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  2. Stable isotope standards and capture by anti-peptide antibodies

    en.wikipedia.org/wiki/Stable_Isotope_Standards...

    SISCAPA is an extension of the well-known gold-standard methods of stable-isotope dilution for quantitation of small molecules by mass spectrometry (MS). [3] Rather than measure an intact protein directly by mass spectrometry, SISCAPA makes use of proteolytic digestion (e.g., with the enzyme trypsin) to cleave sample proteins into smaller peptides ideally suited to quantitation by mass ...

  3. Mass spectrometric immunoassay - Wikipedia

    en.wikipedia.org/wiki/Mass_spectrometric_immunoassay

    Mass spectrometric immunoassay (MSIA) is a rapid method is used to detect and/ or quantify antigens and or antibody analytes. [1] This method uses an analyte affinity (either through antigens or antibodies) isolation to extract targeted molecules and internal standards from biological fluid in preparation for matrix assisted laser desorption ionization-time of flight mass spectrometry (MALDI ...

  4. Immunofluorescence - Wikipedia

    en.wikipedia.org/wiki/Immunofluorescence

    The antibody with the higher affinity for a specific epitope will surpass antibodies with a lower affinity for the same epitope. [ 2 ] [ 3 ] By conjugating the antibody to a fluorophore , the position of the target biomolecule is visualized by exciting the fluorophore and measuring the emission of light in a specific predefined wavelength using ...

  5. Immunoassay - Wikipedia

    en.wikipedia.org/wiki/Immunoassay

    In immunology the particular macromolecule bound by an antibody is referred to as an antigen and the area on an antigen to which the antibody binds is called an epitope. In some cases, an immunoassay may use an antigen to detect for the presence of antibodies, which recognize that antigen, in a solution.

  6. CyTOF - Wikipedia

    en.wikipedia.org/wiki/CyTOF

    Panels can include up to 45 antibodies, as opposed to the 10 that can be done in conventional flow cytometry but require great expertise to design. [15] However, development of spectral flow cytometry has closed the gap between flow and mass cytometry in terms of the maximum number of antibodies that can be used.

  7. Immunoglobulin light chain - Wikipedia

    en.wikipedia.org/wiki/Immunoglobulin_light_chain

    Once set, light chain class remains fixed for the life of the B lymphocyte. In a healthy individual, the total kappa-to-lambda ratio is roughly 2:1 in serum (measuring intact whole antibodies) or 1:1.5 if measuring free light chains, with a highly divergent ratio indicative of neoplasm. The free light chain ratio ranges from 0.26 to 1.65. [1]

  8. Immunostaining - Wikipedia

    en.wikipedia.org/wiki/Immunostaining

    Micrograph of a GFAP immunostained section of a brain tumour.. In biochemistry, immunostaining is any use of an antibody-based method to detect a specific protein in a sample. . The term "immunostaining" was originally used to refer to the immunohistochemical staining of tissue sections, as first described by Albert Coons in 1941.

  9. Mass cytometry - Wikipedia

    en.wikipedia.org/wiki/Mass_cytometry

    Mass cytometry is a mass spectrometry technique based on inductively coupled plasma mass spectrometry and time of flight mass spectrometry used for the determination of the properties of cells . [ 1 ] [ 2 ] In this approach, antibodies are conjugated with isotopically pure elements , and these antibodies are used to label cellular proteins.