Area of research
Store at 2-8 deg C
Optimal conditions to be determined by end-user
AntiPhosphatidic Acid is an indirect solid phase enzyme immunometric assays (ELISA). It is designed for the quantitative measurement of IgG or IgM class autoantibodies directed against negativelycharged phospholipids. The microplate is coated with highly purified Phosphatidic Acid. AntiPhospholipid autoantibodies require beta2Glycoprotein I as a cofactor for binding. The microplate is therefore saturated with human beta2Glycoprotein I. The microplates can be divided into 12 modules of 8 wells each or can be used completely for 96 determinations. Each well can be separated from the module ("breakaway"). The binding of present autoantibodies, formation of the sandwich complexes and enzymatic colour reaction take place during three different reaction phases.
E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays,E05 478 566 350 170 or Enzyme-Linked Immunosorbent Assays,Immunoglobulin M, or IgM for short, is a basic antibody that is produced by B cells. IgM is by far the physically largest antibody in the human circulatory system. It is the first antibody to appear in response to initial exposure to an antigen
ELISA Enzyme-linked immunosorbent assays Code 90320007 SNOMED
Immunoglobulin gamma, IgG, mouse monoclonal H&L chain clones or rabbit, goat polyclonal antibodies have 4 parts. There are 2 heavy chains, 2 light chains. The IgG antibody has 2 antigen binding sites. They represent 70% or more of serum antibodies. This antibody can be antigen purified or protein A or G purified. For storage sodium azide is added or you can call us to request azide free antibody preparations. These will need colder storage temperatures.