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Alternative name
SNARE-associated protein Snapin ELISA KIT; Biogenesis of lysosome-related organelles complex 1 subunit 7 ELISA KIT; BLOC-1 subunit 7 ELISA KIT; Synaptosomal-associated protein 25-binding protein ELISA KIT; SNAP-associated proteinSNAPIN ELISA KIT; BLOC1S7 ELISA KIT; SNAP25BP ELISA KIT; SNAPAP ELISA KIT; BLOC-1 subunit 7 ELISA KIT; SNAP-associated protein ELISA KIT
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Catalog
E035562
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species
Human
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GeneSNAPAP
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Standard Curve
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Other Species
Mouse SNAPAP ELISA Kit
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SpecificityThis assay has high sensitivity and excellent specificity for detection of SNAPAP. No significant cross-reactivity or interference between SNAPAP and analogues was observed.
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SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
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SensitivityThe minimum detectable dose of human SNAPAP is typically less than 0.066ng/mL. The sensitivity of this assay, or Lower Limit of Detection (LLD) was defined as the lowest protein concentration that could be differentiated from zero. It was determined by ad
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Intended UseHuman SNAPAP ELISA Kit allows for the in vitro quantitative determination of SNAPAP , 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 microtiter plate provided in this kit has been pre-coated with an antibody specific to SNAPAP. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to SNAPAP. 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 SNAPAP, 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 SNAPAP in the samples is then determined by comparing the O.D. of the samples to the standard curve.
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