Supernatant was collected from mock- and VZV-infected qHPNCs (3 DPI), centrifuged, and flash frozen. The supernatant was thawed and added at 100% to uninfected qHPNCs or HCECs and replenished every 24 hours for 3 days. Coverslips were fixed and analyzed by immunofluorescence antibody assay (IFA) for adherens junction proteins.
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.