"Blood Protein Electrophoresis" - Books

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Select item 44036681.

StatPearls [Internet].

Treasure Island (FL): StatPearls Publishing; 2026 Jan-.

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Select item 34012942.

Endotext [Internet].

Feingold KR, Adler RA, Ahmed SF, et al., editors.

South Dartmouth (MA): MDText.com, Inc.; 2000-.

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Select item 14589843.

GeneReviews® [Internet].

Adam MP, Bick S, Mirzaa GM, et al., editors.

Seattle (WA): University of Washington, Seattle; 1993-2026.

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Select item 30271644.

Serum Free Light Chain Analysis for the Diagnosis, Management, and Prognosis of Plasma Cell Dyscrasias: Future Research Needs: Identification of Future Research Needs From Comparative Effectiveness Review No. 73 [Internet].

Rao M, Lamont JL, Chan J, et al.

Rockville (MD): Agency for Healthcare Research and Quality (US); 2012 Sep. (Future Research Needs Papers, No. 23.)

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Select item 14152805.

Madame Curie Bioscience Database [Internet].

Austin (TX): Landes Bioscience; 2000-2013.

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Select item 32149406.

Conference on Hemoglobin: 2–3 May 1957.

National Academy of Sciences (US) and National Research Council (US) Division of Medical Sciences.

Washington (DC): National Academies Press (US); 1958.

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Select item 49535407.

Suspected cancer: recognition and referral.

London: National Institute for Health and Care Excellence (NICE); 2026 Jan 12. (NICE Clinical Guidelines, No. 12.)

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Select item 31697308.

Biologic Markers in Reproductive Toxicology.

National Research Council (US) Subcommittee on Reproductive and Neurodevelopmental Toxicology.

Washington (DC): National Academies Press (US); 1989.

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Select item 14453429.

Clinical Methods: The History, Physical, and Laboratory Examinations. 3rd edition.

Walker HK, Hall WD, Hurst JW, editors.

Boston: Butterworths; 1990.

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Select item 144161810.

Helicobacter pylori: Physiology and Genetics.

Mobley HLT, Mendz GL, Hazell SL, editors.

Washington (DC): ASM Press; 2001.

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Select item 189578811.

Molecular Biology of the Cell. 4th edition.

Alberts B, Johnson A, Lewis J, et al.

New York: Garland Science; 2002.

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Select item 434169612.

Some Thyrotropic Agents.

IARC Working Group on the Evaluation of Carcinogenic Risks to Humans.

Lyon (FR): International Agency for Research on Cancer; 2001. (IARC Monographs on the Evaluation of Carcinogenic Risks to Humans, No. 79.)

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Select item 166869013.

Holland-Frei Cancer Medicine. 6th edition.

Kufe DW, Pollock RE, Weichselbaum RR, et al., editors.

Hamilton (ON): BC Decker; 2003.

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Select item 282152414.

PDQ Cancer Information Summaries [Internet].

Bethesda (MD): National Cancer Institute (US); 2002-.

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Select item 434989615.

Some Antiviral and Antineoplastic Drugs, and Other Pharmaceutical Agents.

IARC Working Group on the Evaluation of Carcinogenic Risks to Humans.

Lyon (FR): International Agency for Research on Cancer; 2000. (IARC Monographs on the Evaluation of Carcinogenic Risks to Humans, No. 76.)

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Select item 307786216.

Enterococci: From Commensals to Leading Causes of Drug Resistant Infection [Internet].

Gilmore MS, Clewell DB, Ike Y, et al., editors.

Boston: Massachusetts Eye and Ear Infirmary; 2014-.

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Select item 412734417.

Cobalt in Hard Metals and Cobalt Sulfate, Gallium Arsenide, Indium Phosphide and Vanadium Pentoxide.

IARC Working Group on the Evaluation of Carcinogenic Risks to Humans.

Lyon (FR): International Agency for Research on Cancer; 2006. (IARC Monographs on the Evaluation of Carcinogenic Risks to Humans, No. 86.)

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Select item 292056818.

The Clinical Effectiveness and Cost-Effectiveness of Bortezomib and Thalidomide in Combination Regimens with an Alkylating Agent and a Corticosteroid for the First-Line Treatment of Multiple Myeloma: A Systematic Review and Economic Evaluation.

Picot J, Cooper K, Bryant J, et al.

Southampton (UK): NIHR Journals Library; 2011 Dec. (Health Technology Assessment, No. 15.41.)

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Select item 422694219.

Some Drugs and Herbal Products.

IARC Working Group on the Evaluation of Carcinogenic Risks to Humans.

Lyon (FR): International Agency for Research on Cancer; 2016. (IARC Monographs on the Evaluation of Carcinogenic Risks to Humans, No. 108.)

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Select item 320041820.

Mammography and Beyond: Developing Technologies for the Early Detection of Breast Cancer.

Institute of Medicine (US) and National Research Council (US) Committee on Technologies for the Early Detection of Breast Cancer; Nass SJ, Henderson IC, Lashof JC, editors.

Washington (DC): National Academies Press (US); 2001.

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Figure 2-11

Methods of protein identification and detection. A, Immune (Western) blotting. A complex mixture of proteins can be separated by size using electrophoresis (SDS-PAGE). The separated proteins are then transferred to a nitrocellulose or nylon filter in an electric field, maintaining their size-specific spatial orientation on the filter. Antibodies directed against one specific protein (in this case, the gray ellipsoid) in the original mixture are added to the filter and bind to the specific protein. Bound antibodies can be radiolabeled or enzymatically labeled themselves, or they can be visualized by incubating the filter with labeled anti-immunoglobulin antibodies. B, Immunoprecipitation. A complex mixture of radiolabeled proteins (indicated by different geometric shapes) is incubated with antibodies specific for one of those proteins (in this case, the gray ellipsoid). After the antibodies have bound to their protein, small polystyrene or agarose beads containing staphylococcal protein A are added to the mixture. Protein A binds to the antibodies, and when centrifuged, the beads to which the protein A is bound will sediment to the bottom of the centrifuge tube, taking along the antibodies and the specific protein to which they have bound. The unbound proteins remain in the supernatant and can be removed. After boiling to dissociate the protein A/antibody/protein complex, specifically precipitated radiolabeled protein can be visualized by electrophoresis (SDS-PAGE) and autoradiography. C, Enzyme-linked immunosorbent assay (ELISA). To perform ELISA assays, one needs to develop two independent antibodies that bind to the protein to be detected (gray ellipsoid in this example) with high specificity and affinity. One of these antibodies then is coupled to a plate that is then incubated with the protein mix to be analyzed (this can be tissue, blood, or other body fluid). The specifically bound protein is retained on the plate and is detected with the second antibody generated against it that is coupled to an enzyme or isotope allowing quantitation of the bound protein. ELISA assays are usually very sensitive and can detect picomolar amounts of proteins.

Gene Expression: Protein Analysis.

Kufe DW, Pollock RE, Weichselbaum RR, et al., editors. Holland-Frei Cancer Medicine. 6th edition. Hamilton (ON): BC Decker; 2003.