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. 2019 Oct 28;9:15389. doi: 10.1038/s41598-019-51849-8

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© The Author(s) 2019

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/.

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SDS and heat are primary contributors to protein loss during the stripping process. Four sets of triplicate BMPA hydrogels with immobilized RNase-488 were exposed to (i) photobleaching only (control), (ii) just detergent (2% SDS), (iii) just heat (55–57 °C temperatures), or (iv) detergent and heat (2% SDS + 55–57 °C heat). At round 8, the combination of the detergent and heat condition had the greatest fluorescence intensity loss (61.1% ± 7.7%).