Rat oxidized lowdensity lipoprotein ELISA Kit from MyBioSource.com

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Rat oxidized lowdensity lipoprotein ELISA Kit

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Description

For Samples: Cell culture fluid & body fluid & tissue homogenate serum or blood plasma

Intended Uses: This OX-LDL ELISA kit is intended for laboratory research use only and not for use in diagnostic or therapeutic procedures. The stop solution changes the color from blue to yellow and the intensity of the color is measured at 450 nm using a spectrophotometer. In order to measure the concentration of OX-LDL in the sample, this OX-LDL ELISA Kit includes a set of calibration standards. The calibration standards are assayed at the same time as the samples and allow the operator to produce a standard curve of Optical Density versus OX-LDL concentration. The concentration of in the samples is then determined by comparing the O.D. of the samples to the standard curve.

Principle of the Assay: The coated well immunoenzymatic assay for the quantitative measurement of OX-LDL utilizes a polyclonal anti-OX-LDL antibody and an OX-LDL-HRP conjugate. The assay sample and buffer are incubated together with OX-LDL-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the OX-LDL concentration since OX-LDL from samples and OX-LDL-HRP conjugate compete for the anti-OX-LDL antibody binding site. Since the number of sites is limited, as more sites are occupied by OX-LDL from the sample, fewer sites are left to bind OX-LDL-HRP conjugate. Standards of known OX-LDL concentrations are run concurrently with the samples being assayed and a standard curve is plotted relating the intensity of the color (O.D.) to the concentration of OX-LDL. The OX-LDL concentration in each sample is interpolated from this standard curve