Method for realizing in-vitro preservation of cattleya germplasm resources and recovering growth after preservation
An in vitro preservation and Cattleya technology, applied in the field of plant tissue culture, can solve the problems of large manpower and material resources, cross-contamination, genetic variation, etc., and achieve the effect of prolonging the storage time, strong regeneration ability, and stable genetic genes
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Embodiment 1
[0026] A method for in vitro preservation of Cattleya germplasm resources and recovery of growth after preservation, the specific steps are as follows:
[0027] (1) Peel the shoot tips from the newly grown pseudobulbs of Cattleya, and place them on the surface of the protocorm induction medium supplemented with 0.5 mg / L 6-benzyl adenine in VW medium to cultivate protocorms.
[0028] Among them, the peeling method of the stem tip is as follows: select a pseudobulb with a length of 5cm, wash the surface dust with tap water, peel off the outermost leaf, scrub with alcohol with a volume concentration of 75% for 3 seconds, and put it in a mass concentration of 0.1 % mercuric chloride solution for 20 minutes, rinsed with sterile water for 3 times, air-dried or blotted with filter paper to dry the surface water, and peeled off the shoot tips with a size of about 0.5 mm under a microscope.
[0029] Place the tip of the shoot on the surface of the protocorm induction medium in the test...
Embodiment 2
[0043] A method for in vitro preservation of Cattleya germplasm resources and recovery of growth after preservation, the specific steps are as follows:
[0044] (1) Peel the shoot tips from the newly grown pseudobulbs of Cattleya, and place them on the surface of the protocorm induction medium supplemented with 1 mg / L 6-benzyl adenine in VW medium to cultivate protocorms.
[0045] Among them, the peeling method of the stem tip is as follows: select a pseudobulb with a length of 7cm, wash the surface dust with tap water, peel off the two outermost leaves, scrub with alcohol with a volume concentration of 75% for 4 seconds, and put in a mass concentration of 0.1 % mercuric chloride solution for 20 minutes, rinsed with sterile water for 4 times, air-dried or blotted with filter paper to dry the surface water, and peeled off the shoot tips with a size of about 0.5 mm under a microscope.
[0046] Place the shoot tip on the surface of the protocorm induction medium in the test tube ...
Embodiment 3
[0058] A method for in vitro preservation of Cattleya germplasm resources and recovery of growth after preservation, the specific steps are as follows:
[0059] (1) Peel the shoot tips from the newly grown pseudobulbs of Cattleya, and place them on the surface of the protocorm induction medium supplemented with 0.8 mg / L 6-benzyl adenine in VW medium to cultivate protocorms.
[0060] Among them, the peeling method of the stem tip is as follows: select a pseudobulb with a length of 6cm, wash the surface dust with tap water, peel off the outermost leaf, scrub with alcohol with a volume concentration of 75% for 4 seconds, and put it in a mass concentration of 0.1 % mercuric chloride solution for 20 minutes, rinsed with sterile water for 3 times, air-dried or blotted with filter paper to dry the surface water, and peeled off the shoot tips with a size of about 0.5mm under a microscope.
[0061] Place the shoot tip on the surface of the protocorm induction medium in the test tube or...
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