BBa_B0010
1
BBa_B0010
T1 from E. coli rrnB
2003-11-19T12:00:00Z
2015-08-31T04:07:20Z
Transcriptional terminator consisting of a 64 bp stem-loop.
false
false
_1_
0
24
7
In stock
false
true
Randy Rettberg
annotation7018
1
BBa_B0010
range7018
1
1
80
annotation4184
1
stem_loop
range4184
1
12
55
BBa_B0033
1
BBa_B0033
RBS.4 (weaker) -- derivative of BBa_0030
2003-01-31T12:00:00Z
2015-08-31T04:07:20Z
Released HQ 2013
Weaker RBS based on Ron Weiss thesis. Strengths relative to <bb_part>BBa_B0030</bb_part>, <bb_part>BBa_B0031</bb_part>, <bb_part>BBa_B0032</bb_part>.
false
true
_41_44_48_46_1_
0
24
7
In stock
false
Varies from -6 to +1 region from original sequence to accomodate BioBricks suffix ("RBS-3" in figure 4-14 of thesis). <p>No secondary structures are formed in the given RBS region. Users should check for secondary structures induced in the RBS by upstream and downstream elements in the +50 to -50 region, as such structures will greatly affect the strength of the RBS.
Contact info for this part: <a href="mailto:(bchow@media.mit.edu)">Brian Chow</a>
true
Vinay S Mahajan, Voichita D. Marinescu, Brian Chow, Alexander D Wissner-Gross and Peter Carr IAP, 2003.
annotation1713
1
RBS-4\Weaker
range1713
1
1
11
annotation7028
1
BBa_B0033
range7028
1
1
11
annotation1714
1
RBS
range1714
1
7
10
BBa_K581008
1
BBa_K581008
RBS+ccdB+Termintor
2011-09-25T11:00:00Z
2015-07-09T12:57:45Z
Escherichia coli.
Released HQ 2013
This is the cell death protein coding sequence under the control of a relatively weak RBS. It is replicable in non-ccdB resistant strains.
true
false
_752_
4206
8589
9
In stock
false
Use a relatively weak RBS so the coding sequence would be replicable in non-ccdB resistant strains under the putative promoter in VF region.
false
Deng Linna
component2143057
1
BBa_K145151
component2143052
1
BBa_B0033
component2143064
1
BBa_B0015
annotation2143052
1
BBa_B0033
range2143052
1
1
11
annotation2143057
1
BBa_K145151
range2143057
1
18
323
annotation2143064
1
BBa_B0015
range2143064
1
332
460
BBa_K145151
1
ccdB
ccdB coding region
2008-08-06T11:00:00Z
2015-07-08T03:14:50Z
P1010
Released HQ 2013
Coding region for the ccdB (control of cell death) gene.
true
false
_257_
4206
2970
9
In stock
true
just one stop codon in the end
true
Jonas Demeulemeester
annotation1970251
1
start
range1970251
1
1
3
annotation1970252
1
stop
range1970252
1
304
306
annotation1970253
1
cds
range1970253
1
1
303
BBa_K1350000
1
BBa_K1350000
Ccdb E.coli suicide IPTG
2014-09-26T11:00:00Z
2015-05-08T01:10:01Z
"IPTG bomb" kill the E.coli by coding Ccdb toxin protein. The Ccdb come from BBa_K581008(RBS+ccdB+Termintor),and T5-lac Promoter from BBa_K592008
A system designed to kill E.coli when IPTG added . IPTG can efficiently trigger a large numumber of Ccdb protein .And Ccdb protein a can combine with E.coli ,So it can effectively kill the E.coli.
false
false
_1725_
0
20427
9
It's complicated
false
We have been thinking of a way, that way we could eliminate E.coli. Now we Ccdb protein-bound T5-lac and make the controls to suit our needs.
false
JieRui Chen
component2387309
1
BBa_K581008
component2387294
1
BBa_K592008
annotation2387294
1
BBa_K592008
range2387294
1
1
126
annotation2387309
1
BBa_K581008
range2387309
1
135
594
BBa_K592008
1
PT5lac
T5-lac Promoter
2011-09-10T11:00:00Z
2015-05-08T01:12:48Z
Phage T5
Released HQ 2013
T5-lac promoter is a hybrid promoter made from the phage T5 early promoter and lac-operon. It contains three LacI binding sites and remains repressed in LacIq strains where LacI is expressed in high levels. It is inducible by IPTG, and recognizable by E.coli RNA polymerase. Compared to the T7 promoters, T5-lac promoter doesn't require the co-expression of phage polymerase.
false
false
_763_
0
7929
9
In stock
false
The most common DH5alpha and TOP10 used in assembly are not LacI-constitutive (LacIq) strains. Thus, any ORF placed downstream to this promoter will be massively transcribed. Therefore, it's recommended to employ low-copy number plasmids or even LacIq strains when adding genes to this promoter.
false
Erik Lundin
annotation2135658
1
lacOi site
range2135658
1
94
123
annotation2135659
1
-35 signal
range2135659
1
63
68
annotation2135656
1
lacO1 site
range2135656
1
1
26
annotation2135657
1
lacO1 site
range2135657
1
69
86
annotation2127135
1
T5-lac promoter
range2127135
1
1
126
annotation2135661
1
-10 signal
range2135661
1
87
93
BBa_B0012
1
BBa_B0012
TE from coliphageT7
2003-01-31T12:00:00Z
2015-08-31T04:07:20Z
Derived from the TE terminator of T7 bacteriophage between Genes 1.3 and 1.4 <genbank>V01146</genbank>.
Released HQ 2013
Transcription terminator for the <i>E.coli</i> RNA polymerase.
false
false
_1_
0
24
7
In stock
false
<P> <P>Suggested by Sri Kosuri and Drew Endy as a high efficiency terminator. The 5' end cutoff was placed immediately after the TAA stop codon and the 3' end cutoff was placed just prior to the RBS of Gene 1.4 (before AAGGAG).<P> Use anywhere transcription should be stopped when the gene of interest is upstream of this terminator.
false
Reshma Shetty
annotation1687
1
stop
range1687
1
34
34
annotation1690
1
polya
range1690
1
28
41
annotation1686
1
T7 TE
range1686
1
8
27
annotation7020
1
BBa_B0012
range7020
1
1
41
BBa_B0015
1
BBa_B0015
double terminator (B0010-B0012)
2003-07-16T11:00:00Z
2015-08-31T04:07:20Z
Released HQ 2013
Double terminator consisting of BBa_B0010 and BBa_B0012
false
true
_1_
0
24
7
In stock
false
true
Reshma Shetty
component1916612
1
BBa_B0012
component1916610
1
BBa_B0010
annotation1916612
1
BBa_B0012
range1916612
1
89
129
annotation1916610
1
BBa_B0010
range1916610
1
1
80
BBa_B0010_sequence
1
ccaggcatcaaataaaacgaaaggctcagtcgaaagactgggcctttcgttttatctgttgtttgtcggtgaacgctctc
BBa_B0033_sequence
1
tcacacaggac
BBa_K145151_sequence
1
atgcagtttaaggtttacacctataaaagagagagccgttatcgtctgtttgtggatgtacagagtgatattattgacacgcccgggcgacggatggtgatccccctggccagtgcacgtctgctgtcagataaagtctcccgtgaactttacccggtggtgcatatcggggatgaaagctggcgcatgatgaccaccgatatggccagtgtgccggtctccgttatcggggaagaagtggctgatctcagccaccgcgaaaatgacatcaaaaacgccattaacctgatgttctggggaatataa
BBa_K1350000_sequence
1
tgtggaattgtgagcggataacaattacgagcttcatgcacagtgaaatcatgaaaaatttatttgctttgtgagcggataacaattataatatgtggaattgtgagcgctcacaattccacaacgtactagagtcacacaggactactagatgcagtttaaggtttacacctataaaagagagagccgttatcgtctgtttgtggatgtacagagtgatattattgacacgcccgggcgacggatggtgatccccctggccagtgcacgtctgctgtcagataaagtctcccgtgaactttacccggtggtgcatatcggggatgaaagctggcgcatgatgaccaccgatatggccagtgtgccggtctccgttatcggggaagaagtggctgatctcagccaccgcgaaaatgacatcaaaaacgccattaacctgatgttctggggaatataatactagagccaggcatcaaataaaacgaaaggctcagtcgaaagactgggcctttcgttttatctgttgtttgtcggtgaacgctctctactagagtcacactggctcaccttcgggtgggcctttctgcgtttata
BBa_K581008_sequence
1
tcacacaggactactagatgcagtttaaggtttacacctataaaagagagagccgttatcgtctgtttgtggatgtacagagtgatattattgacacgcccgggcgacggatggtgatccccctggccagtgcacgtctgctgtcagataaagtctcccgtgaactttacccggtggtgcatatcggggatgaaagctggcgcatgatgaccaccgatatggccagtgtgccggtctccgttatcggggaagaagtggctgatctcagccaccgcgaaaatgacatcaaaaacgccattaacctgatgttctggggaatataatactagagccaggcatcaaataaaacgaaaggctcagtcgaaagactgggcctttcgttttatctgttgtttgtcggtgaacgctctctactagagtcacactggctcaccttcgggtgggcctttctgcgtttata
BBa_B0012_sequence
1
tcacactggctcaccttcgggtgggcctttctgcgtttata
BBa_K592008_sequence
1
tgtggaattgtgagcggataacaattacgagcttcatgcacagtgaaatcatgaaaaatttatttgctttgtgagcggataacaattataatatgtggaattgtgagcgctcacaattccacaacg
BBa_B0015_sequence
1
ccaggcatcaaataaaacgaaaggctcagtcgaaagactgggcctttcgttttatctgttgtttgtcggtgaacgctctctactagagtcacactggctcaccttcgggtgggcctttctgcgtttata
igem2sbol
1
iGEM to SBOL conversion
Conversion of the iGEM parts registry to SBOL2.1
Chris J. Myers
James Alastair McLaughlin
2017-03-06T15:00:00.000Z