"
Team:British Columbia/Notebook/CRISPR
From 2013.igem.org
| Line 37: | Line 37: | ||
Decoy: | Decoy: | ||
*PAM + spacer (on Amp) | *PAM + spacer (on Amp) | ||
| - | |||
==='''July 4th'''=== | ==='''July 4th'''=== | ||
| Line 46: | Line 45: | ||
'''Results:''' Oligonucleotides were assembled using this protocol. | '''Results:''' Oligonucleotides were assembled using this protocol. | ||
| - | |||
==='''July 5th'''=== | ==='''July 5th'''=== | ||
| Line 55: | Line 53: | ||
'''Results:''' NA | '''Results:''' NA | ||
| - | |||
==='''July 6th'''=== | ==='''July 6th'''=== | ||
| Line 77: | Line 74: | ||
All oligonucleotides were mixed in equimolar amounts at a final concentration of 10 nM each, annealed and ligated and PCR amplified according to the repeat-assembly protocol. | All oligonucleotides were mixed in equimolar amounts at a final concentration of 10 nM each, annealed and ligated and PCR amplified according to the repeat-assembly protocol. | ||
| - | |||
==='''July 10th'''=== | ==='''July 10th'''=== | ||
| Line 86: | Line 82: | ||
'''Results:''' Unsuccessful no bands were seen on the agarose gel. | '''Results:''' Unsuccessful no bands were seen on the agarose gel. | ||
| + | |||
==='''July 10th'''=== | ==='''July 10th'''=== | ||
| Line 129: | Line 126: | ||
'''Results:''' Sequencing results showed that the T4 spacer was correctly assembled into the repeat-spacer-arrays for single and double inserts. Unfortunately, no T7 spacers were incorporated in the assembly. After going over the sequence of the oligonucleotides with Mike, this is most likely because one of the T7 splint sequences was not correctly designed; we accidentally left the PAM site in it (which would have prevented ligation). The splint was redesigned and reordered; also designed and ordered a second set of different T4 and T7 spacers. | '''Results:''' Sequencing results showed that the T4 spacer was correctly assembled into the repeat-spacer-arrays for single and double inserts. Unfortunately, no T7 spacers were incorporated in the assembly. After going over the sequence of the oligonucleotides with Mike, this is most likely because one of the T7 splint sequences was not correctly designed; we accidentally left the PAM site in it (which would have prevented ligation). The splint was redesigned and reordered; also designed and ordered a second set of different T4 and T7 spacers. | ||
| - | |||
| - | |||
<html> | <html> | ||
<a name="julyweek4"></a> | <a name="julyweek4"></a> | ||
| Line 144: | Line 139: | ||
All oligonucleotides were mixed in equimolar amounts at a final concentration of 10 nM each, annealed and ligated and PCR amplified according to the repeat-assembly protocol. | All oligonucleotides were mixed in equimolar amounts at a final concentration of 10 nM each, annealed and ligated and PCR amplified according to the repeat-assembly protocol. | ||
| - | |||
==='''July 23rd'''=== | ==='''July 23rd'''=== | ||
| Line 177: | Line 171: | ||
'''Results:''' Miniprepped overnight cultures from yesterday and send to sequence confirm. | '''Results:''' Miniprepped overnight cultures from yesterday and send to sequence confirm. | ||
| - | |||
| - | |||
<html> | <html> | ||
<a name="julyweek5"></a> | <a name="julyweek5"></a> | ||
| Line 190: | Line 182: | ||
'''Results:''' Based on the sequencing results, the single insert T7, new T4 and T7 and the double T4 and T7 inserts were correctly assembled. The constructs were given to Joe to add promoters and a terminator via standard assembly. | '''Results:''' Based on the sequencing results, the single insert T7, new T4 and T7 and the double T4 and T7 inserts were correctly assembled. The constructs were given to Joe to add promoters and a terminator via standard assembly. | ||
| - | |||
<html> | <html> | ||
Revision as of 07:14, 27 September 2013
iGEM Home
Contents |
Team CRISPR
July 3
List of BioBricks that are/will be on the way:
Cas9:
- Cas9 - Joe and Anna
- pTet -
- const. promoter + Cas9 - Joe
- promoter + Cas9 + Leader + R + spacer + R (on Kan)
- L + R + spacer + R
Target:
- tracerRNA
- repeat + spacer + repeat -
- leader - Ray, Fisal, Dan
Decoy:
- PAM + spacer (on Amp)
July 4th
Experimenter: Cam Strachan
Aim: Phosphorylate and assemble T4, T7, and tracrRNA ordered oligos for decoy plasmids.
Results: Oligonucleotides were assembled using this protocol.
July 5th
Experimenter: Cam Strachan
Aim: Ligated annealed oligos into PSB1C3, cut with E and S, and transform into 10G heat competent cells. Cells were recovered in 300uL and 25uL wa plated along with a no insert control.
Results: NA
July 6th
Experimenter: Cam Strachan
Aim: Select colonies for screening
Results: Approximately 100 colonies were present for both the T4, T7 and tracr RNA spacers with approximately 10 colonies on the background plate. Colony PCR with VF and VR2 confirmed bands at approximately 350bp. 3 colonies from both T4, T7 and tracrRNA plates were sent for Sanger sequencing through genewiz.
July 9th
Experimenter: Cam Strachan
Aim: Phosphorylate, ligate and amplify oligos for T4 and T7 repeat-spacer arrays.
Results: The T4 and T7 spacers, repeat and the Repeat-BB Suffix oligonucleotides were phosphorylated with T4 PNK.
All oligonucleotides were mixed in equimolar amounts at a final concentration of 10 nM each, annealed and ligated and PCR amplified according to the repeat-assembly protocol.
July 10th
Experimenter: Anna Müller
Aim: PCR the cas9 gene from Streptococcus thermophilus cells.
Results: Unsuccessful no bands were seen on the agarose gel.
July 10th
Experimenter: Cam Strachan
Aim: Gel purify assembled sequences.
Results: The PCR product from yesterday was loaded into a 10% TBE-PAGE gel and run at 100V until the blue marker ran off. Bands corresponding to one (148 bp) and two (219 bp) were excised and purified.
July 11th
Experimenter: Cam Strachan
Aim: Finish purification, cut, ligate and transform repeat-spacer assemblies
Results: Gel slurries were filtered and ethanol precipitated and quantified. Products were cut with E+S, ligated into PSB1C3 and transformed.
July 12th
Experimenter: Cam Strachan
Aim: Finish purification, cut, ligate and transform repeat-spacer assemblies
Results: Gel slurries were filtered and ethanol precipitated and quantified. Products were cut with E+S, ligated into PSB1C3 and transformed.
July 15th
Experimenter: Cam Strachan
Aim: Screen/confirm insert length.
Results: 5 colonies from the single insert and 10 colonies from the double insert plate were screened via colony PCR for correct insert length. Three positive colonies from the single insert and 6 positive colonies from the double insert were inoculated for overnight cultures.
July 17th
Experimenter: Cam Strachan
Aim: Figure out why no T7 sequences were assembled.
Results: Sequencing results showed that the T4 spacer was correctly assembled into the repeat-spacer-arrays for single and double inserts. Unfortunately, no T7 spacers were incorporated in the assembly. After going over the sequence of the oligonucleotides with Mike, this is most likely because one of the T7 splint sequences was not correctly designed; we accidentally left the PAM site in it (which would have prevented ligation). The splint was redesigned and reordered; also designed and ordered a second set of different T4 and T7 spacers.
July 22nd
Experimenter: Cam Strachan
Aim: Restart assembly with fixed splint
Results: The repeat-spacer assembly was restarted with the fixed T7 splint and the new spacers and splints. New splints were phosphorylated with T4 PNK.
All oligonucleotides were mixed in equimolar amounts at a final concentration of 10 nM each, annealed and ligated and PCR amplified according to the repeat-assembly protocol.
July 23rd
Experimenter: Cam Strachan
Aim: Gel purify assembled sequences.
Results: The PCR product from yesterday was loaded into a 10% TBE-PAGE gel and run at 100V until the bromophenol blue marker ran off. Bands corresponding to one (148 bp) and two (219 bp) were excised and purified.
July 24th
Experimenter: Cam Strachan
Aim: Cut, ligate and transform repeat-spacer assemblies
Results: Gel purification products were quantified with the Qubit. Single inserts for T7 and the new T4 and T7, and double inserts for T4+T7 (original set) were cut with E+S, ligated into PSB1C3 and transformed.
July 25th
Experimenter: Cam Strachan
Aim: Screen/confirm insert length.
Results: 5 colonies from each of the single insert and 10 colonies from the double insert plates were screened via colony PCR for correct insert length. Two positive colonies from each of the single insert and 6 positive colonies from each of the double inserts were inoculated for overnight cultures.
July 26th
Experimenter: Cam Strachan
Aim: Miniprep and prepare for sequencing
Results: Miniprepped overnight cultures from yesterday and send to sequence confirm.
July 29th
Experimenter: Cam Strachan
Aim: Analyze sequencing results
Results: Based on the sequencing results, the single insert T7, new T4 and T7 and the double T4 and T7 inserts were correctly assembled. The constructs were given to Joe to add promoters and a terminator via standard assembly.
September 22nd
Experimenter: Anna Müller
Aim: Digest T4, T7 spacer sequence with PAM site(decoy construct) with EcoRI and SpeI to later on ligate into plasmid with ampicillin resistance.
Results: will follow.
Aim: Digest PsBIA3 plasmid with ampicillin resistance with EcoRI and SpeI to construct the decoy plasmides.
Results: will follow.
