pCTAP-B

Vector for expressing proteins C-terminally tagged with streptavidin- and calmodulin-binding peptides. For other reading frames, use pCTAP-A or pCTAP-C.

Sequence Author: Agilent Technologies

|Download SnapGene Viewer
Explore Over 2.7k Plasmids: Mammalian Expression Vectors | More Plasmid Sets
No matches
PciI (4481) ApaLI (4167) BsaI (3552) PfoI (3338) BstBI (3245) RsrII (3079) BsrDI (2796) PflFI - Tth111I (2681) MscI (2645) PluTI (2566) SfoI (2564) NarI (2563) KasI (2562) StuI (2384) BseRI (2381) SfiI (2338) CMV enhancer NdeI (240) SnaBI (346) NheI (597) BmtI (601) Eco53kI (653) SacI (655) AleI (661) SacII (662) BstXI (663) NotI (668) SrfI (682) BamHI (687) PstI (703) EcoRI (705) EcoRV (713) HindIII (717) SalI (732) AccI (733) PaeR7I - PspXI - XhoI (739) BbsI (778) PmlI (798) BspEI (898) BsmBI - Esp3I (939) PspOMI (984) ApaI (988) T7 promoter PvuI (1066) BclI * (1220) MfeI (1313) HpaI (1326) BtsI - BtsαI (1402) MluI (1449) SV40 promoter pCTAP-B 4533 bp
PciI  (4481)
1 site
A C A T G T T G T A C A

PciI is inhibited by nonionic detergents.
ApaLI  (4167)
1 site
G T G C A C C A C G T G
BsaI  (3552)
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.
PfoI  (3338)
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.
BstBI  (3245)
1 site
T T C G A A A A G C T T
RsrII  (3079)
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.
BsrDI  (2796)
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.
PflFI  (2681)
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  (2681)
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.
MscI  (2645)
1 site
T G G C C A A C C G G T
PluTI  (2566)
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.
SfoI  (2564)
1 site
G G C G C C C C G C G G
NarI  (2563)
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.
KasI  (2562)
1 site
G G C G C C C C G C G G
StuI  (2384)
1 site
A G G C C T T C C G G A
BseRI  (2381)
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.
SfiI  (2338)
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.
NdeI  (240)
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.
SnaBI  (346)
1 site
T A C G T A A T G C A T
NheI  (597)
1 site
G C T A G C C G A T C G
BmtI  (601)
1 site
G C T A G C C G A T C G
Eco53kI  (653)
1 site
G A G C T C C T C G A G
SacI  (655)
1 site
G A G C T C C T C G A G
AleI  (661)
1 site
C A C N N N N G T G G T G N N N N C A C
SacII  (662)
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.
BstXI  (663)
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.
NotI  (668)
1 site
G C G G C C G C C G C C G G C G
SrfI  (682)
1 site
G C C C G G G C C G G G C C C G
BamHI  (687)
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.
PstI  (703)
1 site
C T G C A G G A C G T C
EcoRI  (705)
1 site
G A A T T C C T T A A G
EcoRV  (713)
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.
HindIII  (717)
1 site
A A G C T T T T C G A A
SalI  (732)
1 site
G T C G A C C A G C T G
AccI  (733)
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.
PaeR7I  (739)
1 site
C T C G A G G A G C T C

PaeR7I does not recognize the sequence CTCTCGAG.
PspXI  (739)
1 site
V C T C G A G B B G A G C T C V
XhoI  (739)
1 site
C T C G A G G A G C T C
BbsI  (778)
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.
PmlI  (798)
1 site
C A C G T G G T G C A C
BspEI  (898)
1 site
T C C G G A A G G C C T
BsmBI  (939)
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  (939)
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.
PspOMI  (984)
1 site
G G G C C C C C C G G G
ApaI  (988)
1 site
G G G C C C C C C G G G

ApaI can be used between 25°C and 37°C.
PvuI  (1066)
1 site
C G A T C G G C T A G C
BclI  (1220)
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.
MfeI  (1313)
1 site
C A A T T G G T T A A C
HpaI  (1326)
1 site
G T T A A C C A A T T G
BtsI  (1402)
1 site
G C A G T G N N C G T C A C
BtsαI  (1402)
1 site
G C A G T G N N C G T C A C

Sticky ends from different BtsαI sites may not be compatible.
MluI  (1449)
1 site
A C G C G T T G C G C A
NeoR/KanR
2435 .. 3229  =  795 bp
264 amino acids  =  29.0 kDa
Product: aminoglycoside phosphotransferase from Tn5
confers resistance to neomycin, kanamycin, and G418 (Geneticin)
NeoR/KanR
2435 .. 3229  =  795 bp
264 amino acids  =  29.0 kDa
Product: aminoglycoside phosphotransferase from Tn5
confers resistance to neomycin, kanamycin, and G418 (Geneticin)
ori
3837 .. 4425  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
ori
3837 .. 4425  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
f1 ori
1455 .. 1910  =  456 bp
f1 bacteriophage origin of replication; arrow indicates direction of (+) strand synthesis
f1 ori
1455 .. 1910  =  456 bp
f1 bacteriophage origin of replication; arrow indicates direction of (+) strand synthesis
SV40 promoter
2043 .. 2400  =  358 bp
SV40 enhancer and early promoter
SV40 promoter
2043 .. 2400  =  358 bp
SV40 enhancer and early promoter
CMV enhancer
66 .. 370  =  305 bp
human cytomegalovirus immediate early enhancer
CMV enhancer
66 .. 370  =  305 bp
human cytomegalovirus immediate early enhancer
SBP
763 .. 876  =  114 bp
38 amino acids  =  4.3 kDa
Product: streptavidin-binding peptide
selected from a peptide library; binds streptavidin with nanomolar affinity
SBP
763 .. 876  =  114 bp
38 amino acids  =  4.3 kDa
Product: streptavidin-binding peptide
selected from a peptide library; binds streptavidin with nanomolar affinity
CBP
904 .. 981  =  78 bp
26 amino acids  =  3.0 kDa
Product: calmodulin-binding peptide
derived from skeletal muscle myosin light chain kinase; binds calmodulin with nanomolar affinity in the presence of calcium
CBP
904 .. 981  =  78 bp
26 amino acids  =  3.0 kDa
Product: calmodulin-binding peptide
derived from skeletal muscle myosin light chain kinase; binds calmodulin with nanomolar affinity in the presence of calcium
CMV promoter
371 .. 574  =  204 bp
human cytomegalovirus (CMV) immediate early promoter
CMV promoter
371 .. 574  =  204 bp
human cytomegalovirus (CMV) immediate early promoter
SV40 poly(A) signal
1327 .. 1448  =  122 bp
SV40 polyadenylation signal
SV40 poly(A) signal
1327 .. 1448  =  122 bp
SV40 polyadenylation signal
AmpR promoter
1937 .. 2039  =  103 bp
AmpR promoter
1937 .. 2039  =  103 bp
MCS
651 .. 744  =  94 bp
multiple cloning site
MCS
651 .. 744  =  94 bp
multiple cloning site
HSV TK poly(A) signal
3461 .. 3508  =  48 bp
herpesvirus thymidine kinase polyadenylation signal
HSV TK poly(A) signal
3461 .. 3508  =  48 bp
herpesvirus thymidine kinase polyadenylation signal
T3 promoter
620 .. 638  =  19 bp
promoter for bacteriophage T3 RNA polymerase
T3 promoter
620 .. 638  =  19 bp
promoter for bacteriophage T3 RNA polymerase
T7 promoter
1035 .. 1053  =  19 bp
promoter for bacteriophage T7 RNA polymerase
T7 promoter
1035 .. 1053  =  19 bp
promoter for bacteriophage T7 RNA polymerase
stop codons
997 .. 1007  =  11 bp
stop codons in all three reading frames
stop codons
997 .. 1007  =  11 bp
stop codons in all three reading frames
ORF:  3250 .. 3699  =  450 bp
ORF:  149 amino acids  =  16.3 kDa
ORF:  2435 .. 3229  =  795 bp
ORF:  264 amino acids  =  29.0 kDa
ORF:  2607 .. 2993  =  387 bp
ORF:  128 amino acids  =  14.6 kDa
ORF:  453 .. 764  =  312 bp
ORF:  103 amino acids  =  11.0 kDa
ORF:  2744 .. 3280  =  537 bp
ORF:  178 amino acids  =  19.9 kDa
ORF:  3455 .. 3688  =  234 bp
ORF:  77 amino acids  =  8.6 kDa
Click here to try SnapGene

Download pCTAP-B.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

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

Individual Sequences & Maps

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.