Specifications
- Pk:96 Tests
- Assay duration:Multiple steps
- Assay Type:Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Rat
- Target protein:68 kDa Neurofilament/NF-L
- Description:Rat 68kDa Neurofilament/NF-L ELISA kit
- Sample type:Serum, plasma, tissue homogenates and other biological fluids
- Cross reactivity:Rat 68kDa Neurofilament/NF-L ELISA Kit exhibits high specificity and excellent specificity for the detection of rat 68kDa Neurofilament/NF-L. No significant cross-reactivity or interference between 68kDa Neurofilament/NF-L and analogues was observed.
- Detection method:Colorimetric
- Time to Results:4 h 30 min
- Assay Principle:Quantitative
- Shelf life:Store for 6 months at 4 °C
- Detection range:15,625 - 1000 pg/ml
- Storage temperature:4 °C
- Sample volume:100 μl
- Sensitivity:9,375 pg/ml
- Regulatory status:RUO
Specifications
About this item
Rat 68kDa Neurofilament/NF-L ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rat 68kDa Neurofilament/NF-L in serum, plasma, tissue homogenates, and other biological fluids.
- Ready To Use ELISA Kit
- Detection Range: 15,625 to 1000 pg/ml
- Sensitivity: 9,375 pg/ml
- Sample Type: Serum, plasma, tissue homogenates, and other biological fluids
- Assay Precision: Intra - Assay: CV <8%, Inter - Assay: CV <10%
Rat 68kDa Neurofilament / NF-L ELISA Kit (A79558) employs the sandwich enzyme immunoassay technique for the quantitative measurement of rat 68kDa Neurofilament / NF-L in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for 68kDa Neurofilament / NF-L has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the 68kDa Neurofilament / NF-L 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-68kDa Neurofilament / NF-L Antibody, which binds the captured 68kDa Neurofilament / NF-L 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 68kDa Neurofilament / NF-L captured in each well. The concentration of 68kDa Neurofilament / NF-L can then be calculated by reading the O.D. absorbance at 450nm in a microplate reader and referring to the standard curve.