Prostate Specific Antigen(PSA) ELISA

The Calbiotech, Inc (CBI) PSA ELISA Kit is intended for the quantitative measurement of PSA in human serum.


Catalog No Size
Product Catalog No: PS235T Pack Size: 96 Tests

Pack Size:
Pack Size:
Pack Size:
Pack Size:

Category:
Summary

Prostate Specific Antigen (PSA) is a single chain glycoprotein produced by epithelial cells of the prostate gland. PSA is useful in the management of patients with prostate cancer. The measurement of serum PSA has become the most accepted test to indicate men who are at risk of having prostate cancer and who should be examined by other tests. Using a cut-off of 4 ng/ml, 92% of men over 50 years of age with malignant prostatic tissues, 8% of healthy men and 28% of men with benign prostate hyperplasia (BPH) test positive for PSA. Three major forms of PSA exist in the serum: free PSA, bound PSA and complex PSA. Bound PSA is found in higher concentrations in patients with prostate cancer; whereas, free PSA is detected in higher concentrations in patients with BPH. If the free PSA to total PSA ratio is >25%, it is unlikely that the patient has prostate cancer; whereas, if free PSA is <16% then prostate cancer is likely to be the cause. Serial measurement of PSA concentration in the serum is an important tool in monitoring patients with prostatic cancer and determining the potential and actual effectiveness of surgery or other therapies, or may allow for earlier discovery of residual or recurrent carcinoma after radical prostatectomy or radiotherapy. Current indications suggest that men over 50 years should be screened with digital rectal examination and PSA. Men with a high risk of prostate cancer, such as a family history or of African heritage, should begin annual testing at age 40 years. If both are normal, the patient can be followed with annual evaluations and monitoring to determine the rate of change. Slight elevations in PSA (4.1 ng/ml to 10.0 ng/ml) warrant a transrectal ultrasound (TRUS) to evaluate prostate volume and echogenicity of the gland. Hypo-echogenic lesions should be biopsied. Elevated PSA density (>0.15 ng/ml/cc), very high PSA (>10 ng/ml) or a free-to-total PSA ratio of <16% warrants systemic biopsy.

Test Principle

The PSA ELISA kit is a solid phase assay based on a streptavidin-biotin principle. The standards, samples and a reagent mixture of Anti-PSA Enzyme and Biotin conjugates (conjugate reagent) are added into the wells, coated with Streptavidin. PSA in the patient’s serum forms a sandwich between two highly specific Anti-PSA antibodies, labeled with Biotin and HRP. Simultaneously, the biotinylated antibody is immobilized onto the well through a high affinity Streptavidin-Biotin interaction. Unbound protein and excess biotin/enzyme conjugated reagent are washed off, by washing buffer. Upon the addition of the substrate, the intensity of color developed is directly proportional to the concentration of PSA in the samples. A standard curve is prepared relating color intensity to the concentration of the PSA.

Order Enquiry

Order Enquiry Form

References
  1. Espana F; Sanchez-Cuenca J; Estelles A; Gilabert J; Griffin JH; Heeb MJ. Quantitative immunoassay for complexes of prostate-specific antigen with alpha2-macroglobulin. Clin Chem 1996; 42(4):545-50.
  2. Corey E; Wegner SK; Stray JE; Corey MJ; Arfman EW; Lange PH; Vessella RL. Characterization of 10 new monoclonal antibodies against prostate-specific antigen by analysis of affinity, specificity and function in sandwich assays. Int J Cancer 1997; 71(6):1019-28.
  3. Barak M; Cohen M; Mecz Y; Stein A; Rashkovitzki R; Laver B; Lurie A. The additional value of free prostate specific antigen to the battery of age-dependent prostate-specific antigen, prostate-specific antigen density and velocity. Eur J Clin Chem Clin Biochem 1997; 35(6): 475-81.
  4. Vogl M; Muller MM; Holtl W. Clinical usefulness of percentage of free serum prostate specific antigen. Clin Chim Acta 1997; 258(1):79-90.
  5. Stenman UH; Leinonen J; Zhang WM. Problems in the determination of prostate specific antigen. Eur J Clin Chem Clin Biochem 1996; 34(9):735-40.
Documents
Enquiry