- Pk:96 Tests
- Assay duration:Multiple steps
- Assay Type:Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Human
- Target protein:Laminin alpha 4/LAMA4
- Description:Human Laminin alpha 4/LAMA4 ELISA kit
- Sample type:Serum, plasma, tissue homogenates and other biological fluids
- Cross reactivity:Human Laminin alpha 4/LAMA4 ELISA kit exhibits high specificity and excellent specificity for the detection of human Laminin alpha 4/LAMA4. No significant cross-reactivity or interference between Laminin alpha 4/LAMA4 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:78,125 - 5000 pg/ml
- Storage temperature:4 °C
- Sample volume:100 μl
- Sensitivity:46,875 pg/ml
- Regulatory status:RUO
Human Laminin alpha 4/LAMA4 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human Laminin alpha 4/LAMA4 in serum, plasma, tissue homogenates, and other biological fluids.
- Ready to use ELISA kit
- Detection range: 78,125 to 5000 pg/ml
- Sensitivity: 46,875 pg/ml
- Sample type: Serum, plasma, tissue homogenates, and other biological fluids
- Assay precision: Intra assay: CV <8%, Inter assay: CV <10%
Human Laminin alpha 4 / LAMA4 employs the sandwich enzyme immunoassay technique for the quantitative measurement of human Laminin alpha 4 / LAMA4 in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for Laminin alpha 4 / LAMA4 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Laminin alpha 4 / LAMA4 present in each sample is bound to the wells by the immobilised antibody. Following incubation, the wells are washed and then incubated with Biotinylated Anti-Laminin alpha 4 / LAMA4 Antibody, which binds the captured Laminin alpha 4 / LAMA4 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 visualise 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 Laminin alpha 4 / LAMA4 captured in each well. The concentration of Laminin alpha 4 / LAMA4 can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.