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Product Details
| Cat # +Size | E4958-100 |
|---|---|
| Size | 96 assays |
| Detection Method | Absorbance (450 nm) |
| Species Reactivity | Universal |
| Applications | Competitive ELISA kit to quantitatively measure Doramectin in milk and yogurt samples |
| Features & Benefits | ● This ELISA kit is used for in vitro quantitative determination of Doramectin
● Detection Limit: 1ppb for yogurt, raw and finished milk ● Cross reaction: Doramectin 100%, Abamectin 300%, Ivermectin 227%, Eprinomectin 300% ● Sensitivity: 0.1ppb |
| Kit Components | ● Micro ELISA Plate
Sample Diluent A ● Sample Diluent B ● Plate Sealer ● Standard (S0 – S5) ● HRP Conjugate ● Antibody working solution ● Milk Precipitant ● Substrate A ● Substrate B ● Stop Solution ● Wash Buffer (20X) |
| Storage Conditions | 4ºC |
| Shipping Conditions | Gel Pack |
| USAGE | For Research Use Only! Not For Use in Humans. |
Details
Doramectin is a macrocyclic lactone obtained from the fermentation of soil organism Streptomyces avermitilis. It belongs to the class of Avermectins and is structurally similar to Ivermectin. Due to its anthelmintic and insecticidal properties, it is widely used to treat parasitic infections in animals and also used as a pesticide in agriculture to prevent insect attacks on crops. The mode of action of the drug is that it binds to and opens the glutamine gated chloride channel on the invertebrate muscle cells and neurons. This causes an increased influx of chloride ions into the cells which lead to hyperpolarization of the membranes, and ultimately resulting in paralysis and death of the invertebrates. Doramectin is prohibited to be used in dairy-producing animals as the accumulation of the drug in milk residues may pose a health risk in humans. BioVision’s Doramectin ELISA kit is used to quantitatively measure Doramectin in milk and yogurt samples. The kit is based on the Competitive ELISA principle. Samples and standards are added to the microwell plate that is pre-coated with an antigen and competes for binding to the anti-Doramectin antibody. The HRP conjugate is added to each well and any unattached conjugates are washed off using Wash Buffer. The HRP enzymatic reaction is detected by the addition of substrate reagents. Finally, the reaction is terminated with an acidic stop solution. The color developed is inversely proportional to the concentration of Doramectin in the samples.
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