Team:Warsaw/Calendar-Main/5 September 2009
From 2009.igem.org
(Difference between revisions)
Line 26: | Line 26: | ||
* Isolate the plasmids containing previously described constructs | * Isolate the plasmids containing previously described constructs | ||
Methods: | Methods: | ||
- | Plasmids were isolated using the A&A plasmid mini kit. Detailed procedure of the isolation is described[http://aabiot.com/products/dna_purification/plasmid_dna/plasmid_mini/protocol_plasmid_mini.pdf | + | Plasmids were isolated using the A&A plasmid mini kit. Detailed procedure of the isolation is described[http://aabiot.com/products/dna_purification/plasmid_dna/plasmid_mini/protocol_plasmid_mini.pdf here] |
Task 3: | Task 3: | ||
* Digest previously isolated plasmids and verify the correctness of the ligation: | * Digest previously isolated plasmids and verify the correctness of the ligation: | ||
Line 40: | Line 40: | ||
* Digest was performed 90 minutes | * Digest was performed 90 minutes | ||
Results: | Results: | ||
+ | |||
'''Comments:''' | '''Comments:''' | ||
* All samples of cro CDS on [http://partsregistry.org/Part:pSB1A3<span style="color: black">pSB1A3</span>] are only empty plasmids | * All samples of cro CDS on [http://partsregistry.org/Part:pSB1A3<span style="color: black">pSB1A3</span>] are only empty plasmids |
Revision as of 00:29, 7 September 2009
Acquiring the internaline A gene from Listeria monocytogenes st. EDG-e genome
Jarek
Tasks:
- Electrophoretical segregation of PCR products from previous day in 0,8% agarosis gel
- Preparation of another PCR reaction with L.monocytogenes genome DNA
Results:
- I propably took the wrong genome DNA sample for the previous reaction, there are products but none of them has the correct length.
Assembly of endosomal detection operon
Marcin
Task 1:
- Prepare the bacterial cultures for isolation of following constructs:
- [http://partsregistry.org/Part:pSB1A3pSB1A3] plasmid containing cro coding sequence
- [http://partsregistry.org/Part:pSB1A3pSB1A3] plasmid containing p53 coding sequence
Task 2:
- Isolate the plasmids containing previously described constructs
Methods: Plasmids were isolated using the A&A plasmid mini kit. Detailed procedure of the isolation is described[http://aabiot.com/products/dna_purification/plasmid_dna/plasmid_mini/protocol_plasmid_mini.pdf here] Task 3:
- Digest previously isolated plasmids and verify the correctness of the ligation:
Methods:
- Reaction mixture composition:
2 μl purified plasmid DNA product 0.5 μl XbaI (Fermentas) 0.5 μl PstI (Fermentas) 2 μl Buffer Tango (Fermentas) 15 μl MQ water
- Digest was performed 90 minutes
Results:
Comments:
- All samples of cro CDS on [http://partsregistry.org/Part:pSB1A3pSB1A3] are only empty plasmids
- Samples of Bax CDS have biobricks but I am unable to determine whether this biobricks is Bax CDS or [http://partsregistry.org/Part:BBa_E0010BBa_E0010] due to contamination with the latter one. It is obligated to prepare another digestion to reveal the identity of the insert
|
|
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
|
|