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Xenobiotica
the fate of foreign compounds in biological systems
Volume 50, 2020 - Issue 5
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Correction

Correction

This article refers to:
Phase II enzyme induction by α-lipoic acid through phosphatidylinositol 3-kinase-dependent C/EBPs activation

Article title: Phase II enzyme induction by α-lipoic acid through phosphatidylinositol 3-kinase-dependent C/EBPs activation

Authors: Ki, SH & Kim, SG

Journal: Xenobiotica

Bibliometrics: Volume 38, Number 6, pages 587–604

DOI: http://dx.doi.org/10.1080/00498250802126920

When the above article was published, was incorrect.

Figure 3B. Immunocytochemistry. C/EBPα, C/EBPβ, and C/EBPδ were immunochemically localized using their specific antibodies. The same fields were counter-stained with DAPI to verify the location and integrity of nuclei.

Figure 3B. Immunocytochemistry. C/EBPα, C/EBPβ, and C/EBPδ were immunochemically localized using their specific antibodies. The same fields were counter-stained with DAPI to verify the location and integrity of nuclei.

The correct figure is shown here:

Confocal microscopy

Briefly, H4IIE cells were grown on a coverslip and fixed in a 4% paraformaldehyde solution, followed by permeabilization with 0.1% Triton X-100. The cell samples were immunostained with antibodies directed against C/EBPα (sc-61), C/EBPβ (sc-150), and C/EBPδ (sc-515028) overnight, followed by incubation with either Alexa Fluor® 555 goat anti-rabbit or anti-mouse IgG (Invitrogen). After incubation, the samples were cover-slipped with mounting media. The samples were examined using a laser-scanning confocal microscope (A1, Nikon instruments Inc., NY, USA).

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