Cordyceps sinensis host hepialus armoricanus egg shell softening and decoloring method and softening and decoloing agent
A technology of Cordyceps sinensis host and bat moth, which is applied in animal husbandry and other fields to achieve the effect of cheap ingredients and simple operation
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Embodiment 1
[0021] Embodiment 1 softening decolorization experiment
[0022] Put 1.5-2 grams of chlorine dioxide powder (chlorine dioxide content 10%) into 100mL of 50% ethanol aqueous solution (prepared and used now, absolute ethanol and water 1:1), quickly put the bat moth eggs to be tested After adding the above solution, the eggs gradually degenerate from black to brown and finally translucent light yellow. After 15-30 minutes, the softening and decolorization of egg shells is completed.
[0023] The present invention also uses different softeners and treatment methods to treat bat moth egg shells, and finds that the existing silkworm egg shell treatment methods are not suitable for bat moth eggs.
[0024] Table 1: Comparison of the effects of different softeners on the soft shell of bat moth eggs:
[0025]
[0026]
[0027] The inventor of the present invention has not obtained the softening and decolorizing method of bat moth ovum by researching various softening and decolori...
Embodiment 2
[0028] Embodiment 2 tissue section research
[0029] Get 1 gram of chlorine dioxide powder and dissolve in 60mL ethanol aqueous solution, ethanol: water=2:1, take the bat moth eggs in the early and middle stages of development and put them into the above solution, the eggs gradually change color, after 30min the eggs become light yellow, decolorized and softened After completion, the tissues were sectioned after rinsing three times with 0.9% saline.
[0030] Tissue sectioning method: the eggs were fixed with Carnoy`s Fluid for 24 hours, and then dehydrated, permeated and embedded in paraffin according to the conventional paraffin section method. The tangential direction was longitudinal section and the section thickness was 4.5 μM, patch (at a temperature of 42°C) and dry for more than 1.5 hours (the oven temperature is set at 55°C), then stained with hematoxylin-eosin counterstaining method, sealed with neutral gum, and placed in a Leica DM2500 upright microscope Observe and...
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