Theileria equi immunoblotting detecting method and method for preparing kit
A technology of equine worm disease and detection kit, which is applied in the detection of equine worm disease serum antibody by immunoblotting test, and in the field of equine worm blot detection (Babesiosis equine), which can solve the problem of equine Theileria diagnostic kit and other issues, to achieve the effect of saving consumption, shortening the cycle, and reducing the amount of reagents
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Embodiment 1
[0056] Example 1 :Preparation of Western Blot Diagnosis Kit for Martell's Disease
[0057] Reagent preparation:
[0058] 1. 1x VYM’s buffer:
[0059] CaCl 2 .2H 2 O 0.016 g
[0060] KCl 0.400 g
[0061] KH 2 PO 4 1.415 g
[0062] MgSO 4 .7H 2 O 0.154 g
[0063] Na 2 HPO 4 0.077 g
[0064] NaCl 7.077 g
[0065] Glucose 20.500 g
[0066] ddH 2 O 1 L
[0067] After stirring and dissolving, add Adenine 0.0423 g and Guanosine 0.0708 g, adjust the pH to 7.0-7.2, vacuum filter (0.22 μm), and store at 4°C for later use.
[0068] 2. HL2A-FBS culture medium:
[0069] HL-1 medium 35 mL
[0070] Fetal bovine serum 10 mL
[0071] HB101 supplement 1 mL
[0072] Hepes 0.238 g
[0073] L-glutamine(100x) 1 mL
[0074] Hypoxanthine(20mmol) 0.5 mL
[0075] Gentamicin 1 mL
[0076] Antibiotic-antimycotic(100x) 1 mL
[0077] Stir magnetically for 5 min, adjust the pH to 7.2, vacuum filter (0.22 μm), and store at 4°C for later use.
[0078] 3. PI buffer:
[0079] Tris 3.03 g
[0080] Deionized water 500mL
[0081] S...
Embodiment 2
[0106] Example 2 : Western Blot Detection of Matele's Disease
[0107] Reagent preparation:
[0108] 1. 10x running buffer:
[0109] Tris 121.1 g
[0110] Glycine 570 g
[0111] Distilled water 4 L
[0112] 2. Transfer buffer:
[0113] 10x running buffer 100 mL
[0114] Methanol 200 mL
[0115] Distilled water 700 mL
[0116] 3、 Blocking fluid : Phosphate buffer containing 0.2% Tween-20, 10% skimmed milk powder
[0117] 4. Washing solution: Phosphate buffer containing 0.2% Tween-20
[0118] Take the NuPAGE 4%-12% Bis-Tris gel plate, wash the gel wells with 1 x SDS Running Buffer three times; place the gel plate face forward in the core rack of the Mini-Cell vertical electrophoresis system and lock it tightly. Add 200 mL 1 x SDS Running Buffer and 500 μL NuPAGE Antioxidant to the electrophoresis tank and mix well. Add 600 mL 1 x SDS Running Buffer to the lower tank. Add 7 μL to 10 μL of protein molecular weight standard marker (Marker) and the antigen sample obtained in Example 1 into the ...
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