Difference between revisions of "Part:BBa K3503008"
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<h2>Fire retardant test of K3503008</h2> | <h2>Fire retardant test of K3503008</h2> | ||
<p>The test subject was in the size of bed sheet in 300*130mm and the average Moisture content% is 13.55%-14.37%. As demonstrated on Fig 3, all of our engineered flame retardant displayed a significant improvement compared with the water control.</p> | <p>The test subject was in the size of bed sheet in 300*130mm and the average Moisture content% is 13.55%-14.37%. As demonstrated on Fig 3, all of our engineered flame retardant displayed a significant improvement compared with the water control.</p> | ||
− | <img src=""> | + | <img src="https://2020.igem.org/wiki/images/9/9c/T--Puiching_Macau--bedsheet_chart.png"> |
<div class="legend">Figure 3. Vertical Burning Test using bedsheet. | <div class="legend">Figure 3. Vertical Burning Test using bedsheet. | ||
− | <img src=""> | + | <img src="https://2020.igem.org/wiki/images/2/2e/T--Puiching_Macau--wood.png"> |
<div class="legend">Figure 4. Flame retardancy test using wood. | <div class="legend">Figure 4. Flame retardancy test using wood. | ||
<p>As demonstrated in Fig 4, all of our engineered K3503001, K3503007 and K3507008 flame retardants displayed a significant improvement compared with the water control. </p> | <p>As demonstrated in Fig 4, all of our engineered K3503001, K3503007 and K3507008 flame retardants displayed a significant improvement compared with the water control. </p> | ||
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Revision as of 19:47, 26 October 2020
CBD-alpha casein-His
This is a composite part designed to improve the fire retardancy with mussel cellulose binding domain (K1321014). The protein sequence in this part is based on Alpha s1 casein (K2924026) Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BamHI site found at 1357
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Successful expression of K3503008
In order to validate the protein expression of K3503001, K3503007 and K3503008, we performed SDS-PAGE (coomassie blue staining) and Western blot analysis. To make K3503001, K3503007 and K3503008 easily detectable via Western Blot, we designed our constructs to include a “His tag” which is targeted by a commercially available antibody. With the SDS-PAGE and western blot (anti-his for his-tagged protein), we found successful expression of K3503001, K3503007 and K3503008.
Before performing the SDS-PAGE, we grew up our engineered E. coli cells containing a plasmid with K3503001, K3503007 and K3503008 under control of the T7 promoter. Cells were induced with0.1mM IPTG until either OD0.4 (wavelength: 600nm) at 30°C. After expression, cells were then lysed according to our protein extraction protocol, and supernatant and pellet were collected for the SDS-PAGE.
(a)
- Lane1: Bio rad protein dual color ladder;
- Lane2: pet11a
- Lane3: K3503001
- Lane4:K3503001 with 0.1mM IPTG induction
- Lane5: K3503007
- Lane6: K3503007 with 0.1mM IPTG induction
- Lane7: K3503008
- Lane8:K3503008 with 0.1mM IPTG induction
Fire retardant test of K3503008
The test subject was in the size of bed sheet in 300*130mm and the average Moisture content% is 13.55%-14.37%. As demonstrated on Fig 3, all of our engineered flame retardant displayed a significant improvement compared with the water control.
As demonstrated in Fig 4, all of our engineered K3503001, K3503007 and K3507008 flame retardants displayed a significant improvement compared with the water control.