Buffer type |
Buffer comparisons |
No of expts |
OPT buffer selection |
HM buffer selection |
Equilibration |
No buffer < GA-BK |
3 of 3 |
GA-BK |
P-BK2 |
P-BK1 < GA-BK |
4 of 6 |
|
P-BK2 = GA-BK |
2 of 2 |
Resuspension |
P-P1 > GA-A1 |
3 of 4 |
P-P1 |
P-P1 |
Lysis |
P-P2 < GA-A2 |
3 of 4 |
GA-A2 |
P-P2 |
Neutralization |
P-P3-1 < GA-A3 |
3 of 4 |
GA-A3 |
P-P3-2 |
P-P3-2 < GA-A3 |
2 of 4 |
Pre-wash |
P-W1 = GA-W1 |
2 of 4 |
P-W1 |
P-W1 |
Wash |
P-W2-1 > GA-W2 |
3 of 4 |
P-W2-1 |
P-W2-1 |
P-W2-2 < GA-W2 |
2 of 4 |
Elution |
P-EB1 = GA-EB |
2 of 4 |
P-EB2 |
P-EB2 |
P-EB2 > GA-EB |
3 of 4 |
P-EB3 < GA-EB |
3 of 3 |
[DNA] concentrations were measured in three separate readings using IMPLEN
Nanophotometer P330. Independent T-test was used to determine the statistical
significance of the differences between test buffers and generic brand A buffers.
Differences in [DNA] were determined when p<0.05 |