pTK-Gaussia Luc

Control vector for constitutive low-level expression of secreted Gaussia luciferase under control of the HSV TK promoter.

Sequence Author: Thermo Fisher (Pierce)

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SpeI (1) PaqCI (5597) EcoRV (5303) ApaI (4963) PspOMI (4959) DrdI (4617) MauBI (4021) ScaI (3504) FspI (3246) AfeI (3074) BsmI (2857) PaeR7I - XhoI (7) HindIII (20) BspQI - SapI (155) PpuMI (337) BsaI (404) PvuII (549) BstBI (671) MluI (731) BamHI (778) BsaBI * (821) NotI (1350) BseRI (1915) BclI * (1970) PflFI - Tth111I (2090) BsiWI (2104) RsrII (2164) BstEII (2182) BsmBI - Esp3I (2440) DraIII (2619) NgoMIV (2720) NaeI (2722) pTK-Gaussia Luc 5627 bp
SpeI  (1)
1 site
A C T A G T T G A T C A
PaqCI  (5597)
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.
EcoRV  (5303)
1 site
G A T A T C C T A T A G

EcoRV is reportedly more prone than its isoschizomer Eco32I to delete a base after cleavage.
ApaI  (4963)
1 site
G G G C C C C C C G G G

ApaI can be used between 25°C and 37°C.
PspOMI  (4959)
1 site
G G G C C C C C C G G G
DrdI  (4617)
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.
MauBI  (4021)
1 site
C G C G C G C G G C G C G C G C
ScaI  (3504)
1 site
A G T A C T T C A T G A
FspI  (3246)
1 site
T G C G C A A C G C G T
AfeI  (3074)
1 site
A G C G C T T C G C G A
BsmI  (2857)
1 site
G A A T G C N C T T A C G N

Sticky ends from different BsmI sites may not be compatible.
PaeR7I  (7)
1 site
C T C G A G G A G C T C

PaeR7I does not recognize the sequence CTCTCGAG.
XhoI  (7)
1 site
C T C G A G G A G C T C
HindIII  (20)
1 site
A A G C T T T T C G A A
BspQI  (155)
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  (155)
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.
PpuMI  (337)
1 site
R G G W C C Y Y C C W G G R

Sticky ends from different PpuMI sites may not be compatible.
BsaI  (404)
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.
PvuII  (549)
1 site
C A G C T G G T C G A C
BstBI  (671)
1 site
T T C G A A A A G C T T
MluI  (731)
1 site
A C G C G T T G C G C A
BamHI  (778)
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.
BsaBI  (821)
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.
NotI  (1350)
1 site
G C G G C C G C C G C C G G C G
BseRI  (1915)
1 site
G A G G A G ( N ) 8 N N C T C C T C ( N ) 8

Sticky ends from different BseRI sites may not be compatible.
BseRI quickly loses activity at 37°C.
Prolonged incubation with BseRI may lead to degradation of the DNA.
BclI  (1970)
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.
PflFI  (2090)
1 site
G A C N N N G T C C T G N N N C A G

The 1-base overhangs produced by PflFI may be hard to ligate.
Sticky ends from different PflFI sites may not be compatible.
Tth111I  (2090)
1 site
G A C N N N G T C C T G N N N C A G

The 1-base overhangs produced by Tth111I may be hard to ligate.
Sticky ends from different Tth111I sites may not be compatible.
BsiWI  (2104)
1 site
C G T A C G G C A T G C

BsiWI is typically used at 55°C, but is 50% active at 37°C.
RsrII  (2164)
1 site
C G G W C C G G C C W G G C

Efficient cleavage requires at least two copies of the RsrII recognition sequence.
Sticky ends from different RsrII sites may not be compatible.
For full activity, add fresh DTT.
BstEII  (2182)
1 site
G G T N A C C C C A N T G G

Sticky ends from different BstEII sites may not be compatible.
BstEII is typically used at 60°C, but is 50% active at 37°C.
BsmBI  (2440)
1 site
C G T C T C N G C A G A G N ( N ) 4

Sticky ends from different BsmBI sites may not be compatible.
BsmBI-v2 is an improved version of BsmBI.
Esp3I  (2440)
1 site
C G T C T C N G C A G A G N ( N ) 4

Sticky ends from different Esp3I sites may not be compatible.
DraIII  (2619)
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.
NgoMIV  (2720)
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  (2722)
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.
AmpR
2951 .. 3811  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 2:  
   2951 .. 3742  =  792 bp
   263 amino acids  =  28.9 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
2951 .. 3811  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 1:  signal sequence  
   3743 .. 3811  =  69 bp
   23 amino acids  =  2.6 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
2951 .. 3811  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
HSV TK promoter
26 .. 777  =  752 bp
herpes simplex virus thymidine kinase promoter
HSV TK promoter
26 .. 777  =  752 bp
herpes simplex virus thymidine kinase promoter
PuroR
2048 .. 2647  =  600 bp
199 amino acids  =  21.5 kDa
Product: puromycin N-acetyltransferase
confers resistance to puromycin
PuroR
2048 .. 2647  =  600 bp
199 amino acids  =  21.5 kDa
Product: puromycin N-acetyltransferase
confers resistance to puromycin
ori
4075 .. 4663  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
ori
4075 .. 4663  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
hGLuc
791 .. 1348  =  558 bp
185 amino acids  =  19.9 kDa
Product: secreted Gaussia luciferase
human codon-optimized
hGLuc
791 .. 1348  =  558 bp
185 amino acids  =  19.9 kDa
Product: secreted Gaussia luciferase
human codon-optimized
SV40 promoter
1605 .. 1934  =  330 bp
SV40 enhancer and early promoter
SV40 promoter
1605 .. 1934  =  330 bp
SV40 enhancer and early promoter
SV40 poly(A) signal
2777 .. 2898  =  122 bp
SV40 polyadenylation signal
SV40 poly(A) signal
2777 .. 2898  =  122 bp
SV40 polyadenylation signal
bGH poly(A) signal
1371 .. 1482  =  112 bp
bovine growth hormone polyadenylation signal
bGH poly(A) signal
1371 .. 1482  =  112 bp
bovine growth hormone polyadenylation signal
pause site
5536 .. 5627  =  92 bp
RNA polymerase II transcriptional pause signal from the human α2 globin gene
pause site
5536 .. 5627  =  92 bp
RNA polymerase II transcriptional pause signal from the human α2 globin gene
EM7 promoter
1982 .. 2029  =  48 bp
synthetic bacterial promoter
EM7 promoter
1982 .. 2029  =  48 bp
synthetic bacterial promoter
lac operator
5405 .. 5421  =  17 bp
The lac repressor binds to the lac operator to inhibit transcription in E. coli. This inhibition can be relieved by adding lactose or isopropyl-β-D-thiogalactopyranoside (IPTG).
lac operator
5405 .. 5421  =  17 bp
The lac repressor binds to the lac operator to inhibit transcription in E. coli. This inhibition can be relieved by adding lactose or isopropyl-β-D-thiogalactopyranoside (IPTG).
SV40 ori
1785 .. 1920  =  136 bp
SV40 origin of replication
SV40 ori
1785 .. 1920  =  136 bp
SV40 origin of replication
ORF:  350 .. 1348  =  999 bp
ORF:  332 amino acids  =  36.4 kDa
ORF:  2048 .. 2647  =  600 bp
ORF:  199 amino acids  =  21.5 kDa
ORF:  3081 .. 3347  =  267 bp
ORF:  88 amino acids  =  9.3 kDa
ORF:  2208 .. 2534  =  327 bp
ORF:  108 amino acids  =  12.0 kDa
ORF:  2951 .. 3811  =  861 bp
ORF:  286 amino acids  =  31.6 kDa
ORF:  112 .. 1059  =  948 bp
ORF:  315 amino acids  =  34.0 kDa
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