Lincomycin assay kit and method for making the same
A detection kit, the technology of lincomycin, applied in the field of determination of biological immunological methods, can solve the problems of complicated detection, time-consuming, expensive instruments, etc., and achieve the effect of simple operation, rapid response and convenient use
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Embodiment 1
[0038] Embodiment 1: the preparation of lincomycin detection kit
[0039] 1. Preparation of Lincomycin-Conjugated Bovine Serum Albumin
[0040] Coupling lincomycin with bovine serum albumin, and synthesizing lincomycin-conjugated bovine serum albumin as immunogen and coating.
[0041] 2. Preparation of lincomycin monoclonal antibody
[0042] Lincomycin monoclonal antibody was prepared by immunizing BALB / C mice with lincomycin-conjugated bovine serum albumin.
[0043] 3. Preparation of colloidal gold
[0044] Take 0.01% chloroauric acid aqueous solution, heat to boil. Quickly add 1ml of 1% trisodium citrate aqueous solution as needed, continue to boil for about 5min, orange-red appears. The colloidal gold particles thus produced have a size of 20-40 nm.
[0045] 4. Preparation of Colloidal Gold Pads
[0046] Take 5ml of colloidal gold solution with a particle size of 20-40nm, and use 0.2mol / L K 2 CO 3 Adjust the pH value of the colloidal gold solution to 8.0, and place ...
Embodiment 2
[0056] Embodiment 2: the detection of lincomycin detection kit
[0057] 1. Sample handling
[0058] Serum: extract the serum, centrifuge or stand still and take the clear supernatant for use;
[0059] Urine: Use urine to test directly. If the urine is visibly turbid, it needs to be centrifuged, filtered, or the supernatant should be tested after it settles;
[0060] Milk: centrifuge at 3000r / min at 4°C for 15min, remove the upper layer of fat and then detect it.
[0061] Honey and eggs: Use 0.01mol / L PBS with pH 7.5 to make a 1:2 suspension of the sample to be tested, shake for 10 minutes, centrifuge at 3000r / min for 15 minutes, and take the supernatant for testing.
[0062] Tissue samples: Take 5-10g of tissue samples and mash them, add 20-30ml (0.01mol / L, pH 7.5) PBS, shake for 10min, react in a 37°C incubator for 30min, then bathe in water for 10min, at 4°C, 3000r / min Centrifuge for 15 minutes, remove the upper layer of fat, and take the supernatant for detection.
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