pJET1.2 blunt

Linearized positive selection cloning vector with a lethal insert that allows for efficient recovery of blunt-ended PCR products.

Sequence Author: Thermo Fisher (Fermentas)

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HomePlasmidsBasic Cloning VectorspJET1.2 blunt
PstI (2612) XmnI (2223) ScaI (2104) TatI (2102) PvuI (1994) FspI (1846) NmeAIII (1772) BglI (1744) BsrFI (1704) BpmI (1694) BsaI (1685) BmrI (1664) AhdI (1624) AlwNI (1147) PspFI (1039) BbsI (2654) DraIII (2728) BfuAI - BspMI (2813) pJET1.2 forward sequencing primer (2913 .. 2935) EagI - NotI (2932) BspEI (2946) AvaI - BsoBI - PaeR7I - PspXI - XhoI (2955) <EcoRV> (2974) <EcoRV> (0) XbaI (6) BtgI - NcoI - StyI (37) BspDI - ClaI (47) pJET1.2 reverse sequencing primer (34 .. 57) HindIII (253) BbvCI - Bpu10I (347) BsmI (351) BsmBI - Esp3I (374) PmeI (393) MfeI (521) BspQI - SapI (615) DrdI (839) BseYI (1035) pJET1.2/blunt 2974 bp
PstI  (2612)
1 site		 C T G C A G G A C G T C
XmnI  (2223)
1 site		 G A A N N N N T T C C T T N N N N A A G
ScaI  (2104)
1 site		 A G T A C T T C A T G A
TatI  (2102)
1 site		 W G T A C W W C A T G W
PvuI  (1994)
1 site		 C G A T C G G C T A G C
FspI  (1846)
1 site		 T G C G C A A C G C G T
NmeAIII  (1772)
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).
BglI  (1744)
1 site		 G C C N N N N N G G C C G G N N N N N C C G
Sticky ends from different BglI sites may not be compatible.
BsrFI  (1704)
1 site		 R C C G G Y Y G G C C R
Cleavage may be enhanced when more than one copy of the BsrFI recognition sequence is present.
After cleavage, BsrFI can remain bound to DNA and alter its electrophoretic mobility.
BpmI  (1694)
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.
BsaI  (1685)
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.
BmrI  (1664)
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.
AhdI  (1624)
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.
AlwNI  (1147)
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  (1039)
1 site		 C C C A G C G G G T C G
BbsI  (2654)
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.
DraIII  (2728)
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.
BfuAI  (2813)
1 site		 A C C T G C ( N ) 4 T G G A C G ( N ) 4 ( N ) 4
Efficient cleavage requires at least two copies of the BfuAI recognition sequence.
Sticky ends from different BfuAI sites may not be compatible.
BfuAI is typically used at 50°C, but is 50% active at 37°C.
BspMI  (2813)
1 site		 A C C T G C ( N ) 4 T G G A C G ( N ) 4 ( N ) 4
Efficient cleavage requires at least two copies of the BspMI recognition sequence.
Sticky ends from different BspMI sites may not be compatible.
EagI  (2932)
1 site		 C G G C C G G C C G G C
NotI  (2932)
1 site		 G C G G C C G C C G C C G G C G
BspEI  (2946)
1 site		 T C C G G A A G G C C T
AvaI  (2955)
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  (2955)
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.
PaeR7I  (2955)
1 site		 C T C G A G G A G C T C
PaeR7I does not recognize the sequence CTCTCGAG.
PspXI  (2955)
1 site		 V C T C G A G B B G A G C T C V
XhoI  (2955)
1 site		 C T C G A G G A G C T C
End  (2974)
0 sites
Start  (0)
0 sites
XbaI  (6)
1 site		 T C T A G A A G A T C T
BtgI  (37)
1 site		 C C R Y G G G G Y R C C
Sticky ends from different BtgI sites may not be compatible.
NcoI  (37)
1 site		 C C A T G G G G T A C C
StyI  (37)
1 site		 C C W W G G G G W W C C
Sticky ends from different StyI sites may not be compatible.
BspDI  (47)
1 site		 A T C G A T T A G C T A
ClaI  (47)
1 site		 A T C G A T T A G C T A
HindIII  (253)
1 site		 A A G C T T T T C G A A
BbvCI  (347)
1 site		 C C T C A G C G G A G T C G
Bpu10I  (347)
1 site		 C C T N A G C G G A N T C G
Cleavage may be enhanced when more than one copy of the Bpu10I recognition sequence is present.
This recognition sequence is asymmetric, so ligating sticky ends generated by Bpu10I will not always regenerate a Bpu10I site.
Sticky ends from different Bpu10I sites may not be compatible.
BsmI  (351)
1 site		 G A A T G C N C T T A C G N
Sticky ends from different BsmI sites may not be compatible.
BsmBI  (374)
1 site		 C G T C T C N G C A G A G N ( N ) 4
Sticky ends from different BsmBI sites may not be compatible.
BsmBI-v2 is an improved version of BsmBI.
Esp3I  (374)
1 site		 C G T C T C N G C A G A G N ( N ) 4
Sticky ends from different Esp3I sites may not be compatible.
PmeI  (393)
1 site		 G T T T A A A C C A A A T T T G
MfeI  (521)
1 site		 C A A T T G G T T A A C
BspQI  (615)
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  (615)
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  (839)
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.
BseYI  (1035)
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.
pJET1.2 forward sequencing primer
23-mer  /  61% GC
1 binding site
2913 .. 2935  =  23 annealed bases
Tm  =  62°C
pJET1.2 reverse sequencing primer
24-mer  /  42% GC
1 binding site
34 .. 57  =  24 annealed bases
Tm  =  58°C
AmpR
1551 .. 2411  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 2:  
   1551 .. 2342  =  792 bp
   263 amino acids  =  28.9 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
1551 .. 2411  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 1:  signal sequence  
   2343 .. 2411  =  69 bp
   23 amino acids  =  2.6 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
1551 .. 2411  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
ori
792 .. 1380  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
ori
792 .. 1380  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
Eco47I/T7
1 .. 382  =  382 bp
127 amino acids  =  14.7 kDa
Product: mutant version of the Eco47I restriction endonuclease
cleaves double-stranded DNA at GGWCC sites in the absence of protective methylation
Eco47I/T7
1 .. 382  =  382 bp
127 amino acids  =  14.7 kDa
Product: mutant version of the Eco47I restriction endonuclease
cleaves double-stranded DNA at GGWCC sites in the absence of protective methylation
Eco47I/T7
2619 .. 2974  =  356 bp
117 amino acids  =  13.7 kDa
Product: mutant version of the Eco47I restriction endonuclease
cleaves double-stranded DNA at GGWCC sites in the absence of protective methylation
Eco47I/T7
2619 .. 2974  =  356 bp
117 amino acids  =  13.7 kDa
Product: mutant version of the Eco47I restriction endonuclease
cleaves double-stranded DNA at GGWCC sites in the absence of protective methylation
AmpR promoter
2412 .. 2516  =  105 bp
AmpR promoter
2412 .. 2516  =  105 bp
lac UV5 promoter
435 .. 465  =  31 bp
3 segments
   Segment 3:  -10  
   435 .. 441  =  7 bp
E. coli lac promoter with an "up" mutation
lac UV5 promoter
435 .. 465  =  31 bp
3 segments
   Segment 2:  
   442 .. 459  =  18 bp
E. coli lac promoter with an "up" mutation
lac UV5 promoter
435 .. 465  =  31 bp
3 segments
   Segment 1:  -35  
   460 .. 465  =  6 bp
E. coli lac promoter with an "up" mutation
lac UV5 promoter
435 .. 465  =  31 bp
3 segments
E. coli lac promoter with an "up" mutation
lac operator
411 .. 427  =  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
411 .. 427  =  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
1 .. 51  =  51 bp
multiple cloning site
MCS
1 .. 51  =  51 bp
multiple cloning site
MCS
2931 .. 2974  =  44 bp
multiple cloning site
MCS
2931 .. 2974  =  44 bp
multiple cloning site
T7 promoter
2908 .. 2926  =  19 bp
promoter for bacteriophage T7 RNA polymerase
T7 promoter
2908 .. 2926  =  19 bp
promoter for bacteriophage T7 RNA polymerase
ORF:  1681 .. 1947  =  267 bp
ORF:  88 amino acids  =  9.2 kDa
ORF:  2 .. 382  =  381 bp
ORF:  127 amino acids  =  14.7 kDa
ORF:  1551 .. 2411  =  861 bp
ORF:  286 amino acids  =  31.6 kDa
ORF:  2619 .. 2972  =  354 bp
ORF:  117 amino acids  =  13.7 kDa  (no start codon)
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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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