Difference between revisions of "Part:BBa K590011"
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===Usage and Biology=== | ===Usage and Biology=== | ||
| − | This is a high copy plasmid backbone which has Chloramphenicol resistance, with pLac promoter and GFP | + | This is a high copy plasmid backbone which has Chloramphenicol resistance, with pLac promoter and GFP. This is a high efficiency Gibson Assembly vector. In a [http://2011.igem.org/Team:Washington/Magnetosomes/GibsonResults pGA vector evaluation, we determined the cloning efficiency by by dividing the # of bright colonies by the (# of total colonies - # of background colonies). The background colonies were determined by a control sample containing 100 picograms of just the pGA backbone |
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| + | On a average of 6 plates, the Gibson efficiency was determined to be 0.991129032 ~ '''99%!'''. | ||
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| + | A comparison was also conducted between the new pGA vectors and the standard pSB vectors. For more information/details, please click [http://2011.igem.org/Team:Washington/Magnetosomes/GibsonResults here!] | ||
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Revision as of 00:48, 28 September 2011
pGA1C3, Gibson assembly plasmid (bglBrick) with pLac-GFP insert
This Gibson Cloning friendly 1C3 plasmid backbone was made by [http://2011.igem.org/Team:Washington UW iGEM Team 2011] as part of the [http://2011.igem.org/Team:Washington/Magnetosomes/GibsonVectors Gibson Assembly toolkit].
Usage and Biology
This is a high copy plasmid backbone which has Chloramphenicol resistance, with pLac promoter and GFP. This is a high efficiency Gibson Assembly vector. In a [http://2011.igem.org/Team:Washington/Magnetosomes/GibsonResults pGA vector evaluation, we determined the cloning efficiency by by dividing the # of bright colonies by the (# of total colonies - # of background colonies). The background colonies were determined by a control sample containing 100 picograms of just the pGA backbone
On a average of 6 plates, the Gibson efficiency was determined to be 0.991129032 ~ 99%!.
A comparison was also conducted between the new pGA vectors and the standard pSB vectors. For more information/details, please click [http://2011.igem.org/Team:Washington/Magnetosomes/GibsonResults here!]
Sequence and Features
- 10INCOMPATIBLE WITH RFC[10]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 2051 - 12INCOMPATIBLE WITH RFC[12]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 2051 - 21INCOMPATIBLE WITH RFC[21]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 2051
Illegal BglII site found at 2066
Illegal BamHI site found at 1
Illegal XhoI site found at 16
Illegal XhoI site found at 1035
Illegal XhoI site found at 1927 - 23INCOMPATIBLE WITH RFC[23]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 2051 - 25INCOMPATIBLE WITH RFC[25]Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 2051 - 1000INCOMPATIBLE WITH RFC[1000]Plasmid lacks a prefix.
Plasmid lacks a suffix.