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An editable high resolution scientific image depicting Viral Plaque Assay Protocol

Viral Plaque Assay Protocol

Description

This template was adapted from the original submission. Edits were made to enhance scientific accuracy, optimal usability and/or to meet industry-leading design standards for science communication. This figure describes a general protocol for performing a viral plaque assay. First, cells are grown to near confluency in a 12 well plate. Once cells reach confluency, media is removed and 50 μL of serially diluted virus is added to each well. Phosphate-buffered saline (PBS) is added to one well as a control. Following 1 hr incubation at 37°C and 5% CO2, 3 ml of growth media overlay agar is added to each well, and the wells are incubated for 48 hrs at 37°C and 5% CO2. Afterwards, 1 ml of 4% PFA is deposited onto the overlay and left for 1 hr at room temperature. Lastly, 1 ml of crystal violet is added to each well and incubated for 5 minutes. Wells can then be rinsed and observed.

Acknowledgements

References

Andersson, T. (2020) Plaque Assay: A Method to Determine Viral Titer as Plaque Forming Units (PFU). Journal. https://www.jove.com/science-education/10514/plaque-assay-method-to-determine-viral-titer-as-plaque-forming-units
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