1. Single Digests: Performed today. Incubated digested samples for 2hrs @ 37C. Refer to table below.
| Gene | 10x Buffer | BSA Protein | H20 | DNA | RE
|
| Promoter | 5.0uL | 0.5uL | 40.4uL | 2.1uL | 2.0uL, SPE
|
| LAMBDAcI | 5.0uL | 0.5uL | 29.5uL | 15.0uL | 1.0uL, XBA 1
|
| LAMBDAcI | 5.0uL | 0.5uL | 29.5uL | 15.0uL | 1.0uL, SPE
|
| Terminator | 5.0uL | 0.5uL | 38.0uL | 4.5uL | 2.0uL, XBA 1
|
|
| NOTE: RE = Restriction Enzyme
|
2. Ligation: Performed today. Heat inactivated enzyme @ 65C for 15 min to kill enzymes.Ligate samples. Incubate ligated samples @ 16C for 1hour. Refer to table below.
| Genes | 10x Buffer | H20 | Base Vector | Insert | DNA Ligase
|
| LAMBDAcI/Terminator | 2.0uL | 10.7uL | 2.0uL (Term.) | 4.3uL (LAMBDAcI) | 1.0uL
|
| Promoter/LAMBDAcI | 2.0uL | 10.7uL | 2.0uL (Pro.) | 4.3uL (LAMBDAcI) | 1.0uL
|
|
| 3. Double Digests
|
| 4. Ligation
|
| 5. Transformation: Transform ligation products.
|
| 6. Make/Pour Ampicillin Plates
|
| 7. Order Primers for Part Sequencing
|
"
