Difference between revisions of "Part:BBa K314103"

Revision as of 04:39, 23 October 2010

Lac induced expression cassette

Lac induced protein expression insert includes f1 origin K314110, Lac I generator K314111, a lac I repressed promoter R0011, 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.

Lac induced, BBa_R0011, constitutive 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:

10
COMPATIBLE WITH RFC[10]
12
COMPATIBLE WITH RFC[12]
21
COMPATIBLE WITH RFC[21]
23
COMPATIBLE WITH RFC[23]
25
INCOMPATIBLE WITH RFC[25]
Illegal NgoMIV site found at 126
1000
COMPATIBLE WITH RFC[1000]

@@ Line 3: / Line 3: @@
 Lac induced protein expression insert includes f1 origin K314110, Lac I generator K314111, a lac I repressed promoter R0011, 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.
+Lac induced, <partinfo>R0011</partinfo>, constitutive 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===
+{| cellpadding="1" cellspacing="8"
+|-
+|[[Image:Washington2010_vector_assay_data.png | 650px]]
+|<partinfo>E0040</partinfo> (GFP) was inserted between S and P using standard BioBrick assembly.  The resulting constructs were grow in DH5a (constitutive promoters <partinfo>BBa_J23100</partinfo> or <partinfo>BBa_J23114</partinfo>, as well as inducible promoter <partinfo>R0011</partinfo>) or BL21(DE3)* (T7 promoter, <partinfo>BBa_K314104</partinfo>) 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.
+|-
+|}