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Alternative name
Peroxisome proliferator-activated receptor delta ELISA KIT; Nuclear hormone receptor 1 ELISA KIT; NUC1 ELISA KIT; Nuclear receptor subfamily 1 group C member 2 ELISA KIT; Peroxisome proliferator-activated receptor beta ELISA KIT; PPAR-betaPpard ELISA KIT; Nr1c2 ELISA KIT; Pparb ELISA KIT; PPAR-delta ELISA KIT; NUC1 ELISA KIT; PPAR-beta ELISA KIT
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Catalog
E063323
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species
Mouse
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GenePPAR-beta
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Other Species
Human PPAR beta ELISA KitHuman PPAR-beta ELISA Kit
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SpecificityThis assay has high sensitivity and excellent specificity for detection of mouse PPAR-beta. No significant cross-reactivity or interference between mouse PPAR-beta and analogues was observed.
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SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
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SensitivityThe minimum detectable dose of mouse PPAR-beta is typically less than 0.078 ng/ml. The sensitivity of this assay, or Lower Limit of Detection (LLD) was defined as the lowest protein concentration that could be differentiated from zero. It was determined t
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Intended UseMouse PPAR-beta ELISA Kit allows for the in vitro quantitative determination of PPAR-beta , concentrations in serum, Plasma , tissue homogenates and Cell culture supernates and Other biological fluids.
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StorageFor 5-7days:Store the whole kit at 4℃
For a Long time :Store the Substrate at 4℃, other reagent should store at -20℃.
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Product Description
specificalPriciple of the assay: This assay employs the quantitative sandwich enzyme immunoassay technique. Antibody specific for PPAR-beta has been pre-coated onto a microplate. Standards and samples are pipetted into the wells and any PPAR-beta present is bound by the immobilized antibody. After removing any unbound substances, a biotin-conjugated antibody specific for PPAR-beta is added to the wells. After washing, avidin conjugated Horseradish Peroxidase (HRP) is added to the wells. Following a wash to remove any unbound avidin-enzyme reagent, a substrate solution is added to the wells and color develops in proportion to the amount of PPAR-beta bound in the initial step. The color development is stopped and the intensity of the color is measured.
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