Viral Vector Design Service
Viral vectors can bring genetic material into cells. The principle is to use the molecular mechanism of viruses to transmit their genomes into other cells for infection. It can occur in a whole living body (in vivo) or in cell culture (in vitro). It can be applied to basic research, gene therapy or vaccine. Genes transferred via viral vectors dominate clinical trials of gene therapy because they are more effective and specific than physical and chemical methods.
Classifications of viral vector
Viral vectors can be divided into two types: integrated and non-integrated viral vectors. Integrated viral vectors can be integrated into the human genome, including lentivirus, adeno-associated virus and retroviral vectors. Non-integrating vectors (such as adenovirus vectors) remain in the nucleus, but are not integrated into chromosomal DNA. Therefore, transgenes are easily lost during cell division, and the expression of foreign genes is transient.
CD BioSciences provides comprehensive viral vectors and cutting-edge viral vector technologies for basic research and preclinical applications, including designing and constructing suitable viral vectors and producing viral vectors from small-scale to large-scale.
- Lentiviral vector design service
Lentivirus is a special type of retrovirus. CD BioSciences provides lentivirus design services to ensure long-term expression and effective transfer without causing inflammation.
- Adenovirus vector design service
CD BioSciences provides lentivirus design services. Its advantage is that it can make most cells easily infected and has a relatively high titer.
- Herpes simplex virus vector design service
CD BioSciences provides lentivirus design services, which can be used for continuous expression and broad-spectrum effects, making it an important candidate virus for gene delivery.
- Vaccinia virus vector design service
CD BioSciences provides vaccinia virus vector design services. Its immunostimulatory properties make vaccinia virus an attractive immunotherapy for cancer treatment.
- Adeno-associated virus vector design service
CD BioSciences provides AAV vectors characterized by molecular engineering and directed evolution to produce powerful delivery vectors with enhanced characteristics for the treatment of human diseases.
Our service items
|Project name||Viral vector design service|
✓ Lentiviral vector design service
✓ Adenovirus vector design service
✓ Herpes simplex virus vector design service
✓ Vaccinia virus vector design service
✓ Adeno-associated virus vector design service
|Product delivery mode||We will complete the project on time according to the agreed time, summarize the experimental data and conclusions, and complete the experimental report.|
Why choose us?
CD BioSciences provides professional viral vector design service to meet the needs of regular customers to identify hits on time and on budget. CD BioSciences relies on world-class cell engineering technology expertise, we provide customers with the best quality one-stop viral vector design service, including the development of experimental programs according to different experimental needs. In addition to designing, constructing and cloning customized plasmids for the production of viral vectors, CD BioSciences also utilizes a variety of technical and scientific talents to provide comprehensive consulting services for the selection of viral vectors for gene therapy. Please feel free to contact us for more detailed information, our scientists will tailor the most reasonable plan for your project.