pMCS-Red Firefly Luc

Intracellular red firefly luciferase vector for cloning a transcriptional regulatory element.

Sequence Author: Thermo Fisher (Pierce)

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HomePlasmidsLuciferase VectorspMCS-Red Firefly Luc
SpeI (1) BfuAI - BspMI - PaqCI (5947) EcoRV (5653) AflII (5300) DrdI (4967) MauBI (4371) NruI (4298) ScaI (3854) PvuI (3744) FspI (3596) AfeI (3424) SalI (3264) BstZ17I (3259) BsmI (3207) Acc65I (13) KpnI (17) Eco53kI (21) MCS SacI (23) PaeR7I - XhoI (25) HindIII (31) BamHI (37) BsrDI (170) BglII (374) PflMI * (543) KflI - PpuMI (723) SbfI (887) MreI (1453) NotI (1700) SV40 promoter AvrII (2269) TspMI - XmaI (2290) SmaI (2292) BsiWI (2454) RsrII (2514) BstEII (2532) SacII (2612) BsmBI - Esp3I (2790) DraIII (2969) pMCS-Red Firefly Luc 5977 bp
SpeI  (1)
1 site		 A C T A G T T G A T C A
BfuAI  (5947)
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  (5947)
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.
PaqCI  (5947)
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.
EcoRV  (5653)
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.
AflII  (5300)
1 site		 C T T A A G G A A T T C
DrdI  (4967)
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.
MauBI  (4371)
1 site		 C G C G C G C G G C G C G C G C
NruI  (4298)
1 site		 T C G C G A A G C G C T
ScaI  (3854)
1 site		 A G T A C T T C A T G A
PvuI  (3744)
1 site		 C G A T C G G C T A G C
FspI  (3596)
1 site		 T G C G C A A C G C G T
AfeI  (3424)
1 site		 A G C G C T T C G C G A
SalI  (3264)
1 site		 G T C G A C C A G C T G
BstZ17I  (3259)
1 site		 G T A T A C C A T A T G
BsmI  (3207)
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.
Acc65I  (13)
1 site		 G G T A C C C C A T G G
KpnI  (17)
1 site		 G G T A C C C C A T G G
Eco53kI  (21)
1 site		 G A G C T C C T C G A G
SacI  (23)
1 site		 G A G C T C C T C G A G
PaeR7I  (25)
1 site		 C T C G A G G A G C T C
PaeR7I does not recognize the sequence CTCTCGAG.
XhoI  (25)
1 site		 C T C G A G G A G C T C
HindIII  (31)
1 site		 A A G C T T T T C G A A
BamHI  (37)
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.
BsrDI  (170)
1 site		 G C A A T G N N C G T T A C
Sticky ends from different BsrDI sites may not be compatible.
BglII  (374)
1 site		 A G A T C T T C T A G A
PflMI  (543)
1 site		 C C A N N N N N T G G G G T N N N N N A C C
* Blocked by Dcm methylation.
Sticky ends from different PflMI sites may not be compatible.
KflI  (723)
1 site		 G G G W C C C C C C W G G G
Sticky ends from different KflI sites may not be compatible.
PpuMI  (723)
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.
SbfI  (887)
1 site		 C C T G C A G G G G A C G T C C
MreI  (1453)
1 site		 C G C C G G C G G C G G C C G C
NotI  (1700)
1 site		 G C G G C C G C C G C C G G C G
AvrII  (2269)
1 site		 C C T A G G G G A T C C
TspMI  (2290)
1 site		 C C C G G G G G G C C C
XmaI  (2290)
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  (2292)
1 site		 C C C G G G G G G C C C
SmaI can be used at 37°C for brief incubations.
BsiWI  (2454)
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.
RsrII  (2514)
1 site		 C G G W C C G G C C W G G C
Efficient cleavage requires at least two copies of the RsrII recognition sequence.
Sticky ends from different RsrII sites may not be compatible.
For full activity, add fresh DTT.
BstEII  (2532)
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.
SacII  (2612)
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.
BsmBI  (2790)
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  (2790)
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.
DraIII  (2969)
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.
Red Firefly Luciferase
49 .. 1695  =  1647 bp
548 amino acids  =  60.1 kDa
Product: intracellular red firefly luciferase
human codon-optimized
Red Firefly Luciferase
49 .. 1695  =  1647 bp
548 amino acids  =  60.1 kDa
Product: intracellular red firefly luciferase
human codon-optimized
AmpR
3301 .. 4161  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 2:  
   3301 .. 4092  =  792 bp
   263 amino acids  =  28.9 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
3301 .. 4161  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
   Segment 1:  signal sequence  
   4093 .. 4161  =  69 bp
   23 amino acids  =  2.6 kDa
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
AmpR
3301 .. 4161  =  861 bp
286 amino acids  =  31.6 kDa
2 segments
Product: β-lactamase
confers resistance to ampicillin, carbenicillin, and related antibiotics
PuroR
2398 .. 2997  =  600 bp
199 amino acids  =  21.5 kDa
Product: puromycin N-acetyltransferase
confers resistance to puromycin
PuroR
2398 .. 2997  =  600 bp
199 amino acids  =  21.5 kDa
Product: puromycin N-acetyltransferase
confers resistance to puromycin
ori
4425 .. 5013  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
ori
4425 .. 5013  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
SV40 promoter
1955 .. 2284  =  330 bp
SV40 enhancer and early promoter
SV40 promoter
1955 .. 2284  =  330 bp
SV40 enhancer and early promoter
SV40 poly(A) signal
3127 .. 3248  =  122 bp
SV40 polyadenylation signal
SV40 poly(A) signal
3127 .. 3248  =  122 bp
SV40 polyadenylation signal
bGH poly(A) signal
1721 .. 1832  =  112 bp
bovine growth hormone polyadenylation signal
bGH poly(A) signal
1721 .. 1832  =  112 bp
bovine growth hormone polyadenylation signal
pause site
5886 .. 5977  =  92 bp
RNA polymerase II transcriptional pause signal from the human α2 globin gene
pause site
5886 .. 5977  =  92 bp
RNA polymerase II transcriptional pause signal from the human α2 globin gene
EM7 promoter
2332 .. 2379  =  48 bp
synthetic bacterial promoter
EM7 promoter
2332 .. 2379  =  48 bp
synthetic bacterial promoter
MCS
1 .. 42  =  42 bp
multiple cloning site
MCS
1 .. 42  =  42 bp
multiple cloning site
lac operator
5755 .. 5771  =  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
5755 .. 5771  =  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).
SV40 ori
2135 .. 2270  =  136 bp
SV40 origin of replication
SV40 ori
2135 .. 2270  =  136 bp
SV40 origin of replication
ORF:  49 .. 1695  =  1647 bp
ORF:  548 amino acids  =  60.1 kDa
ORF:  2398 .. 2997  =  600 bp
ORF:  199 amino acids  =  21.5 kDa
ORF:  3431 .. 3697  =  267 bp
ORF:  88 amino acids  =  9.3 kDa
ORF:  2558 .. 2884  =  327 bp
ORF:  108 amino acids  =  12.0 kDa
ORF:  3301 .. 4161  =  861 bp
ORF:  286 amino acids  =  31.6 kDa
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phRL-SV40
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pGL4.33[luc2P SRE Hygro]
phRL-TK
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pGL4.34[luc2P SRF-RE Hygro]
phRL-TK(Int-)
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pCMV-Gaussia Luc
pGL4.35[luc2P 9XGAL4UAS Hygro]
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pCMV-Gaussia-Dura Luc
pGL4.36[luc2P MMTV Hygro]
pLVX-MetLuc Control
pSF-CMV-Ub-FLuc AscI
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pGL4.37[luc2P ARE Hygro]
pLVX-MetLuc Reporter
pSF-CMV-Ub-RLuc AscI
pCMV-Green Renilla Luc
pGL4.38[luc2P p53 RE Hygro]
pMCS-Cypridina Luc
pSF-CMVe-FLuc
pCMV-Red Firefly Luc
pGL4.39[luc2P ATF6 RE Hygro]
pMCS-Gaussia Luc
pSF-CMVe-RLuc
pCRE-MetLuc2-Reporter
pGL4.40[luc2P MRE Hygro]
pMCS-Gaussia-Dura Luc
pSF-MinProm-FLuc
pFN26A (BIND) hRluc-neo Flexi Vector
pGL4.41[luc2P HSE Hygro]
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pSF-MinProm-RLuc
pGEM-luc
pGL4.42[luc2P HRE Hygro]
pMCS-Red Firefly Luc
pSF-pA-CMVe-FLuc
pGL2-Basic
pGL4.43[luc2P XRE Hygro]
pMetLuc-Mem Control
pSF-pA-CMVe-RLuc
pGL2-Control
pGL4.44[luc2P AP1 RE Hygro]
pMetLuc-Mem Reporter
pSF-pA-MinProm-FLuc
pGL2-Enhancer
pGL4.45[luc2P ISRE Hygro]
pMetLuc2-Control
pSF-pA-MinProm-RLuc
pGL2-Promoter
pGL4.47[luc2P SIE Hygro]
pMetLuc2-Reporter
pSF-pA-PromMCS-FLuc
pGL3-Basic
pGL4.48[luc2P SBE Hygro]
pmirGLO
pSF-pA-PromMCS-RLuc
pGL3-Control
pGL4.49[luc2P TCF-LEF RE Hygro]
pMirTarget
pSF-PromMCS-FLuc
pGL3-Enhancer
pGL4.50[luc2 CMV Hygro]
pNFkB-MetLuc2-Reporter
pSF-PromMCS-RLuc
pGL3-Promoter
pGL4.51[luc2 CMV Neo]
pNL1.1.CMV[Nluc CMV]
pSF-RecA-FLuc
pGL4.10[luc2]
pGL4.52[luc2P STAT5 RE Hygro]
pNL1.1[Nluc]
pSP-luc+NF
pGL4.11[luc2P]
pGL4.70[hRluc]
pNL1.2[NlucP]
pSV40-CLuc
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pGL4.71[hRlucP]
pNL1.3.CMV[secNluc CMV]
pSV40-GLuc
pGL4.13[luc2 SV40]
pGL4.72[hRlucCP]
pNL1.3[secNluc]
pTK-CLuc
pGL4.14[luc2 Hygro]
pGL4.73[hRluc SV40]
pNL2.1[Nluc Hygro]
pTK-Cypridina Luc
pGL4.15[luc2P Hygro]
pGL4.74[hRluc TK]
pNL2.2[NlucP Hygro]
pTK-Gaussia Luc
pGL4.16[luc2CP Hygro]
pGL4.75[hRluc CMV]
pNL2.3[secNluc Hygro]
pTK-Gaussia-Dura Luc
pGL4.17[luc2 Neo]
pGL4.76[hRluc Hygro]
pNL3.1[Nluc minP]
pTK-GLuc
pGL4.18[luc2P Neo]
pGL4.77[hRlucP Hygro]
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pTK-Green Renilla Luc
pGL4.19[luc2CP Neo]
pGL4.78[hRlucCP Hygro]
pNL3.2[NlucP minP]
pTK-Red Firefly Luc
pGL4.20[luc2 Puro]
pGL4.79[hRluc Neo]
pNL3.3[secNluc minP]
pXPG
pGL4.21[luc2P Puro]
pGL4.80[hRlucP Neo]
pRL-CMV

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