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一般說明
Each species-specific library is delivered as two half-libraries (A and B). It is recommended to screen both A and B libraries together, which will include 6 sgRNAs per gene (3 sgRNAs in each library). Both libraries contain 1000 non-targeting control sgRNAs. The A library also targets miRNAs (4 sgRNAs per miRNA).
應用
特點和優勢
- Use CRISPR nucleases to knockout protein-coding genes to assess their function
- Efficiently screen the whole human genome (16,000+ genes) at the bench-top without robotics or specialized equipment
- Numerous built-in enrichment and depletion controls allow researchers to confidently gauge the success of their pooled screening experiments • Lentiviral CRISPRs can infect a broad variety of mammalian cells by transducing a single guide RNA (sgRNA) to a Cas9-expressing mouse cell line to facilitate gene knockout for screening applications.
- Use the dual vector system for the mouse GeCKO version 2 libraries for mouse cell lines that have Cas9 already integrated into the genome.
- Use puromycin gRNA selection after transduction.
準備報告
其他說明
法律資訊
儲存類別代碼
12 - Non Combustible Liquids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
其他客户在看
商品
Lentiviral vector systems prioritize safety features, with design precautions preventing replication. Good handling practices are essential for use.
Lentiviral vector systems prioritize safety features, with design precautions preventing replication. Good handling practices are essential for use.
Lentiviral vector systems prioritize safety features, with design precautions preventing replication. Good handling practices are essential for use.
Lentiviral vector systems prioritize safety features, with design precautions preventing replication. Good handling practices are essential for use.
实验方案
Lentivirus versions of genome modification technologies support successful CRISPR, RNAi, and ORF experiments.
Lentivirus versions of genome modification technologies support successful CRISPR, RNAi, and ORF experiments.
Lentivirus versions of genome modification technologies support successful CRISPR, RNAi, and ORF experiments.
Lentivirus versions of genome modification technologies support successful CRISPR, RNAi, and ORF experiments.
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