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Plasmid Files

pMCentr2 (linearized)

Linearized vector for ligation-independent cloning (LIC) to create a Gateway® entry vector, with a kanamycin resistance marker and a TEV cleavage site.

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pMCentr2 (linearized) Sequence and MappMCentr2 (linearized).dna
Map and Sequence File   
Sequence Author:  Midwest Center for Structural Genomics
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 PciI (1886) DrdI (1784) BssS α I (1713) BciVI (1688) BsiHKAI (1576) ApaLI (1572) AlwNI (1477) AcuI - Eco57MI (1344) PflMI (974) Bpu10I (728) BsmBI (727) AsiSI - PvuI (711) BsrFI (665) EcoNI (623) NspI (1890) BspQI - SapI (2003) BsaHI (2219) AclI (2256) BbsI (2329) HincII - HpaI (2393) AhdI (2441) AflII (2446) AvaI - BsoBI (2452) BmeT110I (2453) PspOMI (2455) EcoO109I (2456) ApaI (2459) MslI (2510) End (2571) Start (0) EcoRV (129) NruI (368) pMCentr2 2571 bp
PciI  (1886)
1 site
A C A T G T T G T A C A

PciI is inhibited by nonionic detergents.
DrdI  (1784)
1 site
G A C N N N N N N G T C C T G N N N N N N C A G

Sticky ends from different DrdI sites may not be compatible.
BssSαI  (1713)
1 site
C A C G A G G T G C T C
BciVI  (1688)
1 site
G T A T C C ( N ) 5 N C A T A G G ( N ) 5

The 1-base overhangs produced by BciVI may be hard to ligate.
Sticky ends from different BciVI sites may not be compatible.
BsiHKAI  (1576)
1 site
G W G C W C C W C G W G

Sticky ends from different BsiHKAI sites may not be compatible.
ApaLI  (1572)
1 site
G T G C A C C A C G T G
AlwNI  (1477)
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.
AcuI  (1344)
1 site
C T G A A G ( N ) 14 N N G A C T T C ( N ) 14

Efficient cleavage requires at least two copies of the AcuI
recognition sequence.
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).
Eco57MI  (1344)
1 site
C T G R A G ( N ) 14 N N G A C Y T C ( N ) 14

Sticky ends from different Eco57MI sites may not be compatible.
After cleavage, Eco57MI can remain bound to DNA and alter its
electrophoretic mobility.
For full activity, add fresh S-adenosylmethionine (SAM).
PflMI  (974)
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.
Bpu10I  (728)
1 site
C C T N A G C G G A N T C G

Efficient cleavage requires at least two copies of the Bpu10I
recognition sequence.
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.
BsmBI  (727)
1 site
C G T C T C N G C A G A G N ( N ) 4

Sticky ends from different BsmBI sites may not be compatible.
AsiSI  (711)
1 site
G C G A T C G C C G C T A G C G
PvuI  (711)
1 site
C G A T C G G C T A G C
BsrFI  (665)
1 site
R C C G G Y Y G G C C R

Efficient cleavage requires at least two copies of the BsrFI
recognition sequence.
After cleavage, BsrFI can remain bound to DNA and alter its
electrophoretic mobility.
EcoNI  (623)
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.
NspI  (1890)
1 site
R C A T G Y Y G T A C R
BspQI  (2003)
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  (2003)
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.
BsaHI  (2219)
1 site
G R C G Y C C Y G C R G

BsaHI is typically used at 37°C, but is even more active at 60°C.
AclI  (2256)
1 site
A A C G T T T T G C A A
BbsI  (2329)
1 site
G A A G A C N N C T T C T G N N ( N ) 4

Sticky ends from different BbsI sites may not be compatible.
BbsI gradually loses activity when stored at -20°C.
HincII  (2393)
1 site
G T Y R A C C A R Y T G
HpaI  (2393)
1 site
G T T A A C C A A T T G
AhdI  (2441)
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.
AflII  (2446)
1 site
C T T A A G G A A T T C

The sticky ends produced by AflII are hard to ligate.
AvaI  (2452)
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  (2452)
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.
BmeT110I  (2453)
1 site
C Y C G R G G R G C Y C
PspOMI  (2455)
1 site
G G G C C C C C C G G G
EcoO109I  (2456)
1 site
R G G N C C Y Y C C N G G R

Sticky ends from different EcoO109I sites may not be compatible.
ApaI  (2459)
1 site
G G G C C C C C C G G G

ApaI can be used between 25°C and 37°C.
MslI  (2510)
1 site
C A Y N N N N R T G G T R N N N N Y A C
End  (2571)
0 sites
Start  (0)
0 sites
EcoRV  (129)
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.
NruI  (368)
1 site
T C G C G A A G C G C T
KanR
286 .. 1095  =  810 bp
269 amino acids  =  30.8 kDa
Product: aminoglycoside phosphotransferase
confers resistance to kanamycin in bacteria or G418
(Geneticin®) in eukaryotes
KanR
286 .. 1095  =  810 bp
269 amino acids  =  30.8 kDa
Product: aminoglycoside phosphotransferase
confers resistance to kanamycin in bacteria or G418
(Geneticin®) in eukaryotes
ori
1242 .. 1830  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin
of replication
ori
1242 .. 1830  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin
of replication
attL2
17 .. 116  =  100 bp
recombination site for the Gateway® LR reaction
attL2
17 .. 116  =  100 bp
recombination site for the Gateway® LR reaction
attL1
2461 .. 2560  =  100 bp
recombination site for the Gateway® LR reaction
attL1
2461 .. 2560  =  100 bp
recombination site for the Gateway® LR reaction
rrnB T1 terminator
2279 .. 2365  =  87 bp
transcription terminator T1 from the E. coli rrnB
gene
rrnB T1 terminator
2279 .. 2365  =  87 bp
transcription terminator T1 from the E. coli rrnB
gene
rrnB T2 terminator
2160 .. 2187  =  28 bp
transcription terminator T2 from the E. coli rrnB
gene
rrnB T2 terminator
2160 .. 2187  =  28 bp
transcription terminator T2 from the E. coli rrnB
gene
TEV site
2563 .. 2583  =  21 bp
7 amino acids  =  900.0 Da
Product: tobacco etch virus (TEV) protease
recognition and cleavage site
TEV site
2563 .. 2583  =  21 bp
7 amino acids  =  900.0 Da
Product: tobacco etch virus (TEV) protease
recognition and cleavage site
T7 promoter
134 .. 152  =  19 bp
promoter for bacteriophage T7 RNA polymerase
T7 promoter
134 .. 152  =  19 bp
promoter for bacteriophage T7 RNA polymerase
M13 rev
157 .. 173  =  17 bp
common sequencing primer, one of multiple similar
variants
M13 rev
157 .. 173  =  17 bp
common sequencing primer, one of multiple similar
variants
M13 fwd
2429 .. 2445  =  17 bp
common sequencing primer, one of multiple similar
variants
M13 fwd
2429 .. 2445  =  17 bp
common sequencing primer, one of multiple similar
variants
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