MS 6 7 2017

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Culture 1498 Taq DNA Ligase 200ml.

Culture 1497 sso7d-ToughTaq 8L, induce with IPTG.

Spin down 1946 TdT bovine.

Prepare LB media 20L.

Prepare LB/K agar and LB/K/C agar.

Plasmid transformation. 1942 phi 29, 1601 6His-GST-i3C, 1518 T3 Ligase, 1765 T4 DNA Polymerase.

Wash Ni column (load with 1464 T7 DNA Ligase) with Ni washing buffer / Tris-HCl / Buffer B, dilute and load onto QHP column.

Elute 1464 T7 DNA Ligase with Buffer B 06/07/2017

-0.19
-0.21
-0.02
1.36
2.34
(1~5)
7.36
3.66
1.11
0.65
0.34
(6~10)
0.15
0.09
0.06
0.03
0.01
(11~15)

Collect 4~11.

1708 Cre Recombinase 1:1 dilute with SP Dilution Buffer. SP FF column wash with SP Elution Buffer and SP Wash Buffer, then load Cre onto SP FF column.