Search result for '144 '.
Viewing records 1 to 3 of 3 hits.
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N2105633
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Name: pART7::d-FlincG vector |
Price:
£11.00
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Donor
- University of Bristol Jean Charles Isner
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Stock type: individual line
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Material type: plasmid dna
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Description
The d-FlincG (fluorescence indicator of cGMP) biosensor is based on cpEGFP (circular permutated EGFP), C-terminally fused to the in-tandem regulatory domain of type-I PKG. The N-terminal dimerization domain of the PKG was removed, resulting in d-FlincG with an increased dynamic range (Nausch et al., 2008). In order to express d-FlincG in plants, PKG was subcloned in pART7 under the control of the 35S constitutive promoter. pRSET-A::d-FlincG was kindly provided by Drs Naush and Dostmann (College of Medicine, Department of Pharmacology, University of Vermont) carrying a copy of PKGI with cpEGFP inserted in the middle, and carrying a stop codon. pRSET-A:: d-FlincG was cut with BamHI, and Klenow was applied in the presence of dGTP and dATP. pART7 was cut with XhoI, and Klenow was applied in the presence of dTTP and dCTP. The pART7 and pRSET-A::d-FlincG were subsequently cut with EcoRI, and the released fragments of interest were ligated, with XhoI and BamHI providing compatible cohesive ends. The catalytic subunit of PKGI, which is not translated, was removed by cutting pART7::d-FlincG with the two compatible end enzymes AvrII and XbaI, followed by self-ligation. The NotI fragment of pART7::d-FlincG containing the 35S::d-FlincG construct was subcloned in pGREEN 0229. Three-week-old Arabidopsis plants were transformed using the flower-dipping method according to Clough and Bent (1998). Seeds of these plants were collected and grown on soil for 10 days, and were treated with the herbicide BASTA 7 . After 1 week, BASTA -resistant seedlingswere selected and screened for their GFP expression.
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Phenotype
pART7::delta-Flinc
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N2105634
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Name: pART7::d-FlincG vector |
Price:
£11.00
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Donor
- University of Bristol Jean Charles Isner
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Stock type: individual line
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Material type: plasmid dna
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Description
The d-FlincG (fluorescence indicator of cGMP) biosensor is based on cpEGFP (circular permutated EGFP), C-terminally fused to the in-tandem regulatory domain of type-I PKG. The N-terminal dimerization domain of the PKG was removed, resulting in d-FlincG with an increased dynamic range (Nausch et al., 2008). In order to express d-FlincG in plants, PKG was subcloned in pART7 under the control of the 35S constitutive promoter. pRSET-A::d-FlincG was kindly provided by Drs Naush and Dostmann (College of Medicine, Department of Pharmacology, University of Vermont) carrying a copy of PKGI with cpEGFP inserted in the middle, and carrying a stop codon. pRSET-A:: d-FlincG was cut with BamHI, and Klenow was applied in the presence of dGTP and dATP. pART7 was cut with XhoI, and Klenow was applied in the presence of dTTP and dCTP. The pART7 and pRSET-A::d-FlincG were subsequently cut with EcoRI, and the released fragments of interest were ligated, with XhoI and BamHI providing compatible cohesive ends. The catalytic subunit of PKGI, which is not translated, was removed by cutting pART7::d-FlincG with the two compatible end enzymes AvrII and XbaI, followed by self-ligation. The NotI fragment of pART7::d-FlincG containing the 35S::d-FlincG construct was subcloned in pGREEN 0229. Three-week-old Arabidopsis plants were transformed using the flower-dipping method according to Clough and Bent (1998). Seeds of these plants were collected and grown on soil for 10 days, and were treated with the herbicide BASTA 7 . After 1 week, BASTA -resistant seedlingswere selected and screened for their GFP expression.
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Phenotype
pGREEN0229::delta-Flinc
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N2105635
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Name: Delta-FlincG |
Price:
£11.00
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Donor
- University of Bristol Jean Charles Isner
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Stock type: individual line
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Material type: seed
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Description
The d-FlincG (fluorescence indicator of cGMP) biosensor is based on cpEGFP (circular permutated EGFP), C-terminally fused to the in-tandem regulatory domain of type-I PKG. The N-terminal dimerization domain of the PKG was removed, resulting in d-FlincG with an increased dynamic range (Nausch et al., 2008). In order to express d-FlincG in plants, PKG was subcloned in pART7 under the control of the 35S constitutive promoter. pRSET-A::d-FlincG was kindly provided by Drs Naush and Dostmann (College of Medicine, Department of Pharmacology, University of Vermont) carrying a copy of PKGI with cpEGFP inserted in the middle, and carrying a stop codon. pRSET-A:: d-FlincG was cut with BamHI, and Klenow was applied in the presence of dGTP and dATP. pART7 was cut with XhoI, and Klenow was applied in the presence of dTTP and dCTP. The pART7 and 6pRSET-A::d-FlincG were subsequently cut with EcoRI, and the released fragments of interest were ligated, with XhoI and BamHI providing compatible cohesive ends. The catalytic subunit of PKGI, which is not translated, was removed by cutting pART7::d-FlincG with the two compatible end enzymes AvrII and XbaI, followed by self-ligation. The NotI fragment of pART7::d-FlincG containing the 35S::d-FlincG construct was subcloned in pGREEN 0229. Three-week-old Arabidopsis plants were transformed using the flower-dipping method according to Clough and Bent (1998). Seeds of these plants were collected and grown on soil for 10 days, and were treated with the herbicide BASTA 7 . After 1 week, BASTA -resistant seedlings were selected and screened for their GFP expression.
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