Minnesota/10 July 2008
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!| Reagent !! Buffer !! H20 !! Insert DNA !! LAMBDAcI DNA !! Dephosphor. Base V. !! T4 DNA Ligase | !| Reagent !! Buffer !! H20 !! Insert DNA !! LAMBDAcI DNA !! Dephosphor. Base V. !! T4 DNA Ligase | ||
|- | |- | ||
- | |pro-LAMBDAcI-B.V. ||4.0uL || | + | |pro-LAMBDAcI-B.V. ||4.0uL || 0||promoter 1.0uL ||6.0uL ||10.0uL ||1.0uL |
|- | |- | ||
- | |LAMBDAcI-term-B.V. ||4.0uL || | + | |LAMBDAcI-term-B.V. ||4.0uL || 0||terminator 1.0uL ||6.0uL ||10.0uL ||1.0uL |
|- | |- | ||
- | |Control ||4.0uL || 7.0uL || | + | |Control ||4.0uL || 7.0uL || 0|| 0|| 10.0uL ||1.0uL |
|- | |- | ||
|} | |} |
Revision as of 16:08, 11 July 2008
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1. Dephosphorylation: Continued with double digestion base vector product from 07-09-2008. Used Antartic phosphoylase to dephosphorylate the base vector. Want to dephosphorylate the base vector to prevent it from closing - want it to stay a linear digested product. After dephosphorylation, the base vector was then incubated @ 37C for 30 minutes. Sample was then placed in a heat bath @ 65C for 15 minutes to inactivate enzyme (phosphotase).
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NOTE: Total volume in dephosphorylation = 56.6uL | ||||||||||||||||||||||||||||
2. Run RXN model on Calhoun (super computer). | ||||||||||||||||||||||||||||
3. Dilute base vector culture, allow to grow, then miniprep, then streak plates and make base vector glycerol stocks. | ||||||||||||||||||||||||||||
4. Autoclave dishes | ||||||||||||||||||||||||||||
5. Ligation: Follow table below. When ligation is complete, incubate products @16C for 1 hour. Heat inactivate DNA ligase (enzyme) @ 65C for 15 minutes.
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6. Ligation product Transformations: Transform the ligation products to TOP10 E. Coli cells. Allow growth for 2 hours. Following growth, 200 uL of all four ligation reactions and a control were plated on Kanamycin LB and were incubated at 37 degrees overnight. | ||||||||||||||||||||||||||||
7. Ordered Primers: Ordered primers for possible use in real-time PCR. |
Primer | Sequence |
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F Mcherry for modification | gaattcgcggccgcttctagatggtgagcaagggcgagg |
R Mcherry for modification | TATAAACGCAGAAAGGCCCACCC |
R LAMcI for realtime PCR | GGTTGTGCTTACCCATCTCTCC |
R p22mnt for realtime PCR | ACTCGCTCTGCTCATCGGCG |
R p22cII for realtime PCR | CAATCTACAGTGGTGTCGTGCC |
R GFP for realtime PCR | GAATGTTTCCATCTTCTTTAAAATC |
R mCherry for realtime PCR | GTGATGAACTTCGAGGACGGCG |