pESC-URA

Yeast episomal vector with a URA3 marker, for galactose-regulated expression and tagging of up to two genes.

Sequence Author: Agilent Technologies

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MfeI (6512) BmgBI (6300) XbaI (6199) SnaBI (5862) AhdI (4302) MluI (3164) PfoI (46) NdeI (330) BsgI (363) PstI - SbfI (399) BfuAI - BspMI (402) EcoRV (605) NcoI (622) BsmI (779) StuI (853) Bpu10I (1147) NgoMIV (1676) NaeI (1678) BstXI (2165) PacI (2184) Eco53kI (2190) SacI (2192) BglII (2194) BspDI - ClaI (2224) SpeI (2229) EagI - NotI (2236) EcoRI (2258) AgeI (2553) BstAPI (2805) BamHI (2936) TspMI - XmaI (2963) SmaI - SrfI (2965) SalI (2970) PaeR7I - PspXI - XhoI (3006) HindIII (3013) Acc65I (3019) KpnI (3023) SacII (3026) NheI (3028) BmtI (3032) BsrGI (3157) pESC-URA 6631 bp
MfeI  (6512)
1 site
C A A T T G G T T A A C
BmgBI  (6300)
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.
XbaI  (6199)
1 site
T C T A G A A G A T C T
SnaBI  (5862)
1 site
T A C G T A A T G C A T
AhdI  (4302)
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.
MluI  (3164)
1 site
A C G C G T T G C G C A
PfoI  (46)
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.
NdeI  (330)
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.
BsgI  (363)
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).
PstI  (399)
1 site
C T G C A G G A C G T C
SbfI  (399)
1 site
C C T G C A G G G G A C G T C C
BfuAI  (402)
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  (402)
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.
EcoRV  (605)
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.
NcoI  (622)
1 site
C C A T G G G G T A C C
BsmI  (779)
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.
StuI  (853)
1 site
A G G C C T T C C G G A
Bpu10I  (1147)
1 site
C C T N A G C G G A N T C G

Cleavage may be enhanced when more than one copy of the Bpu10I recognition sequence is present.
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.
NgoMIV  (1676)
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  (1678)
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.
BstXI  (2165)
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.
PacI  (2184)
1 site
T T A A T T A A A A T T A A T T
Eco53kI  (2190)
1 site
G A G C T C C T C G A G
SacI  (2192)
1 site
G A G C T C C T C G A G
BglII  (2194)
1 site
A G A T C T T C T A G A
BspDI  (2224)
1 site
A T C G A T T A G C T A
ClaI  (2224)
1 site
A T C G A T T A G C T A
SpeI  (2229)
1 site
A C T A G T T G A T C A
EagI  (2236)
1 site
C G G C C G G C C G G C
NotI  (2236)
1 site
G C G G C C G C C G C C G G C G
EcoRI  (2258)
1 site
G A A T T C C T T A A G
AgeI  (2553)
1 site
A C C G G T T G G C C A
BstAPI  (2805)
1 site
G C A N N N N N T G C C G T N N N N N A C G

Sticky ends from different BstAPI sites may not be compatible.
BamHI  (2936)
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.
TspMI  (2963)
1 site
C C C G G G G G G C C C
XmaI  (2963)
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.
SmaI  (2965)
1 site
C C C G G G G G G C C C

SmaI can be used at 37°C for brief incubations.
SrfI  (2965)
1 site
G C C C G G G C C G G G C C C G
SalI  (2970)
1 site
G T C G A C C A G C T G
PaeR7I  (3006)
1 site
C T C G A G G A G C T C

PaeR7I does not recognize the sequence CTCTCGAG.
PspXI  (3006)
1 site
V C T C G A G B B G A G C T C V
XhoI  (3006)
1 site
C T C G A G G A G C T C
HindIII  (3013)
1 site
A A G C T T T T C G A A
Acc65I  (3019)
1 site
G G T A C C C C A T G G
KpnI  (3023)
1 site
G G T A C C C C A T G G
SacII  (3026)
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.
NheI  (3028)
1 site
G C T A G C C G A T C G
BmtI  (3032)
1 site
G C T A G C C G A T C G
BsrGI  (3157)
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.
2μ ori
5221 .. 6563  =  1343 bp
yeast 2μ plasmid origin of replication
2μ ori
5221 .. 6563  =  1343 bp
yeast 2μ plasmid origin of replication
AmpR
4229 .. 5089  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 2:  
   4229 .. 5020  =  792 bp
   263 amino acids  =  28.9 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
4229 .. 5089  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 1:  signal sequence  
   5021 .. 5089  =  69 bp
   23 amino acids  =  2.6 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
4229 .. 5089  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
URA3
417 .. 1220  =  804 bp
267 amino acids  =  29.3 kDa
Product: orotidine-5'-phosphate decarboxylase, required for uracil biosynthesis
yeast auxotrophic marker, counterselectable with 5-fluoroorotic acid (5-FOA)
URA3
417 .. 1220  =  804 bp
267 amino acids  =  29.3 kDa
Product: orotidine-5'-phosphate decarboxylase, required for uracil biosynthesis
yeast auxotrophic marker, counterselectable with 5-fluoroorotic acid (5-FOA)
GAL1,10 promoter
2268 .. 2932  =  665 bp
divergent inducible promoter, regulated by Gal4
GAL1,10 promoter
2268 .. 2932  =  665 bp
divergent inducible promoter, regulated by Gal4
ori
3470 .. 4058  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
ori
3470 .. 4058  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
f1 ori
1351 .. 1806  =  456 bp
f1 bacteriophage origin of replication; arrow indicates direction of (+) strand synthesis
f1 ori
1351 .. 1806  =  456 bp
f1 bacteriophage origin of replication; arrow indicates direction of (+) strand synthesis
URA3 promoter
201 .. 416  =  216 bp
URA3 promoter
201 .. 416  =  216 bp
CYC1 terminator
3038 .. 3227  =  190 bp
transcription terminator for CYC1
CYC1 terminator
3038 .. 3227  =  190 bp
transcription terminator for CYC1
ADH1 terminator
1885 .. 2050  =  166 bp
transcription terminator for the S. cerevisiae alcohol dehydrogenase 1 (ADH1) gene
ADH1 terminator
1885 .. 2050  =  166 bp
transcription terminator for the S. cerevisiae alcohol dehydrogenase 1 (ADH1) gene
AmpR promoter
5090 .. 5194  =  105 bp
AmpR promoter
5090 .. 5194  =  105 bp
MCS 2
2936 .. 3033  =  98 bp
multiple cloning site 2
MCS 2
2936 .. 3033  =  98 bp
multiple cloning site 2
MCS 1
2180 .. 2263  =  84 bp
multiple cloning site 1
MCS 1
2180 .. 2263  =  84 bp
multiple cloning site 1
UAS
2484 .. 2601  =  118 bp
upstream activating sequence mediating Gal4-dependent induction
UAS
2484 .. 2601  =  118 bp
upstream activating sequence mediating Gal4-dependent induction
Myc
2979 .. 3008  =  30 bp
10 amino acids  =  1.2 kDa
Product: Myc (human c-Myc oncogene) epitope tag
Myc
2979 .. 3008  =  30 bp
10 amino acids  =  1.2 kDa
Product: Myc (human c-Myc oncogene) epitope tag
FLAG
2198 .. 2221  =  24 bp
8 amino acids  =  1.0 kDa
Product: FLAG® epitope tag, followed by an enterokinase cleavage site
FLAG
2198 .. 2221  =  24 bp
8 amino acids  =  1.0 kDa
Product: FLAG® epitope tag, followed by an enterokinase cleavage site
ORF:  417 .. 1220  =  804 bp
ORF:  267 amino acids  =  29.3 kDa
ORF:  4359 .. 4625  =  267 bp
ORF:  88 amino acids  =  9.2 kDa
ORF:  5256 .. 5546  =  291 bp
ORF:  96 amino acids  =  11.5 kDa
ORF:  452 .. 928  =  477 bp
ORF:  158 amino acids  =  16.8 kDa
ORF:  4229 .. 5089  =  861 bp
ORF:  286 amino acids  =  31.6 kDa
ORF:  6022 .. 6342  =  321 bp
ORF:  106 amino acids  =  12.9 kDa
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