Heavy metal copper monoclonal antibody and preparation method thereof
A technology for cloning antibodies and heavy metals, applied in the fields of botanical equipment and methods, biochemical equipment and methods, chemical instruments and methods, etc., can solve the problems of late start and no research reports, and achieve good repeatability and stability. , the effect of antigen practicability
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Embodiment 1
[0044] The detection of embodiment 1 copper standard solution (Sigma Co.)
[0045] The indirect competitive ELISA method was used to conduct a preliminary exploration of the detection curve. The method is as follows:
[0046] Coating: Dilute the coating antigen bovine serum albumin-1-(4-isothiocyanatophenyl)-B with 10mM, pH7.4N-2-hydroxyethylpiperazine-N-2-ethanesulfonic acid buffer Diaminetetraacetic acid-Cu, add 50 μl / well to a 96-well enzyme-linked microanalysis plate, and place it at 4°C overnight;
[0047] Washing: wash 3 times with PBST;
[0048] Blocking: PBST diluted gelatin to 1% (m / v), 100 μl / well, 1.5 hours at 37°C;
[0049] Washing: wash 3 times with PBST;
[0050] Adding samples: dilute the copper nitrate standard solution step by step with phosphate buffer containing 2mM ethylenediaminetetraacetic acid to 10 -5 μg / ml, 10 -4 μg / ml, 10 -3 μg / ml, 10 -2 μg / ml, 10 -1 μg / ml, 1μg / ml, 10μg / ml, 100μg / ml series concentration, the diluted solution was placed at room...
Embodiment 2
[0057] Detect copper residue in the tap water sample of embodiment 2
[0058] Bovine serum albumin-1-(4-isothiocyanatophenyl)-ethylenediaminetetraacetic acid-Cu 0.4 μg / ml coated microanalysis plate 50 μl / well, copper antibody supernatant diluted 4 times as the working concentration, 1% (m / v) gelatin was used as a blocker, the pH value of the antigen-antibody reaction matrix (N-2-hydroxyethylpiperazine-N-2-ethanesulfonic acid buffer solution) was 5.0, and the ionic strength was 0.15mol / L. 50 μl / well in microassay plate.
[0059] Sample preparation to be tested:
[0060] Tap water sample: measure 100 μl of tap water, add 0.5 μl of 1000ug / ml copper standard solution, and prepare a 5ug / ml liquid sample.
[0061] The above samples were detected by copper ELISA detection method, and the operation was as follows:
[0062] 1) Coating:
[0063] Bovine serum albumin-1-(4-isothiocyanatophenyl)-ethylenediaminetetraacetic acid-Cu 0.4μg / ml Add 50μl to each well of the microanalysis plat...
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