A Stable Troponin Detection Kit
A technology for detecting kits and troponin, which is applied in the field of troponin detection kits, can solve problems such as waste, influence on reagent stability, unfavorable reagent long-term storage, etc., and achieve the effect of enhancing stability
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Embodiment 1
[0023] Embodiment 1 (comparative example)
[0024] Component 1 (R1):
[0025] Component 1 (R1):
[0026] Glycine buffer pH 7.6
[0027] Sodium chloride 150mmol / L
[0028] Surfactant 3g / L
[0029] Component 2 (R2):
[0030] Glycine buffer pH 7.6
[0031] Goat anti-human TnI antibody coated latex particles 3g / L.
[0032] When using, use a fully automatic biochemical analyzer with dual reagent functions, such as Toshiba 40 fully automatic analyzer, etc., and use the dual reagent endpoint method for determination. Place R1 and R2 on the corresponding reagent positions according to the ratio of 3:1, and place distilled water, standards and samples on the corresponding positions of the sample plate. The operation is shown in Table 1:
[0033] Table 1 Detection method of troponin I detection reagent
[0034]
[0035] Calculation: troponin I concentration = (∆A determination ÷ ∆A standard) × C standard
Embodiment 2
[0037] Glycine buffer pH 7.6
[0038] Sodium chloride 150mmol / L
[0039] Alkyl glucoside 3g / L;
[0040] Component 2 (R2):
[0041] MOPOS buffer 25mmol / L
[0042] Goat anti-human TnI antibody coated latex particles 3g / L.
[0043] The method of use is the same as above.
Embodiment 3
[0045] Glycine buffer pH 7.6
[0046] Sodium chloride 250mmol / L
[0047] Alkyl glucoside 3g / L;
[0048] Component 2 (R2):
[0049] MOPOS buffer 50mmol / L
[0050] Goat anti-human TnI antibody coated latex particles 3g / L.
[0051] The method of use is the same as above.
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