pET102 D-TOPO

Bacterial directional TOPO® cloning vector, for tagging a protein N-terminally with His-Patch thioredoxin and C-terminally with V5 and 6xHis.

Sequence Author: Thermo Fisher (Invitrogen)

|Download SnapGene Viewer
Explore Over 2.7k Plasmids: TOPO Cloning Vectors | More Plasmid Sets
No matches
EcoNI (5572) BclI * (5090) BstEII (4922) ApaI (4901) PspOMI (4897) ApoI (4829) BssHII (4693) HpaI (4602) PshAI (4263) EagI (4036) NruI (4005) BfuAI - BspMI (3921) BsmI (3622) MscI * (3533) Bpu10I (3395) PflFI - Tth111I (2758) BsaAI (2752) BstZ17I (2733) AccI (2732) BspQI - SapI (2620) PciI (2503) SphI (5637) SgrAI (5785) BglII (5826) T7 promoter XbaI (5892) RBS AflII (5989) AleI (6030) RsrII (6037) TspMI - XmaI (6129) SmaI (6131) BamHI (6271) enterokinase site Eco53kI (9) SacI (11) HindIII (13) BseRI (34) AgeI (67) 6xHis BlpI (150) T7 terminator ZraI (694) AatII (696) SspI (810) ScaI (1134) PvuI (1246) PstI (1373) AhdI (1615) AlwNI (2094) pET102/D-TOPO® 6311 bp
EcoNI  (5572)
1 site
C C T N N N N N A G G G G A N N N N N T C C

The 1-base overhangs produced by EcoNI may be hard to ligate.
Sticky ends from different EcoNI sites may not be compatible.
BclI  (5090)
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.
BstEII  (4922)
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.
ApaI  (4901)
1 site
G G G C C C C C C G G G

ApaI can be used between 25°C and 37°C.
PspOMI  (4897)
1 site
G G G C C C C C C G G G
ApoI  (4829)
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.
BssHII  (4693)
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.
HpaI  (4602)
1 site
G T T A A C C A A T T G
PshAI  (4263)
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.
EagI  (4036)
1 site
C G G C C G G C C G G C
NruI  (4005)
1 site
T C G C G A A G C G C T
BfuAI  (3921)
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  (3921)
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.
BsmI  (3622)
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.
MscI  (3533)
1 site
T G G C C A A C C G G T
* Blocked by Dcm methylation.
Bpu10I  (3395)
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.
PflFI  (2758)
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  (2758)
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.
BsaAI  (2752)
1 site
Y A C G T R R T G C A Y
BstZ17I  (2733)
1 site
G T A T A C C A T A T G
AccI  (2732)
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.
BspQI  (2620)
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  (2620)
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.
PciI  (2503)
1 site
A C A T G T T G T A C A

PciI is inhibited by nonionic detergents.
SphI  (5637)
1 site
G C A T G C C G T A C G
SgrAI  (5785)
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.
BglII  (5826)
1 site
A G A T C T T C T A G A
XbaI  (5892)
1 site
T C T A G A A G A T C T
AflII  (5989)
1 site
C T T A A G G A A T T C
AleI  (6030)
1 site
C A C N N N N G T G G T G N N N N C A C
RsrII  (6037)
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.
TspMI  (6129)
1 site
C C C G G G G G G C C C
XmaI  (6129)
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  (6131)
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  (6271)
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.
Eco53kI  (9)
1 site
G A G C T C C T C G A G
SacI  (11)
1 site
G A G C T C C T C G A G
HindIII  (13)
1 site
A A G C T T T T C G A A
BseRI  (34)
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.
AgeI  (67)
1 site
A C C G G T T G G C C A
BlpI  (150)
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.
ZraI  (694)
1 site
G A C G T C C T G C A G
AatII  (696)
1 site
G A C G T C C T G C A G
SspI  (810)
1 site
A A T A T T T T A T A A
ScaI  (1134)
1 site
A G T A C T T C A T G A
PvuI  (1246)
1 site
C G A T C G G C T A G C
PstI  (1373)
1 site
C T G C A G G A C G T C
AhdI  (1615)
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.
AlwNI  (2094)
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.
lacI
4377 .. 5459  =  1083 bp
360 amino acids  =  38.6 kDa
Product: lac repressor
The lac repressor binds to the lac operator to inhibit transcription in E. coli. This inhibition can be relieved by adding lactose or isopropyl-β-D-thiogalactopyranoside (IPTG).
lacI
4377 .. 5459  =  1083 bp
360 amino acids  =  38.6 kDa
Product: lac repressor
The lac repressor binds to the lac operator to inhibit transcription in E. coli. This inhibition can be relieved by adding lactose or isopropyl-β-D-thiogalactopyranoside (IPTG).
AmpR
828 .. 1688  =  861 bp
286 amino acids  =  31.5 kDa
2 segments
   Segment 1:  signal sequence  
   828 .. 896  =  69 bp
   23 amino acids  =  2.6 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
828 .. 1688  =  861 bp
286 amino acids  =  31.5 kDa
2 segments
   Segment 2:  
   897 .. 1688  =  792 bp
   263 amino acids  =  28.9 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
828 .. 1688  =  861 bp
286 amino acids  =  31.5 kDa
2 segments
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
ori
1859 .. 2447  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
ori
1859 .. 2447  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
HP-thioredoxin
5935 .. 6264  =  330 bp
110 amino acids  =  11.9 kDa
Product: His-Patch thioredoxin
The histidines at positions 8, 32, and 64 coordinate a divalent cation, allowing HP-thioredoxin to be purified on metal-chelating resins.
HP-thioredoxin
5935 .. 6264  =  330 bp
110 amino acids  =  11.9 kDa
Product: His-Patch thioredoxin
The histidines at positions 8, 32, and 64 coordinate a divalent cation, allowing HP-thioredoxin to be purified on metal-chelating resins.
enterokinase site
6280 .. 6294  =  15 bp
5 amino acids  =  606.5 Da
Product: enterokinase recognition and cleavage site
enterokinase site
6280 .. 6294  =  15 bp
5 amino acids  =  606.5 Da
Product: enterokinase recognition and cleavage site
rop
2874 .. 3065  =  192 bp
63 amino acids  =  7.2 kDa
Product: Rop protein, which maintains plasmids at low copy number
rop
2874 .. 3065  =  192 bp
63 amino acids  =  7.2 kDa
Product: Rop protein, which maintains plasmids at low copy number
AmpR promoter
723 .. 827  =  105 bp
AmpR promoter
723 .. 827  =  105 bp
lacI promoter
5460 .. 5537  =  78 bp
lacI promoter
5460 .. 5537  =  78 bp
V5 tag
22 .. 63  =  42 bp
14 amino acids  =  1.4 kDa
Product: epitope tag from simian virus 5
V5 tag
22 .. 63  =  42 bp
14 amino acids  =  1.4 kDa
Product: epitope tag from simian virus 5
6xHis
73 .. 90  =  18 bp
6 amino acids  =  840.9 Da
Product: 6xHis affinity tag
6xHis
73 .. 90  =  18 bp
6 amino acids  =  840.9 Da
Product: 6xHis affinity tag
T7 terminator
161 .. 208  =  48 bp
transcription terminator for bacteriophage T7 RNA polymerase
T7 terminator
161 .. 208  =  48 bp
transcription terminator for bacteriophage T7 RNA polymerase
lac operator
5865 .. 5889  =  25 bp
The lac repressor binds to the lac operator to inhibit transcription in E. coli. This inhibition can be relieved by adding lactose or isopropyl-β-D-thiogalactopyranoside (IPTG).
lac operator
5865 .. 5889  =  25 bp
The lac repressor binds to the lac operator to inhibit transcription in E. coli. This inhibition can be relieved by adding lactose or isopropyl-β-D-thiogalactopyranoside (IPTG).
T7 promoter
5846 .. 5864  =  19 bp
promoter for bacteriophage T7 RNA polymerase
T7 promoter
5846 .. 5864  =  19 bp
promoter for bacteriophage T7 RNA polymerase
RBS
5919 .. 5925  =  7 bp
ribosome binding site
RBS
5919 .. 5925  =  7 bp
ribosome binding site
ORF:  3097 .. 3465  =  369 bp
ORF:  122 amino acids  =  14.2 kDa
ORF:  5635 .. 5874  =  240 bp
ORF:  79 amino acids  =  8.0 kDa
ORF:  5935 .. 6315  =  381 bp
ORF:  127 amino acids  =  13.6 kDa
ORF:  3899 .. 4594  =  696 bp
ORF:  231 amino acids  =  25.4 kDa
ORF:  5498 .. 5761  =  264 bp
ORF:  87 amino acids  =  9.5 kDa
ORF:  828 .. 1688  =  861 bp
ORF:  286 amino acids  =  31.5 kDa
ORF:  4357 .. 4620  =  264 bp
ORF:  87 amino acids  =  8.9 kDa
ORF:  5209 .. 5709  =  501 bp
ORF:  166 amino acids  =  17.5 kDa
ORF:  5893 .. 6315  =  423 bp
ORF:  140 amino acids  =  16.2 kDa  (no start codon)
ORF:  2874 .. 3098  =  225 bp
ORF:  74 amino acids  =  8.5 kDa
ORF:  3462 .. 3800  =  339 bp
ORF:  112 amino acids  =  12.6 kDa
ORF:  4377 .. 5336  =  960 bp
ORF:  319 amino acids  =  34.1 kDa
ORF:  5706 .. 5933  =  228 bp
ORF:  75 amino acids  =  7.9 kDa
ORF:  161 .. 526  =  366 bp
ORF:  121 amino acids  =  12.9 kDa
ORF:  1292 .. 1558  =  267 bp
ORF:  88 amino acids  =  9.2 kDa
ORF:  3704 .. 4321  =  618 bp
ORF:  205 amino acids  =  21.8 kDa
Click here to try SnapGene

Download pET102 D-TOPO.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

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.