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Phenylethanolamine A ELISA Kit

Competitive ELISA kit for the quantitative measurement of Phenylethanolamine A in Urine, Tissue, Feed samples.

WARNING: This product can expose you to chemicals including TMB, which is [are] known to the State of California to cause cancer.  For more information go to www.P65Warnings.ca.gov.
Catalog #: E4751
$525.00

Product Details

Cat # +Size E4751-100
Size 96 assays
Detection Method Absorbance (450 nm)
Species Reactivity Universal
Applications • Cross-reactivity: PHE A - 100%, Ketrintero - <1%, Albuterol - <1%, Ractopamine - <1%
• Sensitivity: 0.1 ppb (ng/mL)
• Sample recovery rate: Urine - 95%±15%, Tissue/Feed - 85%±15%
• Quantitative measurement of Phenylethanolamine A in Urine, Tissue, Feed samples.
• Detection limit: Urine - 0.1 ppb, Tissue - 0.1 ppb, Feed - 1 ppb
Features & Benefits • Detection limit: Urine - 0.1 ppb, Tissue - 0.1 ppb, Feed - 1 ppb
• Cross-reactivity: PHE A - 100%, Ketrintero - <1%, Albuterol - <1%, Ractopamine - <1%
• Sample recovery rate: Urine - 95%±15%, Tissue/Feed - 85%±15%
• Sensitivity: 0.1 ppb (ng/mL)
• Quantitative measurement of Phenylethanolamine A in Urine, Tissue, Feed samples.
Kit Components Plate Sealer
Stop Solution
Reconstitution Buffer (10x)
Antibody Working Solution
Wash Buffer (20x)
High Concentrated Standard (100 ppb)
Standard
Substrate Reagent A
Substrate Reagent B
HRP Conjugate
ELISA Microtplate
Storage Conditions 4°C
Shipping Conditions Gel Pack
USAGE For Research Use Only! Not For Use in Humans.

Details

Phenylethanolamine is a trace amine with a structure similar to those of other trace phenethylamines as well as the catecholamine neurotransmitters. Phenylethanolamine A ELISA Kit is based on Indirect Competitive ELISA method. It can be used to detect PHE A in urine, tissue, feed samples. The micro-plate provided in this kit has been pre-coated with PHE A. During the reaction, PHE A in the samples or standard competes with PHE A on the solid phase supporter for sites of PHE A antibody. Then Horseradish Peroxidase (HRP) conjugate is added to each micro plate well, and TMB substrate is for color development. There is a negative correlation between the OD value of samples and the concentration of PHE A. The concentration of PHE A in the samples can be calculated by comparing the OD of the samples to the standard curve.


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