Colloidal gold chromatographic test strip for rapidly testing lead ion
A technology for detecting test strips and lead ions, which is applied in the field of immunology, and achieves the effect of being easy to popularize and apply, easy to popularize, and has a wide range of applications
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Embodiment 1
[0016] Embodiment 1, preparation of lead ion colloidal gold chromatography detection test strip
[0017] To make lead ion detection test strips, it is first necessary to prepare a carrier protein coupled to lead ions for the preparation of the corresponding detection line (T line) and antibody; and it is necessary to prepare lead gold-labeled antibody for the preparation of the corresponding gold standard Antibody fiber cotton; in addition, it is necessary to prepare goat anti-mouse IgG antibody for the preparation of the control line (C line).
[0018] 1. Coupling of lead to carrier protein
[0019] Preparation of immunoantigen lead-p-thiocyanbenzyl-ethylenediaminetetraacetic acid-keyhole limpet hemocyanin (Pb-ITCBE-KLH).
[0020] First react 2mg of ITCBE and 4.5mg of KLH protein in 3mL, pH9.4 HEPES (hydroxyethylpiperazine ethylsulfuric acid) buffer solution for 24h, then ultrafilter for 10min at 4°C and 6000r / min Remove uncoupled ITCBE, wash the retentate with HEPES buffer...
Embodiment 2
[0034] Embodiment 2, detection sample pretreatment and sample detection
[0035] Spray the selected concentration of coating antigen and goat anti-mouse IgG on the coating film as the test line (T) and control line (C) respectively, and dry in an oven at 37°C for 10 min. In the same way, a certain concentration of gold-labeled antibody was coated on the binding pad. The test strip is composed of a backing plate, on which a sample pad, a gold standard binding pad, a coating film and an absorbent pad are glued in sequence. Cut the affixed board into 3mm wide strips, and then put the test strips together with the desiccant into an aluminum foil bag and seal them for storage.
[0036] Pre-treatment of test samples into digestive juice: take 1.0 g of homogeneous pork sample, add 2 mL of nitric acid into a polytetrafluoroethylene crucible, and place at room temperature for 4 hours. Transfer the sample to the digestion tube, rinse the crucible with 2 mL of nitric acid several times...
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