Difference between revisions of "Part:BBa K2889000:Design"
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1.3 Ligation of purified IL7-AS-S2 fragments to pSB1C3 vector. | 1.3 Ligation of purified IL7-AS-S2 fragments to pSB1C3 vector. | ||
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IL7-AS-S2 fragments were ligated to PSB1C3 vector. Then we selected the positive clones by PCR and sequencing (Fig 3). | IL7-AS-S2 fragments were ligated to PSB1C3 vector. Then we selected the positive clones by PCR and sequencing (Fig 3). | ||
https://static.igem.org/mediawiki/parts/f/f9/Verify_pSB1C3-IL7-AS-S2_by_sequencing.jpeg | https://static.igem.org/mediawiki/parts/f/f9/Verify_pSB1C3-IL7-AS-S2_by_sequencing.jpeg | ||
Revision as of 12:27, 9 October 2018
pSB1C3-IL7-AS-S2
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 198
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
We wanted to investigate which domain is essential for the function of IL7-AS. We cloned the truncated sequences of IL7-AS (IL7-AS-S2) into pSB1C3 for submitting to IGEM 2018 and inserted IL7-AS-S2 into pCDNA3.1 to study the function.
Source
We cloned the truncated sequences of IL7-AS (IL7-AS-S2,411 bp) from human cells.
1.1 Amplification of IL7-AS-S2 fragments from human cell line. First we amplified IL7-AS-S2 using primers. After that, we purified the PCR products by PCR Purification Kit and digested them with restriction enzymes EcoRI and PstI (Fig 1).
1.2 Digested PSB1C3 vector. We digested the PSB1C3 vectors with EcoRI and PstI (Fig 2).
1.3 Ligation of purified IL7-AS-S2 fragments to pSB1C3 vector.
IL7-AS-S2 fragments were ligated to PSB1C3 vector. Then we selected the positive clones by PCR and sequencing (Fig 3).
References
Roux, B. T., Heward, J. A., Donnelly, L. E., Jones, S. W., and Lindsay, M. A. (2017) Catalog of Differentially Expressed Long Non-Coding RNA following Activation of Human and Mouse Innate Immune Response. Frontiers in immunology 8, 1038