CaMKII-GFP Lentivirus

Lentivirus has many advantages as a gene therapy vector in the field of medicine and bioengineering, which makes it one of the common choices in gene therapy. The following are its main advantages: 1. Wide range of cell infection ability Lentivirus can infect many types of cells, including dividing and non-dividing cells. Compared with other viral vectors (such as adenovirus), lentivirus is particularly suitable for treating diseases involving non-dividing cells, such as neurological diseases or certain myocardial cell damage. 2. Long-term stable expression Lentivirus can integrate the target gene into the genome of the host cell, so that the target gene can be expressed stably for a long time. This feature makes it very useful in the treatment of chronic diseases, genetic diseases, etc. that require long-term gene expression. 3. Low immunogenicity Compared with other viral vectors (such as adenovirus), lentivirus causes relatively weak immune response, so it is more suitable for in vivo gene therapy. Lower immunogenicity helps to avoid strong immune rejection, thereby improving the safety and effectiveness of treatment. 4. Large load capacity Lentivirus has a large gene load capacity and can carry relatively long exogenous genes (usually around 8kb). This makes it suitable for delivering larger therapeutic genes or multiple gene modules. 5. Relatively safe Although lentiviruses integrate into the host genome, their design has been highly modified to make them safer, reducing the risk of random insertions into the genome that may cause cancer or genomic instability. In particular, by removing most of the original viral genes, the replication ability of the lentiviral vector is also completely deleted, reducing safety risks.