ELK5655-48T, Rat LBP(Lipopolysaccharide Binding Protein) ELISA Kit, 48T

ELK5655-48T, Rat LBP(Lipopolysaccharide Binding Protein) ELISA Kit, 48T

ELK5656-48T, Pig TNNI3(Troponin I Type 3, Cardiac) ELISA Kit, 48T

ELK5656-48T, Pig TNNI3(Troponin I Type 3, Cardiac) ELISA Kit, 48T

ELK5655-96T, Rat LBP(Lipopolysaccharide Binding Protein) ELISA Kit, 96T

2.963,10 RON

Rat LBP(Lipopolysaccharide Binding Protein) ELISA Kit

SKU
ELK5655-96T

Alternative Names: LPS-Binding Protein

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.137 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: serum, plasma and other biological fluids

Assay length: 3.5h

Research Area: Infection immunity;

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

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Description

Alternative Names: LPS-Binding Protein

Species: Rat

Assay Type: Sandwich

Sensitivity: 0.137 ng/mL

Standard: 20 ng/mL

Detection range: 0.32-20 ng/mL

Sample type: serum, plasma and other biological fluids

Assay length: 3.5h

Research Area: Infection immunity;

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