pFA6a-GST-kanMX6

Plasmid with a kanMX marker for adding a C-terminal GST tag.
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HomePlasmidsYeast PlasmidspFA6a-GST-kanMX6
BsiWI (25) PvuII (15) NdeI (4732) PfoI (4594) AatII (4483) ZraI (4481) NmeAIII (3709) BpmI (3631) BmrI (3601) BanI (3509) AlwNI (3084) PspFI (2976) BseYI (2972) HpaI (2489) SacII (2437) SfiI (2430) SpeI (2417) EcoRV (2407) SalI (37) F2 (42 .. 61) BamHI (43) AvaI - BsoBI - TspMI - XmaI (48) SmaI (50) PacI (58) BtgZI (181) MscI (270) BsgI (349) BstBI (460) SwaI (490) BclI * (497) AscI - BssHII (739) PsiI (800) BstZ17I (817) BglII (947) BstEII (977) BstXI (994) BmgBI (1030) BseRI (1141) MluI (1194) NcoI - StyI (1334) NruI (1418) AsiSI (1761) PflMI (2024) PmeI (2382) Eco53kI (2389) SacI (2391) EcoRI (2393) R1 (2379 .. 2398) pFA6a-GST-kanMX6 4815 bp
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.
PvuII  (15)
1 site		 C A G C T G G T C G A C
NdeI  (4732)
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  (4594)
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  (4483)
1 site		 G A C G T C C T G C A G
ZraI  (4481)
1 site		 G A C G T C C T G C A G
NmeAIII  (3709)
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  (3631)
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.
BmrI  (3601)
1 site		 A C T G G G ( N ) 4 N T G A C C C ( N ) 4
The 1-base overhangs produced by BmrI may be hard to ligate.
Sticky ends from different BmrI sites may not be compatible.
Unlike most restriction enzymes, BmrI can cleave DNA in the absence of magnesium.
BanI  (3509)
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  (3084)
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.
PspFI  (2976)
1 site		 C C C A G C G G G T C G
BseYI  (2972)
1 site		 C C C A G C G G G T C G
After cleavage, BseYI can remain bound to DNA and alter its electrophoretic mobility.
HpaI  (2489)
1 site		 G T T A A C C A A T T G
SacII  (2437)
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.
SfiI  (2430)
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.
SpeI  (2417)
1 site		 A C T A G T T G A T C A
EcoRV  (2407)
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.
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
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
BsgI  (349)
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).
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
BstZ17I  (817)
1 site		 G T A T A C C A T A T G
BglII  (947)
1 site		 A G A T C T T C T A G A
BstEII  (977)
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.
BstXI  (994)
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.
BmgBI  (1030)
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.
BseRI  (1141)
1 site		 G A G G A G ( N ) 8 N N C T C C T C ( N ) 8
Sticky ends from different BseRI sites may not be compatible.
BseRI quickly loses activity at 37°C.
Prolonged incubation with BseRI may lead to degradation of the DNA.
MluI  (1194)
1 site		 A C G C G T T G C G C A
NcoI  (1334)
1 site		 C C A T G G G G T A C C
StyI  (1334)
1 site		 C C W W G G G G W W C C
Sticky ends from different StyI sites may not be compatible.
NruI  (1418)
1 site		 T C G C G A A G C G C T
AsiSI  (1761)
1 site		 G C G A T C G C C G C T A G C G
PflMI  (2024)
1 site		 C C A N N N N N T G G G G T N N N N N A C C
Sticky ends from different PflMI sites may not be compatible.
PmeI  (2382)
1 site		 G T T T A A A C C A A A T T T G
Eco53kI  (2389)
1 site		 G A G C T C C T C G A G
SacI  (2391)
1 site		 G A G C T C C T C G A G
EcoRI  (2393)
1 site		 G A A T T C C T T A A G
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
2379 .. 2398  =  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.
kanMX
992 .. 2348  =  1357 bp
yeast selectable marker conferring kanamycin resistance
kanMX
992 .. 2348  =  1357 bp
yeast selectable marker conferring kanamycin resistance
AmpR
3488 .. 4348  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 2:  
   3488 .. 4279  =  792 bp
   263 amino acids  =  28.9 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
3488 .. 4348  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 1:  signal sequence  
   4280 .. 4348  =  69 bp
   23 amino acids  =  2.6 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
3488 .. 4348  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
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
2729 .. 3317  =  589 bp
high-copy-number colE1/pMB1/pBR322/pUC origin of replication
ori
2729 .. 3317  =  589 bp
high-copy-number colE1/pMB1/pBR322/pUC origin of replication
ADH1 terminator
758 .. 945  =  188 bp
ADH1 terminator
758 .. 945  =  188 bp
AmpR promoter
4349 .. 4453  =  105 bp
AmpR promoter
4349 .. 4453  =  105 bp
T7 promoter
2453 .. 2471  =  19 bp
promoter for bacteriophage T7 RNA polymerase
T7 promoter
2453 .. 2471  =  19 bp
promoter for bacteriophage T7 RNA polymerase
SP6 promoter
4799 .. 2  =  19 bp
promoter for bacteriophage SP6 RNA polymerase
SP6 promoter
4799 .. 2  =  19 bp
promoter for bacteriophage SP6 RNA polymerase
KanR
1336 .. 2145  =  810 bp
269 amino acids  =  30.7 kDa
Product: aminoglycoside phosphotransferase
confers resistance to kanamycin in bacteria or G418 (Geneticin®) in eukaryotes
KanR
1336 .. 2145  =  810 bp
269 amino acids  =  30.7 kDa
Product: aminoglycoside phosphotransferase
confers resistance to kanamycin in bacteria or G418 (Geneticin®) in eukaryotes
TEF promoter
992 .. 1335  =  344 bp
Ashbya gossypii TEF promoter
TEF promoter
992 .. 1335  =  344 bp
Ashbya gossypii TEF promoter
TEF terminator
2151 .. 2348  =  198 bp
Ashbya gossypii TEF terminator
TEF terminator
2151 .. 2348  =  198 bp
Ashbya gossypii TEF terminator
ORF:  1336 .. 2145  =  810 bp
ORF:  269 amino acids  =  30.7 kDa
ORF:  63 .. 737  =  675 bp
ORF:  224 amino acids  =  26.2 kDa
ORF:  912 .. 1202  =  291 bp
ORF:  96 amino acids  =  10.9 kDa
ORF:  3618 .. 3884  =  267 bp
ORF:  88 amino acids  =  9.2 kDa
ORF:  3488 .. 4348  =  861 bp
ORF:  286 amino acids  =  31.6 kDa
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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

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