Detection card and kit for quantitatively detecting folic acid by immunofluorescence chromatography
An immunofluorescence and quantitative technique, which is applied in the field of biology and immunoassay, can solve the problems of inability to operate on-site, high cost of detection, complicated pretreatment, etc., and achieve the effect of convenient detection, convenient observation, and good repeatability of results
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Embodiment 1
[0044] Such as Figure 1-3 As shown, a test card for the quantitative detection of folic acid by immunofluorescence chromatography, including an upper cover 1 and a lower cover 2, the upper cover 1 and the lower cover 2 are snap-connected to each other, and an accommodation chamber is formed between the upper cover 1 and the lower cover 2 , a test strip is set in the chamber, and the test strip includes a PVC bottom plate 3, a sample pad 4, a blood filter pad 5, a first binding pad 6, a second binding pad 7, a nitrocellulose membrane 8 and an absorbent paper 11, The sample pad 4, the blood filter pad 5, the first binding pad 6, the second binding pad 7, the nitrocellulose membrane 8 and the water-absorbing paper 11 are sequentially overlapped with each other and then pasted on the PVC base plate 3, and overlapped with each other. The size of the sample pad 4 is 1mm, one end of the sample pad 4 is pasted on the PVC base plate 3, the other end of the sample pad 4 is lapped on on...
Embodiment 2
[0067] A kit for the quantitative detection of folic acid by immunofluorescence chromatography, the kit includes a sample dissociation solution and a detection card as described in Example 1, and the sample dissociation solution includes a stabilizer, a denaturant and a neutralizer , stabilizers include 25mM MES, 1% TCEP, 0.5% mercaptoethanol, 0.2% PC300 and 2.5% sodium ascorbate, denaturants include 0.1mM sodium carbonate-sodium bicarbonate buffer, 5% sodium hydroxide, 0.1% methanol and 0.2 %PC300, the neutralizer contains 50mM Tris buffer, 0.9% NaCl and 0.5% casein, and the above percentages are all mass percentages.
[0068] The detection method of the kit is:
[0069] The sample to be tested is serum, whole blood or plasma, and the sample is dissociated with the sample dissociation solution. The sample dissociation process is: mix 25 μL of the stabilizer and 15 μL of the denaturant, add 40 μL of the sample to be tested, let stand at 37°C for 5 minutes, add Mix 50 μL of th...
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