Joint detection kit for feline herpes and feline calicivirus
A technology for feline calicivirus and feline herpesvirus, which is applied in the field of combined detection kits for feline herpes and feline calicivirus, can solve the problems of time-consuming, time-consuming, inability to meet detection requirements, etc., to ensure specificity and reduce interference the effect of competition
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Embodiment 1
[0027] A combined detection kit for feline herpes and feline calicivirus, such as Figure 1 to Figure 3As shown in common, it includes a test card 2, a sample diluent bottle 4 (containing a sample treatment solution) and a sterile cotton swab 5 (packaged in a packaging box 1). The test card 2 is provided with a test strip 3 inside. The paper strip 3 includes a bottom plate 30, a nitrocellulose membrane 31 is arranged on the bottom plate 30, a water absorption pad 32 is arranged above the nitrocellulose membrane 31, and a gold-labeled antibody reaction pad 33 is arranged below the nitrocellulose membrane 31. A sample pad 34 is arranged below the reaction pad 33, and the gold-labeled antibody reaction pad 33 is provided with a feline herpesvirus monoclonal antibody-colloidal gold complex coating and a feline calicivirus monoclonal antibody-colloidal gold complex coating. Calicivirus monoclonal antibody-colloidal gold complex coating 331 is located above feline herpes virus monoc...
Embodiment 2
[0036] The difference from Example 1 is:
[0037] The isolation pad refers to coating the isolation pad treatment solution on the glass fiber and drying it at 37°C for 8 hours; the isolation pad treatment solution contains 0.3wt% Triton X-100 and 0.4wt% Triton X-100 per 1000mL of PBS buffer. Formulated with BSA, the concentration of PBS buffer is 25mM, pH is 7.4.
[0038] The nitrocellulose membrane is provided with a detection line T1 coated with a feline calicivirus monoclonal antibody, a detection line T2 coated with a feline herpes virus monoclonal antibody, and a quality control line coated with a goat anti-cat IgG antibody. Detection line T1, detection line T2 and quality control line refer to diluting feline calicivirus monoclonal antibody to 1.0mg / mL, feline herpes virus monoclonal antibody to 0.85mg / mL, and goat anti-cat IgG with diluent, respectively. To 1.8mg / mL, spray on the nitrocellulose membrane in turn, and then dry.
[0039] The diluent is prepared by contai...
Embodiment 3
[0043] The difference from Example 1 is:
[0044] The isolation pad refers to coating the isolation pad treatment solution on the glass fiber and drying it at 37°C for 8 hours; the isolation pad treatment solution contains 0.4wt% Triton X-100 and 0.5wt% Triton X-100 per 1000mL of PBS buffer. It is formulated with BSA, the concentration of PBS buffer is 25 mM, and the pH is 7.6.
[0045] The nitrocellulose membrane is provided with a detection line T1 coated with a feline calicivirus monoclonal antibody, a detection line T2 coated with a feline herpes virus monoclonal antibody, and a quality control line coated with a goat anti-cat IgG antibody. The detection line T1, the detection line T2 and the quality control line refer to the dilution of feline calicivirus monoclonal antibody to 1.2 mg / mL, feline herpes virus monoclonal antibody to 1.0 mg / mL, goat anti-cat The IgG was diluted to 2.0 mg / mL, sprayed on the nitrocellulose membrane in turn, and dried.
[0046] The diluent is...
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