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Alternative name
Galectin-3 ELISA KIT; 35 kDa lectin ELISA KIT; Carbohydrate-binding protein 35 ELISA KIT; CBP 35 ELISA KIT; Galactose-specific lectin 3 ELISA KIT; Galactoside-binding protein ELISA KIT; GALBP ELISA KIT; IgE-binding protein ELISA KIT; L-31 ELISA KIT; Laminin-binding protein ELISA KIT; Lectin L-29 ELISA KIT; Mac-2 antigenLGALS3 ELISA KIT; MAC2 ELISA KIT; Gal-3 ELISA KIT; CBP 35 ELISA KIT; GALBP ELISA KIT
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Catalog
E015980
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species
Human
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GeneGAL3
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SpecificityThis assay has high sensitivity and excellent specificity for detection of GAL-3. No significant cross-reactivity or interference between GAL-3 and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between GAL-3 and all the analogues, therefore, cross reaction may still exist in some cases.
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SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
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Sensitivity0.1 ng/mL.
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Intended UseHuman GAL3 ELISA Kit allows for the in vitro quantitative determination of GAL3 , 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/FamilyCell Biology
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Product Description
specificalPrinciple of the assay: GAL-3 ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-GAL-3 antibody and an GAL-3-HRP conjugate. The assay sample and buffer are incubated together with GAL-3-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 GAL-3 concentration since GAL-3 from samples and GAL-3-HRP conjugate compete for the anti-GAL-3 antibody binding site. Since the number of sites is limited, as more sites are occupied by GAL-3 from the sample, fewer sites are left to bind GAL-3-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The GAL-3 concentration in each sample is interpolated from this standard curve.
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