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  2. File:Antibody basic unit.svg - Wikipedia

    en.wikipedia.org/wiki/File:Antibody_basic_unit.svg

    One of the two antigen-binding regions is circled: they are formed by the variable regions at the tip of the antibody. The heavy chains have (starting from the N-terminus at the tip) a variable domain (V H ), followed by a constant domain (C H 1), a hinge region, and two more constant domain (C H 2, C H 3).

  3. Immunoassay - Wikipedia

    en.wikipedia.org/wiki/Immunoassay

    Free labeled analyte analog molecules are added to the sample, and their Brownian motion differs when bound to a large antibody (Ab) versus free in solution. The analyte competes for binding to the Ab, and if the labeled analyte binds to the Ab, a signal is produced. The signal intensity is inversely proportional to the analyte concentration. [19]

  4. Immunolabeling - Wikipedia

    en.wikipedia.org/wiki/Immunolabeling

    Immunolabeling - Antigen Detection of Tissue via Tagged Antigen-specific Antibody. Immunolabeling is a biochemical process that enables the detection and localization of an antigen to a particular site within a cell, tissue, or organ.

  5. Antibody - Wikipedia

    en.wikipedia.org/wiki/Antibody

    Each antibody binds to a specific antigen in a highly specific interaction analogous to a lock and key.. An antibody (Ab) or immunoglobulin (Ig) is a large, Y-shaped protein belonging to the immunoglobulin superfamily which is used by the immune system to identify and neutralize antigens such as bacteria and viruses, including those that cause disease.

  6. Immunoglobulin light chain - Wikipedia

    en.wikipedia.org/wiki/Immunoglobulin_light_chain

    An antibody molecule. The two heavy chains are colored red, blue, and purple. The two light chains green and yellow. See also: The immunoglobulin light chain is the small polypeptide subunit of an antibody (immunoglobulin). A typical antibody is composed of two immunoglobulin (Ig) heavy chains and two Ig light chains.

  7. Immune electron microscopy - Wikipedia

    en.wikipedia.org/wiki/Immune_electron_microscopy

    A reaction occurs between the antigen and antibody, causing this label to become visible under the microscope. Scanning electron microscopy is a viable option if the antigen is on the surface of the cell, but transmission electron microscopy may be needed to see the label if the antigen is within the cell. [2]

  8. File:Antibody with CDRs.svg - Wikipedia

    en.wikipedia.org/wiki/File:Antibody_with_CDRs.svg

    The following other wikis use this file: Usage on de.wikipedia.org Complementarity Determining Region; Usage on eu.wikipedia.org Txikipedia:Antigorputz

  9. Primary and secondary antibodies - Wikipedia

    en.wikipedia.org/wiki/Primary_and_secondary...

    A primary antibody can be very useful for the detection of biomarkers for diseases such as cancer, diabetes, Parkinson’s and Alzheimer’s disease and they are used for the study of absorption, distribution, metabolism, and excretion (ADME) and multi-drug resistance (MDR) of therapeutic agents. The primary antibody binds to an antigen (in red).

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