Ultra Nuclease (Tag free) 全能核酸酶

Storage Solution: ≥250U/μl Ultra Nuclease (Tag free)、10mM Tris (pH7.4), 500mM NaCl, 2mM MgCl2, 50% glycerol

1. Sample preparation:

Adherent cells: Remove the medium, clean the cells with PBS, and remove the supernatant.

Suspension cells: Cells were collected by centrifugation, cleaned with PBS, centrifuged at 6,000rpm for 10min, and precipitates were collected.

Escherichia coli: The bacteria were collected by centrifugation, cleaned once with PBS, centrifuged at 8,000rpm for 5min, and precipitates were collected.

2. Sample treatment:

The collected cell precipitates are cleaved according to the ratio of mass (g) to volume (mL) to 1: (10~20). Cells can also be cleaved mechanically or chemically on ice or at room temperature (1g cells are about 109).

3. Enzyme addition:

the proportion of 1g cell precipitation digested by 250Units is required. You can also choose the addition plan according to the recommended dosage in the table above, increase the amount of enzyme within a certain range, and reduce the digestion time accordingly.

4. Supernatant acquisition:

The supernatant of cell lysis solution was obtained by centrifugation at 12,000rpm for 30min, and then subsequent related experiments were conducted.

Recommended reaction condition: