pTRE3G-ZsGreen1

Vector for doxycycline-inducible expression of a gene together with the ZsGreen fluorescent protein.

Sequence Author: Clontech (TaKaRa)

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EcoRI (4695) AatII (4624) ZraI (4622) ScaI (4182) TatI (4180) PvuI (4072) FspI (3924) NmeAIII (3850) BsaI (3763) AlwNI (3225) PspFI (3117) BseYI (3113) DrdI (2917) BspQI - SapI (2693) HpaI (2491) MfeI (2478) AvaI - BsoBI - PaeR7I - PspXI - XhoI (1) KasI (274) NarI (275) SfoI (276) PluTI (278) Eco53kI (292) SacI (294) SalI (383) AccI (384) BclI * (471) PvuII (575) Bpu10I (855) EcoNI (899) BspEI * (1064) EagI (1085) NgoMIV (1087) NaeI (1089) FseI (1091) PspOMI (1206) ApaI (1210) AvrII (1244) BsaAI - PmlI (1409) BfuAI - BspMI - PaqCI (1432) DraIII (1456) Acc65I (1534) KpnI (1538) BtgI (1627) BmgBI (1636) MscI (1671) MluI (1692) NheI (1704) BmtI (1708) PstI - SbfI (1714) BamHI (1716) BsgI (2159) BsaBI * (2390) pTRE3G-ZsGreen1 4700 bp
EcoRI  (4695)
1 site
G A A T T C C T T A A G
AatII  (4624)
1 site
G A C G T C C T G C A G
ZraI  (4622)
1 site
G A C G T C C T G C A G
ScaI  (4182)
1 site
A G T A C T T C A T G A
TatI  (4180)
1 site
W G T A C W W C A T G W
PvuI  (4072)
1 site
C G A T C G G C T A G C
FspI  (3924)
1 site
T G C G C A A C G C G T
NmeAIII  (3850)
1 site
G C C G A G ( N ) 18-19 N N C G G C T C ( N ) 18-19

Efficient cleavage requires at least two copies of the NmeAIII recognition sequence.
Sticky ends from different NmeAIII sites may not be compatible.
For full activity, add fresh S-adenosylmethionine (SAM).
BsaI  (3763)
1 site
G G T C T C N C C A G A G N ( N ) 4

Sticky ends from different BsaI sites may not be compatible.
BsaI can be used between 37°C and 50°C.
AlwNI  (3225)
1 site
C A G N N N C T G G T C N N N G A C

Sticky ends from different AlwNI sites may not be compatible.
PspFI  (3117)
1 site
C C C A G C G G G T C G
BseYI  (3113)
1 site
C C C A G C G G G T C G

After cleavage, BseYI can remain bound to DNA and alter its electrophoretic mobility.
DrdI  (2917)
1 site
G A C N N N N N N G T C C T G N N N N N N C A G

Sticky ends from different DrdI sites may not be compatible.
BspQI  (2693)
1 site
G C T C T T C N C G A G A A G N N N N

Sticky ends from different BspQI sites may not be compatible.
SapI  (2693)
1 site
G C T C T T C N C G A G A A G N N N N

Sticky ends from different SapI sites may not be compatible.
SapI gradually settles in solution, so a tube of SapI should be mixed before removing an aliquot.
HpaI  (2491)
1 site
G T T A A C C A A T T G
MfeI  (2478)
1 site
C A A T T G G T T A A C
AvaI  (1)
1 site
C Y C G R G G R G C Y C

Sticky ends from different AvaI sites may not be compatible.
BsoBI  (1)
1 site
C Y C G R G G R G C Y C

Sticky ends from different BsoBI sites may not be compatible.
BsoBI is typically used at 37°C, but can be used at temperatures up to 65°C.
PaeR7I  (1)
1 site
C T C G A G G A G C T C

PaeR7I does not recognize the sequence CTCTCGAG.
PspXI  (1)
1 site
V C T C G A G B B G A G C T C V
XhoI  (1)
1 site
C T C G A G G A G C T C
KasI  (274)
1 site
G G C G C C C C G C G G
NarI  (275)
1 site
G G C G C C C C G C G G

Efficient cleavage requires at least two copies of the NarI recognition sequence.
SfoI  (276)
1 site
G G C G C C C C G C G G
PluTI  (278)
1 site
G G C G C C C C G C G G

Efficient cleavage requires at least two copies of the PluTI recognition sequence.
Eco53kI  (292)
1 site
G A G C T C C T C G A G
SacI  (294)
1 site
G A G C T C C T C G A G
SalI  (383)
1 site
G T C G A C C A G C T G
AccI  (384)
1 site
G T M K A C C A K M T G

Efficient cleavage with AccI requires ≥13 bp on each side of the recognition sequence.
Sticky ends from different AccI sites may not be compatible.
BclI  (471)
1 site
T G A T C A A C T A G T
* Blocked by Dam methylation.
BclI is typically used at 50-55°C, but is 50% active at 37°C.
PvuII  (575)
1 site
C A G C T G G T C G A C
Bpu10I  (855)
1 site
C C T N A G C G G A N T C G

Cleavage may be enhanced when more than one copy of the Bpu10I recognition sequence is present.
This recognition sequence is asymmetric, so ligating sticky ends generated by Bpu10I will not always regenerate a Bpu10I site.
Sticky ends from different Bpu10I sites may not be compatible.
EcoNI  (899)
1 site
C C T N N N N N A G G G G A N N N N N T C C

The 1-base overhangs produced by EcoNI may be hard to ligate.
Sticky ends from different EcoNI sites may not be compatible.
BspEI  (1064)
1 site
T C C G G A A G G C C T
* Blocked by Dam methylation.
EagI  (1085)
1 site
C G G C C G G C C G G C
NgoMIV  (1087)
1 site
G C C G G C C G G C C G

Efficient cleavage requires at least two copies of the NgoMIV recognition sequence.
NaeI  (1089)
1 site
G C C G G C C G G C C G

Efficient cleavage requires at least two copies of the NaeI recognition sequence.
FseI  (1091)
1 site
G G C C G G C C C C G G C C G G

FseI gradually loses activity when stored at -20°C.
PspOMI  (1206)
1 site
G G G C C C C C C G G G
ApaI  (1210)
1 site
G G G C C C C C C G G G

ApaI can be used between 25°C and 37°C.
AvrII  (1244)
1 site
C C T A G G G G A T C C
BsaAI  (1409)
1 site
Y A C G T R R T G C A Y
PmlI  (1409)
1 site
C A C G T G G T G C A C
BfuAI  (1432)
1 site
A C C T G C ( N ) 4 T G G A C G ( N ) 4 ( N ) 4

Efficient cleavage requires at least two copies of the BfuAI recognition sequence.
Sticky ends from different BfuAI sites may not be compatible.
BfuAI is typically used at 50°C, but is 50% active at 37°C.
BspMI  (1432)
1 site
A C C T G C ( N ) 4 T G G A C G ( N ) 4 ( N ) 4

Efficient cleavage requires at least two copies of the BspMI recognition sequence.
Sticky ends from different BspMI sites may not be compatible.
PaqCI  (1432)
1 site
C A C C T G C ( N ) 4 G T G G A C G ( N ) 4 ( N ) 4

Efficient cleavage requires at least two copies of the PaqCI recognition sequence.
Sticky ends from different PaqCI sites may not be compatible.
Cleavage can be improved with PaqCI Activator.
DraIII  (1456)
1 site
C A C N N N G T G G T G N N N C A C

Sticky ends from different DraIII sites may not be compatible.
Acc65I  (1534)
1 site
G G T A C C C C A T G G
KpnI  (1538)
1 site
G G T A C C C C A T G G
BtgI  (1627)
1 site
C C R Y G G G G Y R C C

Sticky ends from different BtgI sites may not be compatible.
BmgBI  (1636)
1 site
C A C G T C G T G C A G

This recognition sequence is asymmetric, so ligating blunt ends generated by BmgBI will not always regenerate a BmgBI site.
MscI  (1671)
1 site
T G G C C A A C C G G T
MluI  (1692)
1 site
A C G C G T T G C G C A
NheI  (1704)
1 site
G C T A G C C G A T C G
BmtI  (1708)
1 site
G C T A G C C G A T C G
PstI  (1714)
1 site
C T G C A G G A C G T C
SbfI  (1714)
1 site
C C T G C A G G G G A C G T C C
BamHI  (1716)
1 site
G G A T C C C C T A G G

After cleavage, BamHI-HF® (but not the original BamHI) can remain bound to DNA and alter its electrophoretic mobility.
BsgI  (2159)
1 site
G T G C A G ( N ) 14 N N C A C G T C ( N ) 14

Efficient cleavage requires at least two copies of the BsgI recognition sequence.
Sticky ends from different BsgI sites may not be compatible.
For full activity, add fresh S-adenosylmethionine (SAM).
BsaBI  (2390)
1 site
G A T N N N N A T C C T A N N N N T A G
* Blocked by Dam methylation.
AmpR
3629 .. 4489  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 2:  
   3629 .. 4420  =  792 bp
   263 amino acids  =  28.9 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
3629 .. 4489  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 1:  signal sequence  
   4421 .. 4489  =  69 bp
   23 amino acids  =  2.6 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
3629 .. 4489  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
ZsGreen
389 .. 1084  =  696 bp
231 amino acids  =  26.1 kDa
Product: Zoanthus green fluorescent protein
ZsGreen
389 .. 1084  =  696 bp
231 amino acids  =  26.1 kDa
Product: Zoanthus green fluorescent protein
ori
2870 .. 3458  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
ori
2870 .. 3458  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
IRES2
1092 .. 1679  =  588 bp
3 segments
   Segment 1:  
   1092 .. 1667  =  576 bp
internal ribosome entry site (IRES) of the encephalomyocarditis virus (EMCV)
IRES2
1092 .. 1679  =  588 bp
3 segments
   Segment 2:  ATG  
   1668 .. 1670  =  3 bp
internal ribosome entry site (IRES) of the encephalomyocarditis virus (EMCV)
IRES2
1092 .. 1679  =  588 bp
3 segments
   Segment 3:  
   1671 .. 1679  =  9 bp
internal ribosome entry site (IRES) of the encephalomyocarditis virus (EMCV)
IRES2
1092 .. 1679  =  588 bp
3 segments
internal ribosome entry site (IRES) of the encephalomyocarditis virus (EMCV)
TRE3G promoter
4 .. 382  =  379 bp
3rd-generation Tet-responsive promoter that can be activated by binding of Tet-On 3G
TRE3G promoter
4 .. 382  =  379 bp
3rd-generation Tet-responsive promoter that can be activated by binding of Tet-On 3G
SV40 poly(A) signal
2492 .. 2613  =  122 bp
SV40 polyadenylation signal
SV40 poly(A) signal
2492 .. 2613  =  122 bp
SV40 polyadenylation signal
AmpR promoter
4490 .. 4594  =  105 bp
AmpR promoter
4490 .. 4594  =  105 bp
small t intron
1852 .. 1917  =  66 bp
simian virus 40 (SV40) small t antigen intron
small t intron
1852 .. 1917  =  66 bp
simian virus 40 (SV40) small t antigen intron
MCS
1686 .. 1721  =  36 bp
multiple cloning site
MCS
1686 .. 1721  =  36 bp
multiple cloning site
tet operator
12 .. 30  =  19 bp
bacterial operator O2 for the tetR and tetA genes
tet operator
12 .. 30  =  19 bp
bacterial operator O2 for the tetR and tetA genes
tet operator
48 .. 66  =  19 bp
bacterial operator O2 for the tetR and tetA genes
tet operator
48 .. 66  =  19 bp
bacterial operator O2 for the tetR and tetA genes
tet operator
84 .. 102  =  19 bp
bacterial operator O2 for the tetR and tetA genes
tet operator
84 .. 102  =  19 bp
bacterial operator O2 for the tetR and tetA genes
tet operator
120 .. 138  =  19 bp
bacterial operator O2 for the tetR and tetA genes
tet operator
120 .. 138  =  19 bp
bacterial operator O2 for the tetR and tetA genes
tet operator
156 .. 174  =  19 bp
bacterial operator O2 for the tetR and tetA genes
tet operator
156 .. 174  =  19 bp
bacterial operator O2 for the tetR and tetA genes
tet operator
192 .. 210  =  19 bp
bacterial operator O2 for the tetR and tetA genes
tet operator
192 .. 210  =  19 bp
bacterial operator O2 for the tetR and tetA genes
tet operator
228 .. 246  =  19 bp
bacterial operator O2 for the tetR and tetA genes
tet operator
228 .. 246  =  19 bp
bacterial operator O2 for the tetR and tetA genes
ATG
1668 .. 1670  =  3 bp
1 amino acid  =  149.2 Da
Product: start codon for translation from IRES2
ATG
1668 .. 1670  =  3 bp
1 amino acid  =  149.2 Da
Product: start codon for translation from IRES2
ORF:  1996 .. 2469  =  474 bp
ORF:  157 amino acids  =  18.2 kDa
ORF:  35 .. 301  =  267 bp
ORF:  88 amino acids  =  10.5 kDa
ORF:  389 .. 1084  =  696 bp
ORF:  231 amino acids  =  26.1 kDa
ORF:  3759 .. 4025  =  267 bp
ORF:  88 amino acids  =  9.2 kDa
ORF:  3629 .. 4489  =  861 bp
ORF:  286 amino acids  =  31.6 kDa
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