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. 2022 Jan 17;23(2):987. doi: 10.3390/ijms23020987

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© 2022 by the authors.

Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).

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Proteomic analysis of Hacl1⁻^/− mouse tissue. (A) Scatter plot of proteins identified and their fold change in Hacl1^−/− liver, kidney, and brain tissue compared to wild-type. Proteins with 1.5-fold change (p < 0.01) were chosen as significantly differentially regulated. (B) Percentage of differentially expressed proteins in Hacl1^−/− liver and kidney. (C) Hacl1 peptide abundance in mouse liver (* indicates p < 0.01).

Proteomic analysis of Hacl1⁻^/− mouse tissue. (A) Scatter plot of proteins identified and their fold change in Hacl1^−/− liver, kidney, and brain tissue compared to wild-type. Proteins with 1.5-fold change (p < 0.01) were chosen as significantly differentially regulated. (B) Percentage of differentially expressed proteins in Hacl1^−/− liver and kidney. (C) Hacl1 peptide abundance in mouse liver (* indicates p < 0.01).