Horse ANP(Atrial Natriuretic Peptide) ELISA Kit
Alternative Names: ANH; ANF; CDD; Atrial Natriuretic Factor; Atrial Natriuretic Hormone; Atriopeptin; Cardionatrine; Cardiodilatin
Species: Horse
Assay Type: Competitive Inhibition
Sensitivity: 9.17 pg/mL
Standard: 2000 pg/mL
Detection range: 31.25-2000 pg/mL
Sample type: Serum, plasma, tissue homogenates and other biological fluids
Assay length: 2h
Research Area: Endocrinology;Cardiovascular biology;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 Horse ANP protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Horse ANP. 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 Horse ANP 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) |
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Description |
Alternative Names: ANH; ANF; CDD; Atrial Natriuretic Factor; Atrial Natriuretic Hormone; Atriopeptin; Cardionatrine; Cardiodilatin Species: Horse Assay Type: Competitive Inhibition Sensitivity: 9.17 pg/mL Standard: 2000 pg/mL Detection range: 31.25-2000 pg/mL Sample type: Serum, plasma, tissue homogenates and other biological fluids Assay length: 2h Research Area: Endocrinology;Cardiovascular biology;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 Horse ANP protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Horse ANP. 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 Horse ANP in the samples is then determined by comparing the OD of the samples to the standard curve. |