-80℃ for 6 months, avoid repeated freeze-thaw cycles.
Deliverables
1. Delivery of 3 ml of lentiviral vector containing three sgRNAs, with a viral titer greater than 1 × 10^7 TU/ml, and polybrene at 125 µl (8 µg/µl).
2. A report will be provided, including the sgRNA sequences, a schematic diagram of the lentiviral construct, and the selection marker.
3. Genomic amplification primers for the target gene.
CRISPR lentivirus Three in One Explanation
Product Advantages
1. Lower cost: The “three-in-one” product features a more streamlined manufacturing process, reducing production costs for companies and enabling researchers to save on experimental time and funding in this area.
2. Higher quality: Gene knockout is more stable, making it easier to obtain “monoclonal, homozygous” knockout cell lines.
3. Faster turnaround: Our ready-to-use products have already undergone pre‑validation of target sgRNAs.
Product Application
1. Functional deficiency studies: Systematically elucidating the essential roles of genes in physiological and pathological processes.
2. Disease model construction: Generating complete gene‑knockout phenotypes that mimic genetic disorders, cancers, or immune deficiencies.
3. Drug target validation: Using gene knockout approaches to assess the functional dependency and therapeutic potential of candidate targets.
4. Transgenic animal development: Generating gene‑knockout mice and other model organisms.
5. Exploration of drug resistance mechanisms: Identifying key genes associated with drug sensitivity.
