<p>β-actin was used as an internal control. PBMC was used as a positive control. DNase treated RNA without adding reverse transcriptase was used as a negative control (NC).</p
<p>(A and B) K562 cells were treated with 0, 2, 4, 6 or 8 μM NC for 2 days, or 8 μM NC for 0, 4, 8, ...
<p>(<b>A, B</b>) Ovarian cancer cells were treated with siRNA for 48 h, total RNA was extracted for ...
<p>A. Cells derived from treatment-resistant GSC clones were treated with RT (12 Gy or 1.5 Gy) in th...
<p>18S was used as an internal control. Raji was used as a positive control. DNase treated RNA witho...
<p>A, IgG protein was expressed in sarcoma cells. FBS was used as a negative control and human IgG (...
<p>(<b>A</b>) <b>mRNA expression of the </b><b><i>AFAP1L1</i></b><b> gene in sarcoma cell lines.</b>...
<p>(A) RT-PCR analysis showing mRNA expression levels of a panel of chemokines and chemokine recepto...
<p>β-actin was used as a control. Data is shown as fold change which is the normalized expression of...
<p>The expression levels for genes were normalized by their untreated counterparts. Each sample was ...
<p>AID transcription was monitored with RT-PCR in a control cell line, Jurkat, and in a Jurkat-AID c...
<p>(A) RT-PCR analysis showing mRNA expression levels of TLRs 1–10 from untransduced and Ad-transduc...
<p>A. Beas2B cells were transfected with either control siRNA or siRNAs specific to G<sub>α16</sub> ...
<p>The expression levels of WT and R233K AQP0 in HEK 293t cells. Western blots were performed with t...
<p>(A) RT-PCR analysis examined the expression of endogenous Oct3/4, Sox2, Nanog, Klf4, c-Myc, as we...
<p>(<b>A</b>) Total RNA from four human cancer cell lines of different tissues, AZ521 (a human color...
<p>(A and B) K562 cells were treated with 0, 2, 4, 6 or 8 μM NC for 2 days, or 8 μM NC for 0, 4, 8, ...
<p>(<b>A, B</b>) Ovarian cancer cells were treated with siRNA for 48 h, total RNA was extracted for ...
<p>A. Cells derived from treatment-resistant GSC clones were treated with RT (12 Gy or 1.5 Gy) in th...
<p>18S was used as an internal control. Raji was used as a positive control. DNase treated RNA witho...
<p>A, IgG protein was expressed in sarcoma cells. FBS was used as a negative control and human IgG (...
<p>(<b>A</b>) <b>mRNA expression of the </b><b><i>AFAP1L1</i></b><b> gene in sarcoma cell lines.</b>...
<p>(A) RT-PCR analysis showing mRNA expression levels of a panel of chemokines and chemokine recepto...
<p>β-actin was used as a control. Data is shown as fold change which is the normalized expression of...
<p>The expression levels for genes were normalized by their untreated counterparts. Each sample was ...
<p>AID transcription was monitored with RT-PCR in a control cell line, Jurkat, and in a Jurkat-AID c...
<p>(A) RT-PCR analysis showing mRNA expression levels of TLRs 1–10 from untransduced and Ad-transduc...
<p>A. Beas2B cells were transfected with either control siRNA or siRNAs specific to G<sub>α16</sub> ...
<p>The expression levels of WT and R233K AQP0 in HEK 293t cells. Western blots were performed with t...
<p>(A) RT-PCR analysis examined the expression of endogenous Oct3/4, Sox2, Nanog, Klf4, c-Myc, as we...
<p>(<b>A</b>) Total RNA from four human cancer cell lines of different tissues, AZ521 (a human color...
<p>(A and B) K562 cells were treated with 0, 2, 4, 6 or 8 μM NC for 2 days, or 8 μM NC for 0, 4, 8, ...
<p>(<b>A, B</b>) Ovarian cancer cells were treated with siRNA for 48 h, total RNA was extracted for ...
<p>A. Cells derived from treatment-resistant GSC clones were treated with RT (12 Gy or 1.5 Gy) in th...