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ELK6069-96T, Rat NT(Neurotensin) ELISA Kit, 96T
2.963,10 RON
Rat NT(Neurotensin) ELISA Kit
SKU
ELK6069-96T
Alternative Names: NTS; NTS1; NmN-125; NN; Tail peptide Neuromedin N
Species: Rat
Assay Type: Competitive Inhibition
Sensitivity: 15.2 pg/mL
Standard: 3000 pg/mL
Detection range: 46.88-3000 pg/mL
Sample type: Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.
Assay length: 2h
Research Area: Reproductive science;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 Rat NT protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat NT. 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 Rat NT 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: NTS; NTS1; NmN-125; NN; Tail peptide Neuromedin N Species: Rat Assay Type: Competitive Inhibition Sensitivity: 15.2 pg/mL Standard: 3000 pg/mL Detection range: 46.88-3000 pg/mL Sample type: Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids. Assay length: 2h Research Area: Reproductive science;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 Rat NT protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat NT. 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 Rat NT in the samples is then determined by comparing the OD of the samples to the standard curve. |
