Date | Product | Gene | Starting Plasmid | Forward Primer | Reverse Primer | Thermocycler Variables: #cycles / annealing temp / extension time | Gel Picture Comments / Deviations from Protocol | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
6/23 | Q2-BACE2-QXBACE2 | pEXPR BACE2 | iGEM 016 BACE2 C-term primerF | iGEM 017 BACE2 C-term primerR | 30 / 60C / 30s | Gel Picture 6/23 | Diluted primers in water, not TE | 6/23 | ||||
Q1-eYFP-Q2eYFP | pEXPR TRE:eYFP | iGEM 018 eYFP N-term primerF | iGEM 019 eYFP N-term primerR | 30 / 60C / 30s | Picture 6/23 | Diluted primers in water, not TE | 6/23 | |||||
Q1-BACE2-Q2 | BACE2 | pEXPR BACE2 | iGEM 001-2 BACE2 N-term primerF | iGEM 002-2 BACE2 N-term primerR30 / 60C / 30s | Picture 6/23 | Diluted primers in water, not TE | 6/23 | |||||
Q2-eYFP-QX | eYFP | pEXPR TRE:eYFP | iGEM 003-2 YFP C-term primerF | iGEM 004-2 YFP C-term primerR | 30 / 60C / 30s | |||||||
6/ | 23Diluted primers in water, not TE | 6/24 | Q2-BACE2-QXBACE2 | pEXPR BACE2 | iGEM 016 BACE2 C-term primerF | iGEM 017 BACE2 C-term primerR | 35 / 56.2C / 30s | Gel Picture 6/24 | Used 0.6 uL DMSO to reduce risk of hairpins or primer dimers | |||
Q1-eYFP-Q2 | pEXPR TRE:eYFP6/24 | |||||||||||
Q1-eYFPBACE2-Q2 | pEXPR BACE2 | |||||||||||
Q2-eYFP-QX | pEXPR TRE:eYFP | |||||||||||
6/25 | Q1-BACE2-Q2 | pEXPR BACE2 | iGEM 018 eYFP N-term primerF | iGEM 019 eYFP N-term primerR | 35 / | 5650.2C / 30s | Picture 6/24 | Used 0.6 uL DMSO to reduce risk of hairpins or primer dimers | 6/24 | Q1-BACE2-Q2 |
| Gel Picture 6/25 |
Q2-BACE2-QXBACE2 | pEXPR BACE2 | |||||||||||
iGEM 001Q2-2 BACE2 N-term primerF | iGEM 002-2 BACE2 N-term primerR | 35 / 56.2C / 30s | Picture 6/24 | Used 0.6 uL DMSO to reduce risk of hairpins or primer dimers | -QX | pEXPR BACE2 | ||||||
Q1-eYFP-Q2 | pEXPR TRE:eYFP | |||||||||||
6/24 | Q2-eYFP-QXeYFP | pEXPR TRE:eYFP | iGEM 003-2 YFP C-term primerF | iGEM 004-2 YFP C-term primerR | 35 / 56.2C / 30s | Picture 6/24 | Used 0.6 uL DMSO to reduce risk of hairpins or primer dimers | 6/24|||||
6/26 | Q2-BACE2-QX (plus betaine) | pEXPR BACE2 | 30 / 55C / 1m
| Gel Picture 6/26 | ||||||||
Q2-BACE2-QX (plus DMSO) | pEXPR BACE2 | |||||||||||
Q1-BACE2-Q2 (plus betaine) | pEXPR BACE2iGEM 016 | |||||||||||
Q1-BACE2 C-term primerF | iGEM 017 BACE2 C-term primerR | 35 / 56.2C / 30s | Picture 6/24 | -Q2 (plus DMSO) | pEXPR BACE2 | |||||||
6/27 | Q2-BACE1-QX | pEXPR BACE1 | Gel Picture 6/27 | |||||||||
Q2-eYFP-QX | pEXPR eYFP | |||||||||||
6/30 | Used 0.6 uL DMSO to reduce risk of hairpins or primer dimers | 6/24Q1-eYFP-Q2 | pEXPR eYFP | pEXPR TRE:eYFP | iGEM 018 eYFP N-term primerF | iGEM 019 eYFP N-term primerR | 35 / 56.2C / 30s | Picture 6/24 | Used 0.6 uL DMSO to reduce risk of hairpins or primer dimers | |||
6/24 | Q1-BACE2-Q2 | BACE2 | pEXPR BACE2 | iGEM 001-2 BACE2 N-term primerF | iGEM 002-2 BACE2 N-term primerR | 35 / 56.2C / 30s | Picture 6/24 | Used 0.6 uL DMSO to reduce risk of hairpins or primer dimers | 6/24 | Q2-eYFP-QX | eYFP | pEXPR TRE:eYFP | iGEM 003-2 YFP C-term primerF | iGEM 004-2 YFP C-term primerR | 35 / 56.2C / 30s | Picture 6/24 | Used 0.6 uL DMSO to reduce risk of hairpins or primer dimers
Gel Picture 6/30 | ||||||||||||
Q1-BACE1-Q2 | pEXPR BACE1 | |||||||||||
7/9 | Q2-eYFP-QX (for BACE2) | pEXPR eYFP | 35 / 58C / 1m with both DMSO and Betaine | Gel Picture 7/9 | ||||||||
Q1-eYFP-Q2 (for BACE2) | pEXPR eYFP | |||||||||||
Q2-eYFP-QX (for BACE1) | pEXPR eYFP | |||||||||||
Q2-BACE2-QX | pEXPR BACE2 | |||||||||||
Q1-BACE2-QX | pEXPR BACE2 | |||||||||||
Q1-BACE1-QX | pEXPR BACE1 | |||||||||||
7/10 | (miRNA generator stuff) | 35 / 58C / 1m with both DMSO and Betaine | Gel Picture 7/10 | |||||||||
(20 PCR products in all) | ||||||||||||
7/11 | (miRNA generator stuff) | 30 / 61C / 30s | Gel Picture 7/11 | |||||||||
(12 PCR products in all) | ||||||||||||
7/16 | (miRNA generator stuff) | 30 / 63C / 30s | ||||||||||
(12 PCR products in all) |
Ran PCRs according to protocol on NEB website: https://www.neb.com/protocols/2012/09/06/protocol-phusion-high-fidelity-pcr-master-mix-with-hf-buffer-m0531
Used 20 uL reaction. For plasmids, diluted to concentration 1ng/uL in EB buffer and added 1uL of each dilution to a separate PCR mix. Diluted primers from 100uM stocks to 10uM with TE buffer.
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