CyOFP1

Orange-red fluorescent protein that is excitable by cyan light and suitable as an acceptor for blue-emitting luciferase.
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HomePlasmidsFluorescent Protein Genes & PlasmidsCyOFP1
600 400 200 End TatI - BsrGI EciI - MmeI PshAI PflMI - BsaAI BsaHI HincII BfuAI - PaqCI - BspMI BmgBI AcuI BsgI BssSI BssSαI BglI MspA1I BmrI SacI Eco53kI PfoI * BpmI BbsI BstBI Bsu36I BsmI BaeGI - Bme1580I ApaLI BseRI BclI * Start CyOFP1 CyOFP1 702 bp
End  (702)
0 sites
TatI  (695)
1 site		 W G T A C W W C A T G W
BsrGI  (695)
1 site		 T G T A C A A C A T G T
BsrGI is typically used at 37°C, but is even more active at 60°C.
EciI  (692)
1 site		 G G C G G A ( N ) 9 N N C C G C C T ( N ) 9
Sticky ends from different EciI sites may not be compatible.
MmeI  (692)
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).
PshAI  (631)
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.
PflMI  (585)
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.
BsaAI  (585)
1 site		 Y A C G T R R T G C A Y
BsaHI  (575)
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.
HincII  (528)
1 site		 G T Y R A C C A R Y T G
BfuAI  (527)
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.
PaqCI  (527)
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.
BspMI  (527)
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.
BmgBI  (525)
1 site		 C A C G T C G T G C A G
This recognition sequence is asymmetric, so ligating blunt ends generated by BmgBI will not always regenerate a BmgBI site.
AcuI  (517)
1 site		 C T G A A G ( N ) 14 N N G A C T T C ( N ) 14
Cleavage may be enhanced when more than one copy of the AcuI recognition sequence is present.
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).
BsgI  (505)
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).
BssSI  (502)
1 site		 C A C G A G G T G C T C
BssSαI  (502)
1 site		 C A C G A G G T G C T C
BglI  (476)
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.
MspA1I  (460)
1 site		 C M G C K G G K C G M C
BmrI  (433)
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.
SacI  (356)
1 site		 G A G C T C C T C G A G
Eco53kI  (354)
1 site		 G A G C T C C T C G A G
PfoI  (341)
1 site		 T C C N G G A A G G N C C T
* Blocked by Dcm methylation.
Sticky ends from different PfoI sites may not be compatible.
BpmI  (325)
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.
BbsI  (308)
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.
BstBI  (299)
1 site		 T T C G A A A A G C T T
Bsu36I  (266)
1 site		 C C T N A G G G G A N T C C
Sticky ends from different Bsu36I sites may not be compatible.
BsmI  (172)
1 site		 G A A T G C N C T T A C G N
Sticky ends from different BsmI sites may not be compatible.
BaeGI  (91)
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  (91)
1 site		 G K G C M C C M C G K G
Sticky ends from different Bme1580I sites may not be compatible.
ApaLI  (87)
1 site		 G T G C A C C A C G T G
BseRI  (31)
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.
BclI  (23)
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.
Start  (0)
0 sites
CyOFP1
1 .. 702  =  702 bp
234 amino acids  =  26.4 kDa
Product: orange-red fluorescent protein that is excitable by cyan light and suitable as an acceptor for blue-emitting luciferase (Chu et al., 2016)
CyOFP1
1 .. 702  =  702 bp
234 amino acids  =  26.4 kDa
Product: orange-red fluorescent protein that is excitable by cyan light and suitable as an acceptor for blue-emitting luciferase (Chu et al., 2016)
ORF:  1 .. 702  =  702 bp
ORF:  234 amino acids  =  26.4 kDa
ORF:  3 .. 254  =  252 bp
ORF:  83 amino acids  =  9.2 kDa  (no start codon)
ORF:  1 .. 702  =  702 bp
ORF:  234 amino acids  =  24.1 kDa  (no start codon)
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