3h
96T
ELK6173
608 EUR
3h
VLDL-R
50ng/mL
Sandwich
0.31ng/mL
0.781-50ng/mL
Rattus norvegicus
ELISA Enzyme-linked immunosorbent assays Code 90320007 SNOMED
Signal transduction;Metabolic pathway;Endocrinology;Cardiovascular biology;Hepatology;
E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays,E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays
Rats are used to make rat monoclonal anti mouse antibodies. There are less rat- than mouse clones however. Rats genes from rodents of the genus Rattus norvegicus are often studied in vivo as a model of human genes in Sprague-Dawley or Wistar rats.
High and low density proteins are supplied by ELK Biotech in volumes of 1. Other densities are possible.The receptors are ligand binding factors of type 1, 2 or 3 and protein-molecules that receive chemical-signals from outside a cell. When such chemical-signals couple or bind to a receptor, they cause some form of cellular/tissue-response, e.g. a change in the electrical-activity of a cell. In this sense, am olfactory receptor is a protein-molecule that recognizes and responds to endogenous-chemical signals, chemokinesor cytokines e.g. an acetylcholine-receptor recognizes and responds to its endogenous-ligand, acetylcholine. However, sometimes in pharmacology, the term is also used to include other proteins that are drug-targets, such as enzymes, transporters and ion-channels.
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 Very Low Density Lipoprotein Receptor (VLDLR). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Very Low Density Lipoprotein Receptor (VLDLR). 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 Very Low Density Lipoprotein Receptor (VLDLR), 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 Very Low Density Lipoprotein Receptor (VLDLR) in the samples is then determined by comparing the O.D. of the samples to the standard curve.