- Förp.:96 Tests
- Analysens varaktighet:Multiple steps
- Analystyp:Sandwich
- Formatera:Pre-coated
- Primary antibody reactivity:Human
- Target protein:Ferritin Light Chain
- Beskrivning:Human ferritin light chain ELISA kit
- Typ av prov:Serum, plasma, tissue homogenates and other biological fluids
- Korsreaktivitet:Human Ferritin Light Chain ELISA kit exhibits high specificity and excellent specificity for the detection of human Ferritin Light Chain. No significant cross-reactivity or interference between Ferritin Light Chain 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
Human Ferritin Light Chain ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human Ferritin Light Chain 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%
Human Ferritin Light Chain ELISA kit (A79343) employs the sandwich enzyme immunoassay technique for the quantitative measurement of human Ferritin Light Chain in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for Ferritin Light Chain has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Ferritin Light Chain 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-Ferritin Light Chain Antibody, which binds the captured Ferritin Light Chain 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 Ferritin Light Chain captured in each well. The concentration of Ferritin Light Chain can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.