Human Gene AAV Virus

Adeno-Associated Virus (AAV) vectors represent a forefront technology in the delivery of individual human genes for research and therapeutic purposes. Originating from a small, non-pathogenic virus belonging to the Parvoviridae family, AAV vectors have emerged as highly effective tools for gene transfer, owing to their unique features and favorable safety profile. One of the key advantages of AAV vectors is their broad tropism—the ability to infect multiple tissue types. This is largely modulated by the AAV capsid protein, with different serotypes (variations) of AAV demonstrating preferences for different tissues, such as muscle, liver, brain, or retina. Their ability to mediate long-term gene expression in a wide variety of cell types, including non-dividing cells, makes them particularly valuable in both basic science and clinical settings.

With our pioneering retrovirus production platform, Cellomics Technology, LLC, launched our new line of products, ElliteTrust Adeno-Associated Virus (AAV) collection of most individual human genes. AAV virus particles designed to carry individual human genes are an efficient gene delivery tool in the landscape of genetic research and R&D of therapeutic intervention. These engineered vectors leverage the natural ability of AAV viruses to mediate long-term gene expression in a wide variety of cell types, including non-dividing cells, making them particularly valuable in both basic science and clinical settings. For the delivery of individual human genes, the AAV virus vector is constructed to include the gene of interest under the control of a promoter that ensures appropriate expression in the target cells. The AAV virus particles are produced with latest recombinant AAV virus design, rendering them replication-deficient and safe for laboratory use. ElliteTrust AAV virus particles can be ordered individually or in the collection.

All ElliteTrust AAV viruses have been produced with our pioneering production platform and released after passing our strict and complete Quality-Control system. The performance of these AAV virus particles is guaranteed by their high efficiency in gene delivery to your target cells, enabling the study of gene function, regulation, and the development of gene therapies for various diseases. The application of individual human gene AAV virus particles spans basic research, where they are used to dissect gene functions, analyze gene regulatory networks, and model human diseases in cell cultures and animal models. 

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