SBB10Ntbk-DanielSedor: Difference between revisions
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Submitted preparation for thermocycling. | Submitted preparation for thermocycling. | ||
===22 February 2010=== | ===22 February 2010=== | ||
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Prepared two new PCR's according to the [[Template:SBB-Protocols_PCR2 | Cloning by PCR]] protocol. | Prepared two new PCR's according to the [[Template:SBB-Protocols_PCR2 | Cloning by PCR]] protocol. | ||
===24 February 2010=== | ===24 February 2010=== | ||
Mixed 6μL of PCR products sbb10A and sbb10B (2/22 versions) with 4μL of Loading Buffer for the purposes of running a preparative gel (see [[Template:SBB-Protocols_PCR3 | SOEing by PCR]] protocol for more details). Preparative gel results (which can be found [[SBB10_gels#JimH | here]]) were in agreement with the predictions made in the sbb10 construction file for the gp=A and gp=B reactions. Performed the [[Template:SBB-Protocols_Zymo3 | Zymo Gel Purification]] protocol on sbb10A and sbb10B in the same zymo column. | Mixed 6μL of PCR products sbb10A and sbb10B (2/22 versions) with 4μL of Loading Buffer for the purposes of running a preparative gel (see [[Template:SBB-Protocols_PCR3 | SOEing by PCR]] protocol for more details). Preparative gel results (which can be found [[SBB10_gels#JimH | here]]) were in agreement with the predictions made in the sbb10 construction file for the gp=A and gp=B reactions. Performed the [[Template:SBB-Protocols_Zymo3 | Zymo Gel Purification]] protocol on sbb10A and sbb10B in the same zymo column. | ||
===1 March 2010=== | ===1 March 2010=== | ||
Performed [[Template:SBB-Protocols_PCR3 | SOEing PCR]] protocol using sbb10A+sbb10B as a template and DS001 and DS002 as oligos. | Performed [[Template:SBB-Protocols_PCR3 | SOEing PCR]] protocol using sbb10A+sbb10B as a template and DS001 and DS002 as oligos. | ||
===8 March 2010=== | ===8 March 2010=== | ||
Purified the DNA from the 3/1 PCR reaction in accordance with the [[Template:SBB-Protocols_Zymo1 | Regular Zymo Cleanup]] protocol. Due to time limitations, the digestion, ligation, and transformation procedures were left for 3/10. | Purified the DNA from the 3/1 PCR reaction in accordance with the [[Template:SBB-Protocols_Zymo1 | Regular Zymo Cleanup]] protocol. Due to time limitations, the digestion, ligation, and transformation procedures were left for 3/10. | ||
===10 March 2010=== | |||
Filler. |
Revision as of 15:28, 8 March 2010
Construction Files
sbb10: Sleeping beauty (SB100x)
Construction of sbb10 PCR DS001/CA1600 on Bca1587 5-1 (420bp, gp=A) PCR CA1597/DS002 on Bca1587 5-6 (767bp, gp=B) ---------------------------- PCR DS001 and DS002 on A+B (1051 bp, EcoRI/BamHI) Sub into pBjk2741 (EcoRI/BamHI, 2170+910, L) Product is pBjk2741-sb10 {<SB100x!} ---------------------------- DS001 Forward oligo for cloning of <SB100x! CCATAgaattcATGagatctGGTAAATCTAAAGAAATCTCTCAGGAC CA1600 CGAAACGCAGACGAGCTTTTTTGTGACGGTTCTGGAGCAGCGGTTTTTT PCA assembly of sleepingBeauty (Bca1587) CA1597 ATGCTGGAAGAAACCGGTACCAAAGTTTCTATCTCTACCGTTAAACGTG PCA assembly of sleepingBeauty (Bca1587) DS002 Reverse oligo for cloning of <SB100x! ctgatGGATCCttaGTATTTGGTAGCGTTACCTT Part: gatctGGTAAATCTAAAGAAATCTCTCAGGACCTGCGTAAACGTATCGTTGACCTGCACAAATCTGGTTCTTCTCTGGGTGCTATCTCTAAACGTCTGGCTGTTCCGCGTTCTTCTGTTCAGACCATCGTTCGTAAATACAAACA CCACGGTACCACCCAGCCGTCTTACCGTTCTGGTCGTCGTCGTGTTCTGTCTCCGCGTGACGAACGTACCCTGGTTCGTAAAGTTCAGATCAACCCGCGTACCACCGCTAAAGACCTGGTTAAAATGCTGGAAGAAACCGGTACC AAAGTTTCTATCTCTACCGTTAAACGTGTTCTGTACCGTCACAACCTGAAAGGTCACTCTGCTCGTAAAAAACCGCTGCTCCAGAACCGTCACAAAAAAGCTCGTCTGCGTTTCGCTACCGCTCACGGTGACAAAGACCGTACCT TCTGGCGTAACGTTCTGTGGTCTGACGAAACCAAAATCGAACTGTTCGGTCACAACGACCACCGTTACGTTTGGCGTAAAAAAGGTGAAGCTTGCAAACCGAAAAACACCATCCCGACCGTTAAACACGGTGGTGGTTCTATCAT GCTGTGGGGTTGCTTCGCTGCTGGTGGTACCGGTGCTCTGCACAAAATCGACGGTATCATGGACGCTGTTCAGTACGTTGACATCCTGAAACAGCACCTGAAAACCTCTGTTCGTAAACTGAAACTGGGTCGTAAATGGGTTTTC CAGCACGACAACGACCCGAAACACACCTCTAAAGTTGTTGCTAAATGGCTGAAAGACAACAAAGTTAAAGTTCTGGAATGGCCGTCTCAGTCTCCGGACCTGAACCCGATCGAAAACCTGTGGGCTGAACTGAAAAAACGTGTTC GTGCTCGTCGTCCGACCAACCTGACCCAGCTGCACCAGCTGTGCCAGGAAGAATGGGCTAAAATCCACCCGACCTACTGCGAAAAACTGGTTGAAGGTTACCCGAAACGTCTGACCCAGGTTAAACAGTTCAAAGGTAACGCTAC CAAATACTAAG
sbb39: Magnesium-repressed Promoter
Eco/Bam transfer pBjh1601CK-Bjh1380 Sub into pBjk2741-Bca1144 (EcoRI/BamHI, 910+2170, L) Product is pBjk2741-Bjh1380 {PmgtCB}
sbb40: Nuclear localization peptide
Eco/Bam transfer pBjh1601CK-Bjh1858 Sub into pBjk2741-Bca1144 (EcoRI/BamHI, 910+2170, L) Product is pBjk2741-Bjh1858 {<NIS!}
Relevant Protocols
Lab Notes
17 February 2010
Prepared two PCR's according to the Cloning by PCR protocol using oligos DS001/CA1600 (gp=A) and DS002/CA1597 (gp=B) from the sbb10 construction file.
Submitted preparation for thermocycling.
22 February 2010
Mixed 6μL of PCR products sbb10A and sbb10B (2/17 versions) with 4μL of Loading Buffer for the purposes of running a preparative gel (see SOEing by PCR protocol for more details). Preparative gel results (which can be found here) did not agree with the predictions made in the construction file.
Prepared two new PCR's according to the Cloning by PCR protocol.
24 February 2010
Mixed 6μL of PCR products sbb10A and sbb10B (2/22 versions) with 4μL of Loading Buffer for the purposes of running a preparative gel (see SOEing by PCR protocol for more details). Preparative gel results (which can be found here) were in agreement with the predictions made in the sbb10 construction file for the gp=A and gp=B reactions. Performed the Zymo Gel Purification protocol on sbb10A and sbb10B in the same zymo column.
1 March 2010
Performed SOEing PCR protocol using sbb10A+sbb10B as a template and DS001 and DS002 as oligos.
8 March 2010
Purified the DNA from the 3/1 PCR reaction in accordance with the Regular Zymo Cleanup protocol. Due to time limitations, the digestion, ligation, and transformation procedures were left for 3/10.
10 March 2010
Filler.