ELK6431-48T, Human C4d(Complement Component 4d) ELISA Kit, 48T

ELK6431-48T, Human C4d(Complement Component 4d) ELISA Kit, 48T

ELK6432-48T, Rat CHGB(Chromogranin B) ELISA Kit, 48T

ELK6432-48T, Rat CHGB(Chromogranin B) ELISA Kit, 48T

ELK6431-96T, Human C4d(Complement Component 4d) ELISA Kit, 96T

2.963,10 RON

Human C4d(Complement Component 4d) ELISA Kit

SKU
ELK6431-96T

Alternative Names: C4d

Species: Human

Assay Type: Sandwich

Sensitivity: 0.92 ng/mL

Standard: 140 ng/mL

Detection range: 2.19-140 ng/mL

Sample type: serum, plasma and other biological fluids

Assay length: 3.5h

Research Area: Signal transduction;Infection immunity;Hematology;

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 C4d. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human C4d. 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 C4d, 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 C4d in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: C4d

Species: Human

Assay Type: Sandwich

Sensitivity: 0.92 ng/mL

Standard: 140 ng/mL

Detection range: 2.19-140 ng/mL

Sample type: serum, plasma and other biological fluids

Assay length: 3.5h

Research Area: Signal transduction;Infection immunity;Hematology;

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 C4d. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human C4d. 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 C4d, 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 C4d in the samples is then determined by comparing the OD of the samples to the standard curve.