ELK5012-48T, Human ADM2(Adrenomedullin 2) ELISA Kit, 48T

ELK5012-48T, Human ADM2(Adrenomedullin 2) ELISA Kit, 48T

ELK5013-48T, Human D2HGDH(D2-Hydroxyglutarate Dehydrogenase) ELISA Kit, 48T

ELK5013-48T, Human D2HGDH(D2-Hydroxyglutarate Dehydrogenase) ELISA Kit, 48T

ELK5012-96T, Human ADM2(Adrenomedullin 2) ELISA Kit, 96T

2.963,10 RON

Human ADM2(Adrenomedullin 2) ELISA Kit

SKU
ELK5012-96T

Alternative Names: AM2; IMDL; IMDS; Intermedin

Species: Human

Assay Type: Competitive Inhibition

Sensitivity: 91.5 pg/mL

Standard: 20000 pg/mL

Detection range: 312.5-20000 pg/mL

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

Assay length: 2h

Research Area: Endocrinology;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human ADM2 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human ADM2. 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 ADM2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: AM2; IMDL; IMDS; Intermedin

Species: Human

Assay Type: Competitive Inhibition

Sensitivity: 91.5 pg/mL

Standard: 20000 pg/mL

Detection range: 312.5-20000 pg/mL

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

Assay length: 2h

Research Area: Endocrinology;

Test principle: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with Human ADM2 protein. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human ADM2. 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 ADM2 in the samples is then determined by comparing the OD of the samples to the standard curve.