Limba
Romanian
Romanian
English|
ELK5226-96T, Human NMS(Neuromedin S) ELISA Kit, 96T
2.963,10 RON
Human NMS(Neuromedin S) ELISA Kit
SKU
ELK5226-96T
Alternative Names: NM-S
Species: Human
Assay Type: Competitive Inhibition
Sensitivity: 52.5 pg/mL
Standard: 10000 pg/mL
Detection range: 156.25-10000 pg/mL
Sample type: Serum, plasma, tissue homogenates and other biological fluids
Assay length: 2h
Research Area: Signal transduction;Metabolic pathway;Neuro science;Gastroenterology;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 Human NMS protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human NMS. 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 Human NMS in the samples is then determined by comparing the OD of the samples to the standard curve.
| Price | 2.490,00 RON (preturile sunt fara TVA) |
|---|---|
| Description |
Alternative Names: NM-S Species: Human Assay Type: Competitive Inhibition Sensitivity: 52.5 pg/mL Standard: 10000 pg/mL Detection range: 156.25-10000 pg/mL Sample type: Serum, plasma, tissue homogenates and other biological fluids Assay length: 2h Research Area: Signal transduction;Metabolic pathway;Neuro science;Gastroenterology;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 Human NMS protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human NMS. 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 Human NMS in the samples is then determined by comparing the OD of the samples to the standard curve. |
