Detailed Selling Lead Description
Test PrincipleThis ELISA kit is designed to detect furazolidone metabolite (AOZ) based on the principle of indirect-competitive enzyme immunoassay. The microtiter wells are coated with capture BSA-linked antigen. AOZ in sample competes with the antigen coated on the microtiter plate for the antibody. After the addition of horseradish peroxidase labeled anti-antibody, tetramethyl-benzidine (TMB)/peroxide substrate is used and the signal is measured by spectrophotometer. The absorption is inversely proportional to the AOZ concentration in the sample.
Kit Components
1.Microtiter plate with 96 wells coated with coupling antigen
2. Standard solutions (6 bottles×1ml / bottle)
0ppb,0.05ppb,0.15ppb,0.45ppb,1.35ppb,4.05ppb 3.High concentration standard control : (1ml/bottle) 100ppb
4.enzyme-labeled secondary antibody solution 12mlred cap
5. concentrated antibody solution 0.8mlgreen cap
6. solution A 7ml white cap
7. solution B 7ml red cap
8. stop solution 7ml yellow cap
9. 20×concentrated wash solution 40ml transparent cap
10. 2×concentrated extraction solution 50ml blue cap
11. dinitrobenzal-dehyde 15.1mg black cap
Sensitivity, accuracy and precisionTest Sensitivity: 0.05ppb
Detection limit:
Tissue and honey sample0.1ppb
Egg sample0.1ppb
Milk sample0.1ppb
Accuracy:
Tissue samples(muscle and liver) 75±15%
honey sample 90±15%
Egg sample 90±20%
Milk sample 90±10%
Precision:
Variation coefficient of the ELISA kit is less than 10%.