Chemiluminescence immune analysis determination reagent kit for detecting Toxoplasma Gondi IgM antibody
A chemiluminescence and reagent kit technology, applied in the field of medical immunology and in vitro diagnosis, can solve the problems of inconvenient operation of etiology experiments, pollution hazards of radioactive waste, and short validity period of radioimmunization reagents, so as to facilitate the monitoring of the production process and avoid immunological Large loss of activity, avoiding toxic or carcinogenic effects
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Embodiment 1
[0028] Example 1 Preparation of Toxoplasma gondii IgM antibody chemiluminescence immunoassay assay kit of the present invention
[0029] 1. Preparation of negative control and positive control
[0030] 1. Preparation of negative control
[0031] Collect more than 6 normal human sera that are negative for Toxoplasma gondii IgM antibody, HIV (1+2) antibody, HCV antibody, TP antibody, and HBsAg negative by ELISA, filter and sterilize, subpackage, and store at low temperature.
[0032] 2. Preparation of positive control
[0033] Collect more than 6 sera from patients who are positive for Toxoplasma gondii IgM antibody and negative for HIV (1+2) antibody, HCV antibody, TP antibody, and HBsAg by ELISA, filter and sterilize, subpackage, and store at low temperature.
[0034] 2. Preparation of anti-FITC coated microplates
[0035] 1. Coating
[0036] Preparation of coating solution: 5.8g Na 2 HPO 4 12H 2 O and 0.59 g NaH 2 PO 4 2H 2 O was dissolved in double distilled water ...
Embodiment 2
[0084] Example 2 Preparation of Toxoplasma gondii IgM antibody chemiluminescence immunoassay assay kit of the present invention
[0085] Except that the magnetic particles were used as the solid phase carrier, and the anti-FITC was coupled to the surface of the magnetic particles by the glutaraldehyde method, the rest were prepared in the same manner as in Example 1 to prepare the Toxoplasma gondii IgM antibody chemiluminescent immunoassay assay kit.
Embodiment 3
[0086] Embodiment 3 The usage method of the kit of the present invention
[0087] The specific operations of the Toxoplasma gondii IgM antibody chemiluminescence immunoassay assay kit prepared in the above embodiment 1 are as follows:
[0088] 1) Take out the Toxoplasma gondii IgM assay kit (chemiluminescence method) from the refrigerator at 2-8°C, and equilibrate at room temperature for 30 minutes;
[0089] 2) Pre-dilute the sample to be tested with physiological saline at a ratio of 1:1000;
[0090] 3) For each experiment, 3 wells of TOX IgM negative control and 2 wells of positive control were set. Add 50 μl of negative control, positive control and pre-diluted sample to be tested, then add 50 μl of FITC marker to each well, shake and mix well, and incubate at 37°C for 30 minutes;
[0091] 4) Wash 5 times with diluted washing solution, fill each well with washing solution, soak for 10 seconds each time, and finally pat dry on clean absorbent paper;
[0092] 5) Add 100 μl...
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