<p>Cells were treated with basal growth medium (GM) (A) or differentiation medium plus different concentrations of 1, 25 - (OH)<sub>2</sub>D<sub>3</sub>, 100 nM (B), 10 nM (C), 1 nM (D), 0.1 nM (E) or 0.01 nM (F) or differentiation medium (DM) (G). Oil Red O staining was performed on days 2, 4, 6, 8 and 10. Representative day 10 images are shown. Images were collected at 400x magnification. (H): Quantification of lipid accumulation in 3T3-L1 cells. Lipid accumulation was quantified using MetaMorph Image analysis software. Area fractions were collected for each treatment and normalized to control of corresponding time point. Data are means ± SE (n = 3). Different letters represent treatment effects that were significantly different (<i>P</i>...
<p>Oil red O staining of SK-N-BE(2) cells treated with 10058-F4 (60 µM), C-<i>m/z</i> 232 (90 µM), 1...
<p>(A, B) Control cells were grown in the basal culture medium. There was no staining with Oil Red O...
(A) Quantification of lipid content normalized by protein and (B) representative phase-contrast imag...
3T3-L1 preadipocytes were differentiated in D-MEM (1-methyl 3-isobutylxanthine, dexamethasone, and i...
<p>(A) Cells were photographed at days 0, 7 and 21 of their adipocytic differentiation after Oil Red...
<p>hMSCs maintained in adipogenic differentiation medium were stained with Oil Red - O to highlight ...
<p>(A) Microscopic observations of the stained lipid droplets. Treatment conditions were (i) non-ind...
<p>(A) Before and (B) after Oil red O staining. Treatment conditions were (i) non-induced control me...
<p>Cells were incubated in adipogenic differentiation medium without (A and C) and with 100 µg /ml P...
<p>(A) Representative micrographs showing intracellular lipid accumulation in L02 cells as stained b...
<p>(a) After differentiation cells were fixed and stained with oil red-O; images shown are 10x magni...
After 72 hours, lipid accumulation in 3T3-L1 cells treated with Red and Green Kratom (0–10 μg/mL) wa...
<p>A. Oil Red O staining of PGE<sub>2</sub>-treated 3T3-L1 cells. Cells (undifferentiated cells: U) ...
<p>3T3-L1 cells were grown on 35 mm dishes and transfected with Clk1 mutants as labeled. Following 6...
<p>Two-day post-confluent 3T3-L1 preadipocytes were cultured with differentiation medium in the abse...
<p>Oil red O staining of SK-N-BE(2) cells treated with 10058-F4 (60 µM), C-<i>m/z</i> 232 (90 µM), 1...
<p>(A, B) Control cells were grown in the basal culture medium. There was no staining with Oil Red O...
(A) Quantification of lipid content normalized by protein and (B) representative phase-contrast imag...
3T3-L1 preadipocytes were differentiated in D-MEM (1-methyl 3-isobutylxanthine, dexamethasone, and i...
<p>(A) Cells were photographed at days 0, 7 and 21 of their adipocytic differentiation after Oil Red...
<p>hMSCs maintained in adipogenic differentiation medium were stained with Oil Red - O to highlight ...
<p>(A) Microscopic observations of the stained lipid droplets. Treatment conditions were (i) non-ind...
<p>(A) Before and (B) after Oil red O staining. Treatment conditions were (i) non-induced control me...
<p>Cells were incubated in adipogenic differentiation medium without (A and C) and with 100 µg /ml P...
<p>(A) Representative micrographs showing intracellular lipid accumulation in L02 cells as stained b...
<p>(a) After differentiation cells were fixed and stained with oil red-O; images shown are 10x magni...
After 72 hours, lipid accumulation in 3T3-L1 cells treated with Red and Green Kratom (0–10 μg/mL) wa...
<p>A. Oil Red O staining of PGE<sub>2</sub>-treated 3T3-L1 cells. Cells (undifferentiated cells: U) ...
<p>3T3-L1 cells were grown on 35 mm dishes and transfected with Clk1 mutants as labeled. Following 6...
<p>Two-day post-confluent 3T3-L1 preadipocytes were cultured with differentiation medium in the abse...
<p>Oil red O staining of SK-N-BE(2) cells treated with 10058-F4 (60 µM), C-<i>m/z</i> 232 (90 µM), 1...
<p>(A, B) Control cells were grown in the basal culture medium. There was no staining with Oil Red O...
(A) Quantification of lipid content normalized by protein and (B) representative phase-contrast imag...