No discussions found
Start your discussion
Share your thoughts or question with experts in your field
Start a discussion
Found 2 matching solutions for this experiment
pBYR2T-EGFP
Kenji Miura, Graduate School of Life and Environmental Sciences,
Upstream tips |
Protocol tips |
Downstream tips |
|
Briefly, the vectors described above and GFP_pICH18711 kindly provided by Dr. Victor Klimyuk (Icon Genetics GmbH) were transformed into A. tumefaciens GV3101. A. tumefaciens GV3101 harboring the binary vector was grown in L-broth media containing 10 mM MES (pH 5.6), 20 μM acetosyringone, 100 mg/L of kanamycin, 30 mg/L gentamycin, 30 mg/L of rifampin to the stationary phase at 28 °C. After centrifugation, A. tumefaciens was resuspended in the infiltration buffer (10 mM MgCl2, 10 mM MES (pH 5.6), 100 μM acetosyringone) to adjust OD600 = approximately 1. |
|
Protocol tips |
Briefly, the vectors described above and GFP_pICH18711 kindly provided by Dr. Victor Klimyuk (Icon Genetics GmbH) were transformed into A. tumefaciens GV3101. A. tumefaciens GV3101 harboring the binary vector was grown in L-broth media containing 10 mM MES (pH 5.6), 20 μM acetosyringone, 100 mg/L of kanamycin, 30 mg/L gentamycin, 30 mg/L of rifampin to the stationary phase at 28 °C. After centrifugation, A. tumefaciens was resuspended in the infiltration buffer (10 mM MgCl2, 10 mM MES (pH 5.6), 100 μM acetosyringone) to adjust OD600 = approximately 1. |
pJL TRBO-G
Sheng Wang, Key Laboratory of Ministry of Education for Protecti
Upstream tips |
Protocol tips |
Downstream tips |
|
A. tumefaciens GV3101 carrying either pJL TRBO-G or pCBNoX P19, were grown in 4 ml LB medium for 24 h at 28 °C and shaking at 250 rpm. The cultures were then transferred into 100 ml LB medium having 200 μM of acetosyringone (Sigma-Aldrich) grown overnight at 28 °C and shaking at 250 rpm. |
Cells were harvested by centrifugation at 3000 g for 10 min and re-suspended in infiltration buffer (pH 5.6, 10 mM MES, 10 mM MgCl2 and 200 μM acetosyringone) to achieve an OD600 of 0.4. The pJL TRBO-G expression vector was mixed in a 1:1 volume ratio with the gene-silencing suppressor (pCBNoX P19). The mixed Agrobacterium suspensions were incubated in the dark at room temperature for 2–3 h before infiltration. The incubated Agrobacterium suspensions were infiltrated into the abaxial surface of leaves using a 1-ml syringe without needle. The agroinfiltrated plants were incubated in the growth chamber for 4–8 days after which the leaves were harvested. |
Protocol tips |
A. tumefaciens GV3101 carrying either pJL TRBO-G or pCBNoX P19, were grown in 4 ml LB medium for 24 h at 28 °C and shaking at 250 rpm. The cultures were then transferred into 100 ml LB medium having 200 μM of acetosyringone (Sigma-Aldrich) grown overnight at 28 °C and shaking at 250 rpm. |
Downstream tips |
Cells were harvested by centrifugation at 3000 g for 10 min and re-suspended in infiltration buffer (pH 5.6, 10 mM MES, 10 mM MgCl2 and 200 μM acetosyringone) to achieve an OD600 of 0.4. The pJL TRBO-G expression vector was mixed in a 1:1 volume ratio with the gene-silencing suppressor (pCBNoX P19). The mixed Agrobacterium suspensions were incubated in the dark at room temperature for 2–3 h before infiltration. The incubated Agrobacterium suspensions were infiltrated into the abaxial surface of leaves using a 1-ml syringe without needle. The agroinfiltrated plants were incubated in the growth chamber for 4–8 days after which the leaves were harvested. |
Can't find the product you've used to perform this experiment? It would be great if you can help us by
Adding a product!