Preparation method for double-stranded DNA antigen and kit for testing anti-double-stranded-DNA antibody of human serum
A kit and human detection technology, applied in the field of immunization, can solve the problems of reduced specificity of anti-dsDNA antibody detection
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[0093] Therefore, the object of the present invention is to provide a method for preparing a double-stranded DNA antigen for systemic lupus erythematosus detection, comprising:
[0094] (1) Treat the plasmid DNA with buffer P1 containing Tris, EDTA salt and RNase A, centrifuge to remove the supernatant, and then add the buffer P1 to suspend;
[0095] (2) using alkaline buffer solution P2 containing SDS (sodium dodecyl sulfate) and alkali metal ions to process the suspension obtained in step (1); and
[0096](3) Treat the product of step (2) with buffer P3 containing potassium acetate, centrifuge to obtain the supernatant, filter the supernatant, treat it with isopropanol, and centrifuge to obtain the precipitate.
[0097] In the present invention, the recombinant plasmid DNA containing the double-stranded DNA antigen for the detection of systemic lupus erythematosus can be various known recombinant plasmid DNAs containing the double-stranded DNA antigen for the detection of sy...
Embodiment 1
[0159] Example 1: Preparation of double-stranded DNA antigen
[0160] On the basis of the classic alkaline lysis method, optimization and improvement were carried out, and high-purity plasmid DNA was purified from commercially available plasmid DNA. The size of the plasmid was 2.5Kb, and it had a stable DNA double-stranded structure and strong immunogenicity. , using it as the coating antigen of the double-stranded DNA antibody ELISA kit, and the prepared kit has achieved high detection sensitivity and specificity. The plasmid prepared by the method has stable and uniform structure and convenient source, and can meet the technical requirements of the enzyme-linked immunosorbent kit for double-stranded DNA antibodies.
[0161] (1) The specific operation is as follows:
[0162] 1) Take 2mg of plasmid pET-GST (purchased from Shenzhen Qinbaosheng Biotechnology Co., Ltd.) and shake and suspend it with 10ml Buffer P1, 8000g, 4°C, 2min, remove the supernatant, and then add 10ml Buff...
Embodiment 2
[0220] Example 2: Biotin Labeling of Double-Stranded DNA
[0221] The double-stranded DNA antigen prepared in Example 1 was directly mixed with long-arm photosensitive biotin (Beijing Jiakangyuan Technology Development Co., Ltd.), and labeled with a light labeling lamp to prepare biotinylated plasmid dsDNA. The specific preparation method is as follows: add 5 μg / 10 μl of DNA to be labeled into a sterilized EP tube, add 5 μg / μl photobiotin in a dark room, mix well, and place in an ice bath.
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