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Alternative name
Granulocyte-macrophage colony-stimulating factor ELISA KIT; Colony-stimulating factor ELISA KIT; CSF ELISA KIT; Molgramostin ELISA KIT; SargramostimCSF2 ELISA KIT; GMCSF ELISA KIT; GM-CSF ELISA KIT; CSF ELISA KIT
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Catalog
E044233
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species
Mouse
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GeneGM-CSF
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SpecificityThis assay has high sensitivity and excellent specificity for detection of anti-GM-CSF. No significant cross-reactivity or interference between anti-GM-CSF and analogues was observed. NOTE: Limited by current skills and knowledge, it is impossible for us to complete the cross-reactivity detection between anti-GM-CSF 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 U/L.
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Intended UseMouse GM-CSF ELISA Kit allows for the in vitro quantitative determination of GM-CSF , 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/FamilyImmunology
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Product Description
specificalPrinciple of the assay: Anti-GM-CSF ELISA kit applies the competitive enzyme immunoassay technique utilizing a GM-CSF antigen and an anti-GM-CSF-HRP conjugate. The assay sample and buffer are incubated together with anti-GM-CSF-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 anti-GM-CSF concentration since anti-GM-CSF from samples and anti-GM-CSF-HRP conjugate compete for the GM-CSF antigen binding site. Since the number of sites is limited, as more sites are occupied by anti-GM-CSF from the sample, fewer sites are left to bind anti-GM-CSF-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The anti-GM-CSF concentration in each sample is interpolated from this standard curve.
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