In the original publication [1], there were mistakes in Tables 1 and 2. Methods, qRT-PCR. The correct version is as follows:
qRT-PCR: The total RNA from the cells was extracted using TRIzol Reagent (15596018, Invitrogen, Waltham, MA, USA) following the manufacturer’s instructions. A BioTek Synergy HT microplate reader was used to determine RNA concentration. mRNA was quantified with TaqMan real-time qRT-PCR (7500 real-time PCR system, Applied Bio-systems, Foster City, CA, USA) by using a one-step RT-PCR Kit (Bio Rad, Hercules, CA, USA) with GAPDH (human cells) and Actb (mouse tissues) as reference genes in each reaction. The 2−ΔΔCt method was used for comparing the data [17,23]. Primer and probe sequences are listed in Table 1.
Table 1.
Primers and probes for qRT-PCR.
The authors state that the scientific conclusions are unaffected. This correction was approved by the Academic Editor. The original publication has also been updated.
Reference
- Ssengonzi, R.; Wang, Y.; Zhou, J.; Kayashima, Y.; Townley-Tilson, W.H.D.; Rao, B.; Ma, Q.; Maeda-Smithies, N.; Li, F. Inhibitor of DNA Binding Protein 2 (ID2) Mediates the Anti-Proliferative and Pro-Differentiation Effects of Insulin-like Growth Factor-1 (IGF-1). Life 2024, 14, 1663. [Google Scholar] [CrossRef] [PubMed]
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