|
|
Human Fibrinogen ELISA Kit
(96-well plate)
more info
|
350€
|
|
Mouse Fibrinogen ELISA Kit
(96-well plate)
more info
|
350€
|
|
Rat Fibrinogen ELISA Kit
(96-well plate)
more info
|
350€
|
The Human Fibrinogen ELISA kit is designed for detection of human FBG in plasma. This assay employs a quantitative competitive sandwich enzyme immunoassay technique that measures FBG in less than 3 hours. A murine antibody specific for FBG has been pre-coated onto a 96-well microplate with removable strips. FBG in standards and samples is competed by a biotinylated FBG sandwiched by the immobilized antibody and streptavidin-peroxidase conjugate. All unbound material is then washed away and a peroxidase enzyme substrate is added. The color development is stopped and the intensity of the color is measured.
The Mouse Fibrinogen ELISA kit is designed for detection of mouse FBG in cell culture media, and plasma samples. This assay employs a quantitative sandwich enzyme immunoassay technique that measures mouse FBG in 3.5 hours. A polyclonal antibody specific for mouse FBG has been pre-coated onto a 96-well microplate with removable strips. FBG in standards and samples is sandwiched by the immobilized polyclonal antibody and biotinylated polyclonal antibody specific for mouse FBG, which is recognized by a streptavidin-peroxidase conjugate. All unbound material is then washed away and a peroxidase enzyme substrate is added. The color development is stopped and the intensity of the color is measured.The Rat Fibrinogen ELISA kit is designed for detection of rat FBG in cell culture media, and plasma samples. This assay employs a quantitative sandwich enzyme immunoassay technique that measures rat FBG in 3.5 hours. A polyclonal antibody specific for rat FBG has been pre-coated onto a 96-well microplate with removable strips. FBG in standards and samples is sandwiched by the immobilized polyclonal antibody and biotinylated polyclonal antibody specific for rat FBG, which is recognized by a streptavidin-peroxidase conjugate. All unbound material is then washed away and a peroxidase enzyme substrate is added. The color development is stopped and the intensity of the color is measured.
|
