pFA6a-TRP1

Plasmid for yeast gene deletion using the S. cerevisiae TRP1 selectable marker.
Try SnapGene for Free
|Download SnapGene Viewer
Explore Over 2.7k Plasmids: Yeast Plasmids | More Plasmid Sets
No matches
HomePlasmidsYeast PlasmidspFA6a-TRP1
PvuII (15) NdeI (3332) PfoI (3194) EcoO109I (3137) AatII (3083) ZraI (3081) SspI (2965) ScaI (2641) TsoI (2560) PvuI (2531) FspI (2383) NmeAIII (2309) BpmI (2231) BanI (2109) BsiWI (25) PstI (35) SalI (37) F1 (42 .. 61) BamHI (43) AvaI - BsoBI - TspMI - XmaI (48) SmaI (50) PacI (58) AscI - BssHII (63) BglII (70) BsrGI (75) BspEI * (88) PmlI (183) BstZ17I (190) BstAPI (302) XbaI (307) MfeI (363) Bsu36I (465) BstXI (521) BsgI (636) PaqCI (656) PmeI (982) Eco53kI (989) SacI (991) EcoRI (993) R1 (979 .. 998) BspDI - ClaI (1000) SpeI (1017) SfiI (1030) BtgI (1034) SacII (1037) HpaI (1089) BspQI - SapI (1152) AflIII - PciI (1268) AlwNI (1684) pFA6a-TRP1 3415 bp
PvuII  (15)
1 site		 C A G C T G G T C G A C
NdeI  (3332)
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  (3194)
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.
EcoO109I  (3137)
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.
AatII  (3083)
1 site		 G A C G T C C T G C A G
ZraI  (3081)
1 site		 G A C G T C C T G C A G
SspI  (2965)
1 site		 A A T A T T T T A T A A
ScaI  (2641)
1 site		 A G T A C T T C A T G A
TsoI  (2560)
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  (2531)
1 site		 C G A T C G G C T A G C
FspI  (2383)
1 site		 T G C G C A A C G C G T
NmeAIII  (2309)
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  (2231)
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  (2109)
1 site		 G G Y R C C C C R Y G G
Sticky ends from different BanI sites may not be compatible.
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
AscI  (63)
1 site		 G G C G C G C C C C G C G C G G
BssHII  (63)
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.
BglII  (70)
1 site		 A G A T C T T C T A G A
BsrGI  (75)
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  (88)
1 site		 T C C G G A A G G C C T
* Blocked by Dam methylation.
PmlI  (183)
1 site		 C A C G T G G T G C A C
BstZ17I  (190)
1 site		 G T A T A C C A T A T G
BstAPI  (302)
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  (307)
1 site		 T C T A G A A G A T C T
MfeI  (363)
1 site		 C A A T T G G T T A A C
Bsu36I  (465)
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  (521)
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  (636)
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).
PaqCI  (656)
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  (982)
1 site		 G T T T A A A C C A A A T T T G
Eco53kI  (989)
1 site		 G A G C T C C T C G A G
SacI  (991)
1 site		 G A G C T C C T C G A G
EcoRI  (993)
1 site		 G A A T T C C T T A A G
BspDI  (1000)
1 site		 A T C G A T T A G C T A
ClaI  (1000)
1 site		 A T C G A T T A G C T A
SpeI  (1017)
1 site		 A C T A G T T G A T C A
SfiI  (1030)
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  (1034)
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  (1037)
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.
HpaI  (1089)
1 site		 G T T A A C C A A T T G
BspQI  (1152)
1 site		 G C T C T T C N C G A G A A G N N N N
Sticky ends from different BspQI sites may not be compatible.
SapI  (1152)
1 site		 G C T C T T C N C G A G A A G N N N N
Sticky ends from different SapI sites may not be compatible.
SapI gradually settles in solution, so a tube of SapI should be mixed before removing an aliquot.
AflIII  (1268)
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  (1268)
1 site		 A C A T G T T G T A C A
PciI is inhibited by nonionic detergents.
AlwNI  (1684)
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.
F1
20-mer  /  50% GC
1 binding site
42 .. 61  =  20 annealed bases
Tm  =  54°C
Forward primer for gene deletion. 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
979 .. 998  =  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
2088 .. 2948  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 2:  
   2088 .. 2879  =  792 bp
   263 amino acids  =  28.9 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
2088 .. 2948  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 1:  signal sequence  
   2880 .. 2948  =  69 bp
   23 amino acids  =  2.6 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
2088 .. 2948  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
TRP1
224 .. 898  =  675 bp
224 amino acids  =  24.1 kDa
Product: phosphoribosylanthranilate isomerase, required for tryptophan biosynthesis
yeast auxotrophic marker
TRP1
224 .. 898  =  675 bp
224 amino acids  =  24.1 kDa
Product: phosphoribosylanthranilate isomerase, required for tryptophan biosynthesis
yeast auxotrophic marker
ori
1329 .. 1917  =  589 bp
high-copy-number colE1/pMB1/pBR322/pUC origin of replication
ori
1329 .. 1917  =  589 bp
high-copy-number colE1/pMB1/pBR322/pUC origin of replication
TRP1 promoter
76 .. 223  =  148 bp
TRP1 promoter
76 .. 223  =  148 bp
AmpR promoter
2949 .. 3053  =  105 bp
AmpR promoter
2949 .. 3053  =  105 bp
T7 promoter
1053 .. 1071  =  19 bp
promoter for bacteriophage T7 RNA polymerase
T7 promoter
1053 .. 1071  =  19 bp
promoter for bacteriophage T7 RNA polymerase
SP6 promoter
3399 .. 2  =  19 bp
promoter for bacteriophage SP6 RNA polymerase
SP6 promoter
3399 .. 2  =  19 bp
promoter for bacteriophage SP6 RNA polymerase
ORF:  2218 .. 2484  =  267 bp
ORF:  88 amino acids  =  9.2 kDa
ORF:  224 .. 898  =  675 bp
ORF:  224 amino acids  =  24.1 kDa
ORF:  474 .. 755  =  282 bp
ORF:  93 amino acids  =  10.8 kDa
ORF:  2088 .. 2948  =  861 bp
ORF:  286 amino acids  =  31.6 kDa
Click here to try SnapGene

Download pFA6a-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
Download SnapGene

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
Download SnapGene Viewer

Individual Sequences & Maps

bleMX6
pFA6a-kanMX6
pPIC6(alpha) B
pYES2.1-E
hphMX6
pFA6a-kanMX6-PGAL1
pPIC6(alpha) C
pYES2 CT
kanMX
pFA6a-kanMX6-PGAL1-3HA
pPIC9
pYES2 NT A
kanMX2
pFA6a-kanMX6-PGAL1-GFP
pPIC9K
pYES2 NT B
kanMX4
pFA6a-kanMX6-PGAL1-GST
pPICZ A
pYES2 NT C
kanMX6
pFA6a-natMX6
pPICZ B
pYES3 CT
natMX6
pFA6a-TRP1
pPICZ C
pYES6 CT
pAbAi
pFA6a-TRP1-PGAL1
pPICZ(alpha) A
pYM25
pAD-GAL4
pFA6a-TRP1-PGAL1-3HA
pPICZ(alpha) B
pYM26
pAG25
pFA6a-TRP1-PGAL1-GFP
pPICZ(alpha) C
pYM44
pAG29
pFA6a-TRP1-PGAL1-GST
pPink-HC
YCp50
pAG32
pFLD
pPink-LC
YCp50-poly
pAO815
pFLD(alpha)
pPINK(alpha)-HC
YCplac111
patMX4
pGAD-C1
pRS303
YCplac22
pAUR101
pGAD-C2
pRS304
YCplac33
pAUR112
pGAD-C3
pRS305
YEp13
pAUR123
pGADT7 AD
pRS306
YEp24
pAUR224
pGADT7-Rec
pRS313
YEp351
pBridge
pGADT7-Rec (linearized)
pRS314
YEp352
pDH25
pGAPZ A
pRS315
YEp353
pEG202
pGAPZ B
pRS316
YEp354
pESC-HIS
pGAPZ C
pRS403
YEp355
pESC-LEU
pGAPZ(alpha) A
pRS404
YEp356
pESC-TRP
pGAPZ(alpha) B
pRS405
YEp356R
pESC-URA
pGAPZ(alpha) C
pRS406
YEp357
pFA6-kanMX4
pGBD-C1
pRS413
YEp357R
pFA6a
pGBD-C2
pRS414
YEp358
pFA6a-12Pk-kanMX6
pGBD-C3
pRS415
YEp358R
pFA6a-13Myc-His3MX6
pGBDU-C1
pRS416
YEp363
pFA6a-13Myc-kanMX6
pGBDU-C2
pRS423
YEp364
pFA6a-13Myc-TRP1
pGBDU-C3
pRS424
YEp365
pFA6a-3HA-His3MX6
pGBKT7
pRS425
YEp366
pFA6a-3HA-kanMX6
pGilda
pRS426
YEp366R
pFA6a-3HA-TRP1
pHIL-D2
pSpot5
YEp367
pFA6a-5FLAG-kanMX6
pHIL-S1
pSpot6
YEp367R
pFA6a-bleMX6
pJG4-5
pSpot7
YEp368
pFA6a-GFP(S65T)-His3MX6
pKLAC1
pSpot8
YEp368R
pFA6a-GFP(S65T)-kanMX6
pKLAC2
pTEF1 Zeo
YEplac112
pFA6a-GFP(S65T)-TRP1
pOAD
pUCATPH
YEplac181
pFA6a-GST-His3MX6
pOBD2
pY-secSUMOstar
YEplac195
pFA6a-GST-kanMX6
pP-secSUMO3
pY-SUMOstar
YIp351
pFA6a-GST-TRP1
pPIC3
pYC2-E
YIp352
pFA6a-His3MX6
pPIC3.5
pYC2 CT
YIp5
pFA6a-His3MX6-PGAL1
pPIC3.5K
pYC2 NT A
YIplac128
pFA6a-His3MX6-PGAL1-3HA
pPIC6 A
pYC2 NT B
YIplac204
pFA6a-His3MX6-PGAL1-GFP
pPIC6 B
pYC2 NT C
YIplac211
pFA6a-His3MX6-PGAL1-GST
pPIC6 C
pYC6 CT
YRp7
pFA6a-hphMX6
pPIC6(alpha) A
pYES2
alpha-factor secretion signal

Plasmid Sets

Basic Cloning Vectors
I.M.A.G.E. Consortium Plasmids
pET & Duet Vectors (Novagen)
TA and GC Cloning Vectors
Coronavirus Resources
Insect Cell Vectors
pGEX Vectors (GE Healthcare)
TOPO Cloning Vectors
CRISPR Plasmids
Luciferase Vectors
Plant Vectors
Viral Expression & Packaging Vectors
Fluorescent Protein Genes & Plasmids
Lucigen Vectors
Qiagen Vectors
Yeast Plasmids
Gateway® Cloning Vectors
Mammalian Expression Vectors
Structural Genomics Vectors

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.
Try for Free