pET-24b(+)

Bacterial vector with a kanamycin resistance marker for inducible expression of T7-tagged proteins. For other reading frames, use pET-24a(+) or pET-24c(+).

Sequence Author: MilliporeSigma (Novagen)

|Download SnapGene Viewer
Explore Over 2.7k Plasmids: pET & Duet Vectors (Novagen) | More Plasmid Sets
No matches
StyI (57) DraIII (5067) PsiI (4939) AsiSI - PvuI (4366) SmaI (4240) TspMI - XmaI (4238) BspDI - ClaI (4057) NruI (4023) AcuI (3712) AlwNI (3580) BssSI - BssSαI (3337) PciI (3164) BspQI - SapI (3048) TatI (2968) BstZ17I (2935) PflFI - Tth111I (2909) BlpI (80) 6xHis PaeR7I - PspXI - XhoI (158) EagI - NotI (166) HindIII (173) SalI (179) Eco53kI (188) SacI (190) EcoRI (192) BamHI (198) T7 tag NheI (230) BmtI (234) NdeI (237) XbaI (275) lac operator T7 promoter BglII (341) SgrAI (382) SphI (538) BstAPI (746) MluI (1063) BclI * (1077) BstEII (1244) NmeAIII (1269) PspOMI (1270) ApaI (1274) BssHII (1474) EcoRV (1513) HpaI (1569) PshAI (1908) BglI (2127) FspI - FspAI (2145) PpuMI (2170) pET-24b(+) 5309 bp
StyI  (57)
1 site
C C W W G G G G W W C C

Sticky ends from different StyI sites may not be compatible.
DraIII  (5067)
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  (4939)
1 site
T T A T A A A A T A T T
AsiSI  (4366)
1 site
G C G A T C G C C G C T A G C G
PvuI  (4366)
1 site
C G A T C G G C T A G C
SmaI  (4240)
1 site
C C C G G G G G G C C C

SmaI can be used at 37°C for brief incubations.
TspMI  (4238)
1 site
C C C G G G G G G C C C
XmaI  (4238)
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.
BspDI  (4057)
1 site
A T C G A T T A G C T A
ClaI  (4057)
1 site
A T C G A T T A G C T A
NruI  (4023)
1 site
T C G C G A A G C G C T
AcuI  (3712)
1 site
C T G A A G ( N ) 14 N N G A C T T C ( N ) 14

Cleavage may be enhanced when more than one copy of the AcuI recognition sequence is present.
Sticky ends from different AcuI sites may not be compatible.
After cleavage, AcuI can remain bound to DNA and alter its electrophoretic mobility.
For full activity, add fresh S-adenosylmethionine (SAM).
AlwNI  (3580)
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.
BssSI  (3337)
1 site
C A C G A G G T G C T C
BssSαI  (3337)
1 site
C A C G A G G T G C T C
PciI  (3164)
1 site
A C A T G T T G T A C A

PciI is inhibited by nonionic detergents.
BspQI  (3048)
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  (3048)
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.
TatI  (2968)
1 site
W G T A C W W C A T G W
BstZ17I  (2935)
1 site
G T A T A C C A T A T G
PflFI  (2909)
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  (2909)
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.
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.
NheI  (230)
1 site
G C T A G C C G A T C G
BmtI  (234)
1 site
G C T A G C C G A T C G
NdeI  (237)
1 site
C A T A T G G T A T A C

Prolonged incubation with NdeI may lead to removal of additional nucleotides.
XbaI  (275)
1 site
T C T A G A A G A T C T
BglII  (341)
1 site
A G A T C T T C T A G A
SgrAI  (382)
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  (538)
1 site
G C A T G C C G T A C G
BstAPI  (746)
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  (1063)
1 site
A C G C G T T G C G C A
BclI  (1077)
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  (1244)
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.
NmeAIII  (1269)
1 site
G C C G A G ( N ) 18-19 N N C G G C T C ( N ) 18-19

Efficient cleavage requires at least two copies of the NmeAIII recognition sequence.
Sticky ends from different NmeAIII sites may not be compatible.
For full activity, add fresh S-adenosylmethionine (SAM).
PspOMI  (1270)
1 site
G G G C C C C C C G G G
ApaI  (1274)
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  (1474)
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.
EcoRV  (1513)
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.
HpaI  (1569)
1 site
G T T A A C C A A T T G
PshAI  (1908)
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.
BglI  (2127)
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.
FspI  (2145)
1 site
T G C G C A A C G C G T
FspAI  (2145)
1 site
R T G C G C A Y Y A C G C G T R
PpuMI  (2170)
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.
lacI
713 .. 1795  =  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
713 .. 1795  =  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).
KanR
3935 .. 4750  =  816 bp
271 amino acids  =  31.0 kDa
Product: aminoglycoside phosphotransferase
confers resistance to kanamycin
KanR
3935 .. 4750  =  816 bp
271 amino acids  =  31.0 kDa
Product: aminoglycoside phosphotransferase
confers resistance to kanamycin
ori
3225 .. 3813  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
ori
3225 .. 3813  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
f1 ori
4843 .. 5298  =  456 bp
f1 bacteriophage origin of replication; arrow indicates direction of (+) strand synthesis
f1 ori
4843 .. 5298  =  456 bp
f1 bacteriophage origin of replication; arrow indicates direction of (+) strand synthesis
rop
2604 .. 2795  =  192 bp
63 amino acids  =  7.2 kDa
Product: Rop protein
rop
2604 .. 2795  =  192 bp
63 amino acids  =  7.2 kDa
Product: Rop protein
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
T7 tag
206 .. 238  =  33 bp
11 amino acids  =  1.1 kDa
Product: epitope tag from a T7 major capsid protein
T7 tag
206 .. 238  =  33 bp
11 amino acids  =  1.1 kDa
Product: epitope tag from a T7 major capsid protein
lacI promoter
635 .. 712  =  78 bp
lacI promoter
635 .. 712  =  78 bp
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
MCS
158 .. 203  =  46 bp
multiple cloning site
MCS
158 .. 203  =  46 bp
multiple cloning site
lac operator
283 .. 307  =  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
283 .. 307  =  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
308 .. 326  =  19 bp
promoter for bacteriophage T7 RNA polymerase
T7 promoter
308 .. 326  =  19 bp
promoter for bacteriophage T7 RNA polymerase
RBS
247 .. 252  =  6 bp
ribosome binding site
RBS
247 .. 252  =  6 bp
ribosome binding site
ORF:  463 .. 963  =  501 bp
ORF:  166 amino acids  =  17.5 kDa
ORF:  1552 .. 1815  =  264 bp
ORF:  87 amino acids  =  8.9 kDa
ORF:  239 .. 466  =  228 bp
ORF:  75 amino acids  =  7.9 kDa
ORF:  836 .. 1795  =  960 bp
ORF:  319 amino acids  =  34.1 kDa
ORF:  3935 .. 4750  =  816 bp
ORF:  271 amino acids  =  31.0 kDa
ORF:  1851 .. 2207  =  357 bp
ORF:  118 amino acids  =  13.0 kDa
ORF:  2571 .. 2795  =  225 bp
ORF:  74 amino acids  =  8.5 kDa
ORF:  411 .. 674  =  264 bp
ORF:  87 amino acids  =  9.5 kDa
ORF:  1578 .. 1829  =  252 bp
ORF:  83 amino acids  =  9.1 kDa
ORF:  2204 .. 2572  =  369 bp
ORF:  122 amino acids  =  14.2 kDa
ORF:  298 .. 537  =  240 bp
ORF:  79 amino acids  =  8.0 kDa
Click here to try SnapGene

Download pET-24b(+).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.