Method for preparing melittin
A technology of melittin and bee venom, applied in the biological field, can solve the problems of long extraction time, cumbersome preparation process, and long production cycle, and achieve the effects of shortening the preparation time, simplifying the extraction process, and reducing the preparation cost
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Embodiment 1
[0030] ①Removal of bee venom
[0031] Add crude bee venom to a buffer solution with a pH of 4.75 to make the concentration 1.0 mg / mL, and centrifuge at 3000 r / min for 5 min to remove insoluble impurities to obtain a supernatant;
[0032] The crude bee venom is obtained by dissolving the venom discharged from bee stings with distilled water and freeze-drying;
[0033] The buffer is acetic acid-sodium acetate buffer solution;
[0034] The impurity removal is the removal of insoluble substances in the buffer solution.
[0035] ② Separation of melittin
[0036] Pass the supernatant obtained in ① through a Sephadex G-25 column, elute with distilled water, control the flow rate at 28mL / h, measure the molecular weight of each separated component, the molecular weight collected under the Sephadex column is 2840Da The chromatographic components were freeze-dried to obtain solid samples;
[0037] The Sephadex G-25 is represented by the English letter G for dextran, and G reflects th...
Embodiment 2
[0047] ①Removal of bee venom
[0048]Add the crude bee venom to a buffer solution with a pH of 5.25, 1.5mg / mL, and centrifuge at 3200r / min for 6min to remove insoluble impurities to obtain a supernatant;
[0049] The crude bee venom is obtained by dissolving the venom discharged from bee stings with distilled water and freeze-drying;
[0050] The buffer is acetic acid-sodium acetate buffer solution;
[0051] The impurity removal is the removal of insoluble substances in the buffer solution.
[0052] ② Separation of melittin
[0053] Pass the supernatant obtained in ① through a Sephadex G-25 column, elute with distilled water, the flow rate is controlled at 30mL / h, measure the molecular weight of each separated component, and the molecular weight collected under the Sephadex column is 2840Da The chromatographic components were freeze-dried to obtain solid samples;
[0054] The Sephadex G-25 is represented by the English letter G for dextran, and G reflects the crosslinking ...
Embodiment 3
[0064] ①Removal of bee venom
[0065] Add the crude bee venom to a buffer solution with a pH of 4.5, 0.5mg / mL, and centrifuge at 2800r / min for 4min to remove insoluble impurities to obtain a supernatant;
[0066] The crude bee venom is obtained by dissolving the venom discharged from bee stings with distilled water and freeze-drying;
[0067] The buffer is acetic acid-sodium acetate buffer solution;
[0068] The impurity removal is the removal of insoluble substances in the buffer solution.
[0069] ② Separation of melittin
[0070] Pass the supernatant obtained in ① through a Sephadex G-25 column, elute with distilled water, and control the flow rate at 26mL / h, measure the molecular weight of each separated component, and the molecular weight collected under the Sephadex column is 2840Da The chromatographic components were freeze-dried to obtain solid samples;
[0071] The Sephadex G-25 is represented by the English letter G for dextran, and G reflects the crosslinking de...
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