Detection reagent for triglyceride and test paper for triglyceride
A technology for detecting reagents and test strips, which is applied in the direction of material analysis by observing the influence of chemical indicators, and analysis by chemical reaction of materials, etc., can solve problems such as insufficient detection speed, and achieve fast and accurate detection. , the effect of rapid detection
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Embodiment 1
[0057] 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.
[0058] 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.
[0059] Step 3. Prepare the detection reagent according to the ratio: 18KU / L lipoprotein lipase, 20KU / L glycerol kinase, 3KU / L glycerol triphosphate oxidase, 7.5KU / L horseradish peroxidase, 3KU / L ascorbate oxidase, 0.20g / L 4-aminoantipyrine, 0.20g / L chromogenic substance, 0.15mmol / L (pH 5.5) Tris-HCl buffer, 0.80g / L seaweed Sugar, 0.1g / L BSA, 0.15g / L CHAPS. 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 temper...
Embodiment 2
[0063] In this example, the detection reagents include 25KU / L lipoprotein lipase, 30KU / L glycerol kinase, 5KU / L glycerol triphosphate oxidase, 9.0KU / L horseradish peroxidase, 5KU / L ascorbic acid oxidation Enzyme, 0.35g / L 4-aminoantipyrine, 0.30g / L chromogenic substance, 0.25mmol / L (pH 5.5) Tris-HCl buffer, 1.0g / L trehalose, 0.3g / LBSA , 0.25g / L CHAPS, other are all with embodiment 1.
Embodiment 3
[0065] In this example, the detection reagent contains 18KU / L lipoprotein lipase, 30KU / L glycerol kinase, 3KU / L glycerol triphosphate oxidase, 9.0KU / L horseradish peroxidase, 3KU / L ascorbic acid oxidation Enzyme, 0.20g / L 4-aminoantipyrine, 0.25g / L chromogenic substance, 0.20mmol / L (pH 6) Tris-HCl buffer, 1.0g / L trehalose, 0.3g / L BSA, 0.25g / L CHAPS, other are all the same as embodiment 1.
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