pHSG398

pUC-type bacterial cloning vector with a chloramphenicol resistance gene. The MCS is similar but reversed in pHSG396.

Sequence Author: TaKaRa

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AcuI (2073) AlwNI (1941) ApaLI (1839) PspFI (1833) BseYI (1829) HaeII (1773) BciVI (1728) BssSI - BssSαI (1698) DrdI (1633) AflIII - PciI (1525) TaqII (1427) BglI (1390) FspI (1380) PvuI (1361) EarI (1339) HindIII (1235) SphI (1233) BfuAI - BspMI (1230) PstI - SbfI (1227) HincII (1219) AccI (1218) SalI (1217) XbaI (1211) BamHI (1205) SmaI (1202) AvaI - BsoBI - KpnI - TspMI - XmaI (1200) Acc65I (1196) BanII - SacI (1194) Eco53kI (1192) EcoRI (1184) BsaAI (99) MslI (122) Bpu10I (179) TsoI (307) BspEI (402) BsrDI (425) AclI (493) BpmI (528) MscI (673) BtgI - NcoI - StyI (707) SspI (718) TatI (821) ScaI (823) BtsI - BtsαI (1048) pHSG398 2227 bp
AcuI  (2073)
1 site
C T G A A G ( N ) 14 N N G A C T T C ( N ) 14

Cleavage may be enhanced when more than one copy of the AcuI recognition sequence is present.
Sticky ends from different AcuI sites may not be compatible.
After cleavage, AcuI can remain bound to DNA and alter its electrophoretic mobility.
For full activity, add fresh S-adenosylmethionine (SAM).
AlwNI  (1941)
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.
ApaLI  (1839)
1 site
G T G C A C C A C G T G
PspFI  (1833)
1 site
C C C A G C G G G T C G
BseYI  (1829)
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.
HaeII  (1773)
1 site
R G C G C Y Y C G C G R
BciVI  (1728)
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.
BssSI  (1698)
1 site
C A C G A G G T G C T C
BssSαI  (1698)
1 site
C A C G A G G T G C T C
DrdI  (1633)
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.
AflIII  (1525)
1 site
A C R Y G T T G Y R C A

Sticky ends from different AflIII sites may not be compatible.
PciI  (1525)
1 site
A C A T G T T G T A C A

PciI is inhibited by nonionic detergents.
TaqII  (1427)
1 site
G A C C G A ( N ) 9 N N C T G G C T ( N ) 9

Sticky ends from different TaqII sites may not be compatible.
BglI  (1390)
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.
FspI  (1380)
1 site
T G C G C A A C G C G T
PvuI  (1361)
1 site
C G A T C G G C T A G C
EarI  (1339)
1 site
C T C T T C N G A G A A G N N N N

Cleavage may be enhanced when more than one copy of the EarI recognition sequence is present.
Sticky ends from different EarI sites may not be compatible.
HindIII  (1235)
1 site
A A G C T T T T C G A A
SphI  (1233)
1 site
G C A T G C C G T A C G
BfuAI  (1230)
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  (1230)
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.
PstI  (1227)
1 site
C T G C A G G A C G T C
SbfI  (1227)
1 site
C C T G C A G G G G A C G T C C
HincII  (1219)
1 site
G T Y R A C C A R Y T G
AccI  (1218)
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.
SalI  (1217)
1 site
G T C G A C C A G C T G
XbaI  (1211)
1 site
T C T A G A A G A T C T
BamHI  (1205)
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.
SmaI  (1202)
1 site
C C C G G G G G G C C C

SmaI can be used at 37°C for brief incubations.
AvaI  (1200)
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  (1200)
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.
KpnI  (1200)
1 site
G G T A C C C C A T G G
TspMI  (1200)
1 site
C C C G G G G G G C C C
XmaI  (1200)
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.
Acc65I  (1196)
1 site
G G T A C C C C A T G G
BanII  (1194)
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  (1194)
1 site
G A G C T C C T C G A G
Eco53kI  (1192)
1 site
G A G C T C C T C G A G
EcoRI  (1184)
1 site
G A A T T C C T T A A G
BsaAI  (99)
1 site
Y A C G T R R T G C A Y
MslI  (122)
1 site
C A Y N N N N R T G G T R N N N N Y A C
Bpu10I  (179)
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.
TsoI  (307)
1 site
T A R C C A ( N ) 9 N N A T Y G G T ( N ) 9

Sticky ends from different TsoI sites may not be compatible.
After cleavage, TsoI can remain bound to DNA and alter its electrophoretic mobility.
For full activity, add fresh S-adenosylmethionine (SAM).
BspEI  (402)
1 site
T C C G G A A G G C C T
BsrDI  (425)
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.
AclI  (493)
1 site
A A C G T T T T G C A A
BpmI  (528)
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.
MscI  (673)
1 site
T G G C C A A C C G G T
BtgI  (707)
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  (707)
1 site
C C A T G G G G T A C C
StyI  (707)
1 site
C C W W G G G G W W C C

Sticky ends from different StyI sites may not be compatible.
SspI  (718)
1 site
A A T A T T T T A T A A
TatI  (821)
1 site
W G T A C W W C A T G W
ScaI  (823)
1 site
A G T A C T T C A T G A
BtsI  (1048)
1 site
G C A G T G N N C G T C A C
BtsαI  (1048)
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.
CmR
193 .. 852  =  660 bp
219 amino acids  =  25.7 kDa
Product: chloramphenicol acetyltransferase
confers resistance to chloramphenicol
CmR
193 .. 852  =  660 bp
219 amino acids  =  25.7 kDa
Product: chloramphenicol acetyltransferase
confers resistance to chloramphenicol
ori
1586 .. 2174  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
ori
1586 .. 2174  =  589 bp
high-copy-number ColE1/pMB1/pBR322/pUC origin of replication
lacZα
1170 .. 1400  =  231 bp
76 amino acids  =  8.5 kDa
Product: LacZα fragment of β-galactosidase
lacZα
1170 .. 1400  =  231 bp
76 amino acids  =  8.5 kDa
Product: LacZα fragment of β-galactosidase
cat promoter
90 .. 192  =  103 bp
promoter of the E. coli cat gene
cat promoter
90 .. 192  =  103 bp
promoter of the E. coli cat gene
lac promoter
1096 .. 1126  =  31 bp
3 segments
   Segment 1:  -35  
   1096 .. 1101  =  6 bp
promoter for the E. coli lac operon
lac promoter
1096 .. 1126  =  31 bp
3 segments
   Segment 2:  
   1102 .. 1119  =  18 bp
promoter for the E. coli lac operon
lac promoter
1096 .. 1126  =  31 bp
3 segments
   Segment 3:  -10  
   1120 .. 1126  =  7 bp
promoter for the E. coli lac operon
lac promoter
1096 .. 1126  =  31 bp
3 segments
promoter for the E. coli lac operon
lac operator
1134 .. 1150  =  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
1134 .. 1150  =  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
1184 .. 1240  =  57 bp
pUC18/19 multiple cloning site
MCS
1184 .. 1240  =  57 bp
pUC18/19 multiple cloning site
M13 rev
1158 .. 1174  =  17 bp
common sequencing primer, one of multiple similar variants
M13 rev
1158 .. 1174  =  17 bp
common sequencing primer, one of multiple similar variants
M13 fwd
1244 .. 1260  =  17 bp
common sequencing primer, one of multiple similar variants
M13 fwd
1244 .. 1260  =  17 bp
common sequencing primer, one of multiple similar variants
ORF:  193 .. 852  =  660 bp
ORF:  219 amino acids  =  25.7 kDa
ORF:  1170 .. 1400  =  231 bp
ORF:  76 amino acids  =  8.5 kDa
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Download pHSG398.dna file

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