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ELK1814-96T, Human GT(Gastrin) ELISA Kit, 96T
2.963,10 RON
Human GT(Gastrin) ELISA Kit
SKU
ELK1814-96T
Alternative Names: GAST; GAS; Gastrin component I; Big gastrin; Gastrin component II; Gastrin component III; Gastrin 17; Gastrin 34
Species: Human
Assay Type: Competitive Inhibition
Sensitivity: 4.39 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: 2h
Research Area: Metabolic pathway;Endocrinology;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 GT protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human GT. 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 GT 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: GAST; GAS; Gastrin component I; Big gastrin; Gastrin component II; Gastrin component III; Gastrin 17; Gastrin 34 Species: Human Assay Type: Competitive Inhibition Sensitivity: 4.39 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: 2h Research Area: Metabolic pathway;Endocrinology;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 GT protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human GT. 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 GT in the samples is then determined by comparing the OD of the samples to the standard curve. |
