Difference between revisions of "Team:BNU-China/Notebook"

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                <h1>Notebook</h1>
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                <small id="secondary-page-header">This is our Notebook</small>
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                    <h2> Week 1 </h2>
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                    <h3> Wet lab </h3>
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                    <p> We choose the plasmid of kit plate to transform and amplify. We design parts by adding
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                        promoter
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                        <p> We choose the plasmid of kit plate to transform and amplify. We design parts by adding
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                        (BBa_K206000) and RBS(BBa_B0034) to the upstream region of luciferase gene and adding prefix
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                        and
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                            (BBa_K206000) and RBS(BBa_B0034) to the upstream region of luciferase gene and adding prefix
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                        suffix and and we committed the GENEWIZ company to synthesize this gene.
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                            and
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                            suffix and and we committed the GENEWIZ company to synthesize this gene.
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                    <p> We gather and summarize the data of algal bloom case in North China. </p>
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                        <p> We gather and summarize the data of algal bloom case in North China. </p>
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                <h2>Cloning</h2>
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            <h2>Cloning</h2>
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                <h3>PCR</h3>
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            <h3>PCR</h3>
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                <h4>Reaction system:</h4>
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            <h4>Reaction system:</h4>
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Revision as of 20:28, 17 October 2016

Team:BNU-CHINA - 2016.igem.org

Notebook

Notebook

This is our Notebook

Week 1

Wet lab

We choose the plasmid of kit plate to transform and amplify. We design parts by adding promoter (BBa_K206000) and RBS(BBa_B0034) to the upstream region of luciferase gene and adding prefix and suffix and and we committed the GENEWIZ company to synthesize this gene.

We gather and summarize the data of algal bloom case in North China.

Cloning

PCR

Reaction system: