1654 pT7A3-T3 DNA ligase
Cloning of 1654 pT7A3-T3 DNA ligase
[edit]Purpose: Cloning of 1654 pT7A3-T3 DNA ligase
Date: Jan , 2013
Notebook:
Page:
Clone ID: 1654
Experimenters: Shanyi
Results
[edit]contamination by accident(1532-4)
[edit]Cloning
[edit]PCR
Nde1 + Xho1
Colony screen
[edit]Cloning
[edit]PCR using contaminated T3 DNA ligase plasmid DNA as template and the following primers
New_T3_DNA_Lig-Nde1-F A1 cacgcaCATATGATGAACATCTTTAACACC
T3DNALigase-30 CTCGGAACTTCTCGAAGCTAGGGTGTCGCAGGGAGCCGTCCGGGGTCGCTTCCA
T3DNALigase-31 CTAGCTTCGAGAAGTTCCGAGGAACTGAGGACAACCCTCAAGAGAAAATGTAAC
T3DNALigase-32 TGATCGCTCGAGTTACATTTTCTCTTGAGGGTTGT
digest with Nde1 + Xho1
Colony screen
[edit]digest with Nde1 + Xho1
SEND 1654-3 TO SEQUENCE
Protein Expression
[edit]2013/3/29
SHANYI
| Lane |
Name |
Protein Name |
Clone ID |
Host |
Induction |
Purification |
pI/Mw |
| M |
PageRuler Plus Prestained protein ladder |
|
|||||
| 1 |
pT7A3-T4-G32 |
T4-G32 |
1097 |
5 ml, Nico21(DE3)plysN |
0.2 mM IPTG RT o/n |
Ni beads |
4.82 / 33506.43 |
| 2 |
pT7A3-MBP-(3c)-MutM |
MBP-(3c)-MutM |
1138 |
5 ml, |
0.2 mM IPTG RT o/n |
Ni beads |
8.68 / 30290.07+43.6 |
| 3 |
pT7A3-KOD |
KOD |
1458 |
5 ml, |
0.2 mM IPTG RT o/n |
Ni beads |
7.53 / 90022.42 |
| 4 |
pT7A3-UDG |
UDG |
1494 |
5 ml, |
0.2 mM IPTG RT o/n |
Ni beads |
5.45 / 27174.73 |
| 5 |
pT7A3-T7-Endo1 |
T7-Endo1 |
1505 |
5 ml, |
0.2 mM IPTG RT o/n |
Ni beads |
9.54 / 17171.84 |
| 6 |
pT7A3-polyAPol |
polyAPol |
1513 |
5 ml,
Nico21(DE3)plysN |
0.2 mM IPTG RT o/n |
Ni beads |
9.67 / 53870.91 |
| 7 |
pT7A3-T7-Exo |
T7-Exo |
1558 |
5 ml,
Nico21(DE3)plysN |
0.2 mM IPTG RT o/n |
Ni beads |
4.93 / 34502.20 |
| 8 |
pT7A3-MBP-(3C)-Exo-1 |
MBP-(3C)-Exo-1 |
1562 |
5 ml,
Nico21(DE3)plysN |
0.2 mM IPTG RT o/n |
Ni beads |
8.80 / 18143.72 |
| 9 |
pT7A3-MBP-(3C)-RnaseH |
MBP-(3C)-RnaseH |
1573 |
5 ml,
Nico21(DE3)plysN |
0.2 mM IPTG RT o/n |
Ni beads |
8.43 / 17596.99 +43.6 |
| 10 |
pT7A3-MBP-(3c)-E_coli_Endo IV |
MBP-(3c)-E_coli_Endo IV |
1593 |
5 ml,
Nico21(DE3)plysN |
0.2mM IPTG RT o/n |
Ni beads |
5.43 / 31479.53 +43.6 |
| 11 |
pT7A3-T3 DNA ligase |
T3 DNA ligase |
1654 |
5 ml,
Nico21(DE3)plysN |
0.2 mM IPTG RT o/n |
Ni beads |
5.14 / 39350.70 |
Protein Purification
[edit]1. Step gradient on 10 ml HisTrap column
Buffer A: 10 mM imidazole, 20 mM Tris-HCl pH 8.0 , 500 mM NaCl, 0.05 mM EDTA, 1 mM beta-ME
Buffer B: 500 mM imidazole, 20 mM Tris-HCl pH 8, 300 mM NaCl, 0.05 mM EDTA, 1 mM beta-ME
method 64
SDS-PAGE: 2013/4/11
| lane |
1 |
2 |
3 |
4 |
5 |
6 |
7 |
8 |
10 |
11 |
12 | ||||
| clone ID | 1458 |
Marker |
1654 |
1697 | |||||||||||
| name |
pT7A3-KOD |
pT7A3-T3 DNA ligase |
pCold-GST-(3c)-wt3C | ||||||||||||
| host |
Nico21DE3plysN |
Nico21DE3plysN |
Nico21DE3plysN | ||||||||||||
| induction |
0.2 mM IPTG 25oC o/n |
0.2 mM IPTG 25oC o/n
|
0.2 mM IPTG 25oC o/n | ||||||||||||
| purification |
10ml HisTrap HP |
10ml HisTrap HP |
10ml HisTrap HP | ||||||||||||
| MW |
7.53 / 90022.42 |
5.14 / 39350.70 |
21KD/8.47 | ||||||||||||
Combine fraction 31-68, concentrate to 20ml
2. Gel filtration on TSK 250 gel filtration.
Buffer: 50 mM Na-Phosphate, pH 7.4, 200 mM NaCl
SDS-PAGE: 2013-4-17
| lane |
1 |
2 |
3 |
4 |
5 |
6 |
7 |
8 |
9 |
10 |
11 |
12 | ||||
| clone ID | 1458 |
Marker |
1654 |
1711 |
1712 | |||||||||||
| name |
pT7A3-KOD |
pT7A3-T3 DNA ligase |
pET28b-hINFA2 h |
pLambda-hINFA2 | ||||||||||||
| host |
Nico21DE3plysN |
Nico21DE3plysN |
||||||||||||||
| induction |
0.2 mM IPTG 25oC o/n |
0.2 mM IPTG 25oC o/n |
||||||||||||||
| purification |
10ml HisTrap HP(2nd time) |
Bio-Sil TSK 250 |
||||||||||||||
| MW |
7.53 / 90022.42 |
5.14 / 39350.70 |
||||||||||||||
concentrate fraction 28 ~31using spin concentator
3. Dialyze twice overnight.
Dialysis Buffer:20 mM Tris-HCl pH7.5, 50 mM NaCl, 50% Glycerol , 0.1 mM EDTA
4. Store in a buffer (20 mM Tris-HCl pH7.5, 50 mM NaCl, 50% Glycerol, 0.1 mM EDTA, 1mM DTT) at -80oC (T7ligase box).
Concentration : 2 mg/ml


