Parasite rapid enzyme immunoassay method and kit for salmon and trout culture
A technology for detecting kits and parasites, applied in biological testing, measuring devices, material inspection products, etc., can solve the problems of poor specificity, high cost, low efficiency, etc., and achieve the effect of simple preparation method and accurate identification
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Embodiment 1
[0027] This embodiment provides a rapid enzyme immunoassay kit for third-generation salmon and trout cultured worms.
[0028] The detection kit of this embodiment includes: third-generation worm-specific antigen-coated plate, 0.1M phosphate buffer containing 0.5% Tween, enzyme-labeled antigen solution, 30% hydrogen peroxide solution, 2mg / mL tetramethylbenzidine Absolute ethanol solution, 2N sulfuric acid solution, positive control serum and negative control serum.
[0029] In this embodiment, the preparation steps of the three-generation worm-specific antigen-coated plate are as follows:
[0030] Step 1. Prepare soluble antigens of third-generation worms: remove the third-generation worms parasitic on fish under a microscope, and put them in normal saline. When the density of worms reaches 10 6 ~10 7 / mL, centrifuge at 4°C to collect the worms, wash the worms three times with PBS buffer solution of pH 7.0, add 5 times the volume of PBS buffer solution of pH 7.0 to the washed...
Embodiment 2
[0035] This embodiment provides a rapid enzyme immunoassay kit for the cultured salmon and trout.
[0036] The detection kit of this example includes: small melon worm-specific antigen-coated plates, 0.1M phosphate buffer containing 0.5% Tween, enzyme-labeled antigen solution, 30% hydrogen peroxide solution, 2 mg / mL tetramethyl-linked Anhydrous ethanol solution of aniline, 2N sulfuric acid solution, positive control serum and negative control serum.
[0037] In this embodiment, the preparation steps of the small melon worm-specific antigen-coated plate are as follows:
[0038]Step 1. Prepare the soluble antigen of the small melon worms: remove the small melon worms parasitic on the fish under a microscope and put them into physiological saline, and the density of the worms reaches 10 6 ~10 7 / mL, centrifuge at 4°C to collect the worms, wash the worms three times with PBS buffer solution of pH 7.0, add 5 times the volume of PBS buffer solution of pH 7.0 to the washed worms ac...
Embodiment 3
[0043] This embodiment provides a rapid enzyme immunoassay kit for trichomonas in salmon and trout culture.
[0044] The detection kit of this embodiment includes: trichotillotype-specific antigen-coated plate, 0.1M phosphate buffer containing 0.5% Tween, enzyme-labeled antigen solution, 30% hydrogen peroxide solution, 2mg / mL tetramethylbenzidine Absolute ethanol solution, 2N sulfuric acid solution, positive control serum and negative control serum.
[0045] In this embodiment, the preparation steps of the trichotillotype-specific antigen-coated plate are as follows:
[0046] Step 1. Preparation of soluble antigens of Trichomonas worms: Remove the Trichomonas parasitic on the fish body under a microscope and put them in normal saline until the density of the worms reaches 10 6 ~10 7 / mL, centrifuge at 4°C to collect the worms, wash the worms three times with PBS buffer solution of pH 7.0, add 5 times the volume of PBS buffer solution of pH 7.0 to the washed worms according t...
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