Fifty thousand cells seeded in 48-well plates were incubated in the presence of rAAV2/1 at a multiplicity of infection of 103 vg/cell in serum-free medium containing human adenovirus 5 (H5) reference material (ATCC VR-1516; titer 5.8 × 1011 particle forming units (pfu)/ml) (LGC Standards, Teddington, Middlesex, UK) at the multiplicity of infection of 50 particle forming units (pfu)/cell. After 2 hours, the cells were rinsed with serum-supplemented medium and further cultured for 72 hours without passaging in culture medium containing or not Dox at the indicated concentration.
Do you have any questions about this protocol?
Post your question to gather feedback from the community. We will also invite the authors of this article to respond.
Tips for asking effective questions
+ Description
Write a detailed description. Include all information that will help others answer your question including experimental processes, conditions, and relevant images.