Team:Shenzhen SZMS/Lab
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- | [[Team:Shenzhen SZMS|<<Back to main page]] | + | {| class="wikitable" align=center |
- | =Schedule= | + | |align=center width=12.5%|[[Team:Shenzhen SZMS|Home]] |
+ | |align=center width=12.5%|[[Team:Shenzhen SZMS/Team Members|Team Members]] | ||
+ | |align=center width=12.5%|[[Team:Shenzhen SZMS/Project|Project]] | ||
+ | |align=center width=12.5%|[[Team:Shenzhen SZMS/Modelling|Modelling]] | ||
+ | |align=center width=12.5%|[[Team:Shenzhen SZMS/Lab|Lab]] | ||
+ | |align=center width=12.5%|[[Team:Shenzhen SZMS/iGem Safety Q&A|Safety]] | ||
+ | |align=center width=12.5%|[[Team:Shenzhen SZMS/Gallery|Gallery]] | ||
+ | |align=center width=12.5%|[[Team:Shenzhen SZMS#Human Practice|Human Practice]] | ||
+ | |} | ||
+ | |||
+ | [https://2014hs.igem.org/Main_Page<br> <<Back to wiki main page] | ||
+ | ---- | ||
+ | Here you can find out how we build our plasmid. The plasmid map and information of parts used is given in [[Team:Shenzhen SZMS/Project]]. | ||
+ | |||
+ | ==Schedule== | ||
{| class="wikitable" | {| class="wikitable" | ||
|- | |- | ||
!width=50px|No. !!width=300px| Procedure !!width=100px|Backbone !!width=250px| Status of the Plasmid | !width=50px|No. !!width=300px| Procedure !!width=100px|Backbone !!width=250px| Status of the Plasmid | ||
|- | |- | ||
- | + | |1 | |
- | + | |[K115016] Spe1,Pst1 Double Digestion, Electrophoresis detection,DNA refinement;[C0051] X ba1,Pst1Double Digestion, Gel extraction;Combination | |
- | + | |1C3(K115016) | |
- | + | |[K115016+C0051] | |
|- | |- | ||
- | + | |2 | |
- | + | |[J23106] Spe1,Pst1 Double Digestion, Electrophoresis detection,DNA refinement;[K115016+C0051] X ba1,Pst1Double Digestion, Gel extraction;Combination | |
- | + | |1A2(J23106) | |
- | + | |J23106+[K115016+C0051] | |
|- | |- | ||
- | + | |3 | |
- | + | |[J2s3106+ K115016+C0051] EcoR1,Spe1Double Digestion, Electrophoresis detection,DNA refinement;[B0051] EcoR1,Xba1 Electrophoresis detection,DNA refinement;Combination | |
- | + | |1C3(B0015) | |
- | + | |[J23106+K115016+C0051]+B0015 | |
|- | |- | ||
- | + | |4 | |
- | + | |[B0030] Spe1,Pst1 Double Digestion, Electrophoresis detection, DNA refinement;[EC:1.7.7.2] Xba1, Pst1Double Digestion, Gel extraction;Combination | |
- | + | |1A2(B0030) | |
- | + | |B0030+EC:1.7.7.2 | |
|- | |- | ||
- | + | |5 | |
- | + | |[R0051] Spe1, Pst1Double Digestion, Electrophoresis detection,DNA refinement;[B0030+ EC:1.7.7.2] Xba1,Pst1 Double Digestion, Gel extraction;Combination | |
- | + | |1A2(R0051) | |
- | + | |R0051+[B0030+ EC:1.7.7.2] | |
|- | |- | ||
- | + | |6 | |
- | + | |[B0030] Spe1, Pst1Double Digestion, Electrophoresis detection,DNA refinement;[K145015] Xba1,Pst1Double Digestion, Gel extraction; Combination | |
- | + | |1A2(B0030) | |
- | + | |B0030+K145015 | |
|- | |- | ||
- | + | |7 | |
- | + | |[B0030+ K145015] EcoR1, Spe1Double Digestion, Electrophoresis detection,DNA refinement;[B0015] EcoR1, Xba1Double Digestion,Electrophoresis detection,DNA refinement;Combination | |
- | + | |1C3(B0015) | |
- | + | |[B0030+ K145015]+B0015 | |
|- | |- | ||
- | + | |8 | |
- | + | |[R0051+B0030+ EC:1.7.7.2] Spe1, Pst1Double Digestion,Gel extraction;[B0030+ K145015+B0015]Xba1, Pst1 Gel extraction;Combination | |
- | + | |1C3(B0030+K145015+B0015) | |
- | + | |[R0051+B0030+ EC:1.7.7.2]+[B0030+K145015+B0015] | |
|- | |- | ||
- | + | |9 | |
- | + | |[K115017] Spe1, Pst1Double Digestion, Electrophoresis detection,DNA refinement;[C0051] Xba1, Pst1Double Digestion,Gel extraction; Combination | |
- | + | |1C3(K115016) | |
- | + | |[K115017+C0051] | |
|- | |- | ||
- | + | |10 | |
- | + | |[J23106] Spe1,Pst1Double Digestion, Electrophoresis detection,DNA refinement;[K115017+C0051] Xba1, Pst1Double Digestion, Gel extraction;Combination | |
- | + | |1A2(J23106) | |
- | + | |J23106+[K115017+C0051] | |
|- | |- | ||
- | + | |11 | |
- | + | |[J23106+ K115017+C0051] EcoR1, Spe1Double Digestion,Gel extraction;[B0015]EcoR, Xba1Double Digestion, Electrophoresis detection,DNA refinement,Combination | |
- | + | |1C3(B0015) | |
- | + | |[J23106+ K115017+C0051]+B0015 | |
|- | |- | ||
|12 | |12 | ||
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|} | |} | ||
- | =Log Book= | + | ==Log Book== |
{| class="wikitable" | {| class="wikitable" | ||
|- | |- |
Latest revision as of 03:56, 21 June 2014
Home | Team Members | Project | Modelling | Lab | Safety | Gallery | Human Practice |
Here you can find out how we build our plasmid. The plasmid map and information of parts used is given in Team:Shenzhen SZMS/Project.
Schedule
No. | Procedure | Backbone | Status of the Plasmid |
---|---|---|---|
1 | [K115016] Spe1,Pst1 Double Digestion, Electrophoresis detection,DNA refinement;[C0051] X ba1,Pst1Double Digestion, Gel extraction;Combination | 1C3(K115016) | [K115016+C0051] |
2 | [J23106] Spe1,Pst1 Double Digestion, Electrophoresis detection,DNA refinement;[K115016+C0051] X ba1,Pst1Double Digestion, Gel extraction;Combination | 1A2(J23106) | J23106+[K115016+C0051] |
3 | [J2s3106+ K115016+C0051] EcoR1,Spe1Double Digestion, Electrophoresis detection,DNA refinement;[B0051] EcoR1,Xba1 Electrophoresis detection,DNA refinement;Combination | 1C3(B0015) | [J23106+K115016+C0051]+B0015 |
4 | [B0030] Spe1,Pst1 Double Digestion, Electrophoresis detection, DNA refinement;[EC:1.7.7.2] Xba1, Pst1Double Digestion, Gel extraction;Combination | 1A2(B0030) | B0030+EC:1.7.7.2 |
5 | [R0051] Spe1, Pst1Double Digestion, Electrophoresis detection,DNA refinement;[B0030+ EC:1.7.7.2] Xba1,Pst1 Double Digestion, Gel extraction;Combination | 1A2(R0051) | R0051+[B0030+ EC:1.7.7.2] |
6 | [B0030] Spe1, Pst1Double Digestion, Electrophoresis detection,DNA refinement;[K145015] Xba1,Pst1Double Digestion, Gel extraction; Combination | 1A2(B0030) | B0030+K145015 |
7 | [B0030+ K145015] EcoR1, Spe1Double Digestion, Electrophoresis detection,DNA refinement;[B0015] EcoR1, Xba1Double Digestion,Electrophoresis detection,DNA refinement;Combination | 1C3(B0015) | [B0030+ K145015]+B0015 |
8 | [R0051+B0030+ EC:1.7.7.2] Spe1, Pst1Double Digestion,Gel extraction;[B0030+ K145015+B0015]Xba1, Pst1 Gel extraction;Combination | 1C3(B0030+K145015+B0015) | [R0051+B0030+ EC:1.7.7.2]+[B0030+K145015+B0015] |
9 | [K115017] Spe1, Pst1Double Digestion, Electrophoresis detection,DNA refinement;[C0051] Xba1, Pst1Double Digestion,Gel extraction; Combination | 1C3(K115016) | [K115017+C0051] |
10 | [J23106] Spe1,Pst1Double Digestion, Electrophoresis detection,DNA refinement;[K115017+C0051] Xba1, Pst1Double Digestion, Gel extraction;Combination | 1A2(J23106) | J23106+[K115017+C0051] |
11 | [J23106+ K115017+C0051] EcoR1, Spe1Double Digestion,Gel extraction;[B0015]EcoR, Xba1Double Digestion, Electrophoresis detection,DNA refinement,Combination | 1C3(B0015) | [J23106+ K115017+C0051]+B0015 |
12 | [The first part] Spe1,Pst1 Double Digestion;[The second part] Xba1,PstL Double Digestion;Gel extraction; Combination | 1C3(The first part) | 1st+2nd |
13 | [The first and second parts] Spe1、Pst1Double Digestion; [The third part] Xba1、Pst1Double Digestion;Gel extraction; Combination | 1C3(The third part) | 1st +2nd+3rd Done |
Log Book
Date | Event | Results | Problem summary |
---|---|---|---|
Apr.3 | B0015(chl) B0030(chl) Plasmid Transformation | Done (yet this B0030 is single error) | |
Apr.4 | Single clone selected from the work on Apr.3 (In order to be pithy, this process is omitted from the table in all the following daily work) | Done | |
Apr.5 | Plasmid preped and culture restored from the bacterial suspension on Apr.4 (omitted later for pithiness and convenience as well) | Done | |
Apr.6 | K115016(CHL) K115017(CHL) C0051(CHL) transformation | Done | |
May.2 | J23106(AMP) K082003(CHL,as GFP+LVA) transformation (help offered by Mentor Wang) | Done | |
May.5 | Digestion: K115016(S/P) C0051(X/P) C0051(E/S) B0015(E/X) Electrophoresis Gel extraction 16℃ overnight | Done | |
May.6 | Product from 5.5(CHL)transformed | Failed | Might be the problem during the plasmid prep |
May.7 | Plasmid mentioned above repreped | Done | |
May.13 | Digestion: C0051(E/S) B0015(S/P) K082003(E/S) Electrophoresis Gel extraction 16℃ overnight | Done, C0051-B0015 K082003-B0015 gained | |
May.14 | Products from 5.13(CHL)all transformed | Done, C0051-B0015 K082003-B0015 gained | |
May.15 | Gel confirmation (products from 5.14), comparison with gel of B0015 | Done, product longer than the original plasmid | |
May.27 | Digestion: C0051-B0015(X/P) K115016(S/P) K115017(S/P) Electrophoresis Gel extraction Combination Transformation(CHL) | Done, K115016-C0051-B0015 K115017-C0051-B0015 gained. | |
May.28 | B0030(AMP) transformation | Done; informed that R0051 requires PCR in order to get the primer of EC 1.7.7.2 | |
May.29 | Digestion: J23106(S/P) K115016-C0051-B0015(X/P) K115017-C0051-B0015(X/P) Electrophoresis Gel extraction Combination Transformation(AMP) | Done, J23106-K115016-C0051-B0015(27℃CI-protein) J23106-K115017-C0051-B0015(32℃CI-protein) gained. | |
May.30 | The result of sequencing of C0051-B0015 K082003-B0015 received | Correctly combined | |
Jun.2 | Digestion: B0030(S/P) K082003-B0015(X/P) Electrophoresis Gel extraction Combination Transformation(AMP) | Done | |
Jun.8 | The results of sequencing of J23106-K115016-C0051-B0015(27℃CI) and J23106-K115017-C0051-B0015(32℃ CI)received. | Correctly combined | |
Jun.9 | Digestion:B0030-K082003-B0015(E/S) J23106-K115017-C0051-B0015(E/X) Electrophoresis Gel extraction Combination Transformation(AMP) | Done with transformation; Yet failed in the electrophoretic analysis. | Disconnected |
Jun.10 | ciF1 ciF2 ciF3: primers to synthesize EC 1.7.7.2 and PEP (additional PEP R0051-B0030-) gained. | ||
Jun.11 | With the original blue 2X Master Mix PCR round 1,2,3 implemented | Failed; only primer founded in the electrophoretic analysis | |
Jun.12 | Round 1 from 6.11 repeated in the morning; Round 3 PCR with 2X hi-fi Master Mix at noon | Failed in the morning but done in the afternoon; R0051-B0030-1.7.7.2 recycled product gained. | might be the problem of MIX |
Jun.13 | Digestion: 27℃ CI(S/P)R0051-B0030-1.7.7.2(X/P) 32℃ CI(E/X) B0030-K082003-B0015(E/S) Electrophoresis Gel extraction Combination Transformation. | Failed, no culture founded on the dish. | Unknown error; might be the problem of extracted gel. |
Jun.15 | Digestion: 27℃ CI(S/P)R0051-B0030-1.7.7.2(X/P) 32℃ CI(E/X) B0030-K082003-B0015(E/S) Electrophoresis Gel extraction Combination Transformation. | According to the result of electrophoresis, the length of the digested and combined part is the same as that of the primitive plasmid; yet we cannot exclude the problem of plasmid prep; might have failed. | A tube was missed during the digestion yet was made up later; do not know about its possible effect yet. |