1151 pET30b-sso7d-ToughTaq
Cloning of pET30b-sso7d-ToughTaq
[edit]Purpose: Cloning of pET30b-sso7d-ToughTaq by gene synthesis
Date: 2012-06-13
Notebook:
Page:
Clone ID: 1151
Experimenters: Jennifer Truong
Results
[edit]Cloning
[edit]Date: June 13, 2012
Synthesized template in 3 fragments (KTaq1, KTaq1 and KTaq3), PCR with KAPA enzyme for 5 cycles with 15 seconds extension time, conbined them, added first (KTaq1-1) and last (KTaq3-14) oligos , PCR with KAPA enzyme for 20 cycles with 45 seconds extension time. Ran gel (lanes 1-4), supposed to be ~1.7 kb
Reamplified 1151 (see lanes 1-3) in fragments
Lane 1: KTaq1-1 - KTaq1-16 (636 bp)
Lane 2: KTaq2-1 - KTaq2-16 (629 bp)
Lane 3: KTaq3-1 - KTaq3-14 (487 bp)
Unsuccessful
Date: June 14, 2012
Reamplified PCR product, see gel lanes 1-3
Lane 1: KTaq1-1 - KTaq1-16 (636 bp)
Lane 2: KTaq2-1 - KTaq2-16 (629 bp)
Lane 3: KTaq3-1 - KTaq3-14 (487 bp)
Successful amplifacation, cut out each band, purify each, join them together by Gisbon (~1.67 uL of each fragment, ran gel of joined template
Expected size (~1.9 kb)
Subcloing ToughTaq from 1094 pET30b-ToughTaq to pET30b-sso7d-NK 369 using Kpn1 + Xho1
Digested ToughTaq and vector 369 with Kpn + Xho1, cut out bands, and purified DNA.
Ligating over night
Date: June 15, 2012
Transformed the ligated DNA from yesterday with DH5 alpha cells and plated on KAN plates
Also, redid the PCR amplication using PHUSION to join the fragments (1 min 30 sec extension time, 20 cycles) instead of Gibson
Cut out band (~1.9 kb) and purified DNA, Digested ToughTaq and vector 369 with Kpn + Xho1
Cut out the digestion (see lanes 3 and 4), purified and ligated for 2 hours
Transformed the ligated DNA with DH5 alpha cells and plated on KAN plates
Date: June 22, 2012
Combined by Gibson, no band (expected: 1.9kb)
Date: June 25, 2012
Ran gel for PCR product of fragments joined with PCR and ligase
No clear band where it is supposed to be (expected = 1.9 kb)
Colony Screening
[edit]All negative, need to reclone
Digested 1151 with enzymes, incorrect band size (lanes 5 and 6)
Date: June 21, 2012
Digested 1151 with enzymes, did not run gel long enough. Redigest sample 5 (lane 5), may be the correct size?
Redigested samples 5 and 6, band is supposed to be 1.7 kb, may send sample 5 to sequencing
Result intepretation/Summary
[edit]Conclusion
[edit]
Cloning of 1151 pET30b-sso7d-ToughTaq
[edit]Purpose: Cloning of 1151 pET30b-sso7d-ToughTaq
Date: 2012-7-9---2012-7-12
Notebook:0
Page:
Clone ID:1151
Experimenters: yingying
Results
[edit]cloning
[edit]Gene synthesis 3 fragments,
lane1: KTaq1-1+KTaq1-16;
lane2: KTaq2-1+KTaq2-16;
lane3: KTaq3-1+KTaq3-14;
lane1:PCR using phusion
tempalte:PCR1+PCR2+PCR3
primer:KTaq1-1+KTaq3-14;
| lane 3 |
lane 4 | |
| PCR product |
pET30b-sso7d-NK 369 | |
| enzymes |
Kpn1 + Xho1 | |
Colony Screening
[edit]Date: 2012-7-12
Make miniprep and digest with Kpn1 + Xho1
clone 1,2,3,4,5,6,7,8,9 may be right, need to sequence
Result intepretation/Summary
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Conclusion
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