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Aflatoxin B1 ELISA Kit

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Aflatoxin B1 ELISA Kit este un kit ELISA de tip Competitive (quantitative) pentru măsurarea Aflatoxin B1. Are o sensibilitate de 0.02 ng/g or ppb, folosește detecție Colorimetric și se poate folosi pe probe de tip Cereals, feed, milk, milk powder, enzyme, cookies, soy sauce, vinegar, oils, peanuts. Se livrează în mărimea 96T, la prețul de 2.562,18 lei cu TVA.

Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.

Descriere

Aflatoxin B1 ELISA Kit is a competitive Enzyme-Linked Immunosorbent Assay (cELISA) designed for the in vitro quantitative determination of Aflatoxin B1 in cereals, feed, milk, milk powder, enzyme, cookies, soy sauce, vinegar, oils, peanuts.

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Specificații

Mărime
96T
Applications
Competitive ELISA
Sensitivity
0.02 ng/g or ppb
Detection type
Colorimetric
Assay Time
10-40 minutes
Recovery
75-125%
Principiul testului
Aflatoxin B1 ELISA Test Kit (A327176) employs the competitive enzyme immunoassay technique for the quantitative measurement of Aflatoxin B1 in cereals, feed, milk, milk powder, enzyme, cookies, soy sauce, vinegar, oils, peanuts. The 96-well microtiter plate has been pre-coated with Aflatoxin B1. During the incubation, Aflatoxin B1 present in the samples or standards competes with the fixed amount of immobilized Aflatoxin B1 for binding sites of the Anti-Aflatoxin B1 Antibody, a HRP-Conjugated Secondary Antibody is added to the wells at the same time. The more Aflatoxin B1 present in a sample or standard, the less Anti-Aflatoxin B1 Antibody that binds to the plate. Following incubation, unbound HRP-Conjugated Secondary Antibody is removed by washing. Following incubation and washing, TMB substrate solution is then used to visualize the HRP enzymatic reaction by catalysis to produce a blue-coloured product that changes to yellow after addition of acidic stop solution. The density of yellow is inversely proportional to the amount of Aflatoxin B1 present in each sample or standard. The concentration of Aflatoxin B1 can then be calculated by reading the O.D. absorbance at 450nm in a microplate reader and referring to the standard curve.

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