DA (Dopamine) ELISA Kit
Catalog Number: ACE-E0072
Size: 96 tests/kit
Detection Range: 31.25—2000 pg/mL
Sensitivity: 18.75 pg/mL
Datasheet
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Size: 96 tests/kit
Detection Range: 31.25—2000 pg/mL
Sensitivity: 18.75 pg/mL
Datasheet
Request Information
Price on request
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You are enquiring about DA (Dopamine) ELISA Kit
Description:
This ELISA kit applies to the in vitro quantitative determination of DA concentrations in serum, plasma and other biological fluids.
Assay Principles: This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with DA. During the reaction, DA in the sample or standard competes with a fixed amount of DA on the solid phase supporter for sites on the Biotinylated Detection Ab specific to DA. Excess conjugate and unbound sample or standard are washed from the plate, and Avidin conjugated to Horseradish Peroxidase (HRP) are added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of DA in the samples is then determined by comparing the OD of the samples to the standard curve.
Species reactivity:
Universal
Sample Type: Serum, plasma and other biological fluids
Storage instruction: -20˚C and 4˚C for 6 months
This ELISA kit applies to the in vitro quantitative determination of DA concentrations in serum, plasma and other biological fluids.
Assay Principles: This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with DA. During the reaction, DA in the sample or standard competes with a fixed amount of DA on the solid phase supporter for sites on the Biotinylated Detection Ab specific to DA. Excess conjugate and unbound sample or standard are washed from the plate, and Avidin conjugated to Horseradish Peroxidase (HRP) are added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color change is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of DA in the samples is then determined by comparing the OD of the samples to the standard curve.
Species reactivity:
Universal
Sample Type: Serum, plasma and other biological fluids
Storage instruction: -20˚C and 4˚C for 6 months
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