HGH (Human Growth Hormone)

The HGH ELISA is intended for the quantitative determination of human growth hormone (HGH) concentration in human serum.


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Product Catalog No: EIA-1787 Pack Size: 96 Wells

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Test Principle

The HGH ELISA is based on the principle of a solid phase enzyme-linked immunosorbent assay (ELISA). The assay system utilizes a sheep anti-HGH antibody for solid phase (microtiter wells) immobilization and a mouse monoclonal anti-HGH antibody in the antibody-enzyme (horseradish peroxidase) conjugate solution. The test sample is allowed to react simultaneously with the antibodies, resulting in HGH molecules being sandwiched between the solid phase and enzyme-linked antibodies. After a 45 minute incubation at room temperature, the wells are washed with water to remove unbound labeled antibodies. A solution of TMB is added and incubated for 20 minutes, resulting in the development of a blue color. The color development is stopped with the addition of 1N HCl, and the color is changed to yellow and measured spectrophotometrically at 450 nm. The concentration of HGH is directly proportional to the color intensity of the test sample.

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    References
    • Van Wyk, J.J. and Underwood, L.E. Growth Hormone Somatomedins and Growth Failure. Hospital Practice, 13:57; 1978.
    • Fisher, D.A., Evaluation of Anterior Pituitary Function in: Radioimmunoassay Manual. Ed. Nicholas, A.L. and Nelson, J.C.P. 3498 Nichols Institute, 1977.
    • Goldfine, I.D., Medical Treatment of Acromegaly. Annual Review of Medicine. 29:407; 1978.
    • Reichlin, S. et al. Hypothalamic Hormones. Annual Review of Medicine. 27:359; 1976.
    • Rimoin, D.L. and Horton, W.A. Short Stature. J. Pediatrics. 92:523; 1978.
    • Reiter, E., et. at., Variable estimates of serum growth hormone concentrations by different radioassay systems. J. Clin Endocrin. Metab., 66:68; 1988.
    • USA Center for Disease Control/National Institute of Health Manual, “Biosafety in Microbiological and Biomedical Laboratories”, 1984.
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