Enzyme-linked immunosorbent assay kit and preparation method thereof
A preparation method and ELISA plate technology, applied in the field of biomedicine, can solve the problems of lack of FN1 research and the production of a complete set of FN1ELISA kits.
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[0051] 1. Reagents:
[0052] (1) Coating solution (0.02mol / l, sodium carbonate-sodium bicarbonate buffer at pH 9.6): Na 2 CO 3 0.6g, NaHCO 3 1.16g, Na 2 N 3 0.2g, add double distilled water to 1000ml, adjust pH to 9.6.
[0053] (2) Specimen diluent (0.01mol / l PBS containing 8% calf serum pH7.4): NaCl 8.0g, NaH 2 PO 4 2H 2 O 0.3g, Na 2 HPO 4 12H 2 O 2.9g, KCl 0.2g, thimerosal 0.1g, add double distilled water to 1000ml, adjust pH to 7.4.
[0054] (3) Blocking solution (8% calf serum / PBS solution): 80ml calf serum, 0.01mol / l pH7.4 PBS 920ml.
[0055] (4) Washing solution (pH7.4 PBST): NaCl 8.0g, NaH 2 PO 4 2H 2 O 0.3g, Na 2 HPO 4 12H 2 O 2.9g, Tween 20 0.5g, thimerosal 0.1g, add double distilled water to 1000ml, adjust pH to 7.4.
[0056] (5) Enzyme-labeled secondary antibody (HRP-labeled goat anti-rabbit polyclonal antibody): purchased from R&D systems in the United States, and diluted to 1:10000 with PBS before use.
[0057] (6) FN1 protein standard substa...
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