pcDNA5 FRT TO

Genomic integration vector for tetracycline-inducible expression of proteins in mammalian cells.

Sequence Author: Thermo Fisher (Invitrogen)

|Download SnapGene Viewer
Explore Over 2.7k Plasmids: Mammalian Expression Vectors | More Plasmid Sets
No matches
SspI (5018) XmnI (4813) FspI (4436) BsaI (4275) AhdI (4214) PciI (3321) BspQI - SapI (3205) BstZ17I (2942) BsmI (2890) PsiI (2829) PfoI (2745) MfeI (161) Bpu10I (180) NruI (208) MluI (228) CMV enhancer SnaBI (590) tet operator tet operator AflII (975) HindIII (978) Acc65I (984) KpnI (988) BamHI (996) EcoRV (1031) NotI (1046) AvaI - BsoBI - PaeR7I - PspXI - XhoI (1052) EcoO109I - PspOMI (1064) ApaI (1068) BclI * (1082) SphI (1295) FRT MscI (1655) PshAI (1682) BfuAI - BspMI (1968) AsiSI (2019) RsrII (2063) SacII (2435) pcDNA™5/FRT/TO 5137 bp
SspI  (5018)
1 site
A A T A T T T T A T A A
XmnI  (4813)
1 site
G A A N N N N T T C C T T N N N N A A G
FspI  (4436)
1 site
T G C G C A A C G C G T
BsaI  (4275)
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.
AhdI  (4214)
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.
PciI  (3321)
1 site
A C A T G T T G T A C A

PciI is inhibited by nonionic detergents.
BspQI  (3205)
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  (3205)
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.
BstZ17I  (2942)
1 site
G T A T A C C A T A T G
BsmI  (2890)
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.
PsiI  (2829)
1 site
T T A T A A A A T A T T
PfoI  (2745)
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.
MfeI  (161)
1 site
C A A T T G G T T A A C
Bpu10I  (180)
1 site
C C T N A G C G G A N T C G

Cleavage may be enhanced when more than one copy of the Bpu10I recognition sequence is present.
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.
NruI  (208)
1 site
T C G C G A A G C G C T
MluI  (228)
1 site
A C G C G T T G C G C A
SnaBI  (590)
1 site
T A C G T A A T G C A T
AflII  (975)
1 site
C T T A A G G A A T T C
HindIII  (978)
1 site
A A G C T T T T C G A A
Acc65I  (984)
1 site
G G T A C C C C A T G G
KpnI  (988)
1 site
G G T A C C C C A T G G
BamHI  (996)
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.
EcoRV  (1031)
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.
NotI  (1046)
1 site
G C G G C C G C C G C C G G C G
AvaI  (1052)
1 site
C Y C G R G G R G C Y C

Sticky ends from different AvaI sites may not be compatible.
BsoBI  (1052)
1 site
C Y C G R G G R G C Y C

Sticky ends from different BsoBI sites may not be compatible.
BsoBI is typically used at 37°C, but can be used at temperatures up to 65°C.
PaeR7I  (1052)
1 site
C T C G A G G A G C T C

PaeR7I does not recognize the sequence CTCTCGAG.
PspXI  (1052)
1 site
V C T C G A G B B G A G C T C V
XhoI  (1052)
1 site
C T C G A G G A G C T C
EcoO109I  (1064)
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.
PspOMI  (1064)
1 site
G G G C C C C C C G G G
ApaI  (1068)
1 site
G G G C C C C C C G G G

ApaI can be used between 25°C and 37°C.
BclI  (1082)
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.
SphI  (1295)
1 site
G C A T G C C G T A C G
MscI  (1655)
1 site
T G G C C A A C C G G T
PshAI  (1682)
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.
BfuAI  (1968)
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  (1968)
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.
AsiSI  (2019)
1 site
G C G A T C G C C G C T A G C G
RsrII  (2063)
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.
SacII  (2435)
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.
HygR
1658 .. 2680  =  1023 bp
340 amino acids  =  37.9 kDa
Product: aminoglycoside phosphotransferase from E. coli
confers resistance to hygromycin
HygR
1658 .. 2680  =  1023 bp
340 amino acids  =  37.9 kDa
Product: aminoglycoside phosphotransferase from E. coli
confers resistance to hygromycin
AmpR
4141 .. 5001  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 2:  
   4141 .. 4932  =  792 bp
   263 amino acids  =  28.9 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
4141 .. 5001  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 1:  signal sequence  
   4933 .. 5001  =  69 bp
   23 amino acids  =  2.6 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
4141 .. 5001  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
ori
3382 .. 3970  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
ori
3382 .. 3970  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
CMV enhancer
235 .. 614  =  380 bp
human cytomegalovirus immediate early enhancer
CMV enhancer
235 .. 614  =  380 bp
human cytomegalovirus immediate early enhancer
bGH poly(A) signal
1095 .. 1319  =  225 bp
bovine growth hormone polyadenylation signal
bGH poly(A) signal
1095 .. 1319  =  225 bp
bovine growth hormone polyadenylation signal
CMV promoter
615 .. 818  =  204 bp
human cytomegalovirus (CMV) immediate early promoter
CMV promoter
615 .. 818  =  204 bp
human cytomegalovirus (CMV) immediate early promoter
SV40 poly(A) signal
2810 .. 2931  =  122 bp
SV40 polyadenylation signal
SV40 poly(A) signal
2810 .. 2931  =  122 bp
SV40 polyadenylation signal
MCS
968 .. 1077  =  110 bp
multiple cloning site
MCS
968 .. 1077  =  110 bp
multiple cloning site
AmpR promoter
5002 .. 5106  =  105 bp
AmpR promoter
5002 .. 5106  =  105 bp
FRT
1603 .. 1650  =  48 bp
FLP-mediated recombination occurs in the 8-bp core sequence TCTAGAAA (Turan and Bode, 2011).
FRT
1603 .. 1650  =  48 bp
FLP-mediated recombination occurs in the 8-bp core sequence TCTAGAAA (Turan and Bode, 2011).
tet operator
820 .. 838  =  19 bp
bacterial operator O2 for the tetR and tetA genes
tet operator
820 .. 838  =  19 bp
bacterial operator O2 for the tetR and tetA genes
tet operator
841 .. 859  =  19 bp
bacterial operator O2 for the tetR and tetA genes
tet operator
841 .. 859  =  19 bp
bacterial operator O2 for the tetR and tetA genes
ORF:  1316 .. 1582  =  267 bp
ORF:  88 amino acids  =  9.3 kDa
ORF:  1730 .. 2680  =  951 bp
ORF:  316 amino acids  =  35.2 kDa
ORF:  4271 .. 4537  =  267 bp
ORF:  88 amino acids  =  9.2 kDa
ORF:  774 .. 1151  =  378 bp
ORF:  125 amino acids  =  14.5 kDa
ORF:  1631 .. 2413  =  783 bp
ORF:  260 amino acids  =  29.2 kDa
ORF:  4141 .. 5001  =  861 bp
ORF:  286 amino acids  =  31.6 kDa
Click here to try SnapGene

Download pcDNA5 FRT TO.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.