Team:Washington/Protocols/pGA.
From 2011.igem.org
(Difference between revisions)
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- | =pGA | + | =pGA vector Assay= |
- | 1. | + | *Prepare these mixtures on ice |
+ | # Obtain a 40 uL aliquot of BL21 cells. | ||
+ | # Add 120 uL of ice water to the aliquot. | ||
+ | # The total volume is now 160 uL; split evenly among four labeled tubes: INS + BCK, INS + BCK, INSctrl, BCKctrl. | ||
+ | #* INS + BCK tubes (x 2) | ||
+ | #** add 1 uL of 10X pGA Gibson product (1A3 BCK/INS pLacGFP) | ||
+ | #* INSctrl tube | ||
+ | #** add 100 pg of pLacGFP gel extract | ||
+ | #* BCKctrl | ||
+ | #** add 100 pg of 1A3 gel extract | ||
+ | #Repeat steps 1-3 for the comparison vector pSB using the following instead: | ||
+ | #* 1 uL of pSB Gibson product (T19-1A3/pLacGFP) | ||
+ | #* 1 ng INS (pLacGFP- gel extract) | ||
+ | #* 1 ng BCK (T19-1A3- gel extract) | ||
+ | #Once all the samples are ready, begin the [https://2011.igem.org/Team:Washington/Protocols/Elect. transformation]. | ||
+ | #* Rescue each sample in 500 mLs of LB | ||
+ | #*Incubate all samples @ 37oC for ~45 min. | ||
+ | #Plate 50 uL on each sample onto a LB + Chlor + Amp + IPTG plate. | ||
+ | #*1 plate for each control in each vector set. | ||
+ | #*3 plates for ''each'' Gibson product tube in each set. ( 6 plates for each vector set + 2 control plates) |
Revision as of 22:09, 27 September 2011
pGA vector Assay
- Prepare these mixtures on ice
- Obtain a 40 uL aliquot of BL21 cells.
- Add 120 uL of ice water to the aliquot.
- The total volume is now 160 uL; split evenly among four labeled tubes: INS + BCK, INS + BCK, INSctrl, BCKctrl.
- INS + BCK tubes (x 2)
- add 1 uL of 10X pGA Gibson product (1A3 BCK/INS pLacGFP)
- INSctrl tube
- add 100 pg of pLacGFP gel extract
- BCKctrl
- add 100 pg of 1A3 gel extract
- INS + BCK tubes (x 2)
- Repeat steps 1-3 for the comparison vector pSB using the following instead:
- 1 uL of pSB Gibson product (T19-1A3/pLacGFP)
- 1 ng INS (pLacGFP- gel extract)
- 1 ng BCK (T19-1A3- gel extract)
- Once all the samples are ready, begin the transformation.
- Rescue each sample in 500 mLs of LB
- Incubate all samples @ 37oC for ~45 min.
- Plate 50 uL on each sample onto a LB + Chlor + Amp + IPTG plate.
- 1 plate for each control in each vector set.
- 3 plates for each Gibson product tube in each set. ( 6 plates for each vector set + 2 control plates)