DsRed-Express

Rapidly maturing tetrameric DsRed.T1 variant of DsRed fluorescent protein.

Sequence Author: Clontech (TaKaRa)

|Download SnapGene Viewer
No matches
600 400 200 End (678) NmeAIII (674) BssHII (645) AleI (628) BsgI (580) PvuII - MspA1I (564) MscI (547) BstXI (543) PflMI * (519) CsiI - SexAI * (518) EcoO109I (489) MflI * - BstYI (479) HaeII (447) StuI (433) PspFI (429) BseYI (425) BbsI (421) MmeI (416) PstI SbfI (341) BseRI (321) AvaI - BsoBI (262) BmrI (183) AhdI (180) BaeGI - Bme1580I (121) BanI (118) BssSI - BssSαI (73) BanII (61) FspI - FspAI (49) AatII (20) ZraI (18) BsaHI (17) Start (0) DsRed-Express DsRed-Express 678 bp
End  (678)
0 sites
NmeAIII  (674)
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).
BssHII  (645)
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.
AleI  (628)
1 site
C A C N N N N G T G G T G N N N N C A C
BsgI  (580)
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).
PvuII  (564)
1 site
C A G C T G G T C G A C
MspA1I  (564)
1 site
C M G C K G G K C G M C
MscI  (547)
1 site
T G G C C A A C C G G T
BstXI  (543)
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.
PflMI  (519)
1 site
C C A N N N N N T G G G G T N N N N N A C C
* Blocked by Dcm methylation.
Sticky ends from different PflMI sites may not be compatible.
CsiI  (518)
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  (518)
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.
EcoO109I  (489)
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.
MflI  (479)
1 site
R G A T C Y Y C T A G R
* Blocked by Dam methylation.
BstYI  (479)
1 site
R G A T C Y Y C T A G R
HaeII  (447)
1 site
R G C G C Y Y C G C G R
StuI  (433)
1 site
A G G C C T T C C G G A
PspFI  (429)
1 site
C C C A G C G G G T C G
BseYI  (425)
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.
BbsI  (421)
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.
MmeI  (416)
1 site
T C C R A C ( N ) 18 N N A G G Y T G ( N ) 18

Efficient cleavage requires at least two copies of the MmeI recognition sequence.
Sticky ends from different MmeI sites may not be compatible.
For full activity, add fresh S-adenosylmethionine (SAM).
PstI  (341)
1 site
C T G C A G G A C G T C
SbfI  (341)
1 site
C C T G C A G G G G A C G T C C
BseRI  (321)
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.
AvaI  (262)
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  (262)
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.
BmrI  (183)
1 site
A C T G G G ( N ) 4 N T G A C C C ( N ) 4

The 1-base overhangs produced by BmrI may be hard to ligate.
Sticky ends from different BmrI sites may not be compatible.
Unlike most restriction enzymes, BmrI can cleave DNA in the absence of magnesium.
AhdI  (180)
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.
BaeGI  (121)
1 site
G K G C M C C M C G K G

Sticky ends from different BaeGI sites may not be compatible.
Bme1580I  (121)
1 site
G K G C M C C M C G K G

Sticky ends from different Bme1580I sites may not be compatible.
BanI  (118)
1 site
G G Y R C C C C R Y G G

Sticky ends from different BanI sites may not be compatible.
BssSI  (73)
1 site
C A C G A G G T G C T C
BssSαI  (73)
1 site
C A C G A G G T G C T C
BanII  (61)
1 site
G R G C Y C C Y C G R G

Sticky ends from different BanII sites may not be compatible.
FspI  (49)
1 site
T G C G C A A C G C G T
FspAI  (49)
1 site
R T G C G C A Y Y A C G C G T R
AatII  (20)
1 site
G A C G T C C T G C A G
ZraI  (18)
1 site
G A C G T C C T G C A G
BsaHI  (17)
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.
Start  (0)
0 sites
DsRed-Express
1 .. 678  =  678 bp
225 amino acids  =  25.7 kDa
Product: rapidly maturing tetrameric variant of DsRed fluorescent protein (Bevis and Glick, 2002)
mammalian codon-optimized
DsRed-Express
1 .. 678  =  678 bp
225 amino acids  =  25.7 kDa
Product: rapidly maturing tetrameric variant of DsRed fluorescent protein (Bevis and Glick, 2002)
mammalian codon-optimized
ORF:  1 .. 678  =  678 bp
ORF:  225 amino acids  =  25.7 kDa
ORF:  3 .. 677  =  675 bp
ORF:  225 amino acids  =  24.8 kDa  (no start codon)
ORF:  1 .. 678  =  678 bp
ORF:  226 amino acids  =  22.4 kDa  (no start codon)
Click here to try SnapGene

Download DsRed-Express.dna file

SnapGene

SnapGene is the easiest way to plan, visualize and document your everyday molecular biology procedures

  • Fast accurate construct design for all major molecular cloning techniques
  • Validate sequenced constructs using powerful alignment tools
  • Customize plasmid maps with flexible annotation and visualization controls
  • Automatically generate a rich graphical history of every edit and procedure

SnapGene Viewer

SnapGene Viewer is free software that allows molecular biologists to create, browse, and share richly annotated sequence files.

  • Gain unparalleled visibility of your plasmids, DNA and protein sequences
  • Annotate features on your plasmids using the curated feature database
  • Store, search, and share your sequences, files and maps

Individual Sequences & Maps

The maps, notes, and annotations in the zip file on this page are copyrighted material. This material may be used without restriction by academic, nonprofit, and governmental entities, except that the source must be cited as ’’www.snapgene.com/resources’’. Commercial entities must contact GSL Biotech LLC for permission and terms of use.

Discover the most user-friendly molecular biology experience.