ELK5283-48T, Rat C1q(Complement 1q) ELISA Kit, 48T

ELK5283-48T, Rat C1q(Complement 1q) ELISA Kit, 48T

ELK5284-48T, Human UROC1(Urocanase Domain Containing Protein 1) ELISA Kit, 48T

ELK5284-48T, Human UROC1(Urocanase Domain Containing Protein 1) ELISA Kit, 48T

ELK5283-96T, Rat C1q(Complement 1q) ELISA Kit, 96T

2.963,10 RON

Rat C1q(Complement 1q) ELISA Kit

SKU
ELK5283-96T

Alternative Names: C1-q

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.38 ng/mL

Standard: 50 ng/mL

Detection range: 0.79-50 ng/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 C1q. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat C1q. 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 C1q, 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 C1q in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: C1-q

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.38 ng/mL

Standard: 50 ng/mL

Detection range: 0.79-50 ng/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 C1q. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Rat C1q. 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 C1q, 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 C1q in the samples is then determined by comparing the OD of the samples to the standard curve.