Method for detecting morchella mycelium nucleus concentration through nucleus staining
A technology of hickory chick and cell nucleus, which is applied in the field of nuclei staining and detection of hickory chick mycelial nuclei concentration, and can solve the problem of no morel mycelial cell apoptosis
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Embodiment 1
[0030] The method for nuclear staining provided by the invention to detect hickory chick hyphae nuclei enrichment comprises the following steps:
[0031] A) hickory chick mycelia culture, the hickory chick described in the present embodiment is Liumei hickory chick, earlier uses puncher to be covered with Liumei hickory chick mycelium and is positioned at the PDA medium i.e. potato in the dish The edge place of glucose agar medium is perforated, specifically: around the edge position of PDA medium, it is preferred to punch several holes with a diameter of 6mm in an equidistant interval state, then inoculate respectively to the center of the PDA medium plate, and then in the plate Insert four coverslips with the same distance from the center of the petri dish obliquely on the PDA medium inside, and incubate at a constant temperature of 18°C for 100 hours, so that the mycelia of Morchella chinensis will be covered with the coverslips;
[0032] B) for the treatment of the mycel...
Embodiment 2
[0038] The method for nuclear staining provided by the invention to detect hickory chick hyphae nuclei enrichment comprises the following steps:
[0039] A) hickory chick mycelia culture, the hickory chick described in the present embodiment is Liumei hickory chick, earlier uses puncher to be covered with Liumei hickory chick mycelium and is positioned at the PDA medium i.e. potato in the dish Perforate at the edge place of glucose agar medium, specifically: around the edge position of PDA medium preferably punch several holes that are 5mm in diameter with equidistant intervals, then inoculate respectively to the center of PDA medium plate, then in described plate Insert four coverslips with the same distance from the center of the petri dish obliquely on the PDA medium inside, and culture at a constant temperature of 20°C for 80 hours, so that the hyphae of Morchella spp. are covered with the coverslips;
[0040] B) For the treatment of the mycelia of Morchella chinensis, fir...
Embodiment 3
[0045] The method for nuclear staining provided by the invention to detect hickory chick hyphae nuclei enrichment comprises the following steps:
[0046] A) hickory chick mycelia culture, the hickory chick described in the present embodiment is Liumei hickory chick, earlier uses puncher to be covered with Liumei hickory chick mycelium and is positioned at the PDA medium i.e. potato in the dish The edge place of glucose agar medium is perforated, specifically: around the edge position of PDA medium, it is preferred to punch several holes with a diameter of 4mm in an equidistant interval state, then inoculate to the PDA medium plate center respectively, then in the four On the PDA medium in each plate, insert four coverslips at an equal distance from the center of the plate, and culture at a constant temperature of 22° C. for 72 hours, so that the hyphae of Morchella spp. are covered with the coverslips;
[0047] B) For the treatment of the mycelia of Morchella chinensis, first ...
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