| 2. Plating from 6-23-08 transformations again.
|
| a. Since plating of the 6-23 transformations provided no colonies for parts 15-18, the remaining cells from those transformations were re-plated. 75 uL of cell culture was spread on each of two plates for each culture; plates contained LB media and the corresponding antibiotic. A metal spreading tool was used to spread the culture suspension on the plates, and this was sterilized between each sample by dipping it in 100% ethanol (EtOH) and flaming it. 75 uL cell culture was pipetted on, and spread around plate.
|
| b. Plates were placed at 37C in an incubator and allowed to grow overnight.
|
| 3. Sequencing primers ordered on 6-20-08 were picked up. All primers were diluted to mircomoles according to the following additions of sterile H20:
|
| Primer | nmoles | uL H20 added
|
| P22 cII cR | 37.7 | 377.0
|
| P22 cII cF | 36.0 | 360.0
|
| Lambda cI R | 32.40 | 324.0
|
| Lambda cI F | 33.2 | 332.0
|
| P22 MNT R | 32.8 | 328.0
|
| P22 MNT F | 28.2 | 282.0
|
| EYFP R | 43.8 | 438.0
|
| EYFP F | 34.5 | 345.0
|
| pSB 2K3 | 39.6 | 396.0
|
| pSB 1A2 | 31.7 | 317.0
|
| pSB 1AK3 | 40.0 | 400.0
|
| GFP R | 32.1 | 321.0
|
| GFP F | 33.7 | 337.0
|
| mCherry R | 43.9 | 439.0
|
| mCherry F | 28.4 | 284.0
|
| LacI R | 29.4 | 294.0
|
| LacI F | 31.2 | 312.0
|
| a. All primers were spun down prior to opening. The appropriate amount of water was added to resuspend each primer in solutions of 100 ug/uL and 10 ug/uL. The 10 ug/uL solution is our working concentration. Primers were then stored at -20C.
|
| b. 12 uL reactions containing plasmid to be sequenced and the corresponding primer(s) were set up and submitted for sequencing. Each reaction mixture contained 1 ul primer, 1 ul plasmid DNA, and 10 uL dd H2O. All samples were sent for sequencing at the Biomedical Genomics Center at the U of M.
|
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