Difference between revisions of "Part:BBa K590012"

Latest revision as of 23:50, 28 September 2011

pGA4C5, Gibson assembly plasmid (bglBrick) with pLac-GFP insert

This is a Gibson Cloning-friendly 4C5 plasmid backbone that was made by the [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 low copy plasmid backbone which has Chloramphenicol resistance, with pLac promoter and GFP. This plasmid has been altered to conform to [http://dspace.mit.edu/handle/1721.1/46747 RFC 21] standards, with arbitrary, Gibson-friendly sequences placed in between the restriction enzyme sites EcoRI-BglII, and BamHI-PstI.

Sequence and Features

Assembly Compatibility:

10
INCOMPATIBLE WITH RFC[10]
Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 3200
12
INCOMPATIBLE WITH RFC[12]
Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 3200
21
INCOMPATIBLE WITH RFC[21]
Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 3200
Illegal BglII site found at 3215
Illegal BamHI site found at 1
Illegal XhoI site found at 16
23
INCOMPATIBLE WITH RFC[23]
Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 3200
25
INCOMPATIBLE WITH RFC[25]
Plasmid lacks a prefix.
Plasmid lacks a suffix.
Illegal EcoRI site found at 3200
1000
INCOMPATIBLE WITH RFC[1000]
Plasmid lacks a prefix.
Plasmid lacks a suffix.

@@ Line 1: / Line 1: @@
 __NOTOC__
 <partinfo>BBa_K590012 short</partinfo>
-Backbone that is Gibson reaction friendly (Bgl Brick)
+This is a Gibson Cloning-friendly 4C5 plasmid backbone that was made by the [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].
-<!-- Add more about the biology of this part here
 ===Usage and Biology===
+This is a low copy plasmid backbone which has Chloramphenicol resistance, with pLac promoter and GFP.  This plasmid has been altered to conform to [http://dspace.mit.edu/handle/1721.1/46747 RFC 21] standards, with arbitrary, Gibson-friendly sequences placed in between the restriction enzyme sites EcoRI-BglII, and BamHI-PstI.
 <!-- -->