Reagent kit for LgG immunoblotting diagnosis of SARS coronavirus antibody
A diagnostic kit, coronavirus technology, applied in the direction of measuring devices, instruments, scientific instruments, etc., can solve problems such as inappropriate rapid detection of diseases, incorrect test results, complicated experimental techniques, etc., to achieve suitable mass production, high sensitivity, Ease of use
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Embodiment 1
[0045] In this embodiment, the purified SARS coronavirus whole virus lysate antigen is electrophoresed and transferred to a nitrocellulose membrane, and an anti-human IgG line is also used as a quality control line on the membrane to check whether the membrane strip fails. Horseradish peroxidase (HRP)-labeled rabbit anti-human IgG and corresponding chromogenic substrates were used for detection. The manufacturing method of the present embodiment is as follows: a. Antigen preparation Purified SARS coronavirus whole virus antigen uses 0.02M pH7.6 PBS to regulate protein concentration to 10mg / ml. The lysate was added at a volume of 1:2, and lysed at 100°C for 5 minutes. b. Antigen separation (gel electrophoresis)
[0046] 1. Prepare 12% polyacrylamide gel as separating gel and 2.5% polyacrylamide gel as stacking gel.
[0047] 2. Exhaust under negative pressure for 5 minutes.
[0048] 3. Pour plate: first pour the separation glue, the area is 15×15cm 2 , after the separating g...
Embodiment 2
[0066] In this embodiment, the purified SARS coronavirus whole virus lysate antigen is electrophoresed and transferred to a nitrocellulose membrane, and an anti-human IgG line is also used as a quality control line on the membrane to check whether the membrane strip fails. Alkaline phosphatase (ALP)-labeled goat-anti-human IgG antibody and corresponding chromogenic substrate were used for detection. The manufacturing method of this embodiment is basically the same as that of Embodiment 1, the differences are as follows:
[0067] a. Preparation of enzyme-labeled antibody
[0068] Choose imported high-purity alkaline phosphatase (ALP)-labeled goat-anti-human IgG antibody 1mg, according to the drop-mixing results, dilute to the planned volume with 0.02M PBS containing 1.0% BSA, pH7.4, and store at 4°C.
[0069] b. Chromogenic substrate:
[0070] Tris 12.1g
[0071] MgCl 2 0.475g
[0072] NaCl 5.8g
[0073] BCIP 0.4g
[0074] ...
Embodiment 3
[0079] In this example, the purified SARS coronavirus recombinant antigen mixture was electrophoresed and transferred to a nitrocellulose membrane, and an anti-human IgG line was also used as a quality control line on the membrane to check whether the membrane strip failed. Horseradish peroxidase (HRP)-labeled rabbit anti-human IgG and corresponding chromogenic substrates were used for detection. The manufacturing method of this example is the same as that of Example 1 as follows.
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