pCMV-3Tag-6

Mammalian expression vector with a hygromycin resistance marker  for tagging proteins with an N-terminal 3xFLAG epitope.

Sequence Author: Agilent Technologies

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SnaBI (346) NsiI (5) PciI (5189) BseRI (4464) AfeI (4455) PluTI (4395) SfoI (4393) NarI (4392) KasI (4391) KflI - PpuMI (4186) XcmI (4167) HSV TK poly(A) signal AsiSI (3231) BfuAI - BspMI (3180) BsmBI - Esp3I (2935) PshAI (2894) HSV TK promoter BstBI (2718) AhdI (2515) CMV promoter NheI (597) BmtI (601) T3 promoter Eco53kI (653) SacI (655) AleI (661) BstXI (663) NotI (668) ATG 3xFLAG SrfI (757) BamHI (763) EcoRV (789) HindIII (793) BspDI - ClaI (800) SalI (808) AccI (809) AbsI - PaeR7I - PspXI - XhoI (814) PspOMI (823) ApaI (827) stop codons CsiI - SexAI * (850) T7 promoter BclI * (914) bGH poly(A) signal BbsI (1116) SphI (1127) PsiI (1237) NgoMIV (1466) NaeI (1468) AmpR promoter EarI (1716) XmnI (1915) DraI (1937) FspI (2292) pCMV-3Tag-6 5241 bp
SnaBI  (346)
1 site
T A C G T A A T G C A T
NsiI  (5)
1 site
A T G C A T T A C G T A
PciI  (5189)
1 site
A C A T G T T G T A C A

PciI is inhibited by nonionic detergents.
BseRI  (4464)
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.
AfeI  (4455)
1 site
A G C G C T T C G C G A
PluTI  (4395)
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.
SfoI  (4393)
1 site
G G C G C C C C G C G G
NarI  (4392)
1 site
G G C G C C C C G C G G

Efficient cleavage requires at least two copies of the NarI recognition sequence.
KasI  (4391)
1 site
G G C G C C C C G C G G
KflI  (4186)
1 site
G G G W C C C C C C W G G G

Sticky ends from different KflI sites may not be compatible.
PpuMI  (4186)
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.
XcmI  (4167)
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.
AsiSI  (3231)
1 site
G C G A T C G C C G C T A G C G
BfuAI  (3180)
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  (3180)
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.
BsmBI  (2935)
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.
BsmBI-v2 is an improved version of BsmBI.
Esp3I  (2935)
1 site
C G T C T C N G C A G A G N ( N ) 4

Sticky ends from different Esp3I sites may not be compatible.
PshAI  (2894)
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.
BstBI  (2718)
1 site
T T C G A A A A G C T T
AhdI  (2515)
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.
NheI  (597)
1 site
G C T A G C C G A T C G
BmtI  (601)
1 site
G C T A G C C G A T C G
Eco53kI  (653)
1 site
G A G C T C C T C G A G
SacI  (655)
1 site
G A G C T C C T C G A G
AleI  (661)
1 site
C A C N N N N G T G G T G N N N N C A C
BstXI  (663)
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.
NotI  (668)
1 site
G C G G C C G C C G C C G G C G
SrfI  (757)
1 site
G C C C G G G C C G G G C C C G
BamHI  (763)
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.
EcoRV  (789)
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.
HindIII  (793)
1 site
A A G C T T T T C G A A
BspDI  (800)
1 site
A T C G A T T A G C T A
ClaI  (800)
1 site
A T C G A T T A G C T A
SalI  (808)
1 site
G T C G A C C A G C T G
AccI  (809)
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.
AbsI  (814)
1 site
C C T C G A G G G G A G C T C C
PaeR7I  (814)
1 site
C T C G A G G A G C T C

PaeR7I does not recognize the sequence CTCTCGAG.
PspXI  (814)
1 site
V C T C G A G B B G A G C T C V
XhoI  (814)
1 site
C T C G A G G A G C T C
PspOMI  (823)
1 site
G G G C C C C C C G G G
ApaI  (827)
1 site
G G G C C C C C C G G G

ApaI can be used between 25°C and 37°C.
CsiI  (850)
1 site
A C C W G G T T G G W C C A

Sticky ends from different CsiI sites may not be compatible.
SexAI  (850)
1 site
A C C W G G T T G G W C C A
* Blocked by Dcm methylation.
Sticky ends from different SexAI sites may not be compatible.
BclI  (914)
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.
BbsI  (1116)
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.
SphI  (1127)
1 site
G C A T G C C G T A C G
PsiI  (1237)
1 site
T T A T A A A A T A T T
NgoMIV  (1466)
1 site
G C C G G C C G G C C G

Efficient cleavage requires at least two copies of the NgoMIV recognition sequence.
NaeI  (1468)
1 site
G C C G G C C G G C C G

Efficient cleavage requires at least two copies of the NaeI recognition sequence.
EarI  (1716)
1 site
C T C T T C N G A G A A G N N N N

Cleavage may be enhanced when more than one copy of the EarI recognition sequence is present.
Sticky ends from different EarI sites may not be compatible.
XmnI  (1915)
1 site
G A A N N N N T T C C T T N N N N A A G
DraI  (1937)
1 site
T T T A A A A A A T T T
FspI  (2292)
1 site
T G C G C A A C G C G T
HygR
2867 .. 3904  =  1038 bp
345 amino acids  =  38.5 kDa
Product: hygromycin B phosphotransferase
confers resistance to hygromycin
HygR
2867 .. 3904  =  1038 bp
345 amino acids  =  38.5 kDa
Product: hygromycin B phosphotransferase
confers resistance to hygromycin
AmpR
1728 .. 2585  =  858 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 1:  signal sequence  
   1728 .. 1796  =  69 bp
   23 amino acids  =  2.6 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
1728 .. 2585  =  858 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 2:  
   1797 .. 2585  =  789 bp
   263 amino acids  =  28.9 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
1728 .. 2585  =  858 bp
286 amino acids  =  31.6 kDa
2 segments
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
ori
4545 .. 5133  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
ori
4545 .. 5133  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
f1 ori
1141 .. 1596  =  456 bp
f1 bacteriophage origin of replication; arrow indicates direction of (+) strand synthesis
f1 ori
1141 .. 1596  =  456 bp
f1 bacteriophage origin of replication; arrow indicates direction of (+) strand synthesis
CMV enhancer
66 .. 370  =  305 bp
human cytomegalovirus immediate early enhancer
CMV enhancer
66 .. 370  =  305 bp
human cytomegalovirus immediate early enhancer
bGH poly(A) signal
927 .. 1134  =  208 bp
bovine growth hormone polyadenylation signal
bGH poly(A) signal
927 .. 1134  =  208 bp
bovine growth hormone polyadenylation signal
CMV promoter
371 .. 574  =  204 bp
human cytomegalovirus (CMV) immediate early promoter
CMV promoter
371 .. 574  =  204 bp
human cytomegalovirus (CMV) immediate early promoter
HSV TK promoter
2679 .. 2824  =  146 bp
herpes simplex virus thymidine kinase promoter
HSV TK promoter
2679 .. 2824  =  146 bp
herpes simplex virus thymidine kinase promoter
AmpR promoter
1623 .. 1727  =  105 bp
AmpR promoter
1623 .. 1727  =  105 bp
MCS
754 .. 828  =  75 bp
multiple cloning site
MCS
754 .. 828  =  75 bp
multiple cloning site
ATG
679 .. 681  =  3 bp
1 amino acid  =  149.2 Da
Product: start codon
ATG
679 .. 681  =  3 bp
1 amino acid  =  149.2 Da
Product: start codon
3xFLAG
682 .. 753  =  72 bp
24 amino acids  =  3.0 kDa
Product: three tandem FLAG epitope tags
3xFLAG
682 .. 753  =  72 bp
24 amino acids  =  3.0 kDa
Product: three tandem FLAG epitope tags
HSV TK poly(A) signal
3946 .. 3994  =  49 bp
herpesvirus thymidine kinase polyadenylation signal
HSV TK poly(A) signal
3946 .. 3994  =  49 bp
herpesvirus thymidine kinase polyadenylation signal
T3 promoter
620 .. 638  =  19 bp
promoter for bacteriophage T3 RNA polymerase
T3 promoter
620 .. 638  =  19 bp
promoter for bacteriophage T3 RNA polymerase
T7 promoter
874 .. 892  =  19 bp
promoter for bacteriophage T7 RNA polymerase
T7 promoter
874 .. 892  =  19 bp
promoter for bacteriophage T7 RNA polymerase
stop codons
836 .. 846  =  11 bp
stop codons in all three reading frames
stop codons
836 .. 846  =  11 bp
stop codons in all three reading frames
ORF:  2867 .. 3904  =  1038 bp
ORF:  345 amino acids  =  38.5 kDa
ORF:  1728 .. 2597  =  870 bp
ORF:  289 amino acids  =  31.9 kDa
ORF:  4194 .. 4493  =  300 bp
ORF:  99 amino acids  =  11.4 kDa
ORF:  453 .. 680  =  228 bp
ORF:  75 amino acids  =  8.1 kDa
ORF:  2192 .. 2458  =  267 bp
ORF:  88 amino acids  =  9.2 kDa
ORF:  2594 .. 4195  =  1602 bp
ORF:  533 amino acids  =  58.6 kDa
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