pEZ BAC (HpaI linearized)

HpaI-linearized and dephosphorylated BAC vector with inducible copy number, suitable for cloning toxic inserts.

Sequence Author: Lucigen

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HomePlasmidsBasic Cloning VectorspEZ BAC (HpaI linearized)
SacII (6780) FseI (6776) BciVI - MreI (6765) XcmI (6575) XbaI (6065) EcoNI (5791) SmaI (5768) TspMI - XmaI (5766) FspAI (5509) BsrGI (5477) SbfI (5240) BlpI (4779) AfeI (4695) MfeI (4270) NdeI (4254) BstXI (4180) KpnI (4054) Acc65I (4050) PflFI - Tth111I (3989) BseRI (3563) BclI* (3459) T3Te terminatorAscI (7001) NotI (7029) BEZ-F1 (7119 .. 7142) BsrBI (7159) lac operatorHindIII (7236) SphI (7246) <HpaI> (7260) <HpaI> (0) BamHI (7) PmlI (19) EcoRI (24) BEZ-R1 (109 .. 132) KasI (211) NarI (212) SfoI (213) BbeI (215) NotI (241) PmeI (290) EcoO109I - PpuMI (604) DraIII (645) ScaI (1539) BstAPI (1619) BstEII (1652) SexAI* (1656) PciI (1775) AhdI (1776) PspOMI (2289) ApaI - BanII (2293) AccI (2365) PfoI* (2505) SpeI (2535) AleI (2718) pEZ™ BAC 7260 bp
SacII  (6780)
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.
FseI  (6776)
1 site		 G G C C G G C C C C G G C C G G
FseI gradually loses activity when stored at -20°C.
BciVI  (6765)
1 site		 G T A T C C ( N ) 5 N C A T A G G ( N ) 5
The 1-base overhangs produced by BciVI may be hard to ligate.
Sticky ends from different BciVI sites may not be compatible.
MreI  (6765)
1 site		 C G C C G G C G G C G G C C G C
XcmI  (6575)
1 site		 C C A N N N N N N N N N T G G G G T N N N N N N N N N A C C
The 1-base overhangs produced by XcmI may be hard to ligate.
Sticky ends from different XcmI sites may not be compatible.
XbaI  (6065)
1 site		 T C T A G A A G A T C T
EcoNI  (5791)
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.
SmaI  (5768)
1 site		 C C C G G G G G G C C C
SmaI can be used at 37°C for brief incubations.
TspMI  (5766)
1 site		 C C C G G G G G G C C C
XmaI  (5766)
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.
FspAI  (5509)
1 site		 R T G C G C A Y Y A C G C G T R
BsrGI  (5477)
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.
SbfI  (5240)
1 site		 C C T G C A G G G G A C G T C C
BlpI  (4779)
1 site		 G C T N A G C C G A N T C G
Sticky ends from different BlpI sites may not be compatible.
AfeI  (4695)
1 site		 A G C G C T T C G C G A
MfeI  (4270)
1 site		 C A A T T G G T T A A C
NdeI  (4254)
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.
BstXI  (4180)
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.
KpnI  (4054)
1 site		 G G T A C C C C A T G G
Acc65I  (4050)
1 site		 G G T A C C C C A T G G
PflFI  (3989)
1 site		 G A C N N N G T C C T G N N N C A G
The 1-base overhangs produced by PflFI may be hard to ligate.
Sticky ends from different PflFI sites may not be compatible.
Tth111I  (3989)
1 site		 G A C N N N G T C C T G N N N C A G
The 1-base overhangs produced by Tth111I may be hard to ligate.
Sticky ends from different Tth111I sites may not be compatible.
BseRI  (3563)
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.
BclI  (3459)
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  (7001)
1 site		 G G C G C G C C C C G C G C G G
NotI  (7029)
2 sites		 G C G G C C G C C G C C G G C G
BsrBI  (7159)
1 site		 C C G C T C G G C G A G
This recognition sequence is asymmetric, so ligating blunt ends generated by BsrBI will not always regenerate a BsrBI site.
BsrBI is typically used at 37°C, but can be used at temperatures up to 50°C.
HindIII  (7236)
1 site		 A A G C T T T T C G A A
SphI  (7246)
1 site		 G C A T G C C G T A C G
End  (7260)
0 sites
Start  (0)
0 sites
BamHI  (7)
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.
PmlI  (19)
1 site		 C A C G T G G T G C A C
EcoRI  (24)
1 site		 G A A T T C C T T A A G
KasI  (211)
1 site		 G G C G C C C C G C G G
NarI  (212)
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  (213)
1 site		 G G C G C C C C G C G G
BbeI  (215)
1 site		 G G C G C C C C G C G G
Cleavage may be enhanced when more than one copy of the BbeI recognition sequence is present.
NotI  (241)
2 sites		 G C G G C C G C C G C C G G C G
PmeI  (290)
1 site		 G T T T A A A C C A A A T T T G
EcoO109I  (604)
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  (604)
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.
DraIII  (645)
1 site		 C A C N N N G T G G T G N N N C A C
Sticky ends from different DraIII sites may not be compatible.
ScaI  (1539)
1 site		 A G T A C T T C A T G A
BstAPI  (1619)
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.
BstEII  (1652)
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.
SexAI  (1656)
1 site		 A C C W G G T T G G W C C A
* Blocked by Dcm methylation.
Sticky ends from different SexAI sites may not be compatible.
PciI  (1775)
1 site		 A C A T G T T G T A C A
PciI is inhibited by nonionic detergents.
AhdI  (1776)
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.
PspOMI  (2289)
1 site		 G G G C C C C C C G G G
ApaI  (2293)
1 site		 G G G C C C C C C G G G
ApaI can be used between 25°C and 37°C.
BanII  (2293)
1 site		 G R G C Y C C Y C G R G
Sticky ends from different BanII sites may not be compatible.
AccI  (2365)
1 site		 G T M K A C C A K M T G
Efficient cleavage with AccI requires ≥13 bp on each side of the recognition sequence.
Sticky ends from different AccI sites may not be compatible.
PfoI  (2505)
1 site		 T C C N G G A A G G N C C T
* Blocked by Dcm methylation.
Sticky ends from different PfoI sites may not be compatible.
SpeI  (2535)
1 site		 A C T A G T T G A T C A
AleI  (2718)
1 site		 C A C N N N N G T G G T G N N N N C A C
BEZ-F1
24-mer  /  50% GC
1 binding site
7119 .. 7142  =  24 annealed bases
Tm  =  60°C
BEZ-R1
24-mer  /  54% GC
1 binding site
109 .. 132  =  24 annealed bases
Tm  =  63°C
sopA
3356 .. 4531  =  1176 bp
391 amino acids  =  44.1 kDa
Product: partitioning protein for the bacterial F plasmid
sopA
3356 .. 4531  =  1176 bp
391 amino acids  =  44.1 kDa
Product: partitioning protein for the bacterial F plasmid
repE
5110 .. 5865  =  756 bp
251 amino acids  =  29.4 kDa
Product: replication initiation protein for the bacterial F plasmid
repE
5110 .. 5865  =  756 bp
251 amino acids  =  29.4 kDa
Product: replication initiation protein for the bacterial F plasmid
CmR
909 .. 1568  =  660 bp
219 amino acids  =  25.7 kDa
Product: chloramphenicol acetyltransferase
confers resistance to chloramphenicol
CmR
909 .. 1568  =  660 bp
219 amino acids  =  25.7 kDa
Product: chloramphenicol acetyltransferase
confers resistance to chloramphenicol
oriV
6251 .. 6865  =  615 bp
origin of replication for the bacterial F plasmid
oriV
6251 .. 6865  =  615 bp
origin of replication for the bacterial F plasmid
sopC
1839 .. 2312  =  474 bp
centromere-like partitioning region of the bacterial F plasmid
sopC
1839 .. 2312  =  474 bp
centromere-like partitioning region of the bacterial F plasmid
cos
385 .. 783  =  399 bp
lambda cos site; allows packaging into phage lambda particles
cos
385 .. 783  =  399 bp
lambda cos site; allows packaging into phage lambda particles
incC
4857 .. 5107  =  251 bp
incompatibility region of the bacterial F plasmid
incC
4857 .. 5107  =  251 bp
incompatibility region of the bacterial F plasmid
ori2
5956 .. 6175  =  220 bp
secondary origin of replication for the bacterial F plasmid; also known as oriS
ori2
5956 .. 6175  =  220 bp
secondary origin of replication for the bacterial F plasmid; also known as oriS
lacZα
1 .. 201  =  201 bp
66 amino acids  =  7.5 kDa
Product: LacZα fragment of β-galactosidase
lacZα
1 .. 201  =  201 bp
66 amino acids  =  7.5 kDa
Product: LacZα fragment of β-galactosidase
lacZα
7189 .. 7260  =  72 bp
24 amino acids  =  2.7 kDa
Product: LacZα fragment of β-galactosidase
lacZα
7189 .. 7260  =  72 bp
24 amino acids  =  2.7 kDa
Product: LacZα fragment of β-galactosidase
loxP
253 .. 286  =  34 bp
Cre-mediated recombination occurs in the 8-bp core sequence (GCATACAT).
loxP
253 .. 286  =  34 bp
Cre-mediated recombination occurs in the 8-bp core sequence (GCATACAT).
loxP
6960 .. 6993  =  34 bp
Cre-mediated recombination occurs in the 8-bp core sequence (GCATACAT).
loxP
6960 .. 6993  =  34 bp
Cre-mediated recombination occurs in the 8-bp core sequence (GCATACAT).
tonB terminator
305 .. 336  =  32 bp
bidirectional E. coli tonB-P14 transcription terminator
tonB terminator
305 .. 336  =  32 bp
bidirectional E. coli tonB-P14 transcription terminator
lac promoter
7115 .. 7145  =  31 bp
3 segments
   Segment 1:  -35  
   7115 .. 7120  =  6 bp
promoter for the E. coli lac operon
lac promoter
7115 .. 7145  =  31 bp
3 segments
   Segment 2:  
   7121 .. 7138  =  18 bp
promoter for the E. coli lac operon
lac promoter
7115 .. 7145  =  31 bp
3 segments
   Segment 3:  -10  
   7139 .. 7145  =  7 bp
promoter for the E. coli lac operon
lac promoter
7115 .. 7145  =  31 bp
3 segments
promoter for the E. coli lac operon
T3Te terminator
6909 .. 6938  =  30 bp
phage T3 early transcription terminator
T3Te terminator
6909 .. 6938  =  30 bp
phage T3 early transcription terminator
T7Te terminator
1583 .. 1606  =  24 bp
phage T7 early transcription terminator
T7Te terminator
1583 .. 1606  =  24 bp
phage T7 early transcription terminator
lac operator
7153 .. 7169  =  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
7153 .. 7169  =  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).
sopB
2385 .. 3356  =  972 bp
323 amino acids  =  35.4 kDa
Product: partitioning protein for the bacterial F plasmid
sopB
2385 .. 3356  =  972 bp
323 amino acids  =  35.4 kDa
Product: partitioning protein for the bacterial F plasmid
T7 promoter
32 .. 50  =  19 bp
promoter for bacteriophage T7 RNA polymerase
T7 promoter
32 .. 50  =  19 bp
promoter for bacteriophage T7 RNA polymerase
ORF:  3079 .. 3315  =  237 bp
ORF:  78 amino acids  =  8.3 kDa
ORF:  5476 .. 5709  =  234 bp
ORF:  77 amino acids  =  9.1 kDa
ORF:  2 .. 256  =  255 bp
ORF:  84 amino acids  =  9.1 kDa  (no start codon)
ORF:  909 .. 1568  =  660 bp
ORF:  219 amino acids  =  25.7 kDa
ORF:  5110 .. 5865  =  756 bp
ORF:  251 amino acids  =  29.4 kDa
ORF:  2385 .. 3356  =  972 bp
ORF:  323 amino acids  =  35.4 kDa
ORF:  5316 .. 5561  =  246 bp
ORF:  81 amino acids  =  8.9 kDa
ORF:  5646 .. 5876  =  231 bp
ORF:  76 amino acids  =  8.7 kDa
ORF:  2606 .. 3004  =  399 bp
ORF:  132 amino acids  =  15.6 kDa
ORF:  3356 .. 4531  =  1176 bp
ORF:  391 amino acids  =  44.1 kDa
ORF:  6728 .. 6976  =  249 bp
ORF:  82 amino acids  =  8.8 kDa
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Individual Sequences & Maps

BlueScribe
pEASY-T1 (linearized)
pJET1.2
pSMART LCAmp
CAG promoter
pEASY-T1 Simple (linearized)
pJET1.2 blunt
pSMART LCAmp (linearized)
chicken beta-actin promoter
pEASY-T3 (linearized)
pJW168
pSMART LCKan
CLIP-tag
pEASY-T5 Zero (linearized)
pKF 18k-2
pSMART LCKan (linearized)
CMV promoter
pEX-1
pKF 19k-2
pSP64 Poly(A)
GAL1 promoter
pEX-A
pKOV
pSP72
GST
pEX-C-GST
pLATE11 (linearized)
pSP73
HaloTag
pEX-C-His
pLATE31 (linearized)
pSpark Done (linearized)
HSV TK promoter
pEX-K
pLATE51 (linearized)
pSpark I (linearized)
lac operator
pEX-N-GST
pLATE52 (linearized)
pSpark II (linearized)
lac promoter
pEX-N-His
pLEXX-AK
pSpark III (linearized)
lac UV5 promoter
pEX-N-His-GST
pLPS-B (linearized)
pSpark IV (linearized)
lacZ
pEX1
pMAL-c5E
pSpark V (linearized)
lambda
pEX2
pMAL-c5G
pSpot1
LITMUS28
pEX3
pMAL-c5X
pSpot2
LITMUS28i
pEZSeq-Amp
pMAL-c5X-His
pSpot3
LITMUS29
pEZSeq-Amp (linearized)
pMAL-c6T
pSpot4
LITMUS38
pEZSeq-Kan
pMAL-p5E
pSTBlue-1
LITMUS38i
pEZSeq-Kan (linearized)
pMAL-p5G
pSTV28
LITMUS39
pEZ BAC
pMAL-p5X
pSTV29
M13mp18
pEZ BAC (BamHI linearized)
pMCS5
pT7Blue
M13mp19
pEZ BAC (HpaI linearized)
pMiniT
pT7Blue-2
MBP
pF1A T7
pMiniT (linearized)
pT7Blue-3
pACYC177
pF1K T7
pMiniT 2.0
pT7CFE1-CFtag
pACYC184
pF25A ICE T7
pMiniT 2.0 (linearized)
pT7CFE1-CGFP-HA-His
pAN7-1
pF25K ICE T7
pMMB190
pT7CFE1-CGST-HA-His
pANT7_cGST
pF3A WG (BYDV)
pMMB206
pT7CFE1-CHA
pANT7_nHA
pF3K WG (BYDV)
pMMB207
pT7CFE1-CHis
pAUR316
pFC20A HaloTag T7 SP6
pMMB208
pT7CFE1-CMyc
pBC KS(+)
pFC20K HaloTag T7 SP6
pMMB66EH
pT7CFE1-NFtag
pBC KS(-)
pFC30A His6HaloTag T7
pMMB66HE
pT7CFE1-NHA
pBC SK(+)
pFC30K His6HaloTag T7
pMMB67EH
pT7CFE1-NHA-CHis
pBC SK(-)
pFC7A (HQ)
pMMB67HE
pT7CFE1-NHis
pBeloBAC11
pFC7K (HQ)
pNEB193
pT7CFE1-NHis-GST
pBluescript II KS(+)
pFN18A HaloTag T7
pNEB206A (linearized)
pT7CFE1-NHis-GST-CHA
pBluescript II KS(-)
pFN18K HaloTag T7
pOSIP-CH
pT7CFE1-NMyc
pBluescript II SK(+)
pFN19A HaloTag T7 SP6
pOSIP-CO
pTOP Blunt V2 (linearized)
pBluescript II SK(-)
pFN19K HaloTag T7 SP6
pOSIP-CT
pTrcHis A
pBluescript KS(+)
pFN29A His6HaloTag T7
pOSIP-KC
pTrcHis B
pBluescript KS(-)
pFN29K His6HaloTag T7
pOSIP-KH
pTrcHis C
pBluescript SK(+)
pFN2A (GST)
pOSIP-KL
pTrcHis2 A
pBluescript SK(-)
pFN2K (GST)
pOSIP-KO
pTrcHis2 B
pBR322
pFN6A (HQ)
pOSIP-KP
pTrcHis2 C
pBS KS(+)
pFN6K (HQ)
pOSIP-KT
pTV 118N
pBS KS(-)
pGEM-11Zf(+)
pOSIP-TH
pTWV228
pBS SK(+)
pGEM-11Zf(-)
pOSIP-TO
pTXB1
pBS SK(-)
pGEM-3Z
pOSIP-TT
pTYB21
pBS(+)
pGEM-3Zf(+)
pPCR-Script Amp SK(+)
pType IIs
pBS(-)
pGEM-3Zf(-)
pPCR-Script Cam SK(+)
pTZ19R
pBSK(+) Simple-Amp
pGEM-4Z
pPTR I
pTZ19U
pBSK(+) Simple-Kan
pGEM-5Zf(+)
pPTR II
pTZ57R
pcDNA3
pGEM-7Zf(+)
pRACE (linearized)
pUAST
pcDNA3.1(+)
pGEM-7Zf(-)
pRANGER-BTB-1
pUC118
pcDNA3.1(-)
pGEM-9Zf(-)
pRANGER-BTB-2
pUC119
pCold I
pGEM-T
pRANGER-BTB-3
pUC18
pCold II
pGEM-T (linearized)
pRANGER-BTB-5
pUC19
pCold III
pGEM-T Easy
pRHA-109
pUC19L
pCold IV
pGEM-T Easy (linearized)
pRHA-113
pUC57
pCold TF
pGGA
pRHA-67
pUC57-Kan
pCR-XL-2-TOPO
pGGAselect
pRSET A
pUC57-Simple
pCR-XL-2-TOPO (linearized)
PGK promoter
pRSET B
pUCmu
pDD
pGS-21a
pRSET C
pVLT31
pDNR-Dual
pH6HTC His6HaloTag T7
pSB1C3
pVLT33
pDNR-LIB
pH6HTN His6HaloTag T7
pSC101
pVLT35
pE-SUMOpro Amp
pHP45(omega)
pSEAP2-Basic
pYES1L
pE-SUMOpro Kan
pHP45(omega)-Km
pSF-Core
pZErO-2
pE-SUMOpro3 Amp
pHP45(omega)-Tc
pSMART BAC v2.0
SNAP-tag
pE-SUMOpro3 Kan
pHSG298
pSMART BAC v2.0 (BamHI linearized)
SP6 promoter
pE-SUMOstar Amp
pHSG299
pSMART BAC v2.0 (EcoRI linearized)
SV40 promoter
pE-SUMOstar Kan
pHSG396
pSMART BAC v2.0 (HindIII linearized)
T3 promoter
pEASY-Blunt (linearized)
pHSG398
pSMART FOS v2.0 (linearized)
T5 promoter
pEASY-Blunt E1 (linearized)
pHY300PLK
pSMART HCAmp
T7 promoter
pEASY-Blunt E2 (linearized)
pICOz
pSMART HCAmp (linearized)
tac promoter
pEASY-Blunt Simple (linearized)
pInvRecA
pSMART HCKan
trc promoter
pEASY-Blunt Zero (linearized)
pJAZZ-OC
pSMART HCKan (linearized)
phiX174
pEASY-Blunt3 (linearized)
pJAZZ-OK

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

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