Canine Fc Fragment of IgG Binding Protein ELISA Kit | FcgammaBP elisa kit

Canine Fc Fragment of IgG Binding Protein ELISA Kit

Cat. Num. AAA55443

• Reactivity: Canine
• Synonyms: Fc Fragment of IgG Binding Protein; Canine Fc Fragment of IgG Binding Protein ELISA Kit; FcgammaBP elisa kit

• Reactivity: Canine
• Specificity: No significant cross-reactivity or interference between Canine FcgammaBP and analogues was observed.

• Samples: Serum, Plasma, Tissue Homogenate, Feces, Urine and Body Fluids
• Assay Type: Sandwich
• Detection Range: 0.625 ng/ml - 20 ng/ml.
• Sensitivity: 0.1 ng/ml.
• Intended Uses: This Quantitative Sandwich ELISA kit is only for in vitro research use only, not for drug, household, therapeutic applications! It is intended to be determinated FcgammaBP concentrations in Canine serum, plasma and other body fluids. Using Purified Canine FcgammaBP antibody to coat Microelisa Stripplate wells to make solid-phase antibody, then add FcgammaBP and FcgammaBP antibody which has been labeled with HRP to wells, then the reactants become antibody-antigen-antibody-enzyme complex, after washing completely, add TMB substrate solution, TMB substrate becomes blue color under HRP enzyme-catalyzed, reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. The concentration of FcgammaBP in the samples is then determined by comparing the O.D. of the samples to the standard curve.
• Intra-assay Precision: Intra-assay CV (%) is less than 15%.
• Inter-assay Precision: Inter-assay CV (%) is less than 15%. [CV(%) = SD/mean ×100]
• Preparation and Storage: Store all reagents at 2-8 degree C

Related Product Information for FcgammaBP elisa kit

Background: This Quantitative Sandwich ELISA kit is only for in vitro research use only! It is intended to be determinated FcgammaBP concentrations in Canine serum, plasma and other body fluids. Using Purified Canine FcgammaBP antibody to coat Microelisa Stripplate wells to make solid-phase antibody, then add FcgammaBP and FcgammaBP antibody which has been labeled with HRP to wells, then the reactants become antibody-antigen-antibody-enzyme complex, after washing completely, add TMB substrate solution, TMB substrate becomes blue color under HRP enzyme-catalyzed, reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. The concentration of FcgammaBP in the samples is then determined by comparing the O.D. of the samples to the standard curve.