Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2021 Jan 26;7:24. doi: 10.1038/s41420-020-00379-8

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© The Author(s) 2021

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

PMC Copyright notice

Fig. 1 — a Immunofluorescence staining of Viral E protein in HTR-8 (HTR-8/SVneo) cells 72 h postinfection with 0.1 multiplicity of infection (MOI) recombinant MR strain (r-MRV) or PRVABC-59 (PRV) or uninfected vehicle cells. Nuclei were stained with DAPI and ZIKV E protein stained with rabbit polyclonal primary antibody and Alexaflour 488-conjugated ant-rabbit secondary antibody. b Western blot analysis showing increased expression of viral E protein, 16–24 h postinfection when compared to uninfected vehicle cells in JEG-3, JAR, and HTR-8. β-Actin was used as a loading control.