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Alternative name
Pro-neuregulin-1, membrane-bound isoform ELISA KIT; Neuregulin-1Alternative name(s):Acetylcholine receptor-inducing activity ELISA KIT; ARIANRG1 ELISA KIT; GGF ELISA KIT; HGL ELISA KIT; HRGA ELISA KIT; NDF ELISA KIT; SMDF ELISA KIT; Pro-NRG1 ELISA KIT; ARIA ELISA KIT; HRG ELISA KIT
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Catalog
E061311
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species
Mouse
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GeneNRG1
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Standard Curve
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Other Species
Human NRG1 ELISA KitHuman NRG1 a ELISA KitMouse NRG1 a ELISA KitChicken NRG1 ELISA KitRat Nrg1 ELISA Kit
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SpecificityThis assay has high sensitivity and excellent specificity for detection of Neuregulin 1 (NRG1).
No significant cross-reactivity or interference between Neuregulin 1 (NRG1) 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 3.6pg/mL.
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Intended UseMouse NRG1 ELISA Kit allows for the in vitro quantitative determination of NRG1 , 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 Neuregulin 1 (NRG1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Neuregulin 1 (NRG1). 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 Neuregulin 1 (NRG1), 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 Neuregulin 1 (NRG1) in the samples is then determined by comparing the O.D. of the samples to the standard curve.
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