mBaoJin

Bright and photostable monomeric green fluorescent protein derived from StayGold.
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No matches
600 400 200 End (702) AluI (693) PleI - MlyI (654) NmeAIII (653) BstUI (638) BsaJI (629) SfaNI (615) TfiI (594) BstXI (590) AlwNI (574) EarI (560) Cac8I (550) Hpy99I (526) TaiI (524) HpyCH4IV (521) MaeIII - Tsp45I (480) BsmI (478) BmrI (472) BpmI (431) AgeI BsrFI BsaWI (373) BciVI (322) BtgZI (317) PvuI - BsiEI (282) NciI - ScrFI (263) BssKI - StyD4I (261) AcuI (256) SspI (211) BbvI (187) BlsI (177) Fnu4HI (176) TseI - ApeKI (175) BsrGI (145) HpyCH4III (87) NlaIV (63) SwaI (45) BseRI (31) BsaI (9) Start (0) mBaoJin mBaoJin 702 bp
End  (702)
0 sites
AluI  (693)
1 site
A G C T T C G A
PleI  (654)
1 site
G A G T C ( N ) 4 C T C A G ( N ) 4 N

Efficient cleavage requires at least two copies of the PleI recognition sequence.
The 1-base overhangs produced by PleI may be hard to ligate.
Sticky ends from different PleI sites may not be compatible.
MlyI  (654)
1 site
G A G T C ( N ) 5 C T C A G ( N ) 5
NmeAIII  (653)
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).
BstUI  (638)
1 site
C G C G G C G C
BsaJI  (629)
1 site
C C N N G G G G N N C C

Sticky ends from different BsaJI sites may not be compatible.
SfaNI  (615)
1 site
G C A T C ( N ) 5 C G T A G ( N ) 5 ( N ) 4

Cleavage may be enhanced when more than one copy of the SfaNI recognition sequence is present.
Sticky ends from different SfaNI sites may not be compatible.
After cleavage, SfaNI can remain bound to DNA and alter its electrophoretic mobility.
Prolonged incubation with SfaNI may lead to degradation of the DNA.
TfiI  (594)
1 site
G A W T C C T W A G

Sticky ends from different TfiI sites may not be compatible.
After cleavage, TfiI can remain bound to DNA and alter its electrophoretic mobility.
BstXI  (590)
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.
AlwNI  (574)
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.
EarI  (560)
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.
Cac8I  (550)
1 site
G C N N G C C G N N C G
Hpy99I  (526)
1 site
C G W C G G C W G C

Sticky ends from different Hpy99I sites may not be compatible.
TaiI  (524)
1 site
A C G T T G C A
HpyCH4IV  (521)
1 site
A C G T T G C A
MaeIII  (480)
1 site
G T N A C C A N T G

Sticky ends from different MaeIII sites may not be compatible.
Tsp45I  (480)
1 site
G T S A C C A S T G

Sticky ends from different Tsp45I sites may not be compatible.
BsmI  (478)
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.
BmrI  (472)
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.
BpmI  (431)
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.
AgeI  (373)
1 site
A C C G G T T G G C C A
BsrFI  (373)
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.
BsaWI  (373)
1 site
W C C G G W W G G C C W

Cleavage may be enhanced when more than one copy of the BsaWI recognition sequence is present.
BciVI  (322)
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.
BtgZI  (317)
1 site
G C G A T G ( N ) 10 C G C T A C ( N ) 10 ( N ) 4

Sticky ends from different BtgZI sites may not be compatible.
After cleavage, BtgZI can remain bound to DNA and alter its electrophoretic mobility.
BtgZI is typically used at 60°C, but is 75% active at 37°C.
PvuI  (282)
1 site
C G A T C G G C T A G C
BsiEI  (282)
1 site
C G R Y C G G C Y R G C

Sticky ends from different BsiEI sites may not be compatible.
NciI  (263)
1 site
C C S G G G G S C C

The 1-base overhangs produced by NciI may be hard to ligate.
Sticky ends from different NciI sites may not be compatible.
ScrFI  (263)
1 site
C C N G G G G N C C

The 1-base overhangs produced by ScrFI may be hard to ligate.
Sticky ends from different ScrFI sites may not be compatible.
BssKI  (261)
1 site
C C N G G G G N C C

Sticky ends from different BssKI sites may not be compatible.
StyD4I  (261)
1 site
C C N G G G G N C C

Sticky ends from different StyD4I sites may not be compatible.
AcuI  (256)
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).
SspI  (211)
1 site
A A T A T T T T A T A A
BbvI  (187)
1 site
G C A G C ( N ) 8 C G T C G ( N ) 8 ( N ) 4

Efficient cleavage requires at least two copies of the BbvI recognition sequence.
Sticky ends from different BbvI sites may not be compatible.
BlsI  (177)
1 site
G C N G C C G N C G

The 1-base overhangs produced by BlsI may be hard to ligate.
Sticky ends from different BlsI sites may not be compatible.
Fnu4HI  (176)
1 site
G C N G C C G N C G

The 1-base overhangs produced by Fnu4HI may be hard to ligate.
Sticky ends from different Fnu4HI sites may not be compatible.
TseI  (175)
1 site
G C W G C C G W C G

Sticky ends from different TseI sites may not be compatible.
ApeKI  (175)
1 site
G C W G C C G W C G

Sticky ends from different ApeKI sites may not be compatible.
BsrGI  (145)
1 site
T G T A C A A C A T G T

BsrGI is typically used at 37°C, but is even more active at 60°C.
HpyCH4III  (87)
1 site
A C N G T T G N C A

The 1-base overhangs produced by HpyCH4III may be hard to ligate.
Sticky ends from different HpyCH4III sites may not be compatible.
NlaIV  (63)
1 site
G G N N C C C C N N G G
SwaI  (45)
1 site
A T T T A A A T T A A A T T T A

SwaI is typically used at 25°C, but is 50% active at 37°C.
BseRI  (31)
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.
BsaI  (9)
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.
Start  (0)
0 sites
mBaoJin
1 .. 702  =  702 bp
234 amino acids  =  26.6 kDa
Product: bright and photostable monomeric green fluorescent protein derived from StayGold (Zhang et al., 2024)
/vntifkey=21
mBaoJin
1 .. 702  =  702 bp
234 amino acids  =  26.6 kDa
Product: bright and photostable monomeric green fluorescent protein derived from StayGold (Zhang et al., 2024)
/vntifkey=21
ORF:  1 .. 702  =  702 bp
ORF:  234 amino acids  =  26.6 kDa
ORF:  386 .. 700  =  315 bp
ORF:  104 amino acids  =  12.4 kDa  (no start codon)
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Download mBaoJin.dna file

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Individual Sequences & Maps

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