pET-32b(+)

Bacterial vector for expressing thioredoxin fusion proteins with an enterokinase site. For other reading frames, use pET-32a(+) or pET-32c(+).

Sequence Author: MilliporeSigma (Novagen)

|Download SnapGene Viewer
Explore Over 2.7k Plasmids: pET & Duet Vectors (Novagen) | More Plasmid Sets
No matches
T7 terminator DraIII (5657) PsiI (5529) ScaI (4994) PvuI (4884) PstI (4759) BsaI (4575) AhdI (4514) AlwNI (4037) PciI (3621) BspQI - SapI (3505) BstZ17I (3392) PflFI - Tth111I (3366) BlpI (80) 6xHis AvaI - BsoBI - PaeR7I - PspXI - XhoI (158) EagI - NotI (166) HindIII (173) SalI (179) Eco53kI (188) SacI (190) EcoRI (192) BamHI (198) EcoRV (206) NcoI (211) enterokinase site Acc65I (233) KpnI (237) BglII (240) BstBI (267) thrombin site 6xHis MscI (350) RsrII (588) RBS XbaI (728) T7 promoter SgrAI (839) SphI (995) EcoNI (1055) BstAPI (1203) MluI (1520) BclI * (1534) BstEII (1701) PspOMI (1727) ApaI (1731) BssHII (1931) HpaI (2026) PshAI (2365) FspAI (2602) PpuMI (2627) Bpu10I (2727) pET-32b(+) 5899 bp
DraIII  (5657)
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.
PsiI  (5529)
1 site
T T A T A A A A T A T T
ScaI  (4994)
1 site
A G T A C T T C A T G A
PvuI  (4884)
1 site
C G A T C G G C T A G C
PstI  (4759)
1 site
C T G C A G G A C G T C
BsaI  (4575)
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  (4514)
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  (4037)
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.
PciI  (3621)
1 site
A C A T G T T G T A C A

PciI is inhibited by nonionic detergents.
BspQI  (3505)
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  (3505)
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  (3392)
1 site
G T A T A C C A T A T G
PflFI  (3366)
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  (3366)
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.
BlpI  (80)
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.
AvaI  (158)
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  (158)
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  (158)
1 site
C T C G A G G A G C T C

PaeR7I does not recognize the sequence CTCTCGAG.
PspXI  (158)
1 site
V C T C G A G B B G A G C T C V
XhoI  (158)
1 site
C T C G A G G A G C T C
EagI  (166)
1 site
C G G C C G G C C G G C
NotI  (166)
1 site
G C G G C C G C C G C C G G C G
HindIII  (173)
1 site
A A G C T T T T C G A A
SalI  (179)
1 site
G T C G A C C A G C T G
Eco53kI  (188)
1 site
G A G C T C C T C G A G
SacI  (190)
1 site
G A G C T C C T C G A G
EcoRI  (192)
1 site
G A A T T C C T T A A G
BamHI  (198)
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  (206)
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.
NcoI  (211)
1 site
C C A T G G G G T A C C
Acc65I  (233)
1 site
G G T A C C C C A T G G
KpnI  (237)
1 site
G G T A C C C C A T G G
BglII  (240)
1 site
A G A T C T T C T A G A
BstBI  (267)
1 site
T T C G A A A A G C T T
MscI  (350)
1 site
T G G C C A A C C G G T
RsrII  (588)
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.
XbaI  (728)
1 site
T C T A G A A G A T C T
SgrAI  (839)
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.
SphI  (995)
1 site
G C A T G C C G T A C G
EcoNI  (1055)
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.
BstAPI  (1203)
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.
MluI  (1520)
1 site
A C G C G T T G C G C A
BclI  (1534)
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  (1701)
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.
PspOMI  (1727)
1 site
G G G C C C C C C G G G
ApaI  (1731)
1 site
G G G C C C C C C G G G

ApaI can be used between 25°C and 37°C.
BssHII  (1931)
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  (2026)
1 site
G T T A A C C A A T T G
PshAI  (2365)
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.
FspAI  (2602)
1 site
R T G C G C A Y Y A C G C G T R
PpuMI  (2627)
1 site
R G G W C C Y Y C C W G G R

Sticky ends from different PpuMI sites may not be compatible.
Bpu10I  (2727)
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.
lacI
1170 .. 2252  =  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
1170 .. 2252  =  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
4441 .. 5301  =  861 bp
286 amino acids  =  31.5 kDa
2 segments
   Segment 2:  
   4441 .. 5232  =  792 bp
   263 amino acids  =  28.9 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
4441 .. 5301  =  861 bp
286 amino acids  =  31.5 kDa
2 segments
   Segment 1:  signal sequence  
   5233 .. 5301  =  69 bp
   23 amino acids  =  2.6 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
4441 .. 5301  =  861 bp
286 amino acids  =  31.5 kDa
2 segments
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
ori
3682 .. 4270  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
ori
3682 .. 4270  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
6xHis
140 .. 157  =  18 bp
6 amino acids  =  840.9 Da
Product: 6xHis affinity tag
6xHis
140 .. 157  =  18 bp
6 amino acids  =  840.9 Da
Product: 6xHis affinity tag
enterokinase site
218 .. 232  =  15 bp
5 amino acids  =  606.5 Da
Product: enterokinase recognition and cleavage site
enterokinase site
218 .. 232  =  15 bp
5 amino acids  =  606.5 Da
Product: enterokinase recognition and cleavage site
S-Tag
248 .. 292  =  45 bp
15 amino acids  =  1.7 kDa
Product: affinity and epitope tag derived from pancreatic ribonuclease A
S-Tag
248 .. 292  =  45 bp
15 amino acids  =  1.7 kDa
Product: affinity and epitope tag derived from pancreatic ribonuclease A
thrombin site
299 .. 316  =  18 bp
6 amino acids  =  627.7 Da
Product: thrombin recognition and cleavage site
thrombin site
299 .. 316  =  18 bp
6 amino acids  =  627.7 Da
Product: thrombin recognition and cleavage site
6xHis
326 .. 343  =  18 bp
6 amino acids  =  840.9 Da
Product: 6xHis affinity tag
6xHis
326 .. 343  =  18 bp
6 amino acids  =  840.9 Da
Product: 6xHis affinity tag
TrxA
365 .. 691  =  327 bp
109 amino acids  =  11.8 kDa
Product: E. coli thioredoxin
TrxA
365 .. 691  =  327 bp
109 amino acids  =  11.8 kDa
Product: E. coli thioredoxin
f1 ori
5433 .. 5888  =  456 bp
f1 bacteriophage origin of replication; arrow indicates direction of (+) strand synthesis
f1 ori
5433 .. 5888  =  456 bp
f1 bacteriophage origin of replication; arrow indicates direction of (+) strand synthesis
rop
3061 .. 3252  =  192 bp
63 amino acids  =  7.2 kDa
Product: Rop protein
rop
3061 .. 3252  =  192 bp
63 amino acids  =  7.2 kDa
Product: Rop protein
AmpR promoter
5302 .. 5406  =  105 bp
AmpR promoter
5302 .. 5406  =  105 bp
lacI promoter
1092 .. 1169  =  78 bp
lacI promoter
1092 .. 1169  =  78 bp
MCS
158 .. 216  =  59 bp
multiple cloning site
MCS
158 .. 216  =  59 bp
multiple cloning site
T7 terminator
26 .. 73  =  48 bp
transcription terminator for bacteriophage T7 RNA polymerase
T7 terminator
26 .. 73  =  48 bp
transcription terminator for bacteriophage T7 RNA polymerase
lac operator
736 .. 760  =  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
736 .. 760  =  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
761 .. 779  =  19 bp
promoter for bacteriophage T7 RNA polymerase
T7 promoter
761 .. 779  =  19 bp
promoter for bacteriophage T7 RNA polymerase
RBS
700 .. 705  =  6 bp
ribosome binding site
RBS
700 .. 705  =  6 bp
ribosome binding site
ORF:  2308 .. 2664  =  357 bp
ORF:  118 amino acids  =  13.0 kDa
ORF:  3028 .. 3252  =  225 bp
ORF:  74 amino acids  =  8.5 kDa
ORF:  326 .. 1420  =  1095 bp
ORF:  364 amino acids  =  39.8 kDa
ORF:  2009 .. 2272  =  264 bp
ORF:  87 amino acids  =  8.9 kDa
ORF:  4571 .. 4837  =  267 bp
ORF:  88 amino acids  =  9.2 kDa
ORF:  1293 .. 2252  =  960 bp
ORF:  319 amino acids  =  34.1 kDa
ORF:  137 .. 691  =  555 bp
ORF:  184 amino acids  =  19.9 kDa
ORF:  743 .. 994  =  252 bp
ORF:  83 amino acids  =  8.6 kDa
ORF:  868 .. 1131  =  264 bp
ORF:  87 amino acids  =  9.5 kDa
ORF:  2035 .. 2286  =  252 bp
ORF:  83 amino acids  =  9.1 kDa
ORF:  4441 .. 5301  =  861 bp
ORF:  286 amino acids  =  31.5 kDa
ORF:  2661 .. 3029  =  369 bp
ORF:  122 amino acids  =  14.2 kDa
Click here to try SnapGene

Download pET-32b(+).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.