Specifications
- Pk:96 Tests
- Assay duration:Multiple steps
- Assay Type:Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Human
- Target protein:ULBP1
- Description:Human ULBP1 ELISA kit
- Sample type:Serum, plasma, tissue homogenates, and other biological fluids
- Cross reactivity:Human ULBP1 ELISA Kit exhibits high specificity and excellent specificity for the detection of human ULBP1. No significant cross-reactivity or interference between ULBP1 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: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
Human ULBP1 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human ULBP1 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 ULBP1 ELISA kit employs the sandwich enzyme immunoassay technique for the quantitative measurement of human ULBP1 in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for ULBP1 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the ULBP1 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-ULBP1 Antibody, which binds the captured ULBP1 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 ULBP1 captured in each well. The concentration of ULBP1 can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.