CRISPR/cas9 Knockout carrier

Shanghai Chengzhi Biotechnology Inc., provides sgRNA design and clone customization services for genes of interest to customers. sgRNA clones express a single strand of fused sgRNA (formed by fusion of crrna and tracrrna). In the presence of cas9 nuclease, sgRNA can recognize the target DNA sequence and guide cas9 nuclease to cut the target site to form double strand breaks (DSBs). Co transfection of multiple sgRNA clones and one cas9 clone can edit multiple sites in the genome at the same time, making the experimental design more efficient and flexible.

sgRNA design and clone customization service of Shanghai Chengzhi Biotechnology Inc.,

Highly efficient integration of genes into a variety of target cells

Lentivirus system can efficiently transfer genes into living model animals and almost all mammalian cells, including undifferentiated, inactive or stopped growing cells, including neuron cells, primary cells, stem cells. The efficiency of lentivirus transduction is close to 100%. It is an ideal expression vector system.

High expression level of target gene

The expression vector types of lentivirus include n or C-terminal with fusion label or without label. The vector contains sequence elements that can be efficiently packaged, transfected and stably integrated into the genome of the target cell, so that our expression clone can be efficiently expressed in the target cell.

SgRNA efficiency verified

Four sgRNAs were designed for each gene to deliver one sgRNA with the highest efficiency.


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