Detection reagent and test paper for beta-hydroxybutyrate
A technology for detecting reagents and test strips, which is used in measuring devices, material analysis, instruments and other directions by observing the impact on chemical indicators, can solve problems such as insufficient detection speed, and achieve fast and accurate detection, rapid detection, and accurate detection. Effect
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Embodiment 1
[0053] Step 1: Paste double-sided adhesive tape 40 on the reactive base layer 30 made of PET with a certain hardness, and punch holes for later use.
[0054] Step 2: tear off the double-sided adhesive tape on the reaction base layer 40, and paste the reaction film 50 on the double-sided tape 40 of the PET board. The reaction film 50 needs to completely cover the hole 31 on the PET substrate.
[0055] Step 3. Prepare the detection reagent according to the ratio: 3KU / L diaphorase, 9KU / L β-hydroxybutyrate dehydrogenase, 1.2KU / L NAD and 0.6KU / L NBT, 0.08mmol / L L (pH 8.0) Tris-HCl buffer solution, 1.0 g / L g / L trehalose. Add the prepared detection reagent dropwise into the wells of the reaction membrane plate with a dispenser, the weight of each hole is 6mg, and put the membrane plate after dripping into the drying tunnel for drying. The drying temperature is 37°C and the drying time is 20min, and the reaction is obtained. Layer 50.
[0056] Step 4: Paste and completely cover the ...
Embodiment 2
[0059] In this example, the detection reagent contains 3KU / L of diaphorase, 13KU / L of β-hydroxybutyrate dehydrogenase, 2.5KU / L of NAD and 0.6KU / L of NBT, 0.12mmol / L (pH 9.0 ) Tris-HCl buffer solution, 1.5g / L g / L trehalose, and others are the same as in Example 1.
Embodiment 3
[0061] In this example, the detection reagent contains 5KU / L diaphorase, 9KU / L β-hydroxybutyrate dehydrogenase, 1.2KU / L NAD and 1.0KU / L NBT, 0.08mmol / L (pH 8.0) Tris-HCl buffer solution, 1.0g / L g / L trehalose, and others are the same as in Example 1.
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