- Assay duration:Multiple steps
- Assay Type (ELISA with LOV):Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Rat
- Target protein:Somatostatin Receptor 2
- Description:Rat somatostatin receptor 2 ELISA kit
- Size:96 tests
- Sample Type:Serum, plasma, tissue homogenates, and other biological fluids
- Cross Reactivity:Rat Somatostatin Receptor 2 ELISA Kit exhibits high specificity and excellent specificity for the detection of rat Somatostatin Receptor 2. No significant cross-reactivity or interference between Somatostatin Receptor 2 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.:76740-302
Rat Somatostatin Receptor 2 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rat Somatostatin Receptor 2 in serum, plasma, tissue homogenates, and other biological fluids.
- Ready-to-use ELISA kit
- Assay precision: Intra-assay: CV <8%, Inter-assay: CV <10%
Rat Somatostatin Receptor 2 ELISA kit (A303721) employs the sandwich enzyme immunoassay technique for the quantitative measurement of rat Somatostatin Receptor 2 in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for Somatostatin Receptor 2 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Somatostatin Receptor 2 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-Somatostatin Receptor 2 Antibody, which binds the captured Somatostatin Receptor 2 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 Somatostatin Receptor 2 captured in each well. The concentration of Somatostatin Receptor 2 can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.