Resources
Plasmid Files

pGL4.50[luc2/CMV/Hygro]

Vector for creating stable cell lines expressing firefly luciferase under control of the CMV promoter.

To see this sequence with restriction sites, features, and translations, please download
 SnapGene or the free  SnapGene Viewer.

pGL4.50[luc2 CMV Hygro].dna
Map and Sequence File:    Download    Open   
Sequence Author:  Promega
Download Free Trial Get SnapGene Viewer


AarI - BfuAI - BspMI (6570) RVprimer3 (6549 .. 6568) BsmBI (6397) BstZ17I (6065) SacII (5949) PvuI (5925) Bsu36I (5911) BstEII (5480) BstXI - PstI (5477) NotI (5453) AlwNI (5049) ApaLI (4947) BciVI (4836) PciI (4633) RVprimer4 (4434 .. 4453) SalI (4383) BstBI (4369) PmeI (4293) BssHII (4268) XmnI (3295) SfiI (8) AseI (173) NdeI (400) SnaBI (506) Eco53kI (732) SacI (734) SfiI (818) MreI - SgrAI (922) BbvCI (1570) KasI (1806) NarI (1807) SfoI (1808) PluTI (1810) BlpI (1813) DraIII (2005) BpmI (2239) FseI (2535) PsiI (2656) MfeI (2685) BamHI (2778) StuI (3211) AvrII (3212) pGL4.50[luc2/CMV/Hygro] 6600 bp
AarI  (6570)
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 AarI recognition sequence.
Sticky ends from different AarI sites may not be compatible.
After cleavage, AarI can remain bound to DNA and alter its electrophoretic mobility.
BfuAI  (6570)
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  (6570)
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.
BsmBI  (6397)
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.
BstZ17I  (6065)
1 site
G T A T A C C A T A T G
SacII  (5949)
1 site
C C G C G G G G C G C C

Efficient cleavage requires at least two copies of the SacII recognition sequence.
PvuI  (5925)
1 site
C G A T C G G C T A G C
Bsu36I  (5911)
1 site
C C T N A G G G G A N T C C

Sticky ends from different Bsu36I sites may not be compatible.
BstEII  (5480)
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.
BstXI  (5477)
1 site
C C A N N N N N N T G G G G T N N N N N N A C C

Sticky ends from different BstXI sites may not be compatible.
PstI  (5477)
1 site
C T G C A G G A C G T C
NotI  (5453)
1 site
G C G G C C G C C G C C G G C G
AlwNI  (5049)
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.
ApaLI  (4947)
1 site
G T G C A C C A C G T G
BciVI  (4836)
1 site
G T A T C C ( N ) 5 N C A T A G G ( N ) 5

The 1-base overhangs produced by BciVI may be hard to ligate.
Sticky ends from different BciVI sites may not be compatible.
PciI  (4633)
1 site
A C A T G T T G T A C A

PciI is inhibited by nonionic detergents.
SalI  (4383)
1 site
G T C G A C C A G C T G
BstBI  (4369)
1 site
T T C G A A A A G C T T
PmeI  (4293)
1 site
G T T T A A A C C A A A T T T G
BssHII  (4268)
1 site
G C G C G C C G C G C G

BssHII is typically used at 50°C, but is 75% active at 37°C.
XmnI  (3295)
1 site
G A A N N N N T T C C T T N N N N A A G
SfiI  (8)
2 sites
G G C C N N N N N G G C C C C G G N N N N N C C G G

Efficient cleavage requires at least two copies of the SfiI recognition sequence.
Sticky ends from different SfiI sites may not be compatible.
AseI  (173)
1 site
A T T A A T T A A T T A
NdeI  (400)
1 site
C A T A T G G T A T A C

Prolonged incubation with NdeI may lead to removal of additional nucleotides.
SnaBI  (506)
1 site
T A C G T A A T G C A T
Eco53kI  (732)
1 site
G A G C T C C T C G A G
SacI  (734)
1 site
G A G C T C C T C G A G
SfiI  (818)
2 sites
G G C C N N N N N G G C C C C G G N N N N N C C G G

Efficient cleavage requires at least two copies of the SfiI recognition sequence.
Sticky ends from different SfiI sites may not be compatible.
MreI  (922)
1 site
C G C C G G C G G C G G C C G C
SgrAI  (922)
1 site
C R C C G G Y G G Y G G C C R C

Efficient cleavage requires at least two copies of the SgrAI recognition sequence.
BbvCI  (1570)
1 site
C C T C A G C G G A G T C G
KasI  (1806)
1 site
G G C G C C C C G C G G
NarI  (1807)
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  (1808)
1 site
G G C G C C C C G C G G
PluTI  (1810)
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.
BlpI  (1813)
1 site
G C T N A G C C G A N T C G

Sticky ends from different BlpI sites may not be compatible.
DraIII  (2005)
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.
BpmI  (2239)
1 site
C T G G A G ( N ) 14 N N G A C C T C ( N ) 14

Efficient cleavage requires at least two copies of the BpmI recognition sequence.
Sticky ends from different BpmI sites may not be compatible.
After cleavage, BpmI can remain bound to DNA and alter its electrophoretic mobility.
BpmI quickly loses activity at 37°C.
FseI  (2535)
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.
PsiI  (2656)
1 site
T T A T A A A A T A T T
MfeI  (2685)
1 site
C A A T T G G T T A A C
BamHI  (2778)
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.
StuI  (3211)
1 site
A G G C C T T C C G G A
AvrII  (3212)
1 site
C C T A G G G G A T C C
RVprimer3
20-mer  /  50% GC
1 binding site
6549 .. 6568  =  20 annealed bases
Tm  =  54°C
RVprimer4
20-mer  /  65% GC
1 binding site
4434 .. 4453  =  20 annealed bases
Tm  =  61°C
luciferase
859 .. 2511  =  1653 bp
550 amino acids  =  60.6 kDa
Product: firefly luciferase
synthetic luc2 version of the luciferase gene
luciferase
859 .. 2511  =  1653 bp
550 amino acids  =  60.6 kDa
Product: firefly luciferase
synthetic luc2 version of the luciferase gene
HygR
3258 .. 4295  =  1038 bp
345 amino acids  =  38.4 kDa
Product: hygromycin B phosphotransferase
confers resistance to hygromycin
HygR
3258 .. 4295  =  1038 bp
345 amino acids  =  38.4 kDa
Product: hygromycin B phosphotransferase
confers resistance to hygromycin
AmpR
5482 .. 6342  =  861 bp
286 amino acids  =  31.6 kDa
   Segment 2:  
   5482 .. 6273  =  792 bp
   263 amino acids  =  28.9 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
5482 .. 6342  =  861 bp
286 amino acids  =  31.6 kDa
   Segment 1:  signal sequence  
   6274 .. 6342  =  69 bp
   23 amino acids  =  2.6 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
5482 .. 6342  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
ori
4694 .. 5282  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
ori
4694 .. 5282  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
SV40 promoter
2870 .. 3227  =  358 bp
SV40 enhancer and early promoter
SV40 promoter
2870 .. 3227  =  358 bp
SV40 enhancer and early promoter
CMV enhancer
227 .. 530  =  304 bp
human cytomegalovirus immediate early enhancer
CMV enhancer
227 .. 530  =  304 bp
human cytomegalovirus immediate early enhancer
CMV promoter
531 .. 734  =  204 bp
human cytomegalovirus (CMV) immediate early promoter
CMV promoter
531 .. 734  =  204 bp
human cytomegalovirus (CMV) immediate early promoter
SV40 poly(A) signal
2555 .. 2676  =  122 bp
SV40 polyadenylation signal
SV40 poly(A) signal
2555 .. 2676  =  122 bp
SV40 polyadenylation signal
<
pause site
6509 .. 6600  =  92 bp
RNA polymerase II transcriptional pause signal from the human α2 globin gene