pLATE31 (linearized)

Vector for ligation independent cloning (LIC) and tightly regulated bacterial expression of a C-terminally 6xHis-tagged protein.

Sequence Author: Thermo Fisher

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rrnB T1 terminator AatII (4031) ZraI (4029) SspI (3913) ScaI (3589) PvuI (3479) FspI (3331) BglI (3229) AhdI (3109) AlwNI (2632) PciI (2216) BspQI - SapI (2100) NdeI (2039) BstZ17I (1989) AccI (1988) BsaAI (1970) PflFI - Tth111I (1963) PfoI (1860) AfeI (1472) rrnB T2 terminator LIC reverse sequencing primer (4324 .. 4339) lac operator Eco53kI (4342) SacI (4344) Acc65I (4346) KpnI (4350) MauBI (4357) BfuAI - BspMI - PaqCI (4362) SbfI (4373) AscI (4378) LIC forward sequencing primer (4387 .. 4406) T7 promoter LIC reverse sequencing primer (4414 .. 4428) XbaI (4434) SwaI (4459) End (4465) Start (0) 6xHis PmeI (45) StuI (52) SphI (60) PacI (82) LIC reverse sequencing primer (89 .. 112) HindIII (150) BspDI - ClaI (157) BamHI (184) StyI (200) T7 terminator PflMI (255) MluI (673) BclI * (687) BstEII (854) PspOMI (880) ApaI (884) ApoI (948) EcoRV (1123) HpaI (1179) KasI (1312) NarI * (1313) SfoI (1314) PluTI (1316) BspEI * (1407) BsaBI * (1415) pLATE31 4465 bp
AatII  (4031)
1 site
G A C G T C C T G C A G
ZraI  (4029)
1 site
G A C G T C C T G C A G
SspI  (3913)
1 site
A A T A T T T T A T A A
ScaI  (3589)
1 site
A G T A C T T C A T G A
PvuI  (3479)
1 site
C G A T C G G C T A G C
FspI  (3331)
1 site
T G C G C A A C G C G T
BglI  (3229)
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.
AhdI  (3109)
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  (2632)
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  (2216)
1 site
A C A T G T T G T A C A

PciI is inhibited by nonionic detergents.
BspQI  (2100)
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  (2100)
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.
NdeI  (2039)
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.
BstZ17I  (1989)
1 site
G T A T A C C A T A T G
AccI  (1988)
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.
BsaAI  (1970)
1 site
Y A C G T R R T G C A Y
PflFI  (1963)
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  (1963)
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.
PfoI  (1860)
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.
AfeI  (1472)
1 site
A G C G C T T C G C G A
Eco53kI  (4342)
1 site
G A G C T C C T C G A G
SacI  (4344)
1 site
G A G C T C C T C G A G
Acc65I  (4346)
1 site
G G T A C C C C A T G G
KpnI  (4350)
1 site
G G T A C C C C A T G G
MauBI  (4357)
1 site
C G C G C G C G G C G C G C G C
BfuAI  (4362)
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  (4362)
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.
PaqCI  (4362)
1 site
C A C C T G C ( N ) 4 G T G G A C G ( N ) 4 ( N ) 4

Efficient cleavage requires at least two copies of the PaqCI recognition sequence.
Sticky ends from different PaqCI sites may not be compatible.
Cleavage can be improved with PaqCI Activator.
SbfI  (4373)
1 site
C C T G C A G G G G A C G T C C
AscI  (4378)
1 site
G G C G C G C C C C G C G C G G
XbaI  (4434)
1 site
T C T A G A A G A T C T
SwaI  (4459)
1 site
A T T T A A A T T A A A T T T A

SwaI is typically used at 25°C, but is 50% active at 37°C.
End  (4465)
0 sites
Start  (0)
0 sites
PmeI  (45)
1 site
G T T T A A A C C A A A T T T G
StuI  (52)
1 site
A G G C C T T C C G G A
SphI  (60)
1 site
G C A T G C C G T A C G
PacI  (82)
1 site
T T A A T T A A A A T T A A T T
HindIII  (150)
1 site
A A G C T T T T C G A A
BspDI  (157)
1 site
A T C G A T T A G C T A
ClaI  (157)
1 site
A T C G A T T A G C T A
BamHI  (184)
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.
StyI  (200)
1 site
C C W W G G G G W W C C

Sticky ends from different StyI sites may not be compatible.
PflMI  (255)
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.
MluI  (673)
1 site
A C G C G T T G C G C A
BclI  (687)
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  (854)
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  (880)
1 site
G G G C C C C C C G G G
ApaI  (884)
1 site
G G G C C C C C C G G G

ApaI can be used between 25°C and 37°C.
ApoI  (948)
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.
EcoRV  (1123)
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  (1179)
1 site
G T T A A C C A A T T G
KasI  (1312)
1 site
G G C G C C C C G C G G
NarI  (1313)
1 site
G G C G C C C C G C G G
* Blocked by Dcm methylation.
Efficient cleavage requires at least two copies of the NarI recognition sequence.
SfoI  (1314)
1 site
G G C G C C C C G C G G
PluTI  (1316)
1 site
G G C G C C C C G C G G

Efficient cleavage requires at least two copies of the PluTI recognition sequence.
BspEI  (1407)
1 site
T C C G G A A G G C C T
* Blocked by Dam methylation.
BsaBI  (1415)
1 site
G A T N N N N A T C C T A N N N N T A G
* Blocked by Dam methylation.
LIC reverse sequencing primer
24-mer  /  46% GC
3 binding sites
4324 .. 4339  =  16 annealed bases (38% GC)
Tm  =  48°C
LIC forward sequencing primer
20-mer  /  40% GC
1 binding site
4387 .. 4406  =  20 annealed bases
Tm  =  49°C
LIC reverse sequencing primer
24-mer  /  46% GC
3 binding sites
4414 .. 4428  =  15 annealed bases (40% GC)
Tm  =  47°C
LIC reverse sequencing primer
24-mer  /  46% GC
3 binding sites
89 .. 112  =  24 annealed bases
Tm  =  58°C
lacI
323 .. 1405  =  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
323 .. 1405  =  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
3036 .. 3896  =  861 bp
286 amino acids  =  31.5 kDa
2 segments
   Segment 2:  
   3036 .. 3827  =  792 bp
   263 amino acids  =  28.9 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
3036 .. 3896  =  861 bp
286 amino acids  =  31.5 kDa
2 segments
   Segment 1:  signal sequence  
   3828 .. 3896  =  69 bp
   23 amino acids  =  2.6 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
3036 .. 3896  =  861 bp
286 amino acids  =  31.5 kDa
2 segments
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
ori
2277 .. 2865  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
ori
2277 .. 2865  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
rop
1658 .. 1849  =  192 bp
63 amino acids  =  7.2 kDa
Product: Rop protein, which maintains plasmids at low copy number
rop
1658 .. 1849  =  192 bp
63 amino acids  =  7.2 kDa
Product: Rop protein, which maintains plasmids at low copy number
AmpR promoter
3897 .. 4001  =  105 bp
AmpR promoter
3897 .. 4001  =  105 bp
rrnB T1 terminator
4102 .. 4183  =  82 bp
transcription terminator T1 from the E. coli rrnB gene
rrnB T1 terminator
4102 .. 4183  =  82 bp
transcription terminator T1 from the E. coli rrnB gene
lacI promoter
245 .. 322  =  78 bp
lacI promoter
245 .. 322  =  78 bp
T7 terminator
189 .. 236  =  48 bp
transcription terminator for bacteriophage T7 RNA polymerase
T7 terminator
189 .. 236  =  48 bp
transcription terminator for bacteriophage T7 RNA polymerase
tet promoter
146 .. 174  =  29 bp
3 segments
   Segment 3:  -10  
   146 .. 151  =  6 bp
E. coli promoter for tetracycline efflux protein gene
tet promoter
146 .. 174  =  29 bp
3 segments
   Segment 2:  
   152 .. 168  =  17 bp
E. coli promoter for tetracycline efflux protein gene
tet promoter
146 .. 174  =  29 bp
3 segments
   Segment 1:  -35  
   169 .. 174  =  6 bp
E. coli promoter for tetracycline efflux protein gene
tet promoter
146 .. 174  =  29 bp
3 segments
E. coli promoter for tetracycline efflux protein gene
rrnB T2 terminator
4275 .. 4302  =  28 bp
transcription terminator T2 from the E. coli rrnB gene
rrnB T2 terminator
4275 .. 4302  =  28 bp
transcription terminator T2 from the E. coli rrnB gene
lac operator
4406 .. 4430  =  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
4406 .. 4430  =  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
4387 .. 4405  =  19 bp
promoter for bacteriophage T7 RNA polymerase
T7 promoter
4387 .. 4405  =  19 bp
promoter for bacteriophage T7 RNA polymerase
6xHis
2 .. 19  =  18 bp
6 amino acids  =  840.9 Da
Product: 6xHis affinity tag
6xHis
2 .. 19  =  18 bp
6 amino acids  =  840.9 Da
Product: 6xHis affinity tag
lac operator
4320 .. 4336  =  17 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
4320 .. 4336  =  17 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).
RBS
4467 .. 4473  =  7 bp
ribosome binding site
RBS
4467 .. 4473  =  7 bp
ribosome binding site
ORF:  256 .. 573  =  318 bp
ORF:  105 amino acids  =  11.2 kDa
ORF:  1162 .. 1554  =  393 bp
ORF:  130 amino acids  =  14.0 kDa
ORF:  3166 .. 3432  =  267 bp
ORF:  88 amino acids  =  9.2 kDa
ORF:  446 .. 1405  =  960 bp
ORF:  319 amino acids  =  34.1 kDa
ORF:  1625 .. 1849  =  225 bp
ORF:  74 amino acids  =  8.5 kDa
ORF:  1270 .. 1626  =  357 bp
ORF:  118 amino acids  =  13.4 kDa
ORF:  3036 .. 3896  =  861 bp
ORF:  286 amino acids  =  31.5 kDa
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Download pLATE31 (linearized).dna file

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