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pTagYFP-C

Vector for fusing TagYFP to the N-terminus of a partner protein.

To see this sequence with restriction sites, features, and translations, please download
 SnapGene or the free  SnapGene Viewer.

pTagYFP-C.dna
Map and Sequence File:    Download    Open   
Sequence Author:  Evrogen
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PciI (4673) EcoO109I (3853) BsaI (3744) RsrII (3271) BsrDI (2988) PflFI - Tth111I (2873) FspI (2857) MscI (2837) PluTI (2758) SfoI (2756) NarI (2755) KasI (2754) EagI (2661) BspDI * - ClaI * (2595) StuI (2576) SfiI (2530) AseI (7) NdeI (234) SnaBI (340) NheI (591) BmtI (595) AfeI (596) AgeI (600) BmgBI (678) BstEII (795) XmnI (859) Bpu10I (1216) BspEI (1330) BglII (1339) PaeR7I - XhoI (1343) Eco53kI (1348) SacI (1350) HindIII (1352) EcoRI (1359) SalI (1369) Acc65I (1375) KpnI (1379) PspOMI (1383) TspMI - XmaI (1386) ApaI (1387) SmaI (1388) BamHI (1390) XbaI * (1402) BclI * (1412) MfeI (1505) HpaI (1518) Bts α I (1594) MluI (1641) SexAI * (2344) pTagYFP-C 4731 bp
PciI  (4673)
1 site		 A C A T G T T G T A C A
PciI is inhibited by nonionic detergents.
EcoO109I  (3853)
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.
BsaI  (3744)
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.
RsrII  (3271)
1 site		 C G G W C C G G C C W G G C
Efficient cleavage requires at least two copies of the RsrII recognition sequence.
Sticky ends from different RsrII sites may not be compatible.
For full activity, add fresh DTT.
BsrDI  (2988)
1 site		 G C A A T G N N C G T T A C
Sticky ends from different BsrDI sites may not be compatible.
PflFI  (2873)
1 site		 G A C N N N G T C C T G N N N C A G
The 1-base overhangs produced by PflFI may be hard to ligate.
Sticky ends from different PflFI sites may not be compatible.
Tth111I  (2873)
1 site		 G A C N N N G T C C T G N N N C A G
The 1-base overhangs produced by Tth111I may be hard to ligate.
Sticky ends from different Tth111I sites may not be compatible.
FspI  (2857)
1 site		 T G C G C A A C G C G T
MscI  (2837)
1 site		 T G G C C A A C C G G T
PluTI  (2758)
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  (2756)
1 site		 G G C G C C C C G C G G
NarI  (2755)
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  (2754)
1 site		 G G C G C C C C G C G G
EagI  (2661)
1 site		 C G G C C G G C C G G C
BspDI  (2595)
1 site		 A T C G A T T A G C T A
* Blocked by Dam methylation.
ClaI  (2595)
1 site		 A T C G A T T A G C T A
* Blocked by Dam methylation.
StuI  (2576)
1 site		 A G G C C T T C C G G A
SfiI  (2530)
1 site		 G G C C N N N N N G G C C C C G G N N N N N C C G G
Efficient cleavage requires at least two copies of the SfiI recognition sequence.
Sticky ends from different SfiI sites may not be compatible.
AseI  (7)
1 site		 A T T A A T T A A T T A
NdeI  (234)
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.
SnaBI  (340)
1 site		 T A C G T A A T G C A T
NheI  (591)
1 site		 G C T A G C C G A T C G
BmtI  (595)
1 site		 G C T A G C C G A T C G
AfeI  (596)
1 site		 A G C G C T T C G C G A
AgeI  (600)
1 site		 A C C G G T T G G C C A
BmgBI  (678)
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.
BstEII  (795)
1 site		 G G T N A C C C C A N T G G
Sticky ends from different BstEII sites may not be compatible.
BstEII is typically used at 60°C, but is 50% active at 37°C.
XmnI  (859)
1 site		 G A A N N N N T T C C T T N N N N A A G
Bpu10I  (1216)
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.
BspEI  (1330)
1 site		 T C C G G A A G G C C T
BglII  (1339)
1 site		 A G A T C T T C T A G A
PaeR7I  (1343)
1 site		 C T C G A G G A G C T C
PaeR7I does not recognize the sequence CTCTCGAG.
XhoI  (1343)
1 site		 C T C G A G G A G C T C
Eco53kI  (1348)
1 site		 G A G C T C C T C G A G
SacI  (1350)
1 site		 G A G C T C C T C G A G
HindIII  (1352)
1 site		 A A G C T T T T C G A A
EcoRI  (1359)
1 site		 G A A T T C C T T A A G
SalI  (1369)
1 site		 G T C G A C C A G C T G
Acc65I  (1375)
1 site		 G G T A C C C C A T G G
KpnI  (1379)
1 site		 G G T A C C C C A T G G
PspOMI  (1383)
1 site		 G G G C C C C C C G G G
TspMI  (1386)
1 site		 C C C G G G G G G C C C
XmaI  (1386)
1 site		 C C C G G G G G G C C C
Efficient cleavage requires at least two copies of the XmaI recognition sequence.
Full cleavage with XmaI may require a long incubation.
ApaI  (1387)
1 site		 G G G C C C C C C G G G
ApaI can be used between 25°C and 37°C.
SmaI  (1388)
1 site		 C C C G G G G G G C C C
SmaI can be used at 37°C for brief incubations.
BamHI  (1390)
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.
XbaI  (1402)
1 site		 T C T A G A A