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Alternative name
Cytochrome P450 2C23 ELISA KIT; Arachidonic acid epoxygenase ELISA KIT; CYPIIC23Cyp2c23 ELISA KIT; Cyp2c-23 ELISA KIT
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Catalog
E044755
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species
Mouse
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GeneAA
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Other Species
Human AT2R1-AA ELISA KitHuman AGTR2-AA ELISA KitHuman AGTR2 AA ELISA KitHuman AA ELISA KitHuman AA ELISA KitHuman AA NAT ELISA KitHuman AA-NAT ELISA KitHuman LKM-AA ELISA KitHuman PDGF-AA ELISA KitMouse AT1R-AA ELISA KitMouse AGTR2-AA ELISA KitMouse AA-NAT ELISA KitMouse H2-Aa ELISA KitMouse LKM-AA ELISA KitMouse PDGF-AA ELISA KitRat RT1 class I histocompatibility antigen, AA alpha chain ELISA KitBovine AA ELISA KitCanine AA ELISA KitChicken AA ELISA KitGeneral AA ELISA KitPorcine AA ELISA KitRabbit AA ELISA KitRat AA ELISA KitCamel AA ELISA KitGoat AA ELISA KitGuinea Pig AA ELISA KitHamster AA ELISA Kit
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SpecificityThis assay has high sensitivity and excellent specificity for detection of mouse AA. No significant cross-reactivity or interference between mouse AA 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 AA is typically less than 13.797 ng/ml. The sensitivity of this assay, or Lower Limit of Detection (LLD) was defined as the lowest mouse AA concentration that could be differentiated from zero. It was determined the me
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Intended UseMouse AA ELISA Kit allows for the in vitro quantitative determination of AA , 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
specificalPrinciple of the assay: This assay employs the competitive inhibition enzyme immunoassay technique. The microtiter plate provided in this kit has been pre-coated with an antibody specific to AA. Standards or samples are added to the appropriate microtiter plate wells with Horseradish Peroxidase (HRP) conjugated AA. The competitive inhibition reaction is launched between with HRP-conjugated AA and AA in samples. A substrate solution is added to the wells and the color develops in opposite to the amount of AA in the sample. The color development is stopped and the intensity of the color is measured.
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