ELK8650-48T, Rat HA(Histamine) ELISA Kit, 48T

ELK8650-48T, Rat HA(Histamine) ELISA Kit, 48T

ELK8651-48T, Dog PIINP(Procollagen II N-Terminal Propeptide) ELISA Kit, 48T

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ELK8650-96T, Rat HA(Histamine) ELISA Kit, 96T

2.475,20 RON

Rat HA(Histamine) ELISA Kit

SKU
ELK8650-96T

Alternative Names: Histamin

Species: Rat

Assay Type: Competitive Inhibition

Sensitivity: 0.51 ng/mL

Standard: 100 ng/mL

Detection range: 1.57-100 ng/mL

Sample type: serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids

Assay length: 2h

Research Area: Signal transduction;Infection immunity;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Rat HA protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat HA. 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 HA in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: Histamin

Species: Rat

Assay Type: Competitive Inhibition

Sensitivity: 0.51 ng/mL

Standard: 100 ng/mL

Detection range: 1.57-100 ng/mL

Sample type: serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids

Assay length: 2h

Research Area: Signal transduction;Infection immunity;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Rat HA protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat HA. 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 HA in the samples is then determined by comparing the OD of the samples to the standard curve.