Echinococcus granulosus hyperimmune yolk antibody, test strip, preparation method and application
A technology of Echinococcus granulosus, egg yolk antibody, applied to Echinococcus granulosus hyperimmune egg yolk antibody and test strip and preparation, application in reagent or reagent strip or medicine, application in kit, Echinococcus granulosa Ball tapeworm hyperimmune yolk antibody and its preparation field
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Embodiment 1
[0053] Embodiment 1: A kind of Echinococcus granulosus hyperimmune egg yolk antibody is carried out according to the following preparation method: the first step, the preparation of Echinococcus antigenic protein: adopt 0.9% sterilized normal saline or concentration is 0.01mol / L, pH Wash the Echinococcus worm body with sterilized PBS with a value of 7.2 to 7.4, freeze and thaw the washed Echinococcus worm body repeatedly in liquid nitrogen and 37°C for 3 to 5 times, and freeze and thaw the Echinococcus worm body Crush the body, add 50 μL of protein lysate to every 1 mg of the crushed Echinococcus worm body, and then lyse the lysate to obtain the lysate, centrifuge the lysate, take the supernatant after centrifugation, filter the supernatant to sterilize, and sterilize the lysate The protein concentration in the supernatant was adjusted to 1 mg / mL to obtain the Echinococcus antigenic protein;
[0054] The second step, the preparation of the immunogen: the Echinococcus antigenic...
Embodiment 2
[0067] Example 2: Application of a hyperimmune yolk antibody against Echinococcus granulosus in the preparation of reagents or reagent strips or medicines for diagnosing echinococcosis.
Embodiment 3
[0068] Embodiment 3: A kind of freeze-dried hyperimmune egg yolk antibody is carried out according to the following preparation method:
[0069] Step 1, wash the magnetic beads with MEST buffer for 3 times, then add 1ml to 2ml of magnetic beads into 1ml to 2ml of activator and shake to mix evenly. The activator includes 10mg / mL 1-(3-dimethylaminopropyl)- 3-Ethylcarbodiimide hydrochloride solution and 10 mg / mL N-hydroxysuccinimide solution, and then react at room temperature for 15 min to 1 h in the dark at a rotational speed of 150 r / min. Stand still for 5min to 10min, separate the magnetic beads after the reaction with a magnetic stand to obtain activated magnetic beads, discard the supernatant of the reaction solution, and keep the lower layer of the reaction solution.
[0070] Step 2, dissolving the lower layer of the reaction solution with 0.01mol / L PBST buffer solution with a pH value of 5.0 to 7.2 to obtain a lower layer solution, washing the activated magnetic beads at ...
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