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. 2020 Aug 3;11:334. doi: 10.1186/s13287-020-01847-9

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© The Author(s) 2020

Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 4 — Generation and characterization of HLA-A knockout iPSCs. a Clone morphology after electroporation. b DNA sequencing results of knockout cell lines showed the double peak phenomenon. c DNA sequencing results showed the deletion loci. d Western blot analysis revealed HLA-A knocked out in iPSCs. e HLA-A^−/−-iPSCs had alkaline phosphatase activity and were positive for Oct3/4, Sox2, and SSEA4