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Plasmid Files

pGL4.70[hRluc]

Promoterless vector for measuring the activity of promoter and enhancer sequences with a Renilla luciferase assay.

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pGL4.70[hRluc] Sequence and MappGL4.70[hRluc].dna
Map and Sequence File   
Sequence Author:  Promega
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 BsgI (3520) AarI - BfuAI - BspMI (3492) RVprimer3 (3471 .. 3490) poly(A) signal BsmBI (3319) SpeI (3306) BstZ17I (2987) SacII (2871) PvuI (2847) MscI (2711) AhdI (2477) BstEII (2402) BstXI - PstI (2399) AleI (2397) NotI (2375) BspHI (2275) AlwNI (1971) BaeGI - Bme1580I (1873) ApaLI (1869) BciVI (1758) BglI - SfiI (8) Acc65I (14) KpnI (18) Bpu10I (19) Eco53kI (23) SacI (25) NheI (27) BmtI (31) AbsI - PaeR7I - PspXI - XhoI (33) BglII (46) BglI - SfiI (59) HindIII (65) NcoI (98) BglI (100) BstAPI - DraIII (288) NsiI (319) PfoI * (380) XmnI (634) BsaI (640) NruI (761) ZraI (795) PflFI - Tth111I (796) AatII (797) PasI (874) XbaI (1037) FseI (1056) ApoI (1142) AanI - AanI - PsiI (1177) HpaI (1197) MfeI (1206) BamHI (1299) SalI (1305) PshAI (1370) RVprimer4 (1356 .. 1375) BbsI (1384) AfeI (1431) BspQI - SapI (1439) AflIII - PciI (1555) NspI (1559) DrdI (1663) pGL4.70[hRluc] 3522 bp
BsgI  (3520)
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).
AarI  (3492)
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  (3492)
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  (3492)
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  (3319)
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.
SpeI  (3306)
1 site
A C T A G T T G A T C A
BstZ17I  (2987)
1 site
G T A T A C C A T A T G
SacII  (2871)
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  (2847)
1 site
C G A T C G G C T A G C
MscI  (2711)
1 site
T G G C C A A C C G G T
AhdI  (2477)
1 site
G A C N N N N N G T C C T G N N N N N C A G

The 1-base overhangs produced by AhdI may be hard to ligate.
Sticky ends from different AhdI sites may not be compatible.
BstEII  (2402)
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  (2399)
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  (2399)
1 site
C T G C A G G A C G T C
AleI  (2397)
1 site
C A C N N N N G T G G T G N N N N C A C
NotI  (2375)
1 site
G C G G C C G C C G C C G G C G
BspHI  (2275)
1 site
T C A T G A A G T A C T
AlwNI  (1971)
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.
BaeGI  (1873)
1 site
G K G C M C C M C G K G

Sticky ends from different BaeGI sites may not be compatible.
Bme1580I  (1873)
1 site
G K G C M C C M C G K G

Sticky ends from different Bme1580I sites may not be compatible.
ApaLI  (1869)
1 site
G T G C A C C A C G T G
BciVI  (1758)
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.
BglI  (8)
3 sites
G C C N N N N N G G C C G G N N N N N C C G

Sticky ends from different BglI sites may not be compatible.
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.
Acc65I  (14)
1 site
G G T A C C C C A T G G
KpnI  (18)
1 site
G G T A C C C C A T G G
Bpu10I  (19)
1 site
C C T N A G C G G A N T C G

Efficient cleavage requires at least two copies of the Bpu10I
recognition sequence.
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.
Eco53kI  (23)
1 site
G A G C T C C T C G A G
SacI  (25)
1 site
G A G C T C C T C G A G
NheI  (27)
1 site
G C T A G C C G A T C G
BmtI  (31)
1 site
G C T A G C C G A T C G
AbsI  (33)
1 site
C C T C G A G G G G A G C T C C
PaeR7I  (33)
1 site
C T C G A G G A G C T C

PaeR7I does not recognize the sequence CTCTCGAG.
PspXI  (33)
1 site
V C T C G A G B B G A G C T C V
XhoI  (33)
1 site
C T C G A G G A G C T C
BglII  (46)
1 site
A G A T C T T C T A G A
BglI  (59)
3 sites
G C C N N N N N G G C C G G N N N N N C C G

Sticky ends from different BglI sites may not be compatible.
SfiI  (59)
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.
HindIII  (65)
1 site
A A G C T T T T C G A A
NcoI  (98)
1 site
C C A T G G G G T A C C
BglI  (100)
3 sites
G C C N N N N N G G C C G G N N N N N C C G

Sticky ends from different BglI sites may not be compatible.
BstAPI  (288)
1 site
G C A N N N N N T G C C G T N N N N N A C G

Sticky ends from different BstAPI sites may not be compatible.
DraIII  (288)
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.
NsiI  (319)
1 site
A T G C A T T A C G T A
PfoI  (380)
1 site
T C C N G G A A G G N C C T
* Blocked by Dcm methylation.
Sticky ends from different PfoI sites may not be compatible.
XmnI  (634)
1 site
G A A N N N N T T C C T T N N N N A A G
BsaI  (640)
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.
NruI  (761)
1 site
T C G C G A A G C G C T
ZraI  (795)
1 site
G A C G T C C T G C A G
PflFI  (796)
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  (796)
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.
AatII  (797)
1 site
G A C G T C C T G C A G
PasI  (874)
1 site
C C C W G G G G G G W C C C

Sticky ends from different PasI sites may not be compatible.
XbaI  (1037)
1 site
T C T A G A A G A T C T
FseI  (1056)
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.
ApoI  (1142)
1 site
R A A T T Y Y T T A A R

ApoI is typically used at 50°C, but is 50% active at 37°C.
AanI  (1177)
1 site
T T A T A A A A T A T T
AanI  (1177)
1 site
T T A T A A A A T A T T
PsiI  (1177)
1 site
T T A T A A A A T A T T
HpaI  (1197)
1 site
G T T A A C C A A T T G
MfeI  (1206)
1 site
C A A T T G G T T A A C
BamHI  (1299)
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.
SalI  (1305)
1 site
G T C G A C C A G C T G
PshAI  (1370)
1 site
G A C N N N N G T C C T G N N N N C A G

PshAI quickly loses activity at 37°C, but can be used at 25°C for
long incubations.
BbsI  (1384)
1 site
G A A G A C N N C T T C T G N N ( N ) 4

Sticky ends from different BbsI sites may not be compatible.
BbsI gradually loses activity when stored at -20°C.
AfeI  (1431)
1 site
A G C G C T T C G C G A
BspQI  (1439)
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  (1439)
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.
AflIII  (1555)
1 site
A C R Y G T T G Y R C A

Sticky ends from different AflIII sites may not be compatible.
PciI  (1555)
1 site
A C A T G T T G T A C A

PciI is inhibited by nonionic detergents.
NspI  (1559)
1 site
R C A T G Y Y G T A C R
DrdI  (1663)
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.
RVprimer3
20-mer  /  50% GC
1 binding site
3471 .. 3490  =  20 annealed bases
Tm  =  54°C
RVprimer4
20-mer  /  65% GC
1 binding site
1356 .. 1375  =  20 annealed bases
Tm  =  61°C
hRluc
100 .. 1035  =  936 bp
311 amino acids  =  36.0 kDa
Product: Renilla luciferase
human codon-optimized
hRluc
100 .. 1035  =  936 bp
311 amino acids  =  36.0 kDa
Product: Renilla luciferase
human codon-optimized
AmpR
2404 .. 3264  =  861 bp
286 amino acids  =  31.6 kDa
   Segment 2:  
   2404 .. 3195  =  792 bp
   263 amino acids  =  28.9 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and
related antibiotics
AmpR
2404 .. 3264  =  861 bp
286 amino acids  =  31.6 kDa
   Segment 1:  signal sequence  
   3196 .. 3264  =  69 bp
   23 amino acids  =  2.6 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and
related antibiotics
AmpR
2404 .. 3264  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and
related antibiotics
ori
1616 .. 2204  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin
of replication
ori
1616 .. 2204  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin
of replication
SV40 poly(A) signal
1076 .. 1197  =  122 bp
SV40 polyadenylation signal
SV40 poly(A) signal
1076 .. 1197  =  122 bp
SV40 polyadenylation signal
pause site
3431 .. 3522  =  92 bp
RNA polymerase II transcriptional pause signal from
the human α2 globin gene
pause site
3431 .. 3522  =  92 bp
RNA polymerase II transcriptional pause signal from
the human α2 globin gene
MCS
1 .. 70  =  70 bp
multiple cloning site
MCS
1 .. 70  =  70 bp
multiple cloning site
poly(A) signal
3369 .. 3417  =  49 bp
synthetic polyadenylation signal
poly(A) signal
3369 .. 3417  =  49 bp
synthetic polyadenylation signal
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