Specifications
- Conf:96 Tests
- Durata del test:Multiple steps
- Tipo di test:Sandwich
- Formato:Pre-coated
- Primary antibody reactivity:Rabbit
- Target protein:alpha 2 Macroglobulin
- Descrizione:Rabbit alpha 2 macroglobulin ELISA kit
- Tiipo del campione:Serum, plasma, tissue homogenates and other biological fluids
- Reattività incrociata:Rabbit alpha 2 Macroglobulin ELISA kit exhibits high specificity and excellent specificity for the detection of rabbit alpha 2 Macroglobulin. No significant cross-reactivity or interference between alpha 2 Macroglobulin and analogues was observed.
- Metodo di rilevamento:Colorimetric
- Tempo ai risultati:4 h 30 min
- Principio del dosaggio:Quantitative
- Durata a magazzino:Store for 6 months at 4 °C
- Range di rilevamento:6,25 - 400 ng/ml
- Temperatura di conservazione:4 °C
- Volume del campione:100 μl
- Sensibilità:3,75 ng/ml
- Stato regolamentazione:RUO
Specifications
About this item
Rabbit alpha 2 Macroglobulin ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rabbit alpha 2 Macroglobulin 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%
Rabbit alpha 2 Macroglobulin ELISA kit (A75070) employs the sandwich enzyme immunoassay technique for the quantitative measurement of rabbit alpha 2 Macroglobulin in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for alpha 2 Macroglobulin has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the alpha 2 Macroglobulin 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-alpha 2 Macroglobulin Antibody, which binds the captured alpha 2 Macroglobulin 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 alpha 2 Macroglobulin captured in each well. The concentration of alpha 2 Macroglobulin can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.