Method of potato virus eradication
A potato virus removal technology, applied in horticultural methods, botanical equipment and methods, plant preservation, etc., can solve the problem of unfavorable survival of shoot tips and regeneration of differentiated plants, low plant survival rate and virus-free rate, and difficulty in cutting The stem tip and other problems can be solved, and the effect of saving manpower and financial resources, less difficult operation and strong frost resistance
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Embodiment 1
[0013] This embodiment is to test the "Zao Dabai" potato variety. The specific operation method is: select potato materials, carry out multiplication, and then carry out virus detection on the materials, and the method used for detection is the RT-PCR method; then establish a single bud Line materials, the established single-bud line materials are propagated and subcultured, and the materials confirmed to carry the virus are propagated for cryopreservation. The subculture medium is selected: MS basic medium + 0.2mol L -1 6-BA+0.03mol L -1 IAA was cultured for proliferation, the pH of the medium was 5.8, the temperature of the culture room was 22 °C, and the light intensity was 40 μmol m -2 ·s -1 , the light time is 12h·d -1 ; After a certain amount of material has been multiplied, cryopreservation is carried out, that is, the vitrification method is adopted, exercised at a low temperature of 4°C for 6 days, and then pre-cultured in a medium supplemented with dimethyl sulfoxi...
Embodiment 2
[0015] This embodiment is to test "Zhengshu No. 5" potato varieties. The specific operation method is: select potato materials, carry out multiplication, and then carry out virus detection to the materials, and the method used for detection is the RT-PCR method; then establish For single-bud material, the established single-bud material is propagated and subcultured, and the virus-carrying material is confirmed to be multiplied for cryopreservation. The subculture medium is selected: MS basic medium + 0.2mol L -1 6-BA+0.03mol L -1 IAA was cultured for proliferation, the pH of the medium was 5.8, the temperature of the culture room was 23 °C, and the light intensity was 38 μmol m -2 ·s -1 , the light time is 13h·d -1 ; When the material is multiplied to a certain amount, cryopreservation is carried out, that is, the vitrification method is adopted, exercised at a low temperature of 3°C for 7 days, and then placed in a medium supplemented with dimethyl sulfoxide (DMSO) and ace...
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