Moisture-preserving springtail culture matrix and preparation method thereof
A technology for cultivating substrates and moisturizing collembola, which is applied in animal husbandry and other fields, can solve the problems of poison addition experiments, pure culture collembola culture management or test control cannot be effectively guaranteed, collembola culture substrate cannot be carried out, etc., to achieve The effect of stable and balanced humidity and proper proportion
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specific Embodiment approach 1
[0013] Specific embodiment one: In this embodiment, a kind of moisturizing collembola culture substrate is composed of 1-3g of agar powder, 2-3mL of phosphate buffer and 97-98mL of distilled water; wherein the phosphate buffer is composed of 2-20g of KH 2 PO 4 and 1-3g of KOH are added to distilled water to make up to 100mL; wherein the pH of the phosphate buffer is 6.0.
[0014] The moisturizing collembola culture medium of this embodiment has a stable and balanced humidity during the collembola culture process, and does not need to replenish water. After sterilization and ultra-clean operation, it can ensure that the collembola living medium is free of sundries and bacteria, and can purify the collembola. Sexual culture, because the base of the medium is soft and the humidity is suitable, the collembola has no escape and wall climbing phenomenon.
[0015] The proportion of agar powder in the moisture-retaining collembola culture medium of this embodiment is appropriate, and...
specific Embodiment approach 2
[0016] Specific implementation mode two: the preparation method of the moisturizing collembola culture substrate of the present embodiment is as follows: 1. Weigh 2-20g of KH 2 PO 4 and 1-3g of KOH, add distilled water, adjust the pH value of the phosphate buffer to 6.0, and then adjust the volume to 100mL to prepare a phosphate buffer; 2. Weigh 1-3g of agar powder into a beaker, add 2-3mL For the phosphate buffer solution prepared in step 1, dilute to 100mL with distilled water; 3. Seal the beaker with parafilm and put it in a high-pressure steam sterilizer to sterilize at 120°C for 20min; 4. Cool down to 50-60°C after sterilization , pour the culture medium prepared in step 3 into a petri dish in an ultra-clean workbench, and the culture medium is 0.4-0.6cm thick; 5. Put the culture dish in step 4 on the test bench and wait for the culture matrix to cool and solidify. Moisturizing springtail culture substrate.
[0017] The adjustment of the phosphate buffer solution descri...
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