ELK9194-48T, Rat BK(Bradykinin) ELISA Kit, 48T

ELK9194-48T, Rat BK(Bradykinin) ELISA Kit, 48T

ELK9195-48T, GSSG(Oxidized Glutathione) ELISA Kit, 48T

ELK9195-48T, GSSG(Oxidized Glutathione) ELISA Kit, 48T

ELK9194-96T, Rat BK(Bradykinin) ELISA Kit, 96T

2.963,10 RON

Rat BK(Bradykinin) ELISA Kit

SKU
ELK9194-96T

Alternative Names: Bradykinin

Species: Rat

Assay Type: Competitive Inhibition

Sensitivity: 0.48 pg/mL

Standard: 100 pg/mL

Detection range: 1.57-100 pg/mL

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

Assay length: 2h

Research Area: Endocrinology;Cardiovascular biology;Pulmonology;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 BK protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat BK. 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 BK in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: Bradykinin

Species: Rat

Assay Type: Competitive Inhibition

Sensitivity: 0.48 pg/mL

Standard: 100 pg/mL

Detection range: 1.57-100 pg/mL

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

Assay length: 2h

Research Area: Endocrinology;Cardiovascular biology;Pulmonology;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 BK protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat BK. 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 BK in the samples is then determined by comparing the OD of the samples to the standard curve.