Specifications
- Assay duration:Multiple steps
- Assay Type (ELISA with LOV):Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Human
- Target protein:Natriuretic Peptides A
- Description:Human natriuretic peptides A ELISA kit
- Size:96 tests
- Sample Type:Serum, plasma, tissue homogenates and other biological fluids
- Cross Reactivity:Human Natriuretic Peptides A ELISA kit exhibits high specificity and excellent specificity for the detection of human Natriuretic Peptides A. No significant cross-reactivity or interference between Natriuretic Peptides A 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:7.813 - 500 pg/ml
- Storage Temperature:4 °C
- Sample Volume:100 μl
- Sensitivity:4.688 pg/ml
- Regulatory Status:RUO
- Cat. No.:76741-176
Specifications
About this item
Human Natriuretic Peptides A ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human Natriuretic Peptides A in serum, plasma, tissue homogenates, and other biological fluids.
- Ready to use ELISA kit
- Detection range: 7.813 to 500 pg/ml
- Sensitivity: 4.688 pg/ml
- Sample type: Serum, plasma, tissue homogenates, and other biological fluids
- Assay precision: Intra assay: CV <8%, Inter assay: CV <10%
Human Natriuretic Peptides A ELISA kit (A77685) employs the sandwich enzyme immunoassay technique for the quantitative measurement of human Natriuretic Peptides A in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for Natriuretic Peptides A has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Natriuretic Peptides A 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-Natriuretic Peptides A Antibody, which binds the captured Natriuretic Peptides A 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 Natriuretic Peptides A captured in each well. The concentration of Natriuretic Peptides A can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.