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Alternative name
TNF-alpha-receptor-like protein ELISA KIT; TNF-alpha-receptor-like proteinVAC_TP3_003 ELISA KIT;
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Catalog
E038677
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species
Human
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GeneTP5
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SpecificityThis assay has high sensitivity and excellent specificity for detection of Human TP5. No significant cross-reactivity or interference between Human TP5 and analogues was observed. Note: Limited by current skills and knowledge, it is impossible for us to complete the cross- reactivity detection between Human TP5 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 TP5 ELISA Kit allows for the in vitro quantitative determination of TP5 , 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 TP5 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 TP5. During the reaction, Human TP5 in the sample or standard competes with a fixed amount of Human TP5 on the solid phase supporter for sites on the Biotinylated Detection Ab specific to Human TP5. 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 TP5 in the samples is then determined by comparing the O.D. of the samples to the standard curve.
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