ELK4209-96T, Human ENdog(Endonuclease G, Mitochondrial) ELISA Kit, 96T

ELK4209-96T, Human ENdog(Endonuclease G, Mitochondrial) ELISA Kit, 96T

ELK4210-96T, Human AP17(Apelin 17) ELISA Kit, 96T

ELK4210-96T, Human AP17(Apelin 17) ELISA Kit, 96T

ELK4210-48T, Human AP17(Apelin 17) ELISA Kit, 48T

2.142,00 RON

Human AP17(Apelin 17) ELISA Kit

SKU
ELK4210-48T

Alternative Names: APLN17

Species: Human

Assay Type: Competitive Inhibition

Sensitivity: 9.14 pg/mL

Standard: 2000 pg/mL

Detection range: 31.25-2000 pg/mL

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

Assay length: 2h

Research Area: Central nervous system ;cardiovascular system

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human AP17 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human AP17. 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 AP17 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: APLN17

Species: Human

Assay Type: Competitive Inhibition

Sensitivity: 9.14 pg/mL

Standard: 2000 pg/mL

Detection range: 31.25-2000 pg/mL

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

Assay length: 2h

Research Area: Central nervous system ;cardiovascular system

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human AP17 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human AP17. 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 AP17 in the samples is then determined by comparing the OD of the samples to the standard curve.