ELK3091-48T, Human MSLN(Mesothelin) ELISA Kit, 48T

ELK3091-48T, Human MSLN(Mesothelin) ELISA Kit, 48T

ELK3092-48T, Human GRN(Granulin) ELISA Kit, 48T

ELK3092-48T, Human GRN(Granulin) ELISA Kit, 48T

ELK3091-96T, Human MSLN(Mesothelin) ELISA Kit, 96T

2.963,10 RON

Human MSLN(Mesothelin) ELISA Kit

SKU
ELK3091-96T

Alternative Names: SMR; MPF; CAK1; Pre-pro-megakaryocyte-potentiating factor; Megakaryocyte-potentiating factor

Species: Human

Assay Type: Sandwich

Sensitivity: 0.056 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

Sample type: serum, plasma, tissue homogenates and other biological fluids

Assay length: 3.5h

Research Area: Metabolic pathway;

Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human MSLN. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human MSLN. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human MSLN, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. 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 MSLN in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: SMR; MPF; CAK1; Pre-pro-megakaryocyte-potentiating factor; Megakaryocyte-potentiating factor

Species: Human

Assay Type: Sandwich

Sensitivity: 0.056 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

Sample type: serum, plasma, tissue homogenates and other biological fluids

Assay length: 3.5h

Research Area: Metabolic pathway;

Test principle: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human MSLN. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human MSLN. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human MSLN, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. 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 MSLN in the samples is then determined by comparing the OD of the samples to the standard curve.