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. 2020 Sep 30;10:16167. doi: 10.1038/s41598-020-73285-9

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© The Author(s) 2020

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/.

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Comparison of conventional and teabag purification of five different membrane proteins. Each panel shows the results from side-by-side comparison of conventional and teabag purifications, respectively. SDS-PAGE with conventional (left) and teabag (right) purification, and SEC profiles with conventional purification (blue) and teabag purification (red). (a) Human ClC-1 chloride channel; (b) human PAR2; (c) Monodelphis domestica KCC2; (d) Clostridium bolteae MraY; (e) human AQP10. For each pairs of SDS-PAGE images, comparable amounts of protein have been loaded and the brightness and contrast is equal and applied across the entire image, non-cropped SDS-PAGE images are provided in the Supplementary Material.