Difference between revisions of "Part:BBa K3503007"
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<partinfo>BBa_K3503007 short</partinfo> | <partinfo>BBa_K3503007 short</partinfo> | ||
− | + | This is a composite part designed to improve the fire retardancy with mussel adhesion protein K3089023. The protein sequence in this part is based on Alpha s1 casein (K2924026) | |
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<partinfo>BBa_K3503007 parameters</partinfo> | <partinfo>BBa_K3503007 parameters</partinfo> | ||
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+ | <html> | ||
+ | <style> | ||
+ | .legend { | ||
+ | font-size: .9em; | ||
+ | } | ||
+ | p { | ||
+ | text-align: justify; | ||
+ | } | ||
+ | .content img { | ||
+ | max-height:80vh; | ||
+ | max-width:100%; | ||
+ | margin: 0 auto; | ||
+ | clear: both; | ||
+ | } | ||
+ | </style> | ||
+ | <div class="content"> | ||
+ | |||
+ | <h2>Successful expression of K3503007</h2> | ||
+ | <p>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.<br> | ||
+ | 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. | ||
+ | </p> | ||
+ | For more experimental details of the Western Blot and SDS-PAGE, please see <a href="https://2020.igem.org/Team:PuiChing_Macau/Protocol">protocol</a>. | ||
+ | |||
+ | <img src=""> | ||
+ | <div class="legend">Figure 2. Western Blot results of inducible expression of K3503001, K3503007, K3503008 | ||
+ | <br>(a) | ||
+ | <ul> | ||
+ | <li>Lane1: Bio rad protein dual color ladder; | ||
+ | <li>Lane2: pet11a</li> | ||
+ | <li>Lane3: K3503001</li> | ||
+ | <li>Lane4:K3503001 with 0.1mM IPTG induction</li> | ||
+ | <li>Lane5: K3503007</li> | ||
+ | <li>Lane6: K3503007 with 0.1mM IPTG induction</li> | ||
+ | <li>Lane7: K3503008</li> | ||
+ | <li>Lane8:K3503008 with 0.1mM IPTG induction</li> | ||
+ | </ul> | ||
+ | </div> | ||
+ | |||
+ | <h2>Fire retardant test of K3503007</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> | ||
+ | <img src=""> | ||
+ | <div class="legend">Figure 3. Vertical Burning Test using bedsheet. | ||
+ | <img src=""> | ||
+ | <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> | ||
+ | |||
+ | </html> |
Revision as of 15:12, 25 October 2020
mfp5-alpha casein-His
This is a composite part designed to improve the fire retardancy with mussel adhesion protein K3089023. 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 499
Illegal BamHI site found at 727
Illegal BamHI site found at 1525 - 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Successful expression of K3503007
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 K3503007
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.