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Organism | Human |
Product Type | Viral Vector |
Tissue | |
Disease |
Applications
Lentivirus
Provides stable, long-term gene expression; ideal for both dividing and non-dividing cells.
AAV (Adeno-Associated Virus)
Offers high precision and low immunogenicity; perfect for targeted gene therapy.
Adenovirus
Delivers high-efficiency gene transfer; suitable for a broad range of cell types and short-term expression.
Our viral vector technology is revolutionizing research in virology, particularly in the study of nerve cells where traditional gene transfer methods fall short.
This cutting-edge tool, endorsed by esteemed publications like Science (2010) and others (2012), facilitates a myriad of experimental approaches.
We offer a range of recombinant viruses, including adenovirus, AAV (Adeno-Associated Virus), and lentivirus, supplied in high concentrations ideal for in vivo experiments.
These viruses empower researchers with precise control over gene expression for over 50 types of genes.
Moreover, our Cre-lox conditional gene silencing shRNA library, available with Cre On or Cre Off systems, expands research possibilities.
For targeting new genes, we provide Cre On and Cre Off shRNAs alongside our robust Cre On and Cre Off system viral vectors, ensuring comprehensive support for your research endeavors.
Cre-On and Cre-Off shRNAs targeting new genes are also available.
The Cre-On and Cre-Off systems are available for viral vector support. There are two types of vectors below.
@ 2024 . All rights reserved
@ 2024 . All rights reserved
