IgM antibody detection diluent
A diluent and antibody technology, which is applied in the field of immunodiagnosis, can solve the problems of many false positives and poor sensitivity, and achieve the effects of increasing sensitivity, improving false positives, and accurate and sensitive IgM antibody detection results
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Embodiment 1
[0048]A test dilution for IgM antibody chemiluminescence detection, including the following components: 0.05 mol / lph7.5 HEPES buffer, 25 mmol / L arginine, 500 mmol / l KCl, 0.1W / V% Tween 20, 1 W / V% Chapter, 2w / V% mannitol, 1 mol / L urea and 10 mmol / LEDTA.
Embodiment 2
[0050]This embodiment relates to a detection method of a giant cell IgM antibody.
[0051]1. Preparation of the kit.
[0052]SME IgM antibody chemiluminescence immunoassay assay kit: including the following steps:
[0053]1) Preparation of mouse anti-human IgM antibody:
[0054]The mouse anti-human IgM antibody was immunized by naturally extracted human IgM antibody, and B lymphocytes capable of specializing in synthesis anti-human IgM antibodies; then use cell hybridization technology, bone marrow cells and B lymphocytes in the same order First, obtain hybrid myeloma cells, carry out in vitro culture, during culture, hybridoma cells produce and secrete anti-human IgM monoclonal antibody, collect culture supernatant, purified to obtain the desired mouse anti-human IgM monoclonal antibody .
[0055]2) Magnetic bead system: magnetic beads γFE2O3Or Fe3O4The magnetic nanoparticles with the composite of the organic polymer material, with a particle size of 0.1 to 5 μm, with a carboxyl functional group ...
Embodiment 3
[0082]The detection of the giant cell IgM antibody detection reagent in Example 2 was carried out without adding a test diluent as a control group, and the dilution was tested in 50 mM hepes + 0.5 m KCl 1; in the experimental group conditions 1; 0.5 mKCl and 2W / V% mannitol buffer test dilution experimental group conditions 2; a buffer test dilution experimental group condition 3 containing 50 mM hepes was added to 0.5 m kCl, 2W / V% mannitol and 0.025m arginine. 50 mM HEPES was added to 0.5 mKCl, 2W / V% mannitol, 0.025 m arginine and 1M urea buffer test dilution experimental group conditions 4; to add test dilution in Example 1 as experimental group conditions 5, Yin properties control C0, weak male quality control C1 and yang properties control C2, 4 clinical-negative serum samples (negative samples 1-4), as shown in the following table:
[0083]
[0084]
[0085]Compare the signal value deviation of the control group and the five conditions and the signal-to-noise ratio P / N (the ratio...
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