Specifications
- Assay duration:Multiple steps
- Assay Type:Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Human
- Target protein:PHAPI2/APRIL
- Description:Human PHAPI2/APRIL ELISA kit
- Size:96 tests
- Sample type:Serum, plasma, tissue homogenates, and other biological fluids
- Cross reactivity:Human PHAPI2/APRIL ELISA Kit exhibits high specificity and excellent specificity for the detection of human PHAPI2/APRIL. No significant cross-reactivity or interference between PHAPI2/APRIL and analogues was observed.
- Detection method:Colorimetric
- Time to Results:4 h 30 min
- Shelf life:Store for 6 months at 4 °C
- Detection range:31.25 - 2000 pg/ml
- Storage temperature:4 °C
- Sample volume:100 μl
- Sensitivity:18.75 pg/ml
- Regulatory status:RUO
- Cat. no.:76740-760
Specifications
About this item
Human PHAPI2/APRIL ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human PHAPI2/APRIL in serum, plasma, tissue homogenates, and other biological fluids.
- Ready-to-use ELISA kit
- Assay precision: Intra-assay: CV <8%, Inter-assay: CV <10%
Human PHAPI2/APRIL ELISA kit (A303172) employs the sandwich enzyme immunoassay technique for the quantitative measurement of human PHAPI2/APRIL in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for PHAPI2/APRIL has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the PHAPI2/APRIL 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-PHAPI2/APRIL Antibody, which binds the captured PHAPI2/APRIL 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 PHAPI2/APRIL captured in each well. The concentration of PHAPI2/APRIL can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.