3T3-L1 preadipocytes were differentiated in D-MEM (1-methyl 3-isobutylxanthine, dexamethasone, and insulin) medium for 7 days. Triglyceride accumulation visualized by Oil-Red O staining. Mature adipocytes show red large lipid vacuoles that occupied most of the cytoplasm. Original magnification: 400x.</p
<p>Oil Red O staining of cholesterol in renal tissues from control, diabetic (DM), and diabetic neph...
The 3T3-L1 cell line, derived from 3T3 cells, is widely used in biological research on adipose tissu...
<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>Cells were treated with basal growth medium (GM) (A) or differentiation medium plus different con...
<p>A) Non-differentiated cells. B) Cells with ten days of differentiation. C) Cells in <i>oil </i><i...
<p>OP9 cells were incubated in medium containing IO or TGZ for the periods indicated. The cells were...
<p>(A) Phase contrast images of 3T3-L1 cells from induction (day 0) to ten days post-induction. Cell...
<p>(A) Before and (B) after Oil red O staining. Treatment conditions were (i) non-induced control me...
<p>P-values are indicated with ** when p<0.01 and *** when p<0.001, bars without a star were not fou...
<p>(A) The lipid droplet of cells cultured in adipogenic medium for 21 days. (B) Staining was not ob...
<p>Two-day post-confluent 3T3-L1 preadipocytes were cultured with differentiation medium in the abse...
<p>MSC were induced to adipogenic differentiation for 15 days. (<b>A</b>) Oil Red O staining showed ...
<p>The PIP cells were grown at 37°C for 4 days, and subsequently fed with differentiation medium for...
<p>Immortalized non-diabetic preadipocytes (NPADs) and diabetic preadipocytes (DPADs) were incubated...
<p>Oil Red O staining of cholesterol in renal tissues from control, diabetic (DM), and diabetic neph...
The 3T3-L1 cell line, derived from 3T3 cells, is widely used in biological research on adipose tissu...
<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>Cells were treated with basal growth medium (GM) (A) or differentiation medium plus different con...
<p>A) Non-differentiated cells. B) Cells with ten days of differentiation. C) Cells in <i>oil </i><i...
<p>OP9 cells were incubated in medium containing IO or TGZ for the periods indicated. The cells were...
<p>(A) Phase contrast images of 3T3-L1 cells from induction (day 0) to ten days post-induction. Cell...
<p>(A) Before and (B) after Oil red O staining. Treatment conditions were (i) non-induced control me...
<p>P-values are indicated with ** when p<0.01 and *** when p<0.001, bars without a star were not fou...
<p>(A) The lipid droplet of cells cultured in adipogenic medium for 21 days. (B) Staining was not ob...
<p>Two-day post-confluent 3T3-L1 preadipocytes were cultured with differentiation medium in the abse...
<p>MSC were induced to adipogenic differentiation for 15 days. (<b>A</b>) Oil Red O staining showed ...
<p>The PIP cells were grown at 37°C for 4 days, and subsequently fed with differentiation medium for...
<p>Immortalized non-diabetic preadipocytes (NPADs) and diabetic preadipocytes (DPADs) were incubated...
<p>Oil Red O staining of cholesterol in renal tissues from control, diabetic (DM), and diabetic neph...
The 3T3-L1 cell line, derived from 3T3 cells, is widely used in biological research on adipose tissu...
<p>(A) Cells were photographed at days 0, 7 and 21 of their adipocytic differentiation after Oil Red...