Glycosylated hemoglobin immunochromatographic test strip and preparation method thereof, and kit
A technology for glycated hemoglobin and immunochromatographic test strips, applied in the field of glycated hemoglobin immunochromatographic test strips and their preparation, can solve problems such as limited detection of HbA1c, and achieve the effects of short detection time, fast release speed, and quick operation.
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[0046] The present invention also provides a method for preparing any one of the above-mentioned glycosylated hemoglobin immunochromatographic test strips, comprising the following steps:
[0047] S1. Add the sample pad treatment solution to the sample pad and dry it.
[0048] The specific steps are: spray the sample pad treatment solution on the sample pad at a speed of 2-8 μL / cm, and dry it overnight.
[0049] In one embodiment, the sample pad treatment solution is a sample pad diluent containing 0.5-2 mg / mL mouse IgG, 0.5%-1% Evans blue and 0.1-2 mg / mL RBC, and the sample pad diluent is a sample pad diluent containing 0.5%- 3% Tween-20 and 2%-5% BSA (Bovine Serum Albumin) in 0.02M PB buffer (Phosphate Buffer).
[0050] S2. Use fluorescent latex particles to label the coupling complex of the first dog and cat HbA1c monoclonal antibody and the first complex, prepare a fluorescent latex particle-coupling complex labeling solution, and mix the labeling solution and the second ...
Embodiment 1
[0074] Preparation of labeling solution
[0075] 1), preparation of activated fluorescent microsphere solution:
[0076] Cleaning: Use a pipette gun to draw 1mL of fluorescent microsphere solution (containing 10mg of fluorescent microspheres) into a centrifuge tube, centrifuge at 14000rpm for 15min, discard the supernatant, add 1mL of 0.01M Tris buffer, and mix well by ultrasonic to obtain the washed Fluorescent microsphere solution.
[0077] Activation: Add 1 mL of 5 mg / mL N-hydroxysuccinimide and 5 mg / mL 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide to the above washed fluorescent microsphere solution The 0.01M Tris buffer solution of hydrochloride was mixed on a rotary mixer for 20 minutes to obtain an activated fluorescent microsphere solution.
[0078] Termination of activation: Centrifuge the above-mentioned activated fluorescent microspheres at 14000 rpm for 15 min, discard the supernatant, add 1 mL of 0.1M MES buffer containing 0.1% methanol, and ultrasonically mix t...
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