Method for detecting raw pork and detection kit therefor
A technology of raw pork and detection department, which is applied in the field of immunochromatographic assay reagents, achieves the effect of stability and easy acquisition, no decrease in sensitivity, and low price
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[0071] The production method of the polyclonal antibody of the present invention is as follows.
[0072] [Preparation of polyclonal antibody]
[0073] Rabbits were immunized with IgG (commercially available) contained in porcine serum according to a conventional method to obtain antiserum. Rabbit-derived anti-pig IgG antibody was purified from antiserum by salting out with 50% saturated ammonium sulfate, followed by purification and recovery with DEAE column (anion exchange column).
[0074] However, if this rabbit-derived anti-pig IgG antibody is directly used as a detection antibody in an immunochromatographic assay or an ELISA assay, although it will react significantly with raw pork, it will also react with a standard buffer (background), so it cannot Used as a detection antibody. Therefore, no implementation of beef, mutton, chicken. The test results are shown in "Table 1".
[0075] "HamaPhoto" in the table is an abbreviation for "Hamamatsu Densitometer".
[0076] [T...
Embodiment
[0101] The immunochromatography device used in the present invention will be described in detail below, but this is just an example, and the present invention is not limited thereto.
[0102] 1. Fabrication of reaction sites on chromatography media
[0103] On a nitrocellulose membrane (HF180 manufactured by Millipore) of 25 x 2.5 cm using an antibody coater (manufactured by BioDot Co., Ltd.), goat The anti-pig IgG antibody was dried at 42°C for 60 minutes and then at room temperature overnight to make reaction sites on a chromatography medium in which the carbonated buffer contained 5% by weight sucrose and 5% by weight isopropanol.
[0104] 2. Preparation of marker solution
[0105] 0.1 mL of goat-derived anti-pig IgG antibody diluted to a concentration of 0.05 mg / mL with HEPES buffer (pH 7.5) was added to 0.5 mL of colloidal gold suspension (manufactured by Tanaka Precious Metal Industry Co., Ltd., average particle size: 60 nm). The mixture was allowed to stand at room ...
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