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Alternative name
Chitinase-3-like protein 1 ELISA KIT; 39 kDa synovial protein ELISA KIT; Cartilage glycoprotein 39 ELISA KIT; CGP-39 ELISA KIT; GP-39 ELISA KIT; hCGP-39 ELISA KIT; YKL-40CHI3L1 ELISA KIT; CGP-39 ELISA KIT; GP-39 ELISA KIT; hCGP-39 ELISA KIT
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Catalog
E002595
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species
Human
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GeneGP
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Standard Curve
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Other Species
Human alpha1beta-GP ELISA KitHuman beta2 GP ELISA KitHuman beta2-GP ELISA KitHuman gp-39/YKL-40 ELISA KitHuman gp-39 ELISA KitHuman GP-BB ELISA KitHuman GP II ELISA KitHuman GP-II ELISA KitHuman GP MM ELISA KitHuman GP-MM ELISA KitHuman GP-73 ELISA KitHuman P gp ELISA KitHuman P-gp ELISA KitHuman GP II b III a/CD41+CD61 ELISA KitHuman GP- I b IX alpha ELISA KitHuman GP- II b III a ELISA KitHuman GP-IIbIIIa ELISA KitHuman GP-4 ELISA KitHuman GP 4 ELISA KitMouse alpha1beta-GP ELISA KitMouse GP ELISA KitMouse beta2-GP ELISA KitMouse gp-39/YKL-40 ELISA KitMouse gp-39 ELISA KitMouse HC gp-39 ELISA Kit
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SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
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Sensitivity1.0 ng/mL
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Intended UseHuman GP ELISA Kit allows for the in vitro quantitative determination of GP , 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 Categories/FamilySignal Transduction
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Product Description
specificalPrinciple of the Assay: GP-Ab ELISA kit applies the competitive enzyme immunoassay technique utilizing GP antigen and an GP-Ab-HRP conjugate. The assay sample and buffer are incubated together with GP-Ab-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the GP-Ab concentration since GP-Ab from samples and GP-Ab-HRP conjugate compete for the GP antigen binding site. Since the number of sites is limited, as more sites are occupied by GP-Ab from the sample, fewer sites are left to bind GP-Ab-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The GP-Ab concentration in each sample is interpolated from this standard curve.
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