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. 2018 May 15;4:23. doi: 10.1038/s41421-018-0020-7

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© The Author(s) 2018

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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Fig. 1 — a Morphology of immortalized marmoset fetal liver cell line MHPCs at passage 30 (scale bar = 100 µm). b Growth curve of MHPCs at passages 30 and 80, and isolated primary cells. Primary refers to isolated primary cells. Data represent mean ± sem (n = 3). The calculation was based on the online software http://www.doubling-time.com/compute.php. c G-band staining analysis of MHPCs at passage 30 showed a normal 46 XY karyotype. d Confocal microscopic images for DAPI staining of the choromosomes during mitosis. e Measurement of telomere lengths in MHPCs at passages 30 and 80 with Q-FISH. Data represent mean ± sem (n = 30)