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Thrombopoietin (Rat) ELISA Kit

A sandwich ELISA kit for in vitro quantitative determination of rat TPO concentrations in serum, plasma and other biological fluids.
Catalog #: E4734
$525.00

Product Details

Cat # +Size E4734-100
Size 100 assays
Detection Method Absorbance (450 nm)
Species Reactivity Rat
Features & Benefits Specificity: No significant cross-reactivity or interference between Rat TPO and analogues was observed.
Sensitivity: 18.75 pg/ml
Detection Range: 31.25 - 2000 pg/ml
Coefficient of variation is < 10%.
Kit Components • Standard
• Wash Buffer (25x)
• Micro ELISA Plate
• Biotinylated Detection Ab (100x)
• HRP Conjugate (100x)
• Plate Sealer
• HRP Conjugate Diluent
• Standard & Sample Diluent
• Stop Solution
• Substrate Reagent
• Biotinylated Detection Antibody Diluent
Storage Conditions 4°C
Shipping Conditions Gel Pack
USAGE For Research Use Only! Not For Use in Humans.

Details

TPO is a lineage-specific growth factor, produced in the liver, kidney and skeletal muscle. It stimulates the proliferation and maturation of megakaryocytes and promotes increased circulating levels of platelets in vivo. TPO signals through the c-mpl receptor and acts as an important regulator of circulating platelets. BioVision's ELISA kit is based on the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to rat TPO. Standards or samples are added to the micro ELISA plate and combined with the specific antibody. Then a biotinylated detection antibody specific for rat TPO and Avidin-Horseradish Peroxidase (HRP) conjugate are added successively to each micro plate well and incubated. On addition of substrate those wells that contain rat TPO, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm. The concentration of rat TPO in the samples can be calculated by comparing the OD of the samples to the standard curve.


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