pTurboRFP-PRL

Promoterless TurboRFP reporter vector.

Sequence Author: Evrogen

|Download SnapGene Viewer
No matches
AfeI (14) AflIII - PciI (4069) EcoO109I (3249) PfoI (2926) RsrII (2667) BsrDI (2384) PflFI - Tth111I (2269) FspI (2253) PluTI (2154) SfoI (2152) NarI (2151) KasI (2150) BglII (27) PaeR7I - XhoI (31) Eco53kI (36) SacI (38) HindIII (40) EcoRI (47) PstI (56) SalI (57) AccI (58) Acc65I (63) KpnI (67) SacII (70) PspOMI (71) TspMI - XmaI (74) ApaI (75) SmaI (76) BamHI (78) AgeI (84) BclI * (107) BsrGI (134) BbsI (392) BsgI (589) PshAI (724) ScaI (757) NotI (795) XbaI * (805) MfeI (901) HpaI (914) AflII (1033) CsiI - SexAI * (1740) BseRI (1969) StuI (1972) BspDI * - ClaI * (1991) pTurboRFP-PRL 4127 bp
AfeI  (14)
1 site
A G C G C T T C G C G A
AflIII  (4069)
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  (4069)
1 site
A C A T G T T G T A C A

PciI is inhibited by nonionic detergents.
EcoO109I  (3249)
1 site
R G G N C C Y Y C C N G G R

Sticky ends from different EcoO109I sites may not be compatible.
PfoI  (2926)
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  (2667)
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.
BsrDI  (2384)
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  (2269)
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  (2269)
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  (2253)
1 site
T G C G C A A C G C G T
PluTI  (2154)
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.
SfoI  (2152)
1 site
G G C G C C C C G C G G
NarI  (2151)
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.
KasI  (2150)
1 site
G G C G C C C C G C G G
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
PstI  (56)
1 site
C T G C A G G A C G T C
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.
PspOMI  (71)
1 site
G G G C C C C C C G G G
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.
ApaI  (75)
1 site
G G G C C C C C C G G G

ApaI can be used between 25°C and 37°C.
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
BclI  (107)
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.
BsrGI  (134)
1 site
T G T A C A A C A T G T

BsrGI is typically used at 37°C, but is even more active at 60°C.
BbsI  (392)
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.
BsgI  (589)
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).
PshAI  (724)
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.
ScaI  (757)
1 site
A G T A C T T C A T G A
NotI  (795)
1 site
G C G G C C G C C G C C G G C G
XbaI  (805)
1 site
T C T A G A A G A T C T
* Blocked by Dam methylation.
MfeI  (901)
1 site
C A A T T G G T T A A C
HpaI  (914)
1 site
G T T A A C C A A T T G
AflII  (1033)
1 site
C T T A A G G A A T T C
CsiI  (1740)
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  (1740)
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.
BseRI  (1969)
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.
StuI  (1972)
1 site
A G G C C T T C C G G A
BspDI  (1991)
1 site
A T C G A T T A G C T A
* Blocked by Dam methylation.
ClaI  (1991)
1 site
A T C G A T T A G C T A
* Blocked by Dam methylation.
NeoR/KanR
2023 .. 2817  =  795 bp
264 amino acids  =  29.0 kDa
Product: aminoglycoside phosphotransferase from Tn5
confers resistance to neomycin, kanamycin, and G418 (Geneticin)
NeoR/KanR
2023 .. 2817  =  795 bp
264 amino acids  =  29.0 kDa
Product: aminoglycoside phosphotransferase from Tn5
confers resistance to neomycin, kanamycin, and G418 (Geneticin)
TurboRFP
97 .. 792  =  696 bp
231 amino acids  =  26.1 kDa
Product: red fluorescent protein from Entacmaea quadricolor
mammalian codon-optimized
TurboRFP
97 .. 792  =  696 bp
231 amino acids  =  26.1 kDa
Product: red fluorescent protein from Entacmaea quadricolor
mammalian codon-optimized
ori
3425 .. 4013  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
ori
3425 .. 4013  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
f1 ori
1043 .. 1498  =  456 bp
f1 bacteriophage origin of replication; arrow indicates direction of (+) strand synthesis
f1 ori
1043 .. 1498  =  456 bp
f1 bacteriophage origin of replication; arrow indicates direction of (+) strand synthesis
SV40 promoter
1631 .. 1988  =  358 bp
SV40 enhancer and early promoter
SV40 promoter
1631 .. 1988  =  358 bp
SV40 enhancer and early promoter
SV40 poly(A) signal
915 .. 1036  =  122 bp
SV40 polyadenylation signal
SV40 poly(A) signal
915 .. 1036  =  122 bp
SV40 polyadenylation signal
AmpR promoter
1525 .. 1629  =  105 bp
AmpR promoter
1525 .. 1629  =  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
3049 .. 3096  =  48 bp
herpesvirus thymidine kinase polyadenylation signal
HSV TK poly(A) signal
3049 .. 3096  =  48 bp
herpesvirus thymidine kinase polyadenylation signal
SV40 ori
1839 .. 1974  =  136 bp
SV40 origin of replication
SV40 ori
1839 .. 1974  =  136 bp
SV40 origin of replication
ORF:  97 .. 792  =  696 bp
ORF:  231 amino acids  =  26.1 kDa
ORF:  2023 .. 2817  =  795 bp
ORF:  264 amino acids  =  29.0 kDa
ORF:  2195 .. 2581  =  387 bp
ORF:  128 amino acids  =  14.6 kDa
ORF:  2838 .. 3287  =  450 bp
ORF:  149 amino acids  =  16.3 kDa
ORF:  198 .. 443  =  246 bp
ORF:  81 amino acids  =  9.1 kDa
ORF:  2332 .. 2868  =  537 bp
ORF:  178 amino acids  =  19.8 kDa
ORF:  3043 .. 3276  =  234 bp
ORF:  77 amino acids  =  8.6 kDa
Click here to try SnapGene

Download pTurboRFP-PRL.dna file

SnapGene

SnapGene is the easiest way to plan, visualize and document your everyday molecular biology procedures

  • Fast accurate construct design for all major molecular cloning techniques
  • Validate sequenced constructs using powerful alignment tools
  • Customize plasmid maps with flexible annotation and visualization controls
  • Automatically generate a rich graphical history of every edit and procedure

SnapGene Viewer

SnapGene Viewer is free software that allows molecular biologists to create, browse, and share richly annotated sequence files.

  • Gain unparalleled visibility of your plasmids, DNA and protein sequences
  • Annotate features on your plasmids using the curated feature database
  • Store, search, and share your sequences, files and maps

Individual Sequences & Maps

The maps, notes, and annotations in the zip file on this page are copyrighted material. This material may be used without restriction by academic, nonprofit, and governmental entities, except that the source must be cited as ’’www.snapgene.com/resources’’. Commercial entities must contact GSL Biotech LLC for permission and terms of use.

Discover the most user-friendly molecular biology experience.