pTurboGFP-PRL

Promoterless TurboGFP reporter vector.

Sequence Author: Evrogen

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No matches
AflIII - PciI (4072) ApaLI (3758) BsaI (3143) PfoI (2929) RsrII (2670) MslI (2591) BsrDI (2387) PflFI - Tth111I (2272) FspI (2256) MscI (2236) AfeI (14) BglII (27) PaeR7I - XhoI (31) Eco53kI (36) SacI (38) HindIII (40) EcoRI (47) SalI (57) AccI (58) Acc65I (63) KpnI (67) SacII (70) TspMI - XmaI (74) SmaI (76) BamHI (78) AgeI (84) BlpI (271) PflMI (282) XmnI (334) FseI (440) PaqCI (548) NotI (798) XbaI * (808) MfeI (904) HpaI (917) BtsI - BtsαI (993) AflII (1036) DraIII (1270) CsiI - SexAI * (1743) BglI - SfiI (1929) StuI (1975) BspDI * - ClaI * (1994) pTurboGFP-PRL 4130 bp
AflIII  (4072)
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  (4072)
1 site
A C A T G T T G T A C A

PciI is inhibited by nonionic detergents.
ApaLI  (3758)
1 site
G T G C A C C A C G T G
BsaI  (3143)
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.
PfoI  (2929)
1 site
T C C N G G A A G G N C C T

Sticky ends from different PfoI sites may not be compatible.
RsrII  (2670)
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.
MslI  (2591)
1 site
C A Y N N N N R T G G T R N N N N Y A C
BsrDI  (2387)
1 site
G C A A T G N N C G T T A C

Sticky ends from different BsrDI sites may not be compatible.
PflFI  (2272)
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  (2272)
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.
FspI  (2256)
1 site
T G C G C A A C G C G T
MscI  (2236)
1 site
T G G C C A A C C G G T
AfeI  (14)
1 site
A G C G C T T C G C G A
BglII  (27)
1 site
A G A T C T T C T A G A
PaeR7I  (31)
1 site
C T C G A G G A G C T C

PaeR7I does not recognize the sequence CTCTCGAG.
XhoI  (31)
1 site
C T C G A G G A G C T C
Eco53kI  (36)
1 site
G A G C T C C T C G A G
SacI  (38)
1 site
G A G C T C C T C G A G
HindIII  (40)
1 site
A A G C T T T T C G A A
EcoRI  (47)
1 site
G A A T T C C T T A A G
SalI  (57)
1 site
G T C G A C C A G C T G
AccI  (58)
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.
Acc65I  (63)
1 site
G G T A C C C C A T G G
KpnI  (67)
1 site
G G T A C C C C A T G G
SacII  (70)
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.
TspMI  (74)
1 site
C C C G G G G G G C C C
XmaI  (74)
1 site
C C C G G G G G G C C C

Cleavage may be enhanced when more than one copy of the XmaI recognition sequence is present.
SmaI  (76)
1 site
C C C G G G G G G C C C

SmaI can be used at 37°C for brief incubations.
BamHI  (78)
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.
AgeI  (84)
1 site
A C C G G T T G G C C A
BlpI  (271)
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.
PflMI  (282)
1 site
C C A N N N N N T G G G G T N N N N N A C C

Sticky ends from different PflMI sites may not be compatible.
XmnI  (334)
1 site
G A A N N N N T T C C T T N N N N A A G
FseI  (440)
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.
PaqCI  (548)
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.
NotI  (798)
1 site
G C G G C C G C C G C C G G C G
XbaI  (808)
1 site
T C T A G A A G A T C T
* Blocked by Dam methylation.
MfeI  (904)
1 site
C A A T T G G T T A A C
HpaI  (917)
1 site
G T T A A C C A A T T G
BtsI  (993)
1 site
G C A G T G N N C G T C A C
BtsαI  (993)
1 site
G C A G T G N N C G T C A C

Sticky ends from different BtsαI sites may not be compatible.
AflII  (1036)
1 site
C T T A A G G A A T T C
DraIII  (1270)
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.
CsiI  (1743)
1 site
A C C W G G T T G G W C C A

Sticky ends from different CsiI sites may not be compatible.
SexAI  (1743)
1 site
A C C W G G T T G G W C C A
* Blocked by Dcm methylation.
Sticky ends from different SexAI sites may not be compatible.
BglI  (1929)
1 site
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  (1929)
1 site
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.
StuI  (1975)
1 site
A G G C C T T C C G G A
BspDI  (1994)
1 site
A T C G A T T A G C T A
* Blocked by Dam methylation.
ClaI  (1994)
1 site
A T C G A T T A G C T A
* Blocked by Dam methylation.
NeoR/KanR
2026 .. 2820  =  795 bp
264 amino acids  =  29.0 kDa
Product: aminoglycoside phosphotransferase from Tn5
confers resistance to neomycin, kanamycin, and G418 (Geneticin)
NeoR/KanR
2026 .. 2820  =  795 bp
264 amino acids  =  29.0 kDa
Product: aminoglycoside phosphotransferase from Tn5
confers resistance to neomycin, kanamycin, and G418 (Geneticin)
TurboGFP
97 .. 795  =  699 bp
232 amino acids  =  25.7 kDa
Product: improved green fluorescent protein from Pontellina plumata
mammalian codon-optimized
TurboGFP
97 .. 795  =  699 bp
232 amino acids  =  25.7 kDa
Product: improved green fluorescent protein from Pontellina plumata
mammalian codon-optimized
ori
3428 .. 4016  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
ori
3428 .. 4016  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
f1 ori
1046 .. 1501  =  456 bp
f1 bacteriophage origin of replication; arrow indicates direction of (+) strand synthesis
f1 ori
1046 .. 1501  =  456 bp
f1 bacteriophage origin of replication; arrow indicates direction of (+) strand synthesis
SV40 promoter
1634 .. 1991  =  358 bp
SV40 enhancer and early promoter
SV40 promoter
1634 .. 1991  =  358 bp
SV40 enhancer and early promoter
SV40 poly(A) signal
918 .. 1039  =  122 bp
SV40 polyadenylation signal
SV40 poly(A) signal
918 .. 1039  =  122 bp
SV40 polyadenylation signal
AmpR promoter
1528 .. 1632  =  105 bp
AmpR promoter
1528 .. 1632  =  105 bp
MCS
12 .. 89  =  78 bp
multiple cloning site of fluorescent protein plasmids
MCS
12 .. 89  =  78 bp
multiple cloning site of fluorescent protein plasmids
HSV TK poly(A) signal
3052 .. 3099  =  48 bp
herpesvirus thymidine kinase polyadenylation signal
HSV TK poly(A) signal
3052 .. 3099  =  48 bp
herpesvirus thymidine kinase polyadenylation signal
SV40 ori
1842 .. 1977  =  136 bp
SV40 origin of replication
SV40 ori
1842 .. 1977  =  136 bp
SV40 origin of replication
ORF:  97 .. 795  =  699 bp
ORF:  232 amino acids  =  25.7 kDa
ORF:  2026 .. 2820  =  795 bp
ORF:  264 amino acids  =  29.0 kDa
ORF:  569 .. 895  =  327 bp
ORF:  108 amino acids  =  11.5 kDa
ORF:  2198 .. 2584  =  387 bp
ORF:  128 amino acids  =  14.6 kDa
ORF:  2841 .. 3290  =  450 bp
ORF:  149 amino acids  =  16.3 kDa
ORF:  4070 .. 218  =  279 bp
ORF:  92 amino acids
ORF:  2335 .. 2871  =  537 bp
ORF:  178 amino acids  =  19.8 kDa
ORF:  3046 .. 3279  =  234 bp
ORF:  77 amino acids  =  8.6 kDa
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Download pTurboGFP-PRL.dna file

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