Difference between revisions of "Part:BBa K314103"
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<partinfo>BBa_K314103 short</partinfo> | <partinfo>BBa_K314103 short</partinfo> | ||
− | + | Lactose (IPTG) inducible inducible, <partinfo>R0011</partinfo>, protein expression insert includes f1 origin [https://parts.igem.org/Part:BBa_K314110 K314110], a Lac I generator [https://parts.igem.org/Part:BBa_K314111 K314111], a high expression promoter [https://parts.igem.org/Part:BBa_J23100 J23100], and the Elowitz standard RBS [https://parts.igem.org/Part:BBa_B0034 B0034]. When ligated with a protein coding sequence at the SpeI site the scar site created will create proper spacing for protein expression. | |
===Usage and Biology=== | ===Usage and Biology=== |
Revision as of 04:44, 23 October 2010
Lac induced expression cassette
Lactose (IPTG) inducible inducible, BBa_R0011, protein expression insert includes f1 origin K314110, a Lac I generator K314111, a high expression promoter J23100, and the Elowitz standard RBS B0034. When ligated with a protein coding sequence at the SpeI site the scar site created will create proper spacing for protein expression.
Usage and Biology
BBa_E0040 (GFP) was inserted between S and P using standard BioBrick assembly. The resulting constructs were grow in DH5a (constitutive promoters BBa_J23100 or BBa_J23114, as well as inducible promoter BBa_R0011) or BL21(DE3)* (T7 promoter, BBa_K314104) cells overnight at 298K in either the presence or absence of 0.5mM IPTG. The cells were harvested, washed in PBS, and then fluorescence for the whole cells was measured on a fluorometer (ex. 485, em. 525) and normalized to cell density (OD600). Cells that did not contain GFP were used as a blank. As observed, the addition of IPTG significantly increased the observed fluorescence of the cells. |
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 126
- 1000COMPATIBLE WITH RFC[1000]