Difference between revisions of "Part:BBa K5353061"

 
 
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<partinfo>BBa_K5353061 short</partinfo>
 
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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).
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<p>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).</p>
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<p>The plasmid information.</p>
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    <figure data-ref="1">
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        <img src="https://static.igem.wiki/teams/5353/partsreg/figure-linear.png">
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        <figcaption><b>
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<img src="https://static.igem.wiki/teams/5353/compositepartsreg/1364-plasmid.png">
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        <figcaption><b>
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        </figcaption>
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    </figure>
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</div>
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<p>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).</p>
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<div>
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    <figure data-ref="1">
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        <img src="https://static.igem.wiki/teams/5353/partsreg/table-1.png">
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        <figcaption><b>Table 1.DNA concentrations extracted and purified.
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<img src="https://static.igem.wiki/teams/5353/partsreg/figure-1.png">
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        <figcaption><b>Figure 1. Gel electrophoresis results 1.
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<img src="https://static.igem.wiki/teams/5353/partsreg/figure-2.png">
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        <figcaption><b>Figure 2. Gel electrophoresis results 2.
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        </figcaption>
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    </figure>
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</div>
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<p>The successful infection could be visualized through fluorescence microscopy.(Figure 3.)</p>
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    <figure data-ref="1">
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        <img src="https://static.igem.wiki/teams/5353/compositepartsreg/1364-1.png">
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        <figcaption><b>Figure 3. Expression of green fluorescent protein of the 1364 HEK293T cell.
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        </figcaption>
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    </figure>
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<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here

Latest revision as of 22:13, 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).

Table 1.DNA concentrations extracted and purified.
Figure 1. Gel electrophoresis results 1.
Figure 2. Gel electrophoresis results 2.

The successful infection could be visualized through fluorescence microscopy.(Figure 3.)

Figure 3. Expression of green fluorescent protein of the 1364 HEK293T cell.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 2227
    Illegal XhoI site found at 2626
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 2361
    Illegal AgeI site found at 1739
  • 1000
    COMPATIBLE WITH RFC[1000]