Detection kit of ischemia modified albumins
A technology for detecting kits and albumin, which is applied in the field of clinical testing, can solve problems affecting instrument analysis performance, inconvenient operation, instrument pollution, etc., and achieve the effects of easy promotion and use, strong anti-interference ability, and good stability
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Embodiment 1
[0051] Embodiment 1: the preparation method of kit of the present invention
[0052] According to the following components, the kit is prepared in the form of liquid dual reagents.
[0053] Kit 1. the first of the kit of the present invention consists of a double reagent kit, and its composition is as follows:
[0054] Reagent 1 composition and concentration:
[0055] Good's buffer: 50mM, pH8.0
[0056] Cobalt chloride: 0.3mM,
[0057] TritonX-405: 0.1%;
[0058] Reagent 2 composition and concentration:
[0059]
[0060] Kit 2. The 2nd composition of kit of the present invention is double reagent kit, and its composition is as follows:
[0061] Reagent 1 composition and concentration:
[0062]
[0063] Reagent 2 composition and concentration:
[0064] Good's buffer: 100mM,
[0065] Dithiothreitol: 5mM,
[0066] Tris(2-carboxyethyl)phosphine-hydrochloride: 5mM.
Embodiment 2
[0067] Embodiment 2. The usage method of kit
[0068] The detection method is the rate method.
[0069] 1) provide serum samples,
[0070] 2) After mixing 150 μL reagent 1 and 20 μL serum sample, incubate at 37°C for 5 minutes, and measure the absorbance A1 at 505 nm,
[0071] 3) Add 50 μL of reagent 2, incubate for another 5 minutes, and detect the absorbance A2 at 505 nm for 5 minutes. The concentration of IMA in the sample was thus calculated. Other suitable assays and procedures known in the art may also be used.
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