Difference between revisions of "Team:Munich/engineeringrecbcd.html"

Line 346: Line 346:
 
       <td>Protocol:</td>
 
       <td>Protocol:</td>
 
       <td>
 
       <td>
<a href="https://static.igem.org/mediawiki/2018/b/be/T--Munich--WL1_Agarose-Gel_electrophoresis.pdf" target="_blank">Agarose gel</a>,
+
<a href="https://static.igem.org/mediawiki/2018/b/be/T--Munich--WL1_Agarose-Gel_electrophoresis.pdf" target="_blank">Agarose gel</a>
 
</td>
 
</td>
 
     </tr>
 
     </tr>

Revision as of 21:44, 15 October 2018

PCR amplify RecBCD WT

2018/06/11
Participants: Enikö Baligács, Rita Olenchuk, Julia Mayer
Protocol: PCR, Gel extraction, Restriction digest, PCR purification, Ligation
Notes: RecC: RecC_3'UTR_SapI_rv, RecC_BB-P_XbaI_fw, AT: 71°, ET: 70s
RecBD: RecB_SapI_fw, RecD_BB-S_SpeI_rv, AT: 72°, ET: 108 s
Digests: RecC: SapI & XbaI; RecBD: SapI SpeI
Restriction digest with RecC(WT): SapI & XbaI; RecBD(WT): SapI SpeI
Results: see below

PCR amplify RecBCD His-tag

2018/06/11
Participants: Enikö Baligács, Rita Olenchuk, Julia Mayer
Protocol: PCR, Restriction digest, PCR purification
Notes: RecC: RecC_C-His_5'UTR_BBP_XbaI_fw RecB_5'UTR_SapI_rv AT: 72° ET: 70s
RecBD: RecB_N-His_SapI_fw RecD_C-His_BBS_SpeI_rv AT: 69° ET: 108 s
Digests: RecBD SapI XbaI, RecC-his: SapI XbaI
Results: see below

PCR amplify RecBCD 5' homology regions

2018/06/11
Participants: Enikö Baligács, Rita Olenchuk, Julia Mayer
Protocol: PCR
Notes: RecBCD_KI_5HA_extract_fw RecBCD_KI_5HA_extract_rv AT: 62° ET: 15 s
Results: see below

PCR amplify RecBCD 3' homology regions

2018/06/11
Participants: Enikö Baligács, Rita Olenchuk, Julia Mayer
Protocol: PCR
Notes: RecBCD_KI_3HA_extract_rv RecBCD_KI_3HA_extract_fw AT: 62° ET: 15 s
Results: see below

PCR amplify resistance cassette for RecBCD knockout

2018/06/11
Participants: Enikö Baligács, Rita Olenchuk, Julia Mayer
Protocol: PCR
Notes: CAT_RecBCD-KO_5HA_short_fw CAT_RecBCD-KO_5HA_short_rv AT: 51° ET: 20s
Results: see below

PCR amplify resistance cassette for RecBCD knockout (2)

2018/06/11
Participants: Enikö Baligács, Rita Olenchuk, Julia Mayer
Protocol: PCR
Notes: CAT_RecBCD-KO_5HA_long_fw CAT_RecBCD-KO_5HA_long_rv AT: 55° ET: 20s
Results: see below
something

Redo: PCR amplify RecBD His-tag

2018/06/11
Participants: Enikö Baligács
Protocol: PCR, Agarose Gel, Gelextraction
Notes: RecBD: RecB_N-His_SapI_fw RecD_C-His_BBS_SpeI_rv AT: 69° ET: 108 s
Results: 51,4ng/ul

Assemble pSB1C3_RecBCD-his

2018/06/11
Participants: Enikö Baligács
Protocol: Restriction digest, PCR purification, Ligation
Notes: digest with SapI SpeI

Prepare pSB1C3 backbone

2018/06/11
Participants: Dominic Schwarz
Protocol: Electrocompetent transformation, Mini Prep, Restriction digest, Agarose gel
Notes: template: pSB1C3-J04450 (iGEM BioBrick Kit plate 7 Well 23 O)
Results: agarose gel wasnt prepared properly leading to loss of samples. We decided to redo the experiment

Amplify Lac-Operon parts from pSB1C3 backbone

2018/06/11
Participants: Dominic Schwarz
Protocol: PCR, Agarose gel, Restriction digest
Notes: template: pSB1C3-J04450 (iGEM BioBrick Kit plate 7 Well 23 O)
Digests with: XbaI, SpeI and EcoRI, PstI for future assemblies
Lac Promoter: BBP_EcoRi_fw & LacO_XbaI_rv (57°C, 1min)
Lac terminator: Term_SpeI_fw & BBS_PstI_rv (65°C, 1min)
Results: see below
something

Assemble pSB1C3_lacO_RecBCD_lacT

2018/06/14
Participants: Dominic Schwarz
Protocol: Ligation, Chemical transformation, Mini Prep, Sequencing
Notes: template: pSB1C3-J04450 (iGEM BioBrick Kit plate 7 Well 23 O)
Digests with: XbaI, SpeI and EcoRI, PstI for future assemblies
Results: colonies but sequencing gave no results. We decided to test the PCR primer on a gel. Resequencing with VF2 and VR and blast analysis showed contamination with pBR322. After reevaluating the design of the plasmid with Thomas (supervisor) we realized there is an error. We redesigned the plasmid and plan to assemble it with gibson assembly.

Testing RecBCD Primers

2018/06/22
Participants: Katja Neishsalo
Protocol: Agarose gel
Results: As expected all primers are ok :) PIC

Midi prep pSB1C3_mRFP

2018/07/31
Participants: Sophie von Schönberg, Ariane Krus, Franziska Winzig
Protocol: Midi Prep, Restriction digest, Agarose gel
Notes: we needed lots of backbone and linear DNA for other experiments, which is why we did this DNA preparation. obtained samples were controlled by restriction digest with KpnI, PstI : 500bp, 2672bp