ELK1590-96T, Human C3a(Complement Component 3a) ELISA Kit, 96T

ELK1590-96T, Human C3a(Complement Component 3a) ELISA Kit, 96T

ELK1591-96T, Rat C3a(Complement Component 3a) ELISA Kit, 96T

ELK1591-96T, Rat C3a(Complement Component 3a) ELISA Kit, 96T

ELK1591-48T, Rat C3a(Complement Component 3a) ELISA Kit, 48T

2.142,00 RON

Rat C3a(Complement Component 3a) ELISA Kit

SKU
ELK1591-48T

Alternative Names: Complement Component 3a

Species: Rat

Assay Type: Sandwich

Sensitivity: 2.81 pg/mL

Standard: 400 pg/mL

Detection range: 6.25-400 pg/mL

Sample type: serum, plasma and other biological fluids

Assay length: 3.5h

Research Area: Infection immunity;Immune molecule;Autoimmunity;

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 C3a. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat C3a. 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 C3a, 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 C3a in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: Complement Component 3a

Species: Rat

Assay Type: Sandwich

Sensitivity: 2.81 pg/mL

Standard: 400 pg/mL

Detection range: 6.25-400 pg/mL

Sample type: serum, plasma and other biological fluids

Assay length: 3.5h

Research Area: Infection immunity;Immune molecule;Autoimmunity;

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 C3a. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat C3a. 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 C3a, 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 C3a in the samples is then determined by comparing the OD of the samples to the standard curve.