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Alternative name
Major histocompatibility complex, class II, DQ beta 1 ELISA KIT; Major histocompatibility complex, class II, DQ beta 1HLA-DQB1 ELISA KIT;
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Catalog
E059356
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species
Mouse
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GeneMHCDQb1
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Standard Curve
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SpecificityThis assay has high sensitivity and excellent specificity for detection of Major Histocompatibility Complex Class II DQ Beta 1 (MHCDQb1).
No significant cross-reactivity or interference between Major Histocompatibility Complex Class II DQ Beta 1 (MHCDQb1) and analogues was observed.
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SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
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SensitivityTypically less than 0.065ng/mL.
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Intended UseMouse MHCDQb1 ELISA Kit allows for the in vitro quantitative determination of MHCDQb1 , 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
specificalPrinciple of the Assay: The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Major Histocompatibility Complex Class II DQ Beta 1 (MHCDQb1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Major Histocompatibility Complex Class II DQ Beta 1 (MHCDQb1). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Major Histocompatibility Complex Class II DQ Beta 1 (MHCDQb1), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Major Histocompatibility Complex Class II DQ Beta 1 (MHCDQb1) in the samples is then determined by comparing the O.D. of the samples to the standard curve.
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