A rapid detection kit for chicken infectious bronchitis virus
A detection kit and bronchitis technology, applied in the field of chicken infectious bronchitis virus detection, can solve the problems of easy cross-contamination by RT-PCR, expensive thermal cycle equipment, poor stability, etc., and achieve good reproducibility and high accuracy , the effect of high sensitivity
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Embodiment 1
[0018] A rapid detection kit for chicken infectious bronchitis virus of the present invention comprises: chicken infectious bronchitis N recombinant protein coated microwell reaction plate / strip, stop solution, positive control and negative control, enzyme conjugate, sample dilution Solution, Concentrated Washing Solution, Chromogenic Solution A and Chromogenic Solution B.
[0019] The preparation method of chicken infectious bronchitis N recombinant protein coated microwell reaction plate / strip is as follows: use 0.1mol / L Tris-HCl buffer solution of pH 8 as the coating solution, dilute chicken infectious bronchitis N recombinant protein to 5 μg / mL, add 50 μL / well to the ELISA reaction plate, block at 37°C for 2 hours, coat at 4°C overnight, pat dry, block with 1% bovine serum albumin at 37°C for 3 hours, wash with 20% NaCl solution containing Tween-20 , pat dry, then add 20% sucrose phosphate buffer and keep at room temperature for 2h.
[0020] The sample diluent is a 10% N...
Embodiment 2
[0028] A rapid detection kit for chicken infectious bronchitis virus of the present invention comprises: chicken infectious bronchitis N recombinant protein coated microwell reaction plate / strip, stop solution, positive control and negative control, enzyme conjugate, sample dilution Solution, Concentrated Washing Solution, Chromogenic Solution A and Chromogenic Solution B.
[0029] The preparation method of chicken infectious bronchitis N recombinant protein coated microwell reaction plate / strip is as follows: use 0.1mol / L Tris-HCl buffer solution of pH 8 as the coating solution, dilute chicken infectious bronchitis N recombinant protein to 5 μg / mL, add 50 μL / well to the ELISA reaction plate, block at 37°C for 2 hours, coat at 4°C overnight, pat dry, block with 1% bovine serum albumin at 37°C for 2 hours, wash with 20% NaCl solution containing Tween-20 , pat dry, then add 20% sucrose phosphate buffer and keep at room temperature for 2h.
[0030] The sample diluent is a 10% N...
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