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

. 2024 Apr 8;14:8158. doi: 10.1038/s41598-024-58455-3

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

© The Author(s) 2024

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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.

PMC Copyright notice

Scatterplots of HRP2 (and HRP3, HRP2/3) antigen levels as compared with other Plasmodium antigens. Scatterplots represent data from all 7847 DBS which were assayed by bead-based multiplex assay for Plasmodium antigens. Antigen levels for HRP2/3 versus PfLDH (A), pAldolase (B), and pLDH (C). Red shading indicates DBS with depressed or absent HRP2/3 levels selected for subsequent pfhrp2 and pfhrp3 genotyping based on discordant antigen signal between HRP2 (HRP3) and the pan-Plasmodium antigens aldolase or LDH or the falciparum-specific LDH. It is not only discordance in terms of negative signal to HRP2 and positive to any of the others, but also if the level of HRP2 is lower than the level of the aldolase/LDH antigens, as described in the methods.