pFA6a-GST-TRP1

Plasmid with a TRP1 marker for adding a C-terminal GST tag.
|Download SnapGene Viewer
Explore Over 2.7k Plasmids: Yeast Plasmids | More Plasmid Sets
No matches
PvuII (15) NdeI (4209) PfoI (4071) AatII (3960) ZraI (3958) SspI (3842) TsoI (3437) PvuI (3408) FspI (3260) NmeAIII (3186) BpmI (3108) BanI (2986) AlwNI (2561) HpaI (1966) BsiWI (25) PstI (35) SalI (37) F2 (42 .. 61) BamHI (43) AvaI - BsoBI - TspMI - XmaI (48) SmaI (50) PacI (58) EcoNI (73) BtgZI (181) MscI (270) BstBI (460) SwaI (490) BclI * (497) AscI - BssHII (739) PsiI (800) BglII (947) BsrGI (952) BspEI * (965) PmlI (1060) BstAPI (1179) XbaI (1184) MfeI (1240) Bsu36I (1342) BstXI (1398) PaqCI (1533) PmeI (1859) Eco53kI (1866) SacI (1868) EcoRI (1870) R1 (1856 .. 1875) BspDI - ClaI (1877) SpeI (1894) SfiI (1907) BtgI (1911) SacII (1914) pFA6a-GST-TRP1 4292 bp
PvuII  (15)
1 site
C A G C T G G T C G A C
NdeI  (4209)
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.
PfoI  (4071)
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.
AatII  (3960)
1 site
G A C G T C C T G C A G
ZraI  (3958)
1 site
G A C G T C C T G C A G
SspI  (3842)
1 site
A A T A T T T T A T A A
TsoI  (3437)
1 site
T A R C C A ( N ) 9 N N A T Y G G T ( N ) 9

Sticky ends from different TsoI sites may not be compatible.
After cleavage, TsoI can remain bound to DNA and alter its electrophoretic mobility.
For full activity, add fresh S-adenosylmethionine (SAM).
PvuI  (3408)
1 site
C G A T C G G C T A G C
FspI  (3260)
1 site
T G C G C A A C G C G T
NmeAIII  (3186)
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).
BpmI  (3108)
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.
BanI  (2986)
1 site
G G Y R C C C C R Y G G

Sticky ends from different BanI sites may not be compatible.
AlwNI  (2561)
1 site
C A G N N N C T G G T C N N N G A C

Sticky ends from different AlwNI sites may not be compatible.
HpaI  (1966)
1 site
G T T A A C C A A T T G
BsiWI  (25)
1 site
C G T A C G G C A T G C

BsiWI is typically used at 55°C, but is 50% active at 37°C.
PstI  (35)
1 site
C T G C A G G A C G T C
SalI  (37)
1 site
G T C G A C C A G C T G
BamHI  (43)
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.
AvaI  (48)
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  (48)
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.
TspMI  (48)
1 site
C C C G G G G G G C C C
XmaI  (48)
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  (50)
1 site
C C C G G G G G G C C C

SmaI can be used at 37°C for brief incubations.
PacI  (58)
1 site
T T A A T T A A A A T T A A T T
EcoNI  (73)
1 site
C C T N N N N N A G G G G A N N N N N T C C

The 1-base overhangs produced by EcoNI may be hard to ligate.
Sticky ends from different EcoNI sites may not be compatible.
BtgZI  (181)
1 site
G C G A T G ( N ) 10 C G C T A C ( N ) 10 ( N ) 4

Sticky ends from different BtgZI sites may not be compatible.
After cleavage, BtgZI can remain bound to DNA and alter its electrophoretic mobility.
BtgZI is typically used at 60°C, but is 75% active at 37°C.
MscI  (270)
1 site
T G G C C A A C C G G T
BstBI  (460)
1 site
T T C G A A A A G C T T
SwaI  (490)
1 site
A T T T A A A T T A A A T T T A

SwaI is typically used at 25°C, but is 50% active at 37°C.
BclI  (497)
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.
AscI  (739)
1 site
G G C G C G C C C C G C G C G G
BssHII  (739)
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.
PsiI  (800)
1 site
T T A T A A A A T A T T
BglII  (947)
1 site
A G A T C T T C T A G A
BsrGI  (952)
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.
BspEI  (965)
1 site
T C C G G A A G G C C T
* Blocked by Dam methylation.
PmlI  (1060)
1 site
C A C G T G G T G C A C
BstAPI  (1179)
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.
XbaI  (1184)
1 site
T C T A G A A G A T C T
MfeI  (1240)
1 site
C A A T T G G T T A A C
Bsu36I  (1342)
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.
BstXI  (1398)
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.
PaqCI  (1533)
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.
PmeI  (1859)
1 site
G T T T A A A C C A A A T T T G
Eco53kI  (1866)
1 site
G A G C T C C T C G A G
SacI  (1868)
1 site
G A G C T C C T C G A G
EcoRI  (1870)
1 site
G A A T T C C T T A A G
BspDI  (1877)
1 site
A T C G A T T A G C T A
ClaI  (1877)
1 site
A T C G A T T A G C T A
SpeI  (1894)
1 site
A C T A G T T G A T C A
SfiI  (1907)
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.
BtgI  (1911)
1 site
C C R Y G G G G Y R C C

Sticky ends from different BtgI sites may not be compatible.
SacII  (1914)
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.
F2
20-mer  /  50% GC
1 binding site
42 .. 61  =  20 annealed bases
Tm  =  56°C
Forward primer for C-terminal tagging. This primer includes a BamHI recognition sequence. A gene-specific sequence should be added at the 5' end of the primer.
R1
20-mer  /  40% GC
1 binding site
1856 .. 1875  =  20 annealed bases
Tm  =  53°C
Reverse primer for gene deletion or C-terminal tagging. This primer includes an EcoRI recognition sequence. A gene-specific sequence should be added at the 5' end of the primer.
AmpR
2965 .. 3825  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 2:  
   2965 .. 3756  =  792 bp
   263 amino acids  =  28.9 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
2965 .. 3825  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 1:  signal sequence  
   3757 .. 3825  =  69 bp
   23 amino acids  =  2.6 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
2965 .. 3825  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
TRP1
1101 .. 1775  =  675 bp
224 amino acids  =  24.1 kDa
Product: phosphoribosylanthranilate isomerase, required for tryptophan biosynthesis
yeast auxotrophic marker
TRP1
1101 .. 1775  =  675 bp
224 amino acids  =  24.1 kDa
Product: phosphoribosylanthranilate isomerase, required for tryptophan biosynthesis
yeast auxotrophic marker
GST
63 .. 716  =  654 bp
218 amino acids  =  25.5 kDa
Product: glutathione S-transferase from Schistosoma japonicum
GST
63 .. 716  =  654 bp
218 amino acids  =  25.5 kDa
Product: glutathione S-transferase from Schistosoma japonicum
ori
2206 .. 2794  =  589 bp
high-copy-number colE1/pMB1/pBR322/pUC origin of replication
ori
2206 .. 2794  =  589 bp
high-copy-number colE1/pMB1/pBR322/pUC origin of replication
ADH1 terminator
758 .. 945  =  188 bp
ADH1 terminator
758 .. 945  =  188 bp
TRP1 promoter
953 .. 1100  =  148 bp
TRP1 promoter
953 .. 1100  =  148 bp
AmpR promoter
3826 .. 3930  =  105 bp
AmpR promoter
3826 .. 3930  =  105 bp
T7 promoter
1930 .. 1948  =  19 bp
promoter for bacteriophage T7 RNA polymerase
T7 promoter
1930 .. 1948  =  19 bp
promoter for bacteriophage T7 RNA polymerase
SP6 promoter
4276 .. 2  =  19 bp
promoter for bacteriophage SP6 RNA polymerase
SP6 promoter
4276 .. 2  =  19 bp
promoter for bacteriophage SP6 RNA polymerase
ORF:  1351 .. 1632  =  282 bp
ORF:  93 amino acids  =  10.8 kDa
ORF:  3095 .. 3361  =  267 bp
ORF:  88 amino acids  =  9.2 kDa
ORF:  63 .. 737  =  675 bp
ORF:  224 amino acids  =  26.2 kDa
ORF:  1101 .. 1775  =  675 bp
ORF:  224 amino acids  =  24.1 kDa
ORF:  2965 .. 3825  =  861 bp
ORF:  286 amino acids  =  31.6 kDa
Click here to try SnapGene

Download pFA6a-GST-TRP1.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.