Difference between revisions of "Part:BBa K3041002"
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Coding gene of Suckerin-12 of the <i> Dosidicus gigas </i> (Humboldt squid) codon-optimized for production in <i>E. coli</i>. | Coding gene of Suckerin-12 of the <i> Dosidicus gigas </i> (Humboldt squid) codon-optimized for production in <i>E. coli</i>. | ||
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+ | ==Validation== | ||
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+ | The successfully synthesized suckerins, codon-optimized for E.coli, were PCR amplified using the standard biobrick primers. In Figure 1, the PCR products of these specific suckerins were visualised on agarose gel. Suckerin-12, shows intense bands on agarose gel. | ||
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+ | [[File:PCR suckerin proteins.png]] | ||
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+ | <small><b>Figure 1: Amplified suckerin genes 8, 9 and 12.</b> | ||
+ | Polymerase chain reaction (PCR) products amplified with general prefix and suffix primers, shown by gel electrophoresis. Lane 1: 1kb ladder. PCR product at different concentrations of suckerin-8 (408 bp, lane 2 and 3), suckerin-9 (568 bp, lane 4 and 5), and suckerin-12 (696 bp, lane 6 and 7). The gel confirms the amplification of the desired suckerin proteins.</small> | ||
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Revision as of 08:35, 14 October 2019
Suckerin-12
Coding gene of Suckerin-12 of the Dosidicus gigas (Humboldt squid) codon-optimized for production in E. coli.
Validation
The successfully synthesized suckerins, codon-optimized for E.coli, were PCR amplified using the standard biobrick primers. In Figure 1, the PCR products of these specific suckerins were visualised on agarose gel. Suckerin-12, shows intense bands on agarose gel.
Figure 1: Amplified suckerin genes 8, 9 and 12.
Polymerase chain reaction (PCR) products amplified with general prefix and suffix primers, shown by gel electrophoresis. Lane 1: 1kb ladder. PCR product at different concentrations of suckerin-8 (408 bp, lane 2 and 3), suckerin-9 (568 bp, lane 4 and 5), and suckerin-12 (696 bp, lane 6 and 7). The gel confirms the amplification of the desired suckerin proteins.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 619