Table 1.
Organism | Input | Formaldehyde per sample | DNA purification method | Days for protocola |
---|---|---|---|---|
S. cerevisiae Standardb |
200 mL liquid culture | 5.5 mL | Phenol/chloroform extraction & ethanol precipitation | 3 |
S. cerevisiae Rapid |
20 OD∗mL pellet (from 25 mL culture) | 27 μL | MinElute column | 1.5 |
S. pombe Standardc |
100 mL liquid culture | 2.7 mL | Phenol/chloroform extraction & ethanol precipitation | 3 |
S. pombe Rapid |
20 OD∗mL pellet (from 25 mL culture) | 27 μL | MinElute column | 3 |
N. crassa Standard Ad |
Isolated nuclei from 500 mL conidia | None | MinElute column | 2 |
N. crassa Standard Be |
Isolated chromatin fraction from 50 mL conidia | 275 μL | Phenol/chloroform extraction & ethanol precipitation | 3 |
N. crassa Rapid |
50 mL conidia | 1.4 mL | MinElute column | 1 |
Number of days required to isolate mononucleosomal fragments from starting material (input)