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Technology at Applied Viromics 

Applied Viromics uses its advanced technologies to delivery the best quality viral vectors for your scientific research. Our carefully designed strategies and highly efficient process enable us to save you cost and time. We establish ourselves as reliable provider of viral vectors because of those techniques and our continuous effort to make them better. 

 
Viral vector, no matter it is adenovirus, AAV, retrovirus, or baculovirus, is first generated by introducing its shuttle plasmid into producing cells together with corresponding helper plasmid (or viral genome). Applied Viromics has optimized the viral production systems to completely avoid using helper virus, thus eliminating any chance of helper virus contamination.

Table below gives general description of viral production technologies used at Applied Viromics:

 

Virus Cell Used Plasmids Transfection  1st Stage 2nd Stage
Adenovirus HEK 293 Shuttle+Helper CaPO4 viral seed

amplify

  

AAV HEK 293 Shuttle+Helper CaPO4 viral vector

none

  

Retrovirus HEK 293 Shuttle+Helper CaPO4 viral vector

none

  

Baculovirus Sf9 insect cells Shuttle+wtBac genome Lipid viral plaques

plaque screen  and amplify

 

Toxic genes

Successful generation of viral vector is built upon our extensive knowledge of virology and experience in viral production. However, for toxic genes that kill producer cells, or genes that are found to interfere with viral replication, recombinant viral vectors cannot be made. 

When ordering your viral vector production, please let us know if you are aware of any toxicity of the gene. Besides communicating with you what we find during viral production process, we will repeat once if the first attempt fails. You will be charged 50% of the cost when viral vector can not be made in two attempts due to previously unknown toxicity. We have developed method to control toxic gene expression during viral production stage, and you have the option to try it. However, the chance of success is case-by-case. 

 
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