Difference between revisions of "Part:BBa K4436017"
(→Characterization) |
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===Characterization === | ===Characterization === | ||
− | We | + | We began by preparing a PCR mix on ice, which consisted of: |
+ | |||
32.5 microliters of Water | 32.5 microliters of Water | ||
+ | |||
10 microliters of Q5 Reaction Buffer | 10 microliters of Q5 Reaction Buffer | ||
+ | |||
2.5 Microliters of the Forward Primer | 2.5 Microliters of the Forward Primer | ||
+ | |||
2.5 Microliters of the Reverse Primer | 2.5 Microliters of the Reverse Primer | ||
+ | |||
1 microliter of 0.1ng/microliter PKD3 | 1 microliter of 0.1ng/microliter PKD3 | ||
+ | |||
0.5 Microliters of Q5 DNA Polymerase. | 0.5 Microliters of Q5 DNA Polymerase. | ||
Line 30: | Line 36: | ||
3) Final Extension: 72 C at 120s | 3) Final Extension: 72 C at 120s | ||
+ | |||
4) Hold at 4 C | 4) Hold at 4 C | ||
Finally, we then ran the results on a 1% Agarose Gel to confirm the results. We were expecting a band at 1.1 kB, which was about the size of the pKD3 plasmid. | Finally, we then ran the results on a 1% Agarose Gel to confirm the results. We were expecting a band at 1.1 kB, which was about the size of the pKD3 plasmid. | ||
− | As you can see below, we obtained those results around the first week in August. | + | As you can see below, we obtained those results around the first week in August. The faint band is in the correct location, and while a primer dimer did form (the band at around 120 bp), the PCR was still sucessful. |
[[File:PKD3 PCR 8-4 gel.png]] | [[File:PKD3 PCR 8-4 gel.png]] |
Revision as of 14:06, 12 October 2022
Forward Primer for Lambda Red CsgA Knockout
This is the forward primer for the Lambda Red Knockout of the native csgA in E. Coli.
Usage and Biology
Lambda Red Knockout is a system used by many molecular biologists to knockout single genes or even entire operons (Datsenko and Wanner, 2000). It uses a phage recombinase to replace the native gene in a strain of E. Coli with an antibiotic resistance gene (Datsenko and Wanner, 2000). One of the first few steps of a Lambda Red Knockout is the PCR amplification of a custom primer, with homology to both the antibiotic resistance gene (in the recombinase sites next to it) and the native gene (Datsenko and Wanner, 2000). Accordingly, this primer can be used to amplify the antibiotic resistance gene while allowing for the recombinase to recognize this site and replace the native gene with said gene (Datsenko and Wanner, 2000).
Characterization
We began by preparing a PCR mix on ice, which consisted of:
32.5 microliters of Water
10 microliters of Q5 Reaction Buffer
2.5 Microliters of the Forward Primer
2.5 Microliters of the Reverse Primer
1 microliter of 0.1ng/microliter PKD3
0.5 Microliters of Q5 DNA Polymerase.
We then ran the following PCR Program:
1) Initial Denaturation: 98 C for 30 seconds
2) 30 cycles of PCR
-> 98 C for 10 seconds -> 66 C for 30s -> 66 C for 90 s
3) Final Extension: 72 C at 120s
4) Hold at 4 C
Finally, we then ran the results on a 1% Agarose Gel to confirm the results. We were expecting a band at 1.1 kB, which was about the size of the pKD3 plasmid.
As you can see below, we obtained those results around the first week in August. The faint band is in the correct location, and while a primer dimer did form (the band at around 120 bp), the PCR was still sucessful.
References
Datsenko, Kirill A., and Barry L. Wanner. “One-Step Inactivation of Chromosomal Genes in Escherichia Coli K-12 Using PCR Products.” Proceedings of the National Academy of Sciences, vol. 97, no. 12, 2000, pp. 6640–6645., https://doi.org/10.1073/pnas.120163297. Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]