Reagent composition for immunochromatography of canine coronavirus and detection method
An immunochromatographic detection and immunochromatographic technology, which is applied in the direction of measuring devices, analytical materials, and biological material analysis, can solve the problems that EDTA hemoglobin does not have sufficient effect, shorten the detection time, suppress non-specific reactions, and use less Effect
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Embodiment 1
[0037] Reagent composition for immunochromatography:
[0038]1.1 There is no special requirement for the buffer in the reagent composition for immunochromatography. The buffer types include: acetate buffer, phosphate buffer, boric acid buffer, Tris hydrochloric acid buffer, etc., preferably Tris hydrochloric acid buffer. The concentration is in the range of 0.01-250 mM, preferably in the range of 10-200 mM, more preferably in the range of 30-180 mM. If the concentration is lower than 0.01 mM, the buffering effect is insufficient. When the concentration is above 250mM, the concentration is higher than necessary, resulting in waste.
[0039] 1.2 The chelating agent which is one of the components of the reagent composition for immunochromatography of the present invention is not particularly limited as long as it can be used as a ligand having a plurality of ligands. As a chelating agent in the present invention, a compound containing amino and carboxylic acid functional groups...
Embodiment 2
[0042] Immunoassay test strip device:
[0043] 2.1 Marking pads and sample pads are usually made of glass fiber membrane. The marker pad contains the combination of colloidal gold particles and monoclonal antibody or polyclonal antibody fragments thereof.
[0044] 2.2 Chromatography medium mainly adopts nitrocellulose membrane. The chromatographic medium is marked with monoclonal or polyclonal antibodies for identifying antigens, and secondary antibodies for identifying markers.
[0045] 2.3 Use filter paper as the absorbent pad.
[0046] 2.4 One side of the back plate is coated with adhesive or adhesive tape to make it sticky, and the sample pad part, marker part, chromatographic medium part and water absorption part are attached to the adhesive surface.
[0047] 2.5 Brief description of judgment principle
[0048] After dipping the end of the sample pad (treated with the immunoreagent composition) into the sample, the sample solution swims from bottom to top along the te...
Embodiment 3
[0050] The preparation method of canine coronavirus colloidal gold immunochromatographic detection test strip is as follows:
[0051] 3.1 Preparation of markers
[0052] Add 0.1ml of canine coronavirus antigen monoclonal antibody [phosphate buffer (pH7.4 diluted to 1mg / ml)] in 1ml of colloidal gold solution, let stand at room temperature for 1 minute, then add 100μl of 10% bovine serum For protein (BSA), centrifuge at 8000rpm for 15 minutes after stirring well. After removing the supernatant, the above-mentioned phosphate buffer solution was added to prepare a labeling reagent solution.
[0053] 3.2 Preparation of the judgment part on the chromatographic membrane
[0054] Dilute the monoclonal antibody to canine coronavirus antigen to 1.0mg / ml with phosphate buffer (pH7.4), dilute the secondary antibody to 1.0mg / ml, and draw the two to the chromatographic membrane at the same time by spraying a gold-spraying membrane device Serve, dry and set aside.
[0055] 3.3 Assembly o...
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