Difference between revisions of "Part:BBa K892011"
Line 1: | Line 1: | ||
− | |||
__NOTOC__ | __NOTOC__ | ||
<partinfo>BBa_K892011 short</partinfo> | <partinfo>BBa_K892011 short</partinfo> | ||
− | + | ||
+ | osmY fused to superfolder GFP with a serine-glycine linker, with sfGFP upstream of osmY. This part was made by swapping out the mamI coding sequence from [https://parts.igem.org/wiki/index.php?title=Part:BBa_K590016 BBa_K590016] and replacing it with [https://parts.igem.org/wiki/index.php?title=Part:BBa_K892008 BBa_K892008] using Gibson assembly. This part was characterized using the method outlined in the [http://2012.igem.org/Team:Washington/Protocols/osmY_Assay Washington 2012 wiki], the data summary is shown below. | ||
+ | |||
+ | [[Image:Washington_osmY_Assay_Results.png|border|950px|center|thumb|Each histogram depicts the average normalized fluorescence values for cells plus supernatant, cells only, and supernatant only. The image in the center is a visual representation of the presented data.]] | ||
Latest revision as of 21:47, 3 October 2012
sfGFP-osmY
osmY fused to superfolder GFP with a serine-glycine linker, with sfGFP upstream of osmY. This part was made by swapping out the mamI coding sequence from BBa_K590016 and replacing it with BBa_K892008 using Gibson assembly. This part was characterized using the method outlined in the [http://2012.igem.org/Team:Washington/Protocols/osmY_Assay Washington 2012 wiki], the data summary is shown below.
Sequence and Features
Assembly Compatibility:
- 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 SapI.rc site found at 94