Difference between revisions of "Part:BBa K5353061"
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− | <figcaption><b>Figure | + | <figcaption><b>Figure 3. Expression of green fluorescent protein of the 1364 HEK293T cell. |
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Revision as of 21:41, 1 October 2024
1364 LentiV-MscS/HA: EGFP/Neo
After purify the plasmid DNA through midi-prep, we utilize them to package the lentivirus together with DVPR and VSV-G. We utilize these lentivirus to infect HEK293T cell and the successfully infected cells will express the MscS-HA tag protein. Meanwhile, this plasmid will also express green fluorescent protein (GFP). The MscS could be induced by physical stimulation (such as ultrasound) to induce the calcium overload. The HA tag could be used for Western blot and imaging detection of the MscS protein, while GFP can be used for validation of the lentivirus infection. The lentivirus gene sequence could be integrated into HEK293T cell genome by utilizing G418 selection (by the Neo marker gene).
The plasmid information.
The designed DNA was constructed and we used the midi-prep preparation kit to conduct the plasmid isolation and purification of the plasmid DNA (Table 1). The inserts in each construct were further validated by the PCR reaction (Figure 1. and Figure 2).
The successful infection could be visualized through fluorescence microscopy.(Figure 3.)
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 2227
Illegal XhoI site found at 2626 - 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 2361
Illegal AgeI site found at 1739 - 1000COMPATIBLE WITH RFC[1000]