Preparation method of human TDP-43 monoclonal antibody coating ELISA plate and ELISA detection kit
A TDP-43 and ELISA technology, which is applied to the preparation method of human TDP-43 monoclonal antibody-coated ELISA kits and the field of ELISA detection kits, can solve the problem that the purity and activity of capture antibodies and detection antibodies are difficult to achieve in the kits , the lack of quantitative research on TDP-43, the inability to provide positive controls and internal reference, etc., to achieve the effect of fast detection, convenient use and wide application range
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[0050] 1. Reagents:
[0051] (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.
[0052] (2) Specimen diluent (0.01mol / l PBS at pH 7.4 containing 8% calf serum and 1% anti-human IgG): 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.
[0053] (3) Blocking solution (8% calf serum / PBS solution): 80 ml of calf serum, 920 ml of 0.01 mol / l pH7.4 PBS.
[0054] (4) Wash 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 200.5g, thimerosal 0.1g, add double distilled water to 1000ml, adjust pH to 7.4.
[0055] (5) Enzyme-labeled secondary antibody (HRP-labeled goat anti-rabbit polyclonal antibody): purchased from R&D systems in the United States, and diluted 1:10000 with the sample diluent when used....
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