pT7CFE1-CGST-HA-His

Vector with C-terminal cleavable GST and HA and 6xHis tags, for use in a human in vitro protein expression system.

Sequence Author: Thermo Fisher (Pierce)

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PvuII (4282) PsiI (3849) PfoI (3560) AatII (3449) ZraI (3447) NmeAIII (2675) BpmI (2597) BsaI (2588) AhdI (2527) AvrII (110) HindIII (183) PmlI (275) BfuAI - BspMI - PaqCI (298) Acc65I (400) KpnI (404) PflMI (412) BtgI (492) MscI (536) XcmI (544) NdeI (546) BstXI (547) BamHI (551) EcoRI (557) EcoRV (565) PacI (573) PstI (582) Eco53kI (586) SacI (588) SalI - SgrDI (590) AccI (591) HincII (592) EagI - NotI (597) AvaI - BsoBI - PaeR7I - PspXI - XhoI (605) EcoNI (642) BspQI - SapI (711) BsgI (918) BstBI (1029) SwaI (1059) BclI * (1066) thrombin site 6xHis BglII (1379) PmeI (1423) SpeI (1428) BlpI (1437) BseYI (1938) PspFI (1942) AlwNI (2050) pT7CFE1-CGST-HA-His 4375 bp
PvuII  (4282)
1 site
C A G C T G G T C G A C
PsiI  (3849)
1 site
T T A T A A A A T A T T
PfoI  (3560)
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.
AatII  (3449)
1 site
G A C G T C C T G C A G
ZraI  (3447)
1 site
G A C G T C C T G C A G
NmeAIII  (2675)
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).
BpmI  (2597)
1 site
C T G G A G ( N ) 14 N N G A C C T C ( N ) 14

Efficient cleavage requires at least two copies of the BpmI recognition sequence.
Sticky ends from different BpmI sites may not be compatible.
After cleavage, BpmI can remain bound to DNA and alter its electrophoretic mobility.
BpmI quickly loses activity at 37°C.
BsaI  (2588)
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  (2527)
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.
AvrII  (110)
1 site
C C T A G G G G A T C C
HindIII  (183)
1 site
A A G C T T T T C G A A
PmlI  (275)
1 site
C A C G T G G T G C A C
BfuAI  (298)
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  (298)
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  (298)
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.
Acc65I  (400)
1 site
G G T A C C C C A T G G
KpnI  (404)
1 site
G G T A C C C C A T G G
PflMI  (412)
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.
BtgI  (492)
1 site
C C R Y G G G G Y R C C

Sticky ends from different BtgI sites may not be compatible.
MscI  (536)
1 site
T G G C C A A C C G G T
XcmI  (544)
1 site
C C A N N N N N N N N N T G G G G T N N N N N N N N N A C C

The 1-base overhangs produced by XcmI may be hard to ligate.
Sticky ends from different XcmI sites may not be compatible.
NdeI  (546)
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.
BstXI  (547)
1 site
C C A N N N N N N T G G G G T N N N N N N A C C

Sticky ends from different BstXI sites may not be compatible.
BamHI  (551)
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.
EcoRI  (557)
1 site
G A A T T C C T T A A G
EcoRV  (565)
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.
PacI  (573)
1 site
T T A A T T A A A A T T A A T T
PstI  (582)
1 site
C T G C A G G A C G T C
Eco53kI  (586)
1 site
G A G C T C C T C G A G
SacI  (588)
1 site
G A G C T C C T C G A G
SalI  (590)
1 site
G T C G A C C A G C T G
SgrDI  (590)
1 site
C G T C G A C G G C A G C T G C
AccI  (591)
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.
HincII  (592)
1 site
G T Y R A C C A R Y T G
EagI  (597)
1 site
C G G C C G G C C G G C
NotI  (597)
1 site
G C G G C C G C C G C C G G C G
AvaI  (605)
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  (605)
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  (605)
1 site
C T C G A G G A G C T C

PaeR7I does not recognize the sequence CTCTCGAG.
PspXI  (605)
1 site
V C T C G A G B B G A G C T C V
XhoI  (605)
1 site
C T C G A G G A G C T C
EcoNI  (642)
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.
BspQI  (711)
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  (711)
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.
BsgI  (918)
1 site
G T G C A G ( N ) 14 N N C A C G T C ( N ) 14

Efficient cleavage requires at least two copies of the BsgI recognition sequence.
Sticky ends from different BsgI sites may not be compatible.
For full activity, add fresh S-adenosylmethionine (SAM).
BstBI  (1029)
1 site
T T C G A A A A G C T T
SwaI  (1059)
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.
BclI  (1066)
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.
BglII  (1379)
1 site
A G A T C T T C T A G A
PmeI  (1423)
1 site
G T T T A A A C C A A A T T T G
SpeI  (1428)
1 site
A C T A G T T G A T C A
BlpI  (1437)
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.
BseYI  (1938)
1 site
C C C A G C G G G T C G

After cleavage, BseYI can remain bound to DNA and alter its electrophoretic mobility.
PspFI  (1942)
1 site
C C C A G C G G G T C G
AlwNI  (2050)
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.
AmpR
2454 .. 3314  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 2:  
   2454 .. 3245  =  792 bp
   263 amino acids  =  28.9 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
2454 .. 3314  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 1:  signal sequence  
   3246 .. 3314  =  69 bp
   23 amino acids  =  2.6 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
2454 .. 3314  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
ATG
533 .. 535  =  3 bp
1 amino acid  =  149.2 Da
Product: start codon
ATG
533 .. 535  =  3 bp
1 amino acid  =  149.2 Da
Product: start codon
HRV 3C site
611 .. 634  =  24 bp
8 amino acids  =  902.1 Da
Product: recognition and cleavage site for human rhinovirus 3C and PreScission proteases
HRV 3C site
611 .. 634  =  24 bp
8 amino acids  =  902.1 Da
Product: recognition and cleavage site for human rhinovirus 3C and PreScission proteases
GST
635 .. 1285  =  651 bp
217 amino acids  =  25.4 kDa
Product: glutathione S-transferase from Schistosoma japonicum
GST
635 .. 1285  =  651 bp
217 amino acids  =  25.4 kDa
Product: glutathione S-transferase from Schistosoma japonicum
thrombin site
1292 .. 1309  =  18 bp
6 amino acids  =  627.7 Da
Product: thrombin recognition and cleavage site
thrombin site
1292 .. 1309  =  18 bp
6 amino acids  =  627.7 Da
Product: thrombin recognition and cleavage site
HA
1316 .. 1342  =  27 bp
9 amino acids  =  1.1 kDa
Product: HA (human influenza hemagglutinin) epitope tag
HA
1316 .. 1342  =  27 bp
9 amino acids  =  1.1 kDa
Product: HA (human influenza hemagglutinin) epitope tag
6xHis
1355 .. 1372  =  18 bp
6 amino acids  =  840.9 Da
Product: 6xHis affinity tag
6xHis
1355 .. 1372  =  18 bp
6 amino acids  =  840.9 Da
Product: 6xHis affinity tag
ori
1695 .. 2283  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
ori
1695 .. 2283  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
IRES
70 .. 531  =  462 bp
internal ribosome entry site (IRES) of the encephalomyocarditis virus (EMCV)
IRES
70 .. 531  =  462 bp
internal ribosome entry site (IRES) of the encephalomyocarditis virus (EMCV)
f1 ori
3753 .. 4208  =  456 bp
f1 bacteriophage origin of replication; arrow indicates direction of (+) strand synthesis
f1 ori
3753 .. 4208  =  456 bp
f1 bacteriophage origin of replication; arrow indicates direction of (+) strand synthesis
AmpR promoter
3315 .. 3419  =  105 bp
AmpR promoter
3315 .. 3419  =  105 bp
T7 terminator
1448 .. 1495  =  48 bp
transcription terminator for bacteriophage T7 RNA polymerase
T7 terminator
1448 .. 1495  =  48 bp
transcription terminator for bacteriophage T7 RNA polymerase
poly(A)
1390 .. 1419  =  30 bp
poly(A)
1390 .. 1419  =  30 bp
T7 promoter
1 .. 19  =  19 bp
promoter for bacteriophage T7 RNA polymerase
T7 promoter
1 .. 19  =  19 bp
promoter for bacteriophage T7 RNA polymerase
ORF:  2584 .. 2850  =  267 bp
ORF:  88 amino acids  =  9.2 kDa
ORF:  533 .. 1375  =  843 bp
ORF:  280 amino acids  =  32.3 kDa
ORF:  2454 .. 3314  =  861 bp
ORF:  286 amino acids  =  31.6 kDa
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Download pT7CFE1-CGST-HA-His.dna file

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