Quick detecting method of skeletonema pseudocostatum, and preparation and using methods of test strip
A technology of test strips and sclerophytes, which is applied in the field of immunochromatographic detection of planktonic algae, can solve the problems of no papers and patent reports, etc., and achieve the effect of fast detection and simple operation
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[0061] Two, the concrete steps of the preparation method of the immunochromatographic detection and analysis test paper strip of described Skeletalum pseudosclerosteosa are as follows:
[0062] Through the sample test of known concentration of Skeletalum skeletalum, the concentration of the capture antigen required for detection of the algae cell sample is determined, and the detection line is drawn on the membrane to obtain the immunochromatographic detection and analysis test strip of Sclerosanthra sclerotinum.
[0063] Take out 80-100 μL of the sample solution to be tested, and directly drop it on the sample loading place of the immunochromatographic detection and analysis test strip of Skeletalum costarum, observe the results after 3 minutes at the fastest and an average of about 15 minutes. After reacting with the antibody, the difference in color displayed on the immunochromatographic detection and analysis test strip of Skeletodera costatum was established to establish t...
Embodiment 1
[0066] Example 1: Preparation of Immunogen
[0067] The vigorously growing Skeletalum costatum cell culture solution was fixed overnight with formaldehyde at a final concentration of 2%, centrifuged at 10,000 r / min for 10 min, and fine algae precipitates were collected. The algal cell aggregates were washed once with distilled water and twice with PB 5, and the algal cells were collected by centrifugation each time, and the centrifugation conditions were 10000r / min, 10min. The collected algae cells were divided into 1.5ml Eppendorf tubes, the residual water was shaken off, and stored at -20°C for later use. Take it out just before use, and resuspend it evenly with 5ml of sterile PBS. Obtain a standard solution of algae cells of known cell density. A certain amount of algae cell suspension is mixed with an equal volume of Freund's complete adjuvant and emulsified. The degree of emulsification is as complete as possible, and finally the immune antigen for animal injection is p...
Embodiment 2
[0068] Example 2: Preparation of monoclonal antibodies. See References (Xu Zhikai. Practical Monoclonal Antibody Technology [M]. Xi'an: Shaanxi Science and Technology Press, 1992: 27-36)
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