Furazolidone (AOZ) Rapid Test Strip


Specification

50T/kit  


Principle of Test

The kit is using competitive colloidal gold immunoassay method. Sample is added to sample hole, if there is AOZ in samples, it will combine with marked antibodies, prevent the marked antibodies from combining the Furazolidone antigens of NC nitrocellulose membrane.

If AOZ contents in sample solution are greater than detection limit, the test line will not display color reaction and the result is positive; If AOZ contents in sample solution are less than detection limit, the test line will display purple and the result is negative.


Technique Data

Kit sensitivity: 0.5 ppb (ng/ml)

(Final detection limit = Kit sensitivity × dilution times of the sample)

Detection Limits

Honey, Tissue, Prepared intestine, Liver …………………..0.25ppb


Kit Content

Test strip ………………………… 50T/kit

Sample redissolving solution ………….1 bottle

Derivatization reagent ……………………. 1 bottle

Instruction …………………………..1


Storage Conditions

1.  The kit shall be stored at [2-30℃] in dry environment.

2.   Expiry date: 12 months