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Alternative name
AP-2 complex subunit sigma ELISA KIT; Adaptor protein complex AP-2 subunit sigma ELISA KIT; Adaptor-related protein complex 2 subunit sigma ELISA KIT; Clathrin assembly protein 2 sigma small chain ELISA KIT; Clathrin coat assembly protein AP17 ELISA KIT; Clathrin coat-associated protein AP17 ELISA KIT; HA2 17 kDa subunit ELISA KIT; Plasma membrane adaptor AP-2 17 kDa protein ELISA KIT; Sigma2-adaptinAP2S1 ELISA KIT; AP17 ELISA KIT; CLAPS2 ELISA KIT
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Catalog
E003189
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species
Human
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GeneAP17
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Other Species
Mouse AP17 ELISA Kit
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SpecificityThis assay has high sensitivity and excellent specificity for detection of Human AP17. No significant cross-reactivity or interference between Human AP17 and analogues was observed. Note: Limited by current skills and knowledge, it is impossible for us to complete the cross- reactivity detection between Human AP17 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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Sensitivity0.094ng/mL
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Intended UseHuman AP17 ELISA Kit allows for the in vitro quantitative determination of AP17 , 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 AP17 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 AP17. During the reaction, Human AP17 in the sample or standard competes with a fixed amount of Human AP17 on the solid phase supporter for sites on the Biotinylated Detection Ab specific to Human AP17. 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 AP17 in the samples is then determined by comparing the O.D. of the samples to the standard curve.
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