Difference between revisions of "Part:BBa K4441009"
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<partinfo>BBa_K4441009 short</partinfo> | <partinfo>BBa_K4441009 short</partinfo> | ||
− | + | Sequence used in wetlab experiments: ATCAGTTTGAACAGTTGTCTGG is taken from [1] | |
− | |||
===Usage and Biology=== | ===Usage and Biology=== | ||
+ | This is the sequence for the Backward Loop Primer (LB). The LB primer is designed using the complementary strand corresponding to the region between B1 and B2 [2]. The Lb primer is part of the primer set that detects the BRAF V600E: | ||
+ | TTACTTACACGCCAAGTCAATCATCCACAGAGACCTCAAGAGTAATAATATATTTCTTCATGAAGACCTCACAGTAAAAATAGGTGATTTTGGTCTAGCTACAGAGAAATCTCGATGGA | ||
+ | GTGGGTCCCATCAGTTTGAACAGTTGTCTGGATCCATTTTGTGGATGGCACCAGAAGTCATCAGAATGCAAGATAAAAATCCATACAGCTTTCAGTCAGATGTATATGCATTTGGAATT | ||
+ | GTTCTGTATGAATTGATGACTGGACAGTTACCTTATTCAAACATCAACAACAGGGACCAG | ||
+ | |||
+ | ====Dilutions==== | ||
+ | |||
+ | Storage Primer Concentration: 100 μM | ||
+ | |||
+ | 10X Concentration (Stock): 16 μM | ||
+ | |||
+ | Volume of 10X primer mix: 10 μL | ||
+ | |||
+ | 1X Concentration (Final):1.6 μM | ||
+ | |||
+ | Volume of storage primer needed: 0.4 μL | ||
+ | |||
+ | Mixed with F3, B3, FIP, BIP and LB for a total of 4.4 μL -- Final primer mix | ||
+ | 1 μL of final primer mix is used in the LAMP reaction mix. For more information, visit https://2022.igem.org/Team:Washington | ||
+ | |||
+ | ====Alternative Sequence==== | ||
+ | As this set of primer failed to produce a positive result, we used NEB LAMP Primer Design Tool (https://lamp.neb.com/#!/) to generate an alternative set of primers. Unfortunately, due to time and budgetary constraints, these primers have not been ordered and experimented with yet. | ||
+ | |||
+ | Sequence: ATCAGTTTGAACAGTTGTCTGG | ||
+ | |||
+ | 5′ pos: 129 | ||
+ | |||
+ | 3′ pos: 15 | ||
+ | |||
+ | len: 22 | ||
+ | |||
+ | Tm: 60.59 | ||
+ | |||
+ | 5′ dG: -4.29 | ||
+ | |||
+ | 3′ dG: -5.35 | ||
+ | |||
+ | % GC: 41 | ||
+ | |||
+ | ==Citations== | ||
+ | 1. Papadakis, G., Pantazis, A. K., Fikas, N., Chatziioannidou, S., Tsiakalou, V., Michaelidou, K., ... & Gizeli, E. (2022). Portable real-time colorimetric LAMP-device for rapid quantitative detection of nucleic acids in crude samples. Scientific reports, 12(1), 1-15. | ||
+ | |||
+ | 2. A guide to lamp primer designing - primerexplorer. (n.d.). Retrieved October 12, 2022, from http://primerexplorer.jp/e/v4_manual/pdf/PrimerExplorerV4_Manual_1.pdf | ||
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Latest revision as of 05:32, 12 October 2022
BRAF V600E LB
Sequence used in wetlab experiments: ATCAGTTTGAACAGTTGTCTGG is taken from [1]
Usage and Biology
This is the sequence for the Backward Loop Primer (LB). The LB primer is designed using the complementary strand corresponding to the region between B1 and B2 [2]. The Lb primer is part of the primer set that detects the BRAF V600E: TTACTTACACGCCAAGTCAATCATCCACAGAGACCTCAAGAGTAATAATATATTTCTTCATGAAGACCTCACAGTAAAAATAGGTGATTTTGGTCTAGCTACAGAGAAATCTCGATGGA GTGGGTCCCATCAGTTTGAACAGTTGTCTGGATCCATTTTGTGGATGGCACCAGAAGTCATCAGAATGCAAGATAAAAATCCATACAGCTTTCAGTCAGATGTATATGCATTTGGAATT GTTCTGTATGAATTGATGACTGGACAGTTACCTTATTCAAACATCAACAACAGGGACCAG
Dilutions
Storage Primer Concentration: 100 μM
10X Concentration (Stock): 16 μM
Volume of 10X primer mix: 10 μL
1X Concentration (Final):1.6 μM
Volume of storage primer needed: 0.4 μL
Mixed with F3, B3, FIP, BIP and LB for a total of 4.4 μL -- Final primer mix 1 μL of final primer mix is used in the LAMP reaction mix. For more information, visit https://2022.igem.org/Team:Washington
Alternative Sequence
As this set of primer failed to produce a positive result, we used NEB LAMP Primer Design Tool (https://lamp.neb.com/#!/) to generate an alternative set of primers. Unfortunately, due to time and budgetary constraints, these primers have not been ordered and experimented with yet.
Sequence: ATCAGTTTGAACAGTTGTCTGG
5′ pos: 129
3′ pos: 15
len: 22
Tm: 60.59
5′ dG: -4.29
3′ dG: -5.35
% GC: 41
Citations
1. Papadakis, G., Pantazis, A. K., Fikas, N., Chatziioannidou, S., Tsiakalou, V., Michaelidou, K., ... & Gizeli, E. (2022). Portable real-time colorimetric LAMP-device for rapid quantitative detection of nucleic acids in crude samples. Scientific reports, 12(1), 1-15.
2. A guide to lamp primer designing - primerexplorer. (n.d.). Retrieved October 12, 2022, from http://primerexplorer.jp/e/v4_manual/pdf/PrimerExplorerV4_Manual_1.pdf
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]