Human Gene Retrovirus

One of the key strengths of retrovirus-based vectors is their ability to mediate stable gene transfer, which is particularly valuable for applications requiring long-term gene expression, such as the correction of genetic disorders, making induced pluripotent stem cells, or engineering T cells for cancer immunotherapy. The integration of the transgene into the host genome ensures that the therapeutic effect can be sustained over time, potentially providing a lasting solution to genetic diseases.

With our pioneering retrovirus production platform, Cellomics Technology, LLC launces our new line of product, ElliteTrust MMLV retrovirus collection of most individual human genes. Retrovirus 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 retroviruses to integrate their RNA genome into the DNA of host cells, thereby facilitating the stable expression of the introduced genes. For the delivery of individual human genes, the retrovirus vector is constructed to include the gene of interest under the control of a promoter that ensures appropriate expression in the target cells. The retrovirus particles are produced with latest recombinant lentivirus design, derived from wild-type Moloney Murine Leukemia Virus (MMLV), rendering them replication-deficient and safe for laboratory use. ElliteTrust retrovirus particles can be ordered individually or in collection.

All ElliteTrust retrovirus have been produced with our pioneering production platform and released after passing our strict and complete Quality-Control system. The performance of these retrovirus particles are guaranteed on gene delivery to your target cells with high efficiency, enabling the study of gene function, regulation, and the development of gene therapies for various diseases. The application of individual human gene retrovirus particles spans both 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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