ELK6601-96T, Rat CALU(Calumenin) ELISA Kit, 96T

ELK6601-96T, Rat CALU(Calumenin) ELISA Kit, 96T

ELK6602-96T, Rat IL17F(Interleukin 17F) ELISA Kit, 96T

ELK6602-96T, Rat IL17F(Interleukin 17F) ELISA Kit, 96T

ELK6602-48T, Rat IL17F(Interleukin 17F) ELISA Kit, 48T

2.142,00 RON

Rat IL17F(Interleukin 17F) ELISA Kit

SKU
ELK6602-48T

Alternative Names: IL-17F; ML-1

Species: Rat

Assay Type: Sandwich

Sensitivity: 5.9 pg/mL

Standard: 1000 pg/mL

Detection range: 15.63-1000 pg/mL

Sample type: Serum, plasma and other biological fluids.

Assay length: 3.5h

Research Area: Cytokine;Tumor immunity;Infection immunity;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 Rat IL17F. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat IL17F. 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 Rat IL17F, 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 Rat IL17F in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: IL-17F; ML-1

Species: Rat

Assay Type: Sandwich

Sensitivity: 5.9 pg/mL

Standard: 1000 pg/mL

Detection range: 15.63-1000 pg/mL

Sample type: Serum, plasma and other biological fluids.

Assay length: 3.5h

Research Area: Cytokine;Tumor immunity;Infection immunity;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 Rat IL17F. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat IL17F. 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 Rat IL17F, 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 Rat IL17F in the samples is then determined by comparing the OD of the samples to the standard curve.