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. Author manuscript; available in PMC: 2016 Apr 1.
Published in final edited form as: Curr Protoc Hum Genet. 2015 Apr 1;85:13.11.1–13.11.9. doi: 10.1002/0471142905.hg1311s85

Figure 1.

Figure 1

NSC plating and virus dilution for cell viability and viral progeny production assay. To assess the optimal titer of adenovirus for NSC infection, NSCs can be seeded in the 24 well plate with 2×104 cells in each well followed by different virus titers (from 0.1 to 1,000). Each virus titer should be evaluated in triplicates to minimize experimental errors.