ELK4958-48T, Human DEFa1B(Defensin Alpha 1B) ELISA Kit, 48T

ELK4958-48T, Human DEFa1B(Defensin Alpha 1B) ELISA Kit, 48T

ELK4959-48T, Human IL7(Interleukin 7) ELISA Kit, 48T

ELK4959-48T, Human IL7(Interleukin 7) ELISA Kit, 48T

ELK4958-96T, Human DEFa1B(Defensin Alpha 1B) ELISA Kit, 96T

2.963,10 RON

Human DEFa1B(Defensin Alpha 1B) ELISA Kit

SKU
ELK4958-96T

Alternative Names: HNP-1; DEFA2; MRS; Neutrophil defensin 1

Species: Human

Assay Type: Sandwich

Sensitivity: 14.2 pg/mL

Standard: 2000 pg/mL

Detection range: 31.25-2000 pg/mL

Sample type: Serum, plasma, tissue homogenates and other biological fluids.

Assay length: 3.5h

Research Area: Infection immunity;

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 DEFa1B. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human DEFa1B. 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 DEFa1B, 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 DEFa1B in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: HNP-1; DEFA2; MRS; Neutrophil defensin 1

Species: Human

Assay Type: Sandwich

Sensitivity: 14.2 pg/mL

Standard: 2000 pg/mL

Detection range: 31.25-2000 pg/mL

Sample type: Serum, plasma, tissue homogenates and other biological fluids.

Assay length: 3.5h

Research Area: Infection immunity;

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 DEFa1B. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human DEFa1B. 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 DEFa1B, 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 DEFa1B in the samples is then determined by comparing the OD of the samples to the standard curve.