pET-51b(+)

Bacterial vector for expressing proteins with a cleavable N-terminal Strep-Tag II tag and a C-terminal 10xHis tag.

Sequence Author: MilliporeSigma (Novagen)

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DraIII (4976) PsiI (4848) SspI (4768) AhdI (4564) BsaI (4498) BglI (4446) FspI (4341) PvuI (4195) ScaI (4083) AlwNI (3370) PciI (2954) BspQI - SapI (2838) BstZ17I (2725) PflFI - Tth111I (2699) BlpI (80) AvrII (97) BseRI - Eco53kI (165) SacI (167) EagI - NotI (172) HindIII (179) SalI (185) PshAI (192) ZraI (194) AatII (196) BamHI (198) Acc65I (204) KpnI (208) BstBI (234) Strep-Tag II NcoI (259) ATG XbaI (298) lac operator T7 promoter BspDI * - ClaI * (367) SgrAI (409) SphI (565) EcoNI (625) PflMI (672) BstAPI (773) MluI (1090) BclI * (1104) BstEII (1271) PspOMI (1297) ApaI (1301) BssHII (1501) HpaI (1596) PpuMI (1960) Bpu10I (2060) pET-51b(+) 5218 bp
DraIII  (4976)
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  (4848)
1 site
T T A T A A A A T A T T
SspI  (4768)
1 site
A A T A T T T T A T A A
AhdI  (4564)
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.
BsaI  (4498)
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.
BglI  (4446)
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  (4341)
1 site
T G C G C A A C G C G T
PvuI  (4195)
1 site
C G A T C G G C T A G C
ScaI  (4083)
1 site
A G T A C T T C A T G A
AlwNI  (3370)
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  (2954)
1 site
A C A T G T T G T A C A

PciI is inhibited by nonionic detergents.
BspQI  (2838)
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  (2838)
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  (2725)
1 site
G T A T A C C A T A T G
PflFI  (2699)
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  (2699)
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.
AvrII  (97)
1 site
C C T A G G G G A T C C
BseRI  (165)
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.
Eco53kI  (165)
1 site
G A G C T C C T C G A G
SacI  (167)
1 site
G A G C T C C T C G A G
EagI  (172)
1 site
C G G C C G G C C G G C
NotI  (172)
1 site
G C G G C C G C C G C C G G C G
HindIII  (179)
1 site
A A G C T T T T C G A A
SalI  (185)
1 site
G T C G A C C A G C T G
PshAI  (192)
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.
ZraI  (194)
1 site
G A C G T C C T G C A G
AatII  (196)
1 site
G A C G T C C T G C 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.
Acc65I  (204)
1 site
G G T A C C C C A T G G
KpnI  (208)
1 site
G G T A C C C C A T G G
BstBI  (234)
1 site
T T C G A A A A G C T T
NcoI  (259)
1 site
C C A T G G G G T A C C
XbaI  (298)
1 site
T C T A G A A G A T C T
BspDI  (367)
1 site
A T C G A T T A G C T A
* Blocked by Dam methylation.
ClaI  (367)
1 site
A T C G A T T A G C T A
* Blocked by Dam methylation.
SgrAI  (409)
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  (565)
1 site
G C A T G C C G T A C G
EcoNI  (625)
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.
PflMI  (672)
1 site
C C A N N N N N T G G G G T N N N N N A C C

Sticky ends from different PflMI sites may not be compatible.
BstAPI  (773)
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  (1090)
1 site
A C G C G T T G C G C A
BclI  (1104)
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  (1271)
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  (1297)
1 site
G G G C C C C C C G G G
ApaI  (1301)
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  (1501)
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  (1596)
1 site
G T T A A C C A A T T G
PpuMI  (1960)
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  (2060)
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
740 .. 1822  =  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
740 .. 1822  =  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
3777 .. 4637  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 1:  signal sequence  
   3777 .. 3845  =  69 bp
   23 amino acids  =  2.6 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
3777 .. 4637  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 2:  
   3846 .. 4637  =  792 bp
   263 amino acids  =  28.9 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
3777 .. 4637  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
ori
3015 .. 3603  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
ori
3015 .. 3603  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
f1 ori
4752 .. 5207  =  456 bp
f1 bacteriophage origin of replication; arrow indicates direction of (+) strand synthesis
f1 ori
4752 .. 5207  =  456 bp
f1 bacteriophage origin of replication; arrow indicates direction of (+) strand synthesis
rop
2394 .. 2585  =  192 bp
63 amino acids  =  7.2 kDa
Product: Rop protein
rop
2394 .. 2585  =  192 bp
63 amino acids  =  7.2 kDa
Product: Rop protein
10xHis
110 .. 139  =  30 bp
10 amino acids  =  1.4 kDa
Product: 10xHis affinity tag
10xHis
110 .. 139  =  30 bp
10 amino acids  =  1.4 kDa
Product: 10xHis affinity tag
enterokinase site
209 .. 223  =  15 bp
5 amino acids  =  606.5 Da
Product: enterokinase recognition and cleavage site
enterokinase site
209 .. 223  =  15 bp
5 amino acids  =  606.5 Da
Product: enterokinase recognition and cleavage site
Strep-Tag II
230 .. 253  =  24 bp
8 amino acids  =  1.1 kDa
Product: peptide that binds Strep-Tactin, an engineered form of streptavidin
Strep-Tag II
230 .. 253  =  24 bp
8 amino acids  =  1.1 kDa
Product: peptide that binds Strep-Tactin, an engineered form of streptavidin
ATG
260 .. 262  =  3 bp
1 amino acid  =  149.2 Da
Product: start codon
ATG
260 .. 262  =  3 bp
1 amino acid  =  149.2 Da
Product: start codon
lacI promoter
662 .. 739  =  78 bp
lacI promoter
662 .. 739  =  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
lac operator
306 .. 330  =  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
306 .. 330  =  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
331 .. 349  =  19 bp
promoter for bacteriophage T7 RNA polymerase
T7 promoter
331 .. 349  =  19 bp
promoter for bacteriophage T7 RNA polymerase
RBS
270 .. 275  =  6 bp
ribosome binding site
RBS
270 .. 275  =  6 bp
ribosome binding site
MCS
163 .. 209  =  47 bp
multiple cloning site
MCS
163 .. 209  =  47 bp
multiple cloning site
ORF:  67 .. 990  =  924 bp
ORF:  307 amino acids  =  32.8 kDa
ORF:  1579 .. 1842  =  264 bp
ORF:  87 amino acids  =  8.9 kDa
ORF:  863 .. 1822  =  960 bp
ORF:  319 amino acids  =  34.1 kDa
ORF:  2361 .. 2585  =  225 bp
ORF:  74 amino acids  =  8.5 kDa
ORF:  3777 .. 4637  =  861 bp
ORF:  286 amino acids  =  31.6 kDa
ORF:  1994 .. 2362  =  369 bp
ORF:  122 amino acids  =  14.2 kDa
ORF:  4241 .. 4507  =  267 bp
ORF:  88 amino acids  =  9.2 kDa
ORF:  313 .. 564  =  252 bp
ORF:  83 amino acids  =  8.6 kDa
ORF:  438 .. 701  =  264 bp
ORF:  87 amino acids  =  9.5 kDa
ORF:  1605 .. 1856  =  252 bp
ORF:  83 amino acids  =  9.1 kDa
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