Free Prostate Specific Antigen (fPSA) ELISA Assay Kit

$260.00

The Eagle Biosciences Free Prostate Specific Antigen (fPSA) ELISA Assay Kit (enzyme-linked immunoassay kit) is intended for the direct quantitative determination of Free Prostate Specific Antigen in human serum. The Free Prostate Specific Antigen (fPSA) ELISA Assay Kit is for research use only and not to be used in diagnostic procedures.

SKU: PSF31-K01 Categories: , ,

Free Prostate Specific Antigen (fPSA) ELISA Assay Kit

For Research Use Only

Size: 1×96 wells
Sensitivity: 0.05 ng/mL
Dynamic Range: 0.1–15 ng/mL
Incubation Time: 75 minutes
Sample Type: Serum
Sample Size: 50 μL

Controls Included

Additional Information

Assay Background


Prostate specific antigen (PSA) is a 33-kDa glycoprotein secreted by epithelial cells of the prostate gland. In human serum, PSA is primarily complexed with α1-antichymotrypsin, and to a lesser extent with other serum proteins. Only a small fraction of PSA is present as the free form (free PSA). The expected normal level of PSA in male serum is lower than 4 ng/mL. A rise in the concentration of PSA indicates prostate pathology, including benign prostatic hyperplasia (BPH) and prostate cancer. Free PSA (fPSA) has been studied in attempts to help distinguish BPH from untreated prostate cancer. These studies have shown that the ratio of free PSA / total PSA is lower in untreated prostate cancer than in patients with BPH.

Assay Principle


The principle of the following enzyme immunoassay test follows a typical one-step capture or ‘sandwich’ type assay. The assay makes use of two highly specific monoclonal antibodies: A monoclonal antibody specific for fPSA is immobilized onto the microplate and another monoclonal antibody specific for a different region of fPSA is conjugated to horse radish peroxidase (HRP). fPSA from the sample and standards are allowed to bind simultaneously to the plate and to the HRP conjugate. The washing and decanting steps remove any unbound HRP conjugate. After the washing step, the enzyme substrate is added. The enzymatic reaction is terminated by addition of the stopping solution. The absorbance is measured on a microtiter plate reader. The intensity of the colour formed by the enzymatic reaction is directly proportional to the concentration of fPSA in the sample. A set of standards is used to plot a standard curve from which the amount of fPSA in patient samples and controls can be directly read.

Typical Standard Curve


Manual

Product Manual