Specifications
- VE:96 Tests
- Testdauer:Multiple steps
- Testtyp:Sandwich
- Format:Pre-coated
- Reaktivität der primären Antikörper:Rat
- Target protein:alpha 1 Microglobulin
- Bezeichnung:Rat alpha 1 microglobulin ELISA kit
- Probentyp:Serum, plasma, tissue homogenates and other biological fluids
- Kreuzreaktivität:Rat alpha 1 Microglobulin ELISA Kit exhibits high specificity and excellent specificity for the detection of rat alpha 1 Microglobulin. No significant cross-reactivity or interference between alpha 1 Microglobulin and analogues was observed.
- Erkennungsmethode:Colorimetric
- Time to Results:4 h 30 min
- Testprinzip:Quantitative
- Shelf life:Store for 6 months at 4 °C
- Erfassungsbereich:6,25 - 400 ng/ml
- Lagertemperatur:4 °C
- Probenvolumen:100 μl
- Empfindlichkeit:3,75 ng/ml
- Regulatory status:RUO
Specifications
About this item
Rat alpha 1 Microglobulin ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rat alpha 1 Microglobulin in serum, plasma, tissue homogenates, and other biological fluids.
- Ready To Use ELISA Kit
- Detection Range: 6,25 to 400 ng/ml
- Sensitivity: 3,75 ng/ml
- Sample Type: Serum, plasma, tissue homogenates, and other biological fluids
- Assay Precision: Intra - Assay: CV <8%, Inter - Assay: CV <10%
Rat alpha 1 Microglobulin ELISA Kit (A78985) employs the sandwich enzyme immunoassay technique for the quantitative measurement of rat alpha 1 Microglobulin in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for alpha 1 Microglobulin has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the alpha 1 Microglobulin 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-alpha 1 Microglobulin Antibody, which binds the captured alpha 1 Microglobulin 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 alpha 1 Microglobulin captured in each well. The concentration of alpha 1 Microglobulin can then be calculated by reading the O.D. absorbance at 450nm in a microplate reader and referring to the standard curve.