constructs to transfection and single clone generation of a
wide range of cells, including difficult-to-transfect and tumor cell lines.


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