1392 pAAV-VP16-EBNA1c
Cloning of 1348 pLVX-EF1-VP16-EBNA1c
[edit]Purpose: Cloning of 1348 pLVX-EF1-VP16-EBNA1c
Date: 2012-9-7---2012-9-12
Notebook:
Page:
Clone ID: 1348
Experimenters: yingying lu
Results
[edit]Cloning
[edit]Date:
Gene synthesis this VP16 fragment
PCR out EBNA1C from 371 pCEP4 E02S CK2M EN2L, ~950 bp
9/7/2012:
PCR
9/8/2012 Digestion for cloning
Lane 2, 4, 6: TagGFP amplified with TagGFP-EcoR1-BamH1-F & TaqGFP-R3 using 110 pLVX-TagGFP as template as template
Lane #9: TagRFP amplified with TagRFP-EcoR1-BamH1-F gtattcgaattcGCGGCCGCggatccGTGTCTAAGGGCGAAGAGCTG
ATG AGC GGG GGC GAGGAGCTGTTCGCCGGCATCG
TagRFP-Xba1-R
(GCAAACTGGGGCACAAACTTAA TCTAGA CGATCAA)
TTG ATC GTC TAG ATT AAG TTT GTG CCC CAG TTT GC
Lane #10: PCR product VP16 + EBNA1c has this configuration: EcoR1 ---VP16--BamH1--EBNA1c--Xho1
Lane #12: A/WSN/33 M15/88E amplified
FluASeg-7-NdeI-F
actagc CAT ATG CAC CAT CAT CAT CAT CAT agtcttctaaccgaggtc
FluASeg-7-Xho1-R
(catcggtctcataggcaaatgCTCGAG atcaga)
tctgatCTCGAGcatttgcctatgagaccgatg
using 61 pHW2000-A/WSN/33 M15/88E as template
| 1 |
2 |
3 |
4 |
5 |
6 |
7 |
8 |
9 |
10 |
11 |
12 |
13 | |
| Plasmid ID |
1333 |
1334 |
1329 |
1330 |
1329 |
1368 |
254 |
1036 | |||||
| Plasmid or DNA Name |
TagGFP |
TagGFP |
TagGFP |
TagRFP |
VP16 + EBNA1c |
A/WSN/33 M15/88E |
|||||||
| Digestion |
EcoR1+ Xba1 |
EcoR1+ Xba1 |
EcoR1+ Xba1 |
EcoR1+ Xba1 |
EcoR1+ Xba1 |
EcoR1+ Xba1 |
EcoR1+ Xba1 |
EcoR1+ Xba1 |
EcoR1+ Xba1 |
BamH1 + Xho1 |
BamH1 + Xho1 |
Nde1 + Xho1 |
Nde1 + Xho1 |
cut out bands as indicated, purify and ligate using T7 ligase + 10X T4 ligase buffer.
transform DH5a
Colony Screening
[edit]2012-9-11
BamH1 + Xho1
no EBNA1c insert
Result intepretation/Summary
[edit]Conclusion
[edit]
== Cloning of 1399 pAAV--EBNA1c
[edit]Purpose: Cloning of 1392 pLVX-EBNA1c
Date: 2012-9-12
Notebook:0
Page:
Clone ID:1392
Experimenters: yingying
Results
[edit]cloning
[edit]lane 7: EBNA1c PCR product
lane 8: 254,pAAV.CMV-MCS, pAAV-MCS
BamH1 + Xho1
Colony Screening
[edit]Date: 2012-9-14
need to sequence: EBNA1c
pick clone 2 to sequence, right
cloning of 1392 pAAV-VP16-EBNA1c
[edit]lane1: VP16 insert
lane2: clone2-1399
EcoR1+BamH1
colony screen
[edit]2012-9-19
mini prep and digest detect EcoR1+BamH1 / BamH1 + Xho1
Result intepretation/Summary
[edit]- <br>
Conclusion
[edit]Note: the cloning vector for assembling VP16-EBNA1c is 254,pAAV.CMV-MCS, pAAV-MCS, not pLVX-EF1. Therefore, need to do subcloning.

