Team:GeorgiaTech/Parts

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<h1>Biobricks and Devices</h1>
<h1>Biobricks and Devices</h1>
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<th width="30%">Name</th><th width="15%">Type</th><th width="40%">Description</th><th width="10%">Length</th>
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<th width="20%">Name</th><th width="20%">Type</th><th width="50%">Description</th><th width="10%">Length</th>
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<tr><td>BBa_K1539001<td>Part<td>Coding sequence has a high efficiency promoter followed by a high efficiency RBS to express fluorescent protein mCherry.<td>814 bp
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<tr><td>BBa_K1539002<td>Part<td>Coding sequence has a low efficiency promoter followed by a low efficiency RBS to express fluorescent protein mCherry.<td>814 bp
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<tr><td>BBa_K1539003<td>Part<td>This coding sequence is for the beta subunit for Protein A (composed of three subunits) of the multi-complex enzyme soluble methane monooxyegnase (sMMO). The gene has been codon optimized for E. coli.<td>1170 bp
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<tr><td>BBa_K1539005<td>Part<td>This coding sequence is for the gamma subunit for Protein A (composed of three subunits) of the multi-complex enzyme soluble methane monooxyegnase (sMMO). The gene has been codon optimized for E. coli.<td>513 bp
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<tr><td>BBa_K1539008<td>Part<td>This coding sequence is for the gene sMMO B, encoding Protein B of the multi-complex enzyme soluble methane monooxyegnase (sMMO). The gene has been codon optimized for E. coli.<td>426 bp
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<tr><td>BBa_K1539013<td>Part<td>This coding sequence is for the gene sMMO C, encoding Protein C of the multi-complex enzyme soluble methane monooxyegnase (sMMO). The gene has been codon optimized for E. coli.<td>1047 bp
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<tr><td>BBa_K1539021<td>Device<td>This primer is used to insert a high efficiency RBS to transcribe genes starting with ATG in E. coli.<td>46 bp
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<tr><td>BBa_K1539034<td>Device<td>This primer is used to insert a low efficiency RBS to transcribe genes starting with ATG in E. coli.<td>46 bp
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<tr><td>BBa_K1539055<td>Device<td>This primer is used to insert a high efficiency promoter to translate E. coli. genes. Must be used after insertion of RBS primer. Use Georgia Tech iGEM RBS primers (BBa_K1539021 or BBa_K1539034) or an RBS primer with a similar design.<td>58 bp
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<tr><td>BBa_K1539089<td>Device<td>This primer is used to insert a low efficiency promoter to translate E. coli. genes. Must be used after insertion of RBS primer. Use Georgia Tech iGEM RBS primers (BBa_K1539021 or BBa_K1539034) or an RBS primer with a similar design.<td>58 bp
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Latest revision as of 05:26, 15 October 2014

Biobricks and Devices

NameTypeDescriptionLength
BBa_K1539001PartCoding sequence has a high efficiency promoter followed by a high efficiency RBS to express fluorescent protein mCherry.814 bp
BBa_K1539002PartCoding sequence has a low efficiency promoter followed by a low efficiency RBS to express fluorescent protein mCherry.814 bp
BBa_K1539003PartThis coding sequence is for the beta subunit for Protein A (composed of three subunits) of the multi-complex enzyme soluble methane monooxyegnase (sMMO). The gene has been codon optimized for E. coli.1170 bp
BBa_K1539005PartThis coding sequence is for the gamma subunit for Protein A (composed of three subunits) of the multi-complex enzyme soluble methane monooxyegnase (sMMO). The gene has been codon optimized for E. coli.513 bp
BBa_K1539008PartThis coding sequence is for the gene sMMO B, encoding Protein B of the multi-complex enzyme soluble methane monooxyegnase (sMMO). The gene has been codon optimized for E. coli.426 bp
BBa_K1539013PartThis coding sequence is for the gene sMMO C, encoding Protein C of the multi-complex enzyme soluble methane monooxyegnase (sMMO). The gene has been codon optimized for E. coli.1047 bp
BBa_K1539021DeviceThis primer is used to insert a high efficiency RBS to transcribe genes starting with ATG in E. coli.46 bp
BBa_K1539034DeviceThis primer is used to insert a low efficiency RBS to transcribe genes starting with ATG in E. coli.46 bp
BBa_K1539055DeviceThis primer is used to insert a high efficiency promoter to translate E. coli. genes. Must be used after insertion of RBS primer. Use Georgia Tech iGEM RBS primers (BBa_K1539021 or BBa_K1539034) or an RBS primer with a similar design.58 bp
BBa_K1539089DeviceThis primer is used to insert a low efficiency promoter to translate E. coli. genes. Must be used after insertion of RBS primer. Use Georgia Tech iGEM RBS primers (BBa_K1539021 or BBa_K1539034) or an RBS primer with a similar design.58 bp

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