Rapid propagation method for botrypus lanuginosus suspension cell
A technology of suspended cells and shaded ferns, applied in the field of plants, achieves the effects of fast growth, simple operation and low energy consumption
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Embodiment 1
[0009] Take the leaves of Pseudomonas tomentosa, soak them in bleaching powder for 3 minutes, remove surface stains and hairs with a brush, wash them with running water for 30 minutes, treat them with mercuric chloride on an ultra-clean workbench for 15 minutes, rinse them with sterile water 5-7 times, and disinfect them Grind the treated leaves of F. tomentosa in a glass homogenizer to make them broken, and then filter the broken tissue with a stainless steel mesh with a pore size of 200 mesh to remove large cell clusters or tissue pieces. The screened broken tissue is inserted into the culture medium Formula is B 5 Suspension cell culture in +NAA0.1mg / L+6-BA1mg / l+200mg / L yeast extract medium, add sucrose 30g / L, pH5-6, light 2000lx, temperature 23℃, inoculate 80mL per 250ml Erlenmeyer flask Liquid, using horizontal oscillation, speed 100-150r / min, amplitude 2-4cm, culture suspension cell liquid for a period of time to remove dead cells and cell debris, insert 2mg / L cerium nit...
Embodiment 2
[0011] Take the leaves of Pseudomonas tomentosa, soak them in bleaching powder for 3 minutes, remove surface stains and hairs with a brush, wash them with running water for 30 minutes, treat them with mercuric chloride on an ultra-clean workbench for 15 minutes, rinse them with sterile water 5-7 times, and disinfect them Grind the treated leaves of F. tomentosa in a glass homogenizer to make them broken, and then filter the broken tissue with a stainless steel mesh with a pore size of 200 mesh to remove large cell clusters or tissue pieces. The screened broken tissue is inserted into the culture medium Formula is B 5 Suspension cell culture in +NAA0.2mg / L+6-BA2mg / l+200mg / L yeast extract medium, add sucrose 30g / L, pH5-6, light 2000lx, temperature 23℃, inoculate 80mL per 250ml Erlenmeyer flask Liquid, using horizontal oscillation, speed 100-150r / min, amplitude 2-4cm, culture suspension cell liquid for a period of time to remove dead cells and cell debris, insert 5mg / L cerium nit...
Embodiment 3
[0013] Take the leaves of Pseudomonas tomentosa, soak them in bleaching powder for 3 minutes, remove surface stains and hairs with a brush, wash them with running water for 30 minutes, treat them with mercuric chloride on an ultra-clean workbench for 15 minutes, rinse them with sterile water 5-7 times, and disinfect them Grind the treated leaves of F. tomentosa in a glass homogenizer to make them broken, and then filter the broken tissue with a stainless steel mesh with a pore size of 200 mesh to remove large cell clusters or tissue pieces. The screened broken tissue is inserted into the culture medium Formula is B 5 Suspension cell culture in +NAA0.1mg / L+6-BA2mg / l+200mg / L yeast extract medium, add sucrose 30g / L, pH5-6, light 2000lx, temperature 23℃, inoculate 80mL per 250ml Erlenmeyer flask Liquid, using horizontal oscillation, speed 100-150r / min, amplitude 2-4cm, culture suspension cell liquid for a period of time to remove dead cells and cell debris, insert 5mg / L cerium nit...
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