pDsRed2-N1

Vector for fusing DsRed2 to the C-terminus of a partner protein.

Sequence Author: Clontech (TaKaRa)

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AflIII - PciI (4631) ApaLI (4317) PfoI (3488) RsrII (3229) BsrDI (2946) PflFI - Tth111I (2831) PluTI (2716) SfoI (2714) NarI (2713) KasI (2712) BspDI * - ClaI * (2553) SfiI (2488) AseI (7) NdeI (234) SnaBI (340) NheI (591) BmtI (595) AfeI (596) BglII (609) PaeR7I - XhoI (613) Eco53kI (618) SacI (620) HindIII (622) EcoRI (629) SalI (639) AccI (640) Acc65I (645) KpnI (649) SacII (652) PspOMI (653) TspMI - XmaI (656) ApaI (657) SmaI (658) BamHI (660) AgeI (666) FspAI (727) BstEII (819) AhdI (858) SbfI (1019) BbsI (1099) BstXI (1221) BsgI (1258) AleI (1306) NotI (1357) XbaI * (1367) MfeI (1463) HpaI (1476) BtsI - BtsαI (1552) AflII (1595) DraIII (1829) pDsRed2-N1 4689 bp
AflIII  (4631)
1 site
A C R Y G T T G Y R C A

Sticky ends from different AflIII sites may not be compatible.
PciI  (4631)
1 site
A C A T G T T G T A C A

PciI is inhibited by nonionic detergents.
ApaLI  (4317)
1 site
G T G C A C C A C G T G
PfoI  (3488)
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.
RsrII  (3229)
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  (2946)
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  (2831)
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  (2831)
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.
PluTI  (2716)
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  (2714)
1 site
G G C G C C C C G C G G
NarI  (2713)
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  (2712)
1 site
G G C G C C C C G C G G
BspDI  (2553)
1 site
A T C G A T T A G C T A
* Blocked by Dam methylation.
ClaI  (2553)
1 site
A T C G A T T A G C T A
* Blocked by Dam methylation.
SfiI  (2488)
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
BglII  (609)
1 site
A G A T C T T C T A G A
PaeR7I  (613)
1 site
C T C G A G G A G C T C

PaeR7I does not recognize the sequence CTCTCGAG.
XhoI  (613)
1 site
C T C G A G G A G C T C
Eco53kI  (618)
1 site
G A G C T C C T C G A G
SacI  (620)
1 site
G A G C T C C T C G A G
HindIII  (622)
1 site
A A G C T T T T C G A A
EcoRI  (629)
1 site
G A A T T C C T T A A G
SalI  (639)
1 site
G T C G A C C A G C T G
AccI  (640)
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.
Acc65I  (645)
1 site
G G T A C C C C A T G G
KpnI  (649)
1 site
G G T A C C C C A T G G
SacII  (652)
1 site
C C G C G G G G C G C C

Efficient cleavage requires at least two copies of the SacII recognition sequence.
PspOMI  (653)
1 site
G G G C C C C C C G G G
TspMI  (656)
1 site
C C C G G G G G G C C C
XmaI  (656)
1 site
C C C G G G G G G C C C

Cleavage may be enhanced when more than one copy of the XmaI recognition sequence is present.
ApaI  (657)
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  (658)
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  (660)
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.
AgeI  (666)
1 site
A C C G G T T G G C C A
FspAI  (727)
1 site
R T G C G C A Y Y A C G C G T R
BstEII  (819)
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.
AhdI  (858)
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.
SbfI  (1019)
1 site
C C T G C A G G G G A C G T C C
BbsI  (1099)
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.
BstXI  (1221)
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.
BsgI  (1258)
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).
AleI  (1306)
1 site
C A C N N N N G T G G T G N N N N C A C
NotI  (1357)
1 site
G C G G C C G C C G C C G G C G
XbaI  (1367)
1 site
T C T A G A A G A T C T
* Blocked by Dam methylation.
MfeI  (1463)
1 site
C A A T T G G T T A A C
HpaI  (1476)
1 site
G T T A A C C A A T T G
BtsI  (1552)
1 site
G C A G T G N N C G T C A C
BtsαI  (1552)
1 site
G C A G T G N N C G T C A C

Sticky ends from different BtsαI sites may not be compatible.
AflII  (1595)
1 site
C T T A A G G A A T T C
DraIII  (1829)
1 site
C A C N N N G T G G T G N N N C A C

Sticky ends from different DraIII sites may not be compatible.
NeoR/KanR
2585 .. 3379  =  795 bp
264 amino acids  =  29.0 kDa
Product: aminoglycoside phosphotransferase from Tn5
confers resistance to neomycin, kanamycin, and G418 (Geneticin)
NeoR/KanR
2585 .. 3379  =  795 bp
264 amino acids  =  29.0 kDa
Product: aminoglycoside phosphotransferase from Tn5
confers resistance to neomycin, kanamycin, and G418 (Geneticin)
DsRed2
679 .. 1356  =  678 bp
225 amino acids  =  25.8 kDa
Product: improved tetrameric variant of DsRed fluorescent protein
mammalian codon-optimized
DsRed2
679 .. 1356  =  678 bp
225 amino acids  =  25.8 kDa
Product: improved tetrameric variant of DsRed fluorescent protein
mammalian codon-optimized
ori
3987 .. 4575  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
ori
3987 .. 4575  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
f1 ori
1605 .. 2060  =  456 bp
f1 bacteriophage origin of replication; arrow indicates direction of (+) strand synthesis
f1 ori
1605 .. 2060  =  456 bp
f1 bacteriophage origin of replication; arrow indicates direction of (+) strand synthesis
SV40 promoter
2193 .. 2550  =  358 bp
SV40 enhancer and early promoter
SV40 promoter
2193 .. 2550  =  358 bp
SV40 enhancer and early promoter
CMV enhancer
61 .. 364  =  304 bp
human cytomegalovirus immediate early enhancer
CMV enhancer
61 .. 364  =  304 bp
human cytomegalovirus immediate early enhancer
CMV promoter
365 .. 568  =  204 bp
human cytomegalovirus (CMV) immediate early promoter
CMV promoter
365 .. 568  =  204 bp
human cytomegalovirus (CMV) immediate early promoter
SV40 poly(A) signal
1477 .. 1598  =  122 bp
SV40 polyadenylation signal
SV40 poly(A) signal
1477 .. 1598  =  122 bp
SV40 polyadenylation signal
AmpR promoter
2087 .. 2191  =  105 bp
AmpR promoter
2087 .. 2191  =  105 bp
MCS
591 .. 671  =  81 bp
multiple cloning site of fluorescent protein plasmids
MCS
591 .. 671  =  81 bp
multiple cloning site of fluorescent protein plasmids
HSV TK poly(A) signal
3611 .. 3658  =  48 bp
herpesvirus thymidine kinase polyadenylation signal
HSV TK poly(A) signal
3611 .. 3658  =  48 bp
herpesvirus thymidine kinase polyadenylation signal
SV40 ori
2401 .. 2536  =  136 bp
SV40 origin of replication
SV40 ori
2401 .. 2536  =  136 bp
SV40 origin of replication
ORF:  679 .. 1356  =  678 bp
ORF:  225 amino acids  =  25.8 kDa
ORF:  3400 .. 3849  =  450 bp
ORF:  149 amino acids  =  16.3 kDa
ORF:  2585 .. 3379  =  795 bp
ORF:  264 amino acids  =  29.0 kDa
ORF:  2757 .. 3143  =  387 bp
ORF:  128 amino acids  =  14.6 kDa
ORF:  607 .. 1386  =  780 bp
ORF:  259 amino acids  =  26.3 kDa
ORF:  447 .. 731  =  285 bp
ORF:  94 amino acids  =  10.2 kDa
ORF:  2894 .. 3430  =  537 bp
ORF:  178 amino acids  =  19.8 kDa
ORF:  3605 .. 3838  =  234 bp
ORF:  77 amino acids  =  8.6 kDa
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