ELK1593-96T, Rat C5a(Complement Component 5a) ELISA Kit, 96T

ELK1593-96T, Rat C5a(Complement Component 5a) ELISA Kit, 96T

ELK1594-96T, Human C4BPa(C4 Binding Protein Alpha) ELISA Kit, 96T

ELK1594-96T, Human C4BPa(C4 Binding Protein Alpha) ELISA Kit, 96T

ELK1594-48T, Human C4BPa(C4 Binding Protein Alpha) ELISA Kit, 48T

2.142,00 RON

Human C4BPa(C4 Binding Protein Alpha) ELISA Kit

SKU
ELK1594-48T

Alternative Names: C4BP-a; PRP; C4BP; Complement Component 4 Binding Protein,Alpha; Proline-rich protein

Species: Human

Assay Type: Sandwich

Sensitivity: 0.068 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

Sample type: Serum, plasma and other biological fluids

Assay length: 3.5h

Research Area: 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 Human C4BPa. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human C4BPa. 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 C4BPa, 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 C4BPa in the samples is then determined by comparing the OD of the samples to the standard curve.

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Description

Alternative Names: C4BP-a; PRP; C4BP; Complement Component 4 Binding Protein,Alpha; Proline-rich protein

Species: Human

Assay Type: Sandwich

Sensitivity: 0.068 ng/mL

Standard: 10 ng/mL

Detection range: 0.16-10 ng/mL

Sample type: Serum, plasma and other biological fluids

Assay length: 3.5h

Research Area: 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 Human C4BPa. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human C4BPa. 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 C4BPa, 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 C4BPa in the samples is then determined by comparing the OD of the samples to the standard curve.