Kit for detecting autoimmune liver disease related antibody autoantibody to nuclear antigen (ANA) and detection method thereof
An autoimmune, kit-based technology, applied in measurement devices, instruments, scientific instruments, etc., can solve problems such as differences between new and old tissue slices, and difficulty in developing
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Embodiment 1
[0021] The kit (plate type) for detecting autoimmune liver disease-related antibody ANA described in the present invention includes:
[0022] 1. Preparation of target antigen-carrier conjugate: Add 100 μl of target antigen (natural antigen, recombinant antigen, synthetic peptide, HepG2 cell, Hep2 cell, Hela cell or cell lysed antigen) not higher than 10ug / ml to a 96-well plate In the medium, coat at 4°C for 16-24h or at 37°C for 2h, then wash twice with the prepared (PBST) washing solution;
[0023] 2. Blocking: Use 50-200 μl of 0.01-0.1M phosphate buffer containing 0.05-0.5% Tween20, 1-5% BSA, 1-5% Casein, 1-5% peptone, 5-10% sucrose, Block at 4°C for 16-24h or at 37°C for 2h, then shake off excess buffer, place in a dry environment to dry, and seal at 2-8°C for storage;
[0024] 3. Preparation of calibrator, positive control substance and negative control substance: take a clinically determined high-value sample, dilute it with the calibrator diluent (PBS+3%BSA) at a rate o...
Embodiment 2
[0039] The kit (magnetic particles) for detecting autoimmune liver disease-associated antibody ANA described in the present invention includes:
[0040] 1. Preparation of target antigen-carrier conjugates: Take 10mg of magnetic particles, wash them with phosphate buffer for 5 times, add no less than 0.15ml of EDC or (and) NHS or glutaraldehyde (and) activator for 2 hours, wash 3 times, then add 0.1mg of target antigen, shake at room temperature for 2h;
[0041] 2. Blocking: Use 1ml of 0.01-0.1M phosphate buffer containing 0.05-0.5% Tween20, 1-5% BSA, 1-5% Casein, 1-5% peptone, 5-10% sucrose, shake at room temperature Block for 10 minutes, block four times in a row, then add 2ml of blocking solution and store at 2-8°C;
[0042] 3. Preparation of calibrator, positive control substance and negative control substance: take a clinically determined high-value sample, dilute it with the calibrator diluent (PBS+3%BSA) at a rate of not less than 1:50, and take a linear comparison The...
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