Specifications
- Förp.:96 Tests
- Analysens varaktighet:Multiple steps
- Analystyp:Sandwich
- Formatera:Pre-coated
- Primary antibody reactivity:Rat
- Target protein:Fatty Acid Synthase
- Beskrivning:Rat fatty acid synthase ELISA kit
- Typ av prov:Serum, plasma, tissue homogenates and other biological fluids
- Korsreaktivitet:Rat Fatty Acid Synthase ELISA kit exhibits high specificity and excellent specificity for the detection of rat Fatty Acid Synthase. No significant cross-reactivity or interference between Fatty Acid Synthase and analogues was observed.
- Detektionsmetod:Colorimetric
- Time to Results:4 h 30 min
- Analysprincip:Quantitative
- Hållbarhetstid:Store for 6 months at 4 °C
- Detektionsområde:0,313 - 20 ng/ml
- Förvaringstemperatur:4 °C
- Provvolym:100 μl
- Känslighet:0,188 ng/ml
- Regulatory status:RUO
Specifications
About this item
Rat Fatty Acid Synthase ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rat Fatty Acid Synthase in serum, plasma, tissue homogenates, and other biological fluids.
- Ready-To-Use ELISA Kit
- Detection Range: 0,313 - 20 ng/ml
- Sensitivity: 0,188 ng/ml
- Sample Type: Serum, plasma, tissue homogenates, and other biological fluids
- Assay Precision: Intra-Assay: CV <8%, Inter-Assay: CV <10%
Rat Fatty Acid Synthase ELISA kit (A79322) employs the sandwich enzyme immunoassay technique for the quantitative measurement of rat Fatty Acid Synthase in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for Fatty Acid Synthase has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Fatty Acid Synthase present in each sample is bound to the wells by the immobilized antibody. Following incubation, the wells are washed and then incubated with Biotinylated Anti-Fatty Acid Synthase Antibody, which binds the captured Fatty Acid Synthase present in each well. Following incubation, unbound biotinylated detection antibody is removed by washing, and an HRP-Streptavidin conjugate is added to the wells and the microtiter plate is incubated. Following incubation and washing, TMB substrate solution is then used to visualize the HRP enzymatic reaction by catalysis to produce a blue-coloured product that changes to yellow after addition of acidic stop solution. The density of yellow is proportional to the amount of Fatty Acid Synthase captured in each well. The concentration of Fatty Acid Synthase can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.