Upregulation of Pluripotency Markers in Adipose Tissue-Derived Stem Cells by miR-302 and Leukemia Inhibitory Factor

<table>(a) RT-PCR analysis of the expression of pluripotency markers in the freshly isolated (ADSC P0) and third-passaged ADSCs (ADSC P3), (b) quantitative real-time PCR analysis for the expression of<i> OCT4</i>,<i> Sox2</i>, and<i> Nanog</i> mRNAs in the freshly isolated (ADSC P0) and third-passaged ADSCs (ADSC P3) using <i>β</i>-tubulin (<i>Tubb5</i>) mRNA level as an internal control. <svg height="11.375" id="M1" style="vertical-align:-0.30096pt" version="1.1" viewbox="0 0 58.712502 11.375" width="58.712502" xmlns="http://www.w3.org/2000/svg" xmlns:xlink="http://www.w3.org/1999/xlink">
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</svg> was considered as significant.</table>

BioMed Research International

fig2

Figure 2

Figure 2: Upregulation of Pluripotency Markers in Adipose Tissue-Derived Stem Cells by miR-302 and Leukemia Inhibitory Factor 