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Zhongjian Baotai

Beijing Biotai Co., Ltd. and all staff are dedicate-d to providing customers with the best techni-cal solutions, quality products and after-sales services, and strive to promote the developme-nt of China's food safety industry.

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Evergreen Melamine Rapid Test Strip

The Evergreen melamine rapid detection strip adopts colloidal gold immunochromatography technology, which is easy to operate, easy to interpret and does not require any other equipment. It can be used for on-site rapid detection of melamine in milk, milk powder, grain and feed. The detection limit is 0.05ppm, and the detection can be completed in 5 minutes without sample pretreatment, thus meeting the national detection requirements.

Classification:

Evergreen Melamine Rapid Test Strip

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Product number:

ER30121

Specifications:

Article 50

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Product Description

EvergreenMelamine rapid detection strip, using colloidal gold immunochromatography technology, easy to operate, the results are easy to interpret, without any other equipment, can be used for on-site rapid detection of melamine in milk, milk powder, grain, feed, the detection limit is 0.05ppm,5 minutes to complete the detection, without sample pretreatment, to meet the national testing requirements.

 

Principle

The determination of immunochromatography is based on antigen-antibody reaction. Under the adsorption effect, the liquid flows from right to left, and the specific antibody of melamine connected with colloidal gold is found in the binding zone. If there is no melamine in the sample, the colloidal gold complex passes through the detection line (T), colloidal gold will combine with the pre-coated target antigen of the detection line to form an antigen-antibody-colloidal gold complex to form a color band. If there is melamine in the sample, when passing through the binding layer, the colloidal gold will first combine with the antigen in the sample to form an antigen-antibody-colloidal gold complex, which will affect the formation of a color band on the detection line (T) through the inhibition of the detection line area and the pre-coated target antigen on the detection line (T).

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