Area of research
Proteases, Inhibitors, & Enzymes
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Optimal conditions to be determined by end user
An antihuman Granzyme B coating antibody is adsorbed onto microwells. Human Granzyme B present in the sample or standard binds to antibodies adsorbed to the microwells. Following incubation unbound biological components are removed during a wash step and a biotinconjugated antihuman Granzyme B antibody is added and binds to Granzyme B captured by the first antibody. Following incubation unbound biotin conjugated antihuman Granzyme B antibody is removed during a wash step. StreptavidinHRP is added and binds to the biotin conjugated antihuman Granzyme B antibody. Following incubation unbound StreptavidinHRP is removed during a wash step, and substrate solution reactive with HRP is added to the wells. A coloured product is formed in proportion to the amount of human Granzyme B present in the sample or standard. The reaction is terminated by addition of acid and absorbance is measured at 450 nm. A standard curve is prepared from 7 human Granzyme B standard dilutions and human Granzyme B sample concentration determined.
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.
ELISA Enzyme-linked immunosorbent assays Code 90320007 SNOMED