YIp351

Yeast/E. coli integrating shuttle vector with a LEU2 marker. See also YIp352.
Try SnapGene for Free
|Download SnapGene Viewer
Explore Over 2.7k Plasmids: Yeast Plasmids | More Plasmid Sets
No matches
HomePlasmidsYeast PlasmidsYIp351
Eco53kI (23) lac operator BspQI - SapI (4182) DrdI (3963) PspFI (3765) BseYI (3761) AlwNI (3656) AhdI (3177) BsaI (3111) BpmI (3108) NmeAIII (3030) FspI (2954) ScaI (2696) BanII - SacI (25) AvaI - BsoBI - TspMI - XmaI (31) SmaI (33) BamHI (36) XbaI (42) SalI (48) PstI - SbfI (58) SphI (64) HindIII (66) KasI (230) NarI (231) SfoI (232) PluTI (234) BseRI (509) BsrGI (729) PfoI (975) BtgI (988) EcoRV (1103) BstXI (1142) BbsI (1397) AflII (1534) AgeI (1599) BspDI - ClaI (1699) BstEII (1814) EcoO109I - PpuMI (1959) YIp351 4406 bp
Eco53kI  (23)
1 site		 G A G C T C C T C G A G
BspQI  (4182)
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  (4182)
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.
DrdI  (3963)
1 site		 G A C N N N N N N G T C C T G N N N N N N C A G
Sticky ends from different DrdI sites may not be compatible.
PspFI  (3765)
1 site		 C C C A G C G G G T C G
BseYI  (3761)
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.
AlwNI  (3656)
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.
AhdI  (3177)
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.
BsaI  (3111)
1 site		 G G T C T C N C C A G A G N ( N ) 4
Sticky ends from different BsaI sites may not be compatible.
BsaI can be used between 37°C and 50°C.
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.
NmeAIII  (3030)
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).
FspI  (2954)
1 site		 T G C G C A A C G C G T
ScaI  (2696)
1 site		 A G T A C T T C A T G A
BanII  (25)
1 site		 G R G C Y C C Y C G R G
Sticky ends from different BanII sites may not be compatible.
SacI  (25)
1 site		 G A G C T C C T C G A G
AvaI  (31)
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  (31)
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  (31)
1 site		 C C C G G G G G G C C C
XmaI  (31)
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  (33)
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  (36)
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.
XbaI  (42)
1 site		 T C T A G A A G A T C T
SalI  (48)
1 site		 G T C G A C C A G C T G
PstI  (58)
1 site		 C T G C A G G A C G T C
SbfI  (58)
1 site		 C C T G C A G G G G A C G T C C
SphI  (64)
1 site		 G C A T G C C G T A C G
HindIII  (66)
1 site		 A A G C T T T T C G A A
KasI  (230)
1 site		 G G C G C C C C G C G G
NarI  (231)
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.
SfoI  (232)
1 site		 G G C G C C C C G C G G
PluTI  (234)
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.
BseRI  (509)
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.
BsrGI  (729)
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.
PfoI  (975)
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.
BtgI  (988)
1 site		 C C R Y G G G G Y R C C
Sticky ends from different BtgI sites may not be compatible.
EcoRV  (1103)
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.
BstXI  (1142)
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.
BbsI  (1397)
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.
AflII  (1534)
1 site		 C T T A A G G A A T T C
AgeI  (1599)
1 site		 A C C G G T T G G C C A
BspDI  (1699)
1 site		 A T C G A T T A G C T A
ClaI  (1699)
1 site		 A T C G A T T A G C T A
BstEII  (1814)
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.
EcoO109I  (1959)
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.
PpuMI  (1959)
1 site		 R G G W C C Y Y C C W G G R
Sticky ends from different PpuMI sites may not be compatible.
LEU2
759 .. 1853  =  1095 bp
364 amino acids  =  39.2 kDa
Product: 3-isopropylmalate dehydrogenase, required for leucine biosynthesis
yeast auxotrophic marker
LEU2
759 .. 1853  =  1095 bp
364 amino acids  =  39.2 kDa
Product: 3-isopropylmalate dehydrogenase, required for leucine biosynthesis
yeast auxotrophic marker
AmpR
2390 .. 3250  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 1:  signal sequence  
   2390 .. 2458  =  69 bp
   23 amino acids  =  2.6 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
2390 .. 3250  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 2:  
   2459 .. 3250  =  792 bp
   263 amino acids  =  28.9 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
2390 .. 3250  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
ori
3421 .. 4009  =  589 bp
high-copy-number colE1/pMB1/pBR322/pUC origin of replication
ori
3421 .. 4009  =  589 bp
high-copy-number colE1/pMB1/pBR322/pUC origin of replication
LEU2 promoter
1854 .. 2258  =  405 bp
LEU2 promoter
1854 .. 2258  =  405 bp
lacZα
1 .. 303  =  303 bp
100 amino acids  =  11.5 kDa
Product: LacZα fragment of β-galactosidase
lacZα
1 .. 303  =  303 bp
100 amino acids  =  11.5 kDa
Product: LacZα fragment of β-galactosidase
AmpR promoter
2285 .. 2389  =  105 bp
AmpR promoter
2285 .. 2389  =  105 bp
lac promoter
4333 .. 4363  =  31 bp
3 segments
   Segment 1:  -35  
   4333 .. 4338  =  6 bp
promoter for the E. coli lac operon
lac promoter
4333 .. 4363  =  31 bp
3 segments
   Segment 2:  
   4339 .. 4356  =  18 bp
promoter for the E. coli lac operon
lac promoter
4333 .. 4363  =  31 bp
3 segments
   Segment 3:  -10  
   4357 .. 4363  =  7 bp
promoter for the E. coli lac operon
lac promoter
4333 .. 4363  =  31 bp
3 segments
promoter for the E. coli lac operon
lac operator
4371 .. 4387  =  17 bp
The lac repressor binds to the lac operator to inhibit transcription in E. coli. This inhibition can be relieved by adding lactose or isopropyl-β-D-thiogalactopyranoside (IPTG).
lac operator
4371 .. 4387  =  17 bp
The lac repressor binds to the lac operator to inhibit transcription in E. coli. This inhibition can be relieved by adding lactose or isopropyl-β-D-thiogalactopyranoside (IPTG).
MCS
15 .. 71  =  57 bp
pUC19 multiple cloning site
MCS
15 .. 71  =  57 bp
pUC19 multiple cloning site
M13 fwd
75 .. 91  =  17 bp
common sequencing primer, one of multiple similar variants
M13 fwd
75 .. 91  =  17 bp
common sequencing primer, one of multiple similar variants
M13 rev
4395 .. 5  =  17 bp
common sequencing primer, one of multiple similar variants
M13 rev
4395 .. 5  =  17 bp
common sequencing primer, one of multiple similar variants
ORF:  1 .. 303  =  303 bp
ORF:  100 amino acids  =  11.5 kDa
ORF:  2390 .. 3250  =  861 bp
ORF:  286 amino acids  =  31.6 kDa
ORF:  4334 .. 284  =  357 bp
ORF:  118 amino acids  =  13.4 kDa
ORF:  759 .. 1853  =  1095 bp
ORF:  364 amino acids  =  39.2 kDa
ORF:  2854 .. 3120  =  267 bp
ORF:  88 amino acids  =  9.2 kDa
Click here to try SnapGene

Download YIp351.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