Table 1.
Extraction steps | BP1 | BP2 | K | H1 | H2 | S |
---|---|---|---|---|---|---|
Lysis buffer/agent | STES buffer | TN150 buffer | Tissue lysis buffer and protinase K | Distilled water | Aqueous NaOH | TNES buffer and protinase K |
Cell lysis and homogenization | Bead beating | Bead beating | Incubation at 56 °C and vortexing | Boiling | Boiling | Incubation at 56 °C and vortexing |
Extraction and DNA precipitation | Phenol chloroform and cold absolute ethanol | Phenol chloroform and cold absolute ethanol | Mini column and washing buffer | Heat | Heat | Hypertonic NaCl and cold absolute ethanol |
Store in | TE buffer | TE buffer | Elution buffer | Distilled water | Aqueous NaOH | TE buffer |
Approximate time for completion | 7 ½ h | 8 h | 3 h | 25 min | 35 min | 11 h |
BP 1 Bead beater phenol chloroform with STES buffer, BP 2 Bead beater phenol chloroform with TN150 buffer, K DNeasy blood and tissue kit, H 1 Heat treating in distilled water, H 2 Heat treating in NaOH, S Salting out method