pCAMBIA1300

Agrobacterium binary vector for plant transformation, with hygromycin- and kanamycin-resistance genes.

Sequence Author: Cambia

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EcoRI (0) lac operator BstXI (8716) CaMV 35S promoter (enhanced) AatII (7875) ZraI (7873) AsiSI (7536) RsrII (7487) PspXI (6835) BclI * (6320) SacII (6317) PsiI (6189) Bpu10I (6044) EcoO109I - PpuMI (5905) BspHI (5863) BlpI (5713) SspI (5367) NsiI (5329) Eco53kI (8) BanII - SacI (10) Acc65I (12) KpnI (16) BamHI (21) XbaI (27) SalI (33) PstI - SbfI (43) HindIII (51) PmeI (264) BsaBI * (1715) PasI (1722) AclI (2316) BsiWI (3276) NheI (3392) BmtI (3396) BspDI * - ClaI * (3472) EcoNI (3705) BsaI (3795) MreI - SgrAI (4174) KasI (4177) NarI (4178) SfoI (4179) PluTI (4181) BstZ17I (4376) pCAMBIA1300 8959 bp
EcoRI  (0)
1 site
G A A T T C C T T A A G
BstXI  (8716)
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.
AatII  (7875)
1 site
G A C G T C C T G C A G
ZraI  (7873)
1 site
G A C G T C C T G C A G
AsiSI  (7536)
1 site
G C G A T C G C C G C T A G C G
RsrII  (7487)
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.
PspXI  (6835)
1 site
V C T C G A G B B G A G C T C V
BclI  (6320)
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.
SacII  (6317)
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.
PsiI  (6189)
1 site
T T A T A A A A T A T T
Bpu10I  (6044)
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.
EcoO109I  (5905)
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  (5905)
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.
BspHI  (5863)
1 site
T C A T G A A G T A C T
BlpI  (5713)
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.
SspI  (5367)
1 site
A A T A T T T T A T A A
NsiI  (5329)
1 site
A T G C A T T A C G T A
Eco53kI  (8)
1 site
G A G C T C C T C G A G
BanII  (10)
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  (10)
1 site
G A G C T C C T C G A G
Acc65I  (12)
1 site
G G T A C C C C A T G G
KpnI  (16)
1 site
G G T A C C C C A T G G
BamHI  (21)
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  (27)
1 site
T C T A G A A G A T C T
SalI  (33)
1 site
G T C G A C C A G C T G
PstI  (43)
1 site
C T G C A G G A C G T C
SbfI  (43)
1 site
C C T G C A G G G G A C G T C C
HindIII  (51)
1 site
A A G C T T T T C G A A
PmeI  (264)
1 site
G T T T A A A C C A A A T T T G
BsaBI  (1715)
1 site
G A T N N N N A T C C T A N N N N T A G
* Blocked by Dam methylation.
PasI  (1722)
1 site
C C C W G G G G G G W C C C

Sticky ends from different PasI sites may not be compatible.
AclI  (2316)
1 site
A A C G T T T T G C A A
BsiWI  (3276)
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.
NheI  (3392)
1 site
G C T A G C C G A T C G
BmtI  (3396)
1 site
G C T A G C C G A T C G
BspDI  (3472)
1 site
A T C G A T T A G C T A
* Blocked by Dam methylation.
ClaI  (3472)
1 site
A T C G A T T A G C T A
* Blocked by Dam methylation.
EcoNI  (3705)
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.
BsaI  (3795)
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.
MreI  (4174)
1 site
C G C C G G C G G C G G C C G C
SgrAI  (4174)
1 site
C R C C G G Y G G Y G G C C R C

Efficient cleavage requires at least two copies of the SgrAI recognition sequence.
KasI  (4177)
1 site
G G C G C C C C G C G G
NarI  (4178)
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  (4179)
1 site
G G C G C C C C G C G G
PluTI  (4181)
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.
BstZ17I  (4376)
1 site
G T A T A C C A T A T G
pVS1 RepA
2661 .. 3734  =  1074 bp
357 amino acids  =  39.9 kDa
Product: replication protein from Pseudomonas plasmid pVS1
pVS1 RepA
2661 .. 3734  =  1074 bp
357 amino acids  =  39.9 kDa
Product: replication protein from Pseudomonas plasmid pVS1
HygR
6874 .. 7899  =  1026 bp
341 amino acids  =  38.0 kDa
Product: hygromycin B phosphotransferase
confers resistance to hygromycin
HygR
6874 .. 7899  =  1026 bp
341 amino acids  =  38.0 kDa
Product: hygromycin B phosphotransferase
confers resistance to hygromycin
KanR
5339 .. 6133  =  795 bp
264 amino acids  =  31.0 kDa
Product: aminoglycoside phosphotransferase
confers resistance to kanamycin
KanR
5339 .. 6133  =  795 bp
264 amino acids  =  31.0 kDa
Product: aminoglycoside phosphotransferase
confers resistance to kanamycin
CaMV 35S promoter (enhanced)
7967 .. 8644  =  678 bp
cauliflower mosaic virus 35S promoter with a duplicated enhancer region
CaMV 35S promoter (enhanced)
7967 .. 8644  =  678 bp
cauliflower mosaic virus 35S promoter with a duplicated enhancer region
pVS1 StaA
1603 .. 2232  =  630 bp
209 amino acids  =  22.1 kDa
Product: stability protein from Pseudomonas plasmid pVS1
pVS1 StaA
1603 .. 2232  =  630 bp
209 amino acids  =  22.1 kDa
Product: stability protein from Pseudomonas plasmid pVS1
ori
4664 .. 5252  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
ori
4664 .. 5252  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
lacZα
8945 .. 219  =  234 bp
77 amino acids  =  8.6 kDa
Product: LacZα fragment of β-galactosidase
lacZα
8945 .. 219  =  234 bp
77 amino acids  =  8.6 kDa
Product: LacZα fragment of β-galactosidase
pVS1 oriV
3800 .. 3994  =  195 bp
origin of replication for the Pseudomonas plasmid pVS1 (Heeb et al., 2000)
pVS1 oriV
3800 .. 3994  =  195 bp
origin of replication for the Pseudomonas plasmid pVS1 (Heeb et al., 2000)
CaMV poly(A) signal
6660 .. 6834  =  175 bp
cauliflower mosaic virus polyadenylation signal
CaMV poly(A) signal
6660 .. 6834  =  175 bp
cauliflower mosaic virus polyadenylation signal
bom
4338 .. 4478  =  141 bp
basis of mobility region from pBR322
bom
4338 .. 4478  =  141 bp
basis of mobility region from pBR322
lac promoter
8871 .. 8901  =  31 bp
3 segments
   Segment 1:  -35  
   8871 .. 8876  =  6 bp
promoter for the E. coli lac operon
lac promoter
8871 .. 8901  =  31 bp
3 segments
   Segment 2:  
   8877 .. 8894  =  18 bp
promoter for the E. coli lac operon
lac promoter
8871 .. 8901  =  31 bp
3 segments
   Segment 3:  -10  
   8895 .. 8901  =  7 bp
promoter for the E. coli lac operon
lac promoter
8871 .. 8901  =  31 bp
3 segments
promoter for the E. coli lac operon
RB T-DNA repeat
279 .. 303  =  25 bp
right border repeat from nopaline C58 T-DNA
RB T-DNA repeat
279 .. 303  =  25 bp
right border repeat from nopaline C58 T-DNA
LB T-DNA repeat
6558 .. 6582  =  25 bp
left border repeat from nopaline C58 T-DNA
LB T-DNA repeat
6558 .. 6582  =  25 bp
left border repeat from nopaline C58 T-DNA
lac operator
8909 .. 8925  =  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
8909 .. 8925  =  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
8959 .. 56  =  57 bp
pUC18/19 multiple cloning site
MCS
8959 .. 56  =  57 bp
pUC18/19 multiple cloning site
M13 fwd
60 .. 76  =  17 bp
common sequencing primer, one of multiple similar variants
M13 fwd
60 .. 76  =  17 bp
common sequencing primer, one of multiple similar variants
M13 rev
8933 .. 8949  =  17 bp
common sequencing primer, one of multiple similar variants
M13 rev
8933 .. 8949  =  17 bp
common sequencing primer, one of multiple similar variants
ORF:  1603 .. 2232  =  630 bp
ORF:  209 amino acids  =  22.1 kDa
ORF:  6826 .. 7566  =  741 bp
ORF:  246 amino acids  =  27.0 kDa
ORF:  8945 .. 219  =  234 bp
ORF:  77 amino acids  =  8.6 kDa
ORF:  618 .. 1304  =  687 bp
ORF:  228 amino acids  =  25.1 kDa
ORF:  2559 .. 3734  =  1176 bp
ORF:  391 amino acids  =  43.9 kDa
ORF:  5472 .. 5702  =  231 bp
ORF:  76 amino acids  =  8.3 kDa
ORF:  650 .. 1000  =  351 bp
ORF:  116 amino acids  =  12.6 kDa
ORF:  2507 .. 2764  =  258 bp
ORF:  85 amino acids  =  9.6 kDa
ORF:  5339 .. 6133  =  795 bp
ORF:  264 amino acids  =  31.0 kDa
ORF:  1069 .. 1341  =  273 bp
ORF:  90 amino acids  =  9.9 kDa
ORF:  6874 .. 7899  =  1026 bp
ORF:  341 amino acids  =  38.0 kDa
ORF:  8071 .. 8388  =  318 bp
ORF:  105 amino acids  =  11.6 kDa
ORF:  8398 .. 8856  =  459 bp
ORF:  152 amino acids  =  16.9 kDa
ORF:  1341 .. 1655  =  315 bp
ORF:  104 amino acids  =  12.0 kDa
ORF:  2529 .. 3101  =  573 bp
ORF:  190 amino acids  =  20.6 kDa
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