Bovine NEFA (Non-Esterified Fatty Acid) ELISA Kit
€0.00
In stock
SKU
ELK8609
Catalog Number: ELK8609
Reactivity: Bovine
Standard Range: 6.25-400 nmol/ml
Sensitivity: 3.55 nmol/ml
Information
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Reactivity: Bovine
Standard Range: 6.25-400 nmol/ml
Sensitivity: 3.55 nmol/ml
Information
Request Manual
Questions? Contact us!
Test Principle:
This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with NEFA(Non-Esterified Fatty Acid) protein. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to NEFA(Non-Esterified Fatty Acid). Next,Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of NEFA(Non-Esterified Fatty Acid) in the samples is then determined by comparing the OD of the samples to the standard curve.
Research Area: Kidney diseases
Alternative Names:
Non-Esterified Fatty Acid, Non-ester fatty acid, NEFA
Sample Type:
Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.
Assay Type: Competitive Inhibition
Standard: 400nmol/ml
Assay Length: 2h
Assay Length: For Research Use Only
This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with NEFA(Non-Esterified Fatty Acid) protein. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to NEFA(Non-Esterified Fatty Acid). Next,Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of NEFA(Non-Esterified Fatty Acid) in the samples is then determined by comparing the OD of the samples to the standard curve.
Research Area: Kidney diseases
Alternative Names:
Non-Esterified Fatty Acid, Non-ester fatty acid, NEFA
Sample Type:
Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.
Assay Type: Competitive Inhibition
Standard: 400nmol/ml
Assay Length: 2h
Assay Length: For Research Use Only
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