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| Content Provider | Springer Nature Link |
|---|---|
| Author | Kinkel, Adrienne D. Fernyhough, Melinda E. Helterline, Deri L. Vierck, Janet L. Oberg, Karen S. Vance, Tyler J. Hausman, Gary J. Hill, Rodney A. Dodson, Michael V. |
| Copyright Year | 2005 |
| Abstract | Bovine adipofibroblasts, 3T3-L1 cells, L-6 myogenic cells, and sheep satellite cells were allowed to proliferate for 48 h. Oil red-O (ORO) was dissolved in three different solvents isopropanol, propylene glycol and triethyl phosphate. At 48 h, the proliferative cultures were stained with the three stains. ORO stain prepared in both propylene glycol and triethyl phosphate resulted in bright red droplets appearing in all cultures, whereas ORO dissolved in isopropanol was not taken up by any of the cells. These data suggest that certain preparations of ORO may stain cells in non-adipogenic lineages as well as undifferentiated pre-adipocytes. Caution must be exercised when choosing solvents for ORO in differentiation studies using cells of the fat/adipose lineage. |
| Starting Page | 49 |
| Ending Page | 56 |
| Page Count | 8 |
| File Format | |
| ISSN | 09209069 |
| Journal | Cytotechnology |
| Volume Number | 46 |
| Issue Number | 1 |
| e-ISSN | 15730778 |
| Language | English |
| Publisher | Kluwer Academic Publishers |
| Publisher Date | 2005-06-16 |
| Publisher Place | Dordrecht |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | Adipocyte Adipofibroblasts Cell culture Oil red-O Satellite cell Staining Biomedicine general Biotechnology Biochemistry Proteomics Cell Biology |
| Content Type | Text |
| Resource Type | Article |
| Subject | Cell Biology Clinical Biochemistry Bioengineering Biomedical Engineering Biotechnology |
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