Human Fc ELISA Reagent Kit
Condition of sample preparation and optimal sample dilution should be determined experimentally by the investigator.
EK000095-20310: ELISA reagent kit for human Fc protein
The human Fc ELISA Reagent Kit contains the same essential components as the human Fc ELISA Complete Kit (EK000095-HUFC). Thus, the human Fc ELISA Reagent Kit can be used to make the human Fc ELISA kit in house to save more.
Application: for the quantitative determination of human Fc proteins in cell culture supernatants and serum.
This assay is specific for human Fc, and does not cross react with mouse Fc.
1. Capturing antibody
2. Detecting antibody
3. Human Fc protein standard
4. ELISA Protocol
The following reagents are not included in the human Fc ELISA reagent kits and must be provided by the end users:
1. 96-well or 384-well ELISA plates
2. Assay Diluent (PBS + 1% BSA)
3. Wash buffer (PBS + 0.01% Tween20)
4. HRP substrate (TMB)
5. Stop solution (0.5N HCl)
6. Absorbance microplate reader (we recommend BMG LABTECH microplate readers)
Fc is the tail region of an immunoglobulin G (IgG) that interacts with cell surface receptors called Fc receptors and some proteins of the complement system. The ~230 amino acid fragment generally exists as a dimer, although under reduced condition, it exists as a monomer. It is the basis of prolonged pharmacokinetics of antibodies and is commonly used as a fusion to extend half-life of fusion proteins.
This assay employs the quantitative sandwich enzyme immunoassay technique. An affinity purified polyclonal antibody specific for human or mouse Fc has been coated onto a 96-well microplate. Standards, control, and samples are pipetted into the wells and any human or mouse Fc present is bound by the immobilized antibody. After washing away any unbound substances, an enzyme-linked polyclonal antibody specific for human or mouse Fc is added to the wells. Following an incubation and a wash to remove any unbound antibody-enzyme reagent, a substrate solution is added to the wells. The enzyme reaction yields a blue product that turns yellow when the stop solution is added. The intensity of the color measured is in proportion to the amount of human or mouse Fc bound in the initial step. The sample values are then read off the standard curve.