Colloidal gold rapid diagnosis test paper of porcine 2 type torque teno virus antibody and preparation method thereof
A technique for rapid diagnosis of leukovirus, applied in the field of colloidal gold rapid diagnosis test paper for porcine type 2 leptovirus antibody and its preparation, achieving the effects of good sensitivity and specificity, convenient use, and simple structure
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Embodiment 1
[0039] like figure 1 As shown, the colloidal gold rapid diagnostic test paper for porcine type 2 leukovirus antibody of the present invention comprises a PVC base plate 1, a sample pad 2, a colloidal gold binding pad 3, a nitrocellulose membrane 4 and a water-absorbing filter paper 5, and a sample pad 2 , colloidal gold binding pad 3, nitrocellulose membrane 4 and water-absorbing filter paper 5 are sequentially arranged on the PVC base plate 1 according to the chromatography direction, and one end of the sample pad 2 is stacked on the front end of the colloidal gold binding pad 3, and the back of the colloidal gold binding pad 3 The end is stacked on one end of the nitrocellulose membrane 4, and the front end of the water-absorbing filter paper 5 is stacked on the other end of the nitrocellulose membrane 4; the nitrocellulose membrane 4 is sprayed with a detection line 41 and a quality control line 42, respectively. The colloidal gold binding pad consists of a nitrocellulose m...
Embodiment 2
[0046] A colloidal gold rapid diagnostic test paper for porcine type 2 leukovirus antibody is prepared according to the same preparation method as in Example 1. The difference from Example 1 is that the pH value of the colloidal gold used in step 4) was adjusted to 10.0, and the mixing ratio of the dialyzed rTTSuV2 ORF1' protein solution and colloidal gold was 100 μL / 10mL.
Embodiment 3
[0048] A colloidal gold rapid diagnostic test paper for porcine type 2 leukovirus antibody is prepared according to the same preparation method as in Example 1. The difference from Example 1 is that the pH value of the colloidal gold used in step 4) was adjusted to 11.0, and the mixing ratio of the dialyzed rTTSuV2 ORF1' protein solution and colloidal gold was 150 μL / 10mL.
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