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Catalog
E003155
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species
Human
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GeneAP
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Other Species
Human AP ELISA KitHuman AP/3a 5a THP ELISA KitHuman AP/3alpha-5alpha-THP ELISA KitHuman alpha2-AP ELISA KitHuman AP-12 ELISA KitHuman AP-1 ELISA KitMouse AP/3alpha-5alpha-THP ELISA KitMouse alpha2-AP ELISA KitMouse AP ELISA KitMouse AP-1 ELISA KitBovine AP ELISA KitCanine AP ELISA KitChicken AP ELISA KitGeneral AP ELISA KitPorcine AP ELISA KitRabbit AP ELISA KitRat AP ELISA KitCamel AP ELISA KitGoat AP ELISA KitGuinea Pig AP ELISA KitHamster AP ELISA KitHorse AP ELISA KitMonkey AP ELISA KitSheep AP ELISA Kit
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SpecificityThis assay has high sensitivity and excellent specificity for detection of Human AP. No significant cross-reactivity or interference between Human AP and analogues was observed. Note: Limited by current skills and knowledge, it is impossible for us to complete the cross- reactivity detection between Human AP and all the analogues, therefore, cross reaction may still exist.
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SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
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Sensitivity0.938ng/mL
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Intended UseHuman AP ELISA Kit allows for the in vitro quantitative determination of AP , 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
specificalDescription: The kit is a competitive enzyme immunoassay for in vitro quantitative measurement of AP in human serum, plasma and other biological fluids
Principle of the Assay: This ELISA kit uses Competitive-ELISA as the method. The microtiter plate provided in this kit has been pre-coated with Human AP. During the reaction, Human AP in the sample or standard competes with a fixed amount of Human AP on the solid phase supporter for sites on the Biotinylated Detection Ab specific to Human AP. Excess conjugate and unbound sample or standard are washed from the plate, and Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm +/- 2 nm. The concentration of Human AP in the samples is then determined by comparing the O.D. of the samples to the standard curve.
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