ELK3200-48T, Human TREM2(Triggering Receptor Expressed On Myeloid Cells 2) ELISA Kit, 48T

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ELK3200-96T, Human TREM2(Triggering Receptor Expressed On Myeloid Cells 2) ELISA Kit, 96T

2.963,10 RON

Human TREM2(Triggering Receptor Expressed On Myeloid Cells 2) ELISA Kit

SKU
ELK3200-96T

Alternative Names: Trem2a; Trem2b; Trem2c; Triggering receptor expressed on monocytes 2

Species: Human

Assay Type: Sandwich

Sensitivity: 26.2 pg/mL

Standard: 4000 pg/mL

Detection range: 62.5-4000 pg/mL

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

Assay length: 3.5h

Research Area: CD & Adhesion 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 TREM2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human TREM2. 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 TREM2, 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 TREM2 in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: Trem2a; Trem2b; Trem2c; Triggering receptor expressed on monocytes 2

Species: Human

Assay Type: Sandwich

Sensitivity: 26.2 pg/mL

Standard: 4000 pg/mL

Detection range: 62.5-4000 pg/mL

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

Assay length: 3.5h

Research Area: CD & Adhesion 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 TREM2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human TREM2. 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 TREM2, 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 TREM2 in the samples is then determined by comparing the OD of the samples to the standard curve.