Human OxLDL(Oxidized Low Density Lipoprotein) ELISA Kit

 

Human OxLDL(Oxidized Low Density Lipoprotein) ELISA Kit

Size

96T

Catalog no.

ELK8195

Price

608 EUR

Buy at gentaur.com
Assay length

3h

Alternative Names

OL

Sensitivity

6.4pg/mL

Assay Type

Sandwich

Standard

1000pg/mL

Detection range

15.6-1000pg/mL

Research Area

Metabolic pathway;Endocrinology;Cardiovascular biology;

Test

ELISA Enzyme-linked immunosorbent assays Code 90320007 SNOMED

Description

High and low density proteins are supplied by ELK Biotech in volumes of 1. Other densities are possible.

Properties

E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays,E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays,Human proteins, cDNA and human recombinants are used in human reactive ELISA kits and to produce anti-human mono and polyclonal antibodies. Modern humans (Homo sapiens, primarily ssp. Homo sapiens sapiens). Depending on the epitopes used human ELISA kits can be cross reactive to many other species. Mainly analyzed are human serum, plasma, urine, saliva, human cell culture supernatants and biological samples.

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 Oxidized Low Density Lipoprotein (OxLDL). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Oxidized Low Density Lipoprotein (OxLDL). 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 Oxidized Low Density Lipoprotein (OxLDL), 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 Oxidized Low Density Lipoprotein (OxLDL) in the samples is then determined by comparing the O.D. of the samples to the standard curve.