Monkey Total Bilirubin ELISA Kit | TBIL elisa kit
Monkey Total Bilirubin ELISA Kit
Reactivity
Monkey
Synonyms
Total Bilirubin; N/A; Monkey Total Bilirubin ELISA Kit; TBIL elisa kit
Reactivity
Monkey
Specificity
This assay has high sensitivity and excellent specificity for detection of TBB. No significant cross-reactivity or interference between TBB and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between TBB and all the analogues, therefore, cross reaction may still exist in some cases.
Samples
Serum, plasma, cell culture supernatants, body fluid and tissue homogenate
Assay Type
Quantitative Competitive
Sensitivity
0.1 umol/L
Preparation and Storage
Store all reagents at 2-8 degree C.
Standard Curve (Sample)
Related Product Information for TBIL elisa kit
Intended Uses: This TBB ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Monkey TBB. This ELISA kit for research use only, not for therapeutic or test applications!
Principle of the Assay: TBB ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-TBB antibody and an TBB-HRP conjugate. The assay sample and buffer are incubated together with TBB-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the TBB concentration since TBB from samples and TBB-HRP conjugate compete for the anti-TBB antibody binding site. Since the number of sites is limited, as more sites are occupied by TBB from the sample, fewer sites are left to bind TBB-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The TBB concentration in each sample is interpolated from this standard curve.
Principle of the Assay: TBB ELISA kit applies the competitive enzyme immunoassay technique utilizing a polyclonal anti-TBB antibody and an TBB-HRP conjugate. The assay sample and buffer are incubated together with TBB-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the TBB concentration since TBB from samples and TBB-HRP conjugate compete for the anti-TBB antibody binding site. Since the number of sites is limited, as more sites are occupied by TBB from the sample, fewer sites are left to bind TBB-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The TBB concentration in each sample is interpolated from this standard curve.
