ELK3244-48T, Human MIA1(Melanoma Inhibitory Activity Protein 1) ELISA Kit, 48T

ELK3244-48T, Human MIA1(Melanoma Inhibitory Activity Protein 1) ELISA Kit, 48T

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ELK3244-96T, Human MIA1(Melanoma Inhibitory Activity Protein 1) ELISA Kit, 96T

2.963,10 RON

Human MIA1(Melanoma Inhibitory Activity Protein 1) ELISA Kit

SKU
ELK3244-96T

Alternative Names: CD-RAP; Melanoma-derived growth regulatory protein

Species: Human

Assay Type: Sandwich

Sensitivity: 3.1 pg/mL

Standard: 500 pg/mL

Detection range: 7.82-500 pg/mL

Sample type: Serum, plasma and other biological fluids.

Assay length: 3.5h

Research Area: Immune molecule;

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 MIA1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human MIA1. 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 MIA1, 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 MIA1 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: CD-RAP; Melanoma-derived growth regulatory protein

Species: Human

Assay Type: Sandwich

Sensitivity: 3.1 pg/mL

Standard: 500 pg/mL

Detection range: 7.82-500 pg/mL

Sample type: Serum, plasma and other biological fluids.

Assay length: 3.5h

Research Area: Immune molecule;

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 MIA1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human MIA1. 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 MIA1, 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 MIA1 in the samples is then determined by comparing the OD of the samples to the standard curve.