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In Vitro and In Vivo Nonimaging Tests

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Fundamentals of Nuclear Pharmacy
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Abstract

The radioimmunoassay (RIA) method was first developed by S.A. Berson and R.S. Yalow in the late 1950s for the determination of insulin in human serum. The method is employed to determine numerous hormones, enzymes, antigens, and drugs in minute quantities (10-9-10-12Af) in human plasma in order to assess various disease conditions.

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Suggested Reading

  • Chase GC, Rabinowitz JL. Principles of Radioisotope Methodology. 3rd ed. Minneapolis: Burgess; 1970.

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  • Moss AJ Jr, Dalrymple GV, Boyd CM, eds. Practical Radioimmunoassay. St Louis: Mosby; 1976.

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  • Odell WD, Daughaday WH, eds. Principles of Competitive Protein-Binding Assays. Philadelphia: Lippincott; 1974.

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  • Rothfeld B, ed. Nuclear Medicine In Vitro. Philadelphia: Lippincott; 1974.

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  • Thorell JI, Larson SM. Radioimmunoassay and Related Techniques. St Louis: Mosby; 1978.

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© 1998 Springer Science+Business Media New York

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Saha, G.B. (1998). In Vitro and In Vivo Nonimaging Tests. In: Fundamentals of Nuclear Pharmacy. Springer, New York, NY. https://doi.org/10.1007/978-1-4757-2934-4_12

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  • DOI: https://doi.org/10.1007/978-1-4757-2934-4_12

  • Publisher Name: Springer, New York, NY

  • Print ISBN: 978-1-4757-2936-8

  • Online ISBN: 978-1-4757-2934-4

  • eBook Packages: Springer Book Archive

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