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ELK0332-48T, Pig βEP(Beta-Endorphin) ELISA Kit, 48T
2.689,40 RON
Pig βEP(Beta-Endorphin) ELISA Kit
SKU
ELK0332-48T
Alternative Names: Beta EP; b-EP
Species: Pig
Assay Type: Competitive Inhibition
Sensitivity: 4.79 pg/mL
Standard: 1000 pg/mL
Detection range: 15.63-1000 pg/mL
Sample type: Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.
Assay length: 2.5h
Research Area: Signal transduction;Endocrinology;Neuro science;Hormone metabolism;
Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Pig βEP protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Pig βEP. 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 Pig βEP in the samples is then determined by comparing the OD of the samples to the standard curve.
| Price | 2.260,00 RON (preturile sunt fara TVA) |
|---|---|
| Description |
Alternative Names: Beta EP; b-EP Species: Pig Assay Type: Competitive Inhibition Sensitivity: 4.79 pg/mL Standard: 1000 pg/mL Detection range: 15.63-1000 pg/mL Sample type: Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids. Assay length: 2.5h Research Area: Signal transduction;Endocrinology;Neuro science;Hormone metabolism; Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Pig βEP protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Pig βEP. 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 Pig βEP in the samples is then determined by comparing the OD of the samples to the standard curve. |
