<p>(<b>A</b>) Western blots detected expression of β-gal-V5 (112 kDa) and ARP2-V5 (54 kDa) in total cell lysates. (<b>B</b>) Normalized cell viability% of controls was assessed using MTT assays with 2×10<sup>4</sup> cells cultured in the absence of serum or transfected with <i>arp2</i> cDNA. Viability of these two treatment groups were assayed at 16, 24, 48, and 72 h timepoints. (<b>C</b>) Normalized cell viability% of controls assayed using a trypan blue exclusion method. Cells were cultured in the absence of serum or transfected with <i>arp2</i> cDNA and assayed at 16, 24, 48, 72, 96, and 120 h timepoints. Mean values are presented (n = 3, X ± S.E.M), <sup>#</sup><i>p</i><0.05, *<i>p</i><0.01, <sup>¶</sup><i>p</i><0.001 compared to contro...
<p>Hep G2 and SMMC7721 cells were incubated with ARG (0, 1.56, 12.5, 100 μM) for 12 h and 24 h respe...
<p>A. Protein level of Cyt-C was determined by Western blotting. Expression of Cyt-C was quantitated...
<p>Cells were treated by APRTP-Js for 240 s, 480 s and 720 s, and then cultured for 24 h. (A) Cells ...
<p>(<b>A</b>) Western blots detected expression of β-gal-V5 (112 kDa) and ARP2-V5 (54 kDa) in total ...
<p><b>(A) Knockdown of ARP2 protein expression.</b> Replicate monolayers of A549 cells were transfec...
<p>(A) Early apoptosis detection was measured by flow cytometry with an Annexin V apoptosis detectio...
<p>(A) Hep G2, SMMC7721 and LO2 cells treated with ARG (0, 1.56, 12.5, 100 μM) for 24 h were double-...
(A) K562 cells were transfected with control, ARG1 or ARG2 siRNA and incubated at 21% or 1% O2 for 4...
<p>A. Down-regulation of TROP2 induced cell apoptosis in Siha and CaSki cells. Cells were harvested ...
<p>(A, C) RBP2 expression was measured by western blotting. (B, D) Flow cytometry analysis of the ef...
(A) Bax and Bcl-2 protein expression in ARPE-19 under the pro-oxidants conditions treated for 24 h w...
<p><b>A.</b> MDA-MB-231 cells were treated with RL2 (0.2 mg/mL) for the indicated time followed by t...
<p>(A) Loss of cell surface ULBP2 expression in apoptotic compounds-treated cells. Jurkat cells (upp...
<p>(A) Cell viability examined by trypan blue exclusion in LNCaP (LN), LNb4 and PC-3 cells. (B) Dete...
<p>A375 cells were treated with the indicated concentrations of compound <b>1</b> (0.03 to 3 μM) or ...
<p>Hep G2 and SMMC7721 cells were incubated with ARG (0, 1.56, 12.5, 100 μM) for 12 h and 24 h respe...
<p>A. Protein level of Cyt-C was determined by Western blotting. Expression of Cyt-C was quantitated...
<p>Cells were treated by APRTP-Js for 240 s, 480 s and 720 s, and then cultured for 24 h. (A) Cells ...
<p>(<b>A</b>) Western blots detected expression of β-gal-V5 (112 kDa) and ARP2-V5 (54 kDa) in total ...
<p><b>(A) Knockdown of ARP2 protein expression.</b> Replicate monolayers of A549 cells were transfec...
<p>(A) Early apoptosis detection was measured by flow cytometry with an Annexin V apoptosis detectio...
<p>(A) Hep G2, SMMC7721 and LO2 cells treated with ARG (0, 1.56, 12.5, 100 μM) for 24 h were double-...
(A) K562 cells were transfected with control, ARG1 or ARG2 siRNA and incubated at 21% or 1% O2 for 4...
<p>A. Down-regulation of TROP2 induced cell apoptosis in Siha and CaSki cells. Cells were harvested ...
<p>(A, C) RBP2 expression was measured by western blotting. (B, D) Flow cytometry analysis of the ef...
(A) Bax and Bcl-2 protein expression in ARPE-19 under the pro-oxidants conditions treated for 24 h w...
<p><b>A.</b> MDA-MB-231 cells were treated with RL2 (0.2 mg/mL) for the indicated time followed by t...
<p>(A) Loss of cell surface ULBP2 expression in apoptotic compounds-treated cells. Jurkat cells (upp...
<p>(A) Cell viability examined by trypan blue exclusion in LNCaP (LN), LNb4 and PC-3 cells. (B) Dete...
<p>A375 cells were treated with the indicated concentrations of compound <b>1</b> (0.03 to 3 μM) or ...
<p>Hep G2 and SMMC7721 cells were incubated with ARG (0, 1.56, 12.5, 100 μM) for 12 h and 24 h respe...
<p>A. Protein level of Cyt-C was determined by Western blotting. Expression of Cyt-C was quantitated...
<p>Cells were treated by APRTP-Js for 240 s, 480 s and 720 s, and then cultured for 24 h. (A) Cells ...