Table 2.
Effect of different culture conditions on lipid accumulation
| Media type | Interaction | n | Nile Red AFU | SEM |
|---|---|---|---|---|
| Continuous | None | 149 | 33.78 | ± 0.90 |
| 3-Step Sequential | None | 189 | 32.40 | ± 1.00 |
| Continuous | Early (6) | 80 | 39.34 | ± 1.17 |
| 3-Step Sequential | Early (6) | 101 | 37.88 | ± 1.27 |
| Continuous | Late (7) | 69 | 28.21 | ± 1.30 |
| 3-Step Sequential | Late (7) | 88 | 26.91 | ± 1.35 |
| Continuous | Additive | 112 | 29.38 | ± 0.90 |
| 3-Step Sequential | Additive | 163 | 27.82 | ± 0.74 |
| Continuous | No Additive | 37 | 38.18 | ± 1.56 |
| 3-Step Sequential | No Additive | 26 | 36.97 | ± 1.86 |
Embryos were cultured in designated treatment groups, then assessed for lipid content using Nile Red dye and quantified by mean arbitrary fluorescent units (AFU, mean ± SEM). There were no differences in the mean lipid content between the culture groups (P < 0.05).