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Ubigene has modified over 5000 genes from more than 200 cell lines with our exclusive innovation
CRISPR-U™ technology. At the same time, we already provide customers with high quality gene-editing
tools for cell or animal research worldwide.
With 14 years of experience, Ubigene has exclusively innovated and developed 6 product lines,
fullfilling all kinds of needs from researchers. Experiment process simplified, efficiency improved,
achieving our aim of 'Make genome editing easier'!
Lentivirus, different from regular retrovirus, can effectively infect cells in division and non-division, and the infection efficiency is very high, which is several times or even dozens of times that of traditional methods. Lentivirus has a wide range for host and can effectively infect many types of cells, such as neurons, hepatocytes, cardiomyocytes, tumor cells, endothelial cells, stem cells, etc. In addition, it also has the advantages of low immunogenicity and large gene capacity. It is a powerful tool for introducing foreign genes, and Lentivirus is often used to construct stable cell lines. While ensuring the Strong activity, high titer and stable expression of fluorescence/resistance genes of lentivirus vector, Ubigene adopts the third generation lentivirus packaging system for lentivirus packaging to make it safer.