Human ACTAlpha 1 ELISA Kit

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  • Alternative name

    Alpha-1-antichymotrypsin ELISA KIT; Cell growth-inhibiting gene 24/25 protein ELISA KIT; Serpin A3Cleaved into the following chain:Alpha-1-antichymotrypsin His-Pro-lessSERPINA3 ELISA KIT; AACT ELISA KIT; GIG24 ELISA KIT; GIG25 ELISA KIT; ACT ELISA KIT

  • Catalog
  • species
  • GeneACTAlpha 1
  • Standard CurveHuman ACTAlpha 1 ELISA Kit
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Intended UseHuman ACTAlpha 1 ELISA Kit allows for the in vitro quantitative determination of ACTAlpha 1 , concentrations in serum, Plasma , tissue homogenates and Cell culture supernates and Other biological fluids.
  • StorageFor 5-7days:Store the whole kit at 4℃
    For a Long time :Store the Substrate at 4℃, other reagent should store at -20℃.
  • Product Categories/FamilySignal Transduction
  • Product Description
    For Samples: Cell culture fluid & body fluid & tissue homogenate Serum or blood plasma Intended Uses: This ACTA1 ELISA kit is intended for laboratory research use only and not for use in diagnostic or therapeutic procedures. The stop solution changes the color from blue to yellow and the intensity of the color is measured at 450 nm using a spectrophotometer. In order to measure the concentration of ACTA1 in the sample, this ACTA1 ELISA Kit includes a set of calibration standards. The calibration standards are assayed at the same time as the samples and allow the operator to produce a standard curve of Optical Density versus ACTA1 concentration. The concentration of in the samples is then determined by comparing the O.D. of the samples to the standard curve. Principle of the Assay: The coated well immunoenzymatic assay for the quantitative measurement of ACTA1 utilizes a multiclonal anti-ACTA1 antibody and an ACTA1-HRP conjugate. The assay sample and buffer are incubated together with ACTA1-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 ACTA1 concentration since ACTA1 from samples and ACTA1-HRP conjugate compete for the anti-ACTA1 antibody binding site. Since the number of sites is limited, as more sites are occupied by ACTA1 from the sample, fewer sites are left to bind ACTA1-HRP conjugate. Standards of known ACTA1 concentrations are run concurrently with the samples being assayed and a standard curve is plotted relating the intensity of the color (Optical Density) to the concentration of ACTA1. The ACTA1 concentration in each sample is interpolated from this standard curve.

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