High-performance small and dense low-density lipoprotein cholesterol detection kit
A technology for low-density lipoprotein and detection kits, which can be used in the determination/inspection of microorganisms, biochemical equipment and methods, etc., and can solve problems such as transformation
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Embodiment 1
[0023] The raw materials of a high-performance small and dense low-density lipoprotein cholesterol detection kit include by weight: Reagent A: Good's buffer 90mmol / L, cholesterol esterase 1ku / L, cholesterol oxidase 1ku / L, phospholipase 0.7ku / L, catalase 400ku / L and N-ethyl-N-(2-hydroxy-3-sulfopropyl)-3-methylaniline sodium salt (TOOS) 1mmol / L; Reagent B: Good's buffer 90mmol / L, peroxidase 2ku / L, 4-aminoantipyrine 3mmol / L and sodium azide 0.04%, the pH value of Good's buffer is 7.0, the phospholipase is sphingomyelinase, the peroxidase The pH is 6.8.
[0024] In the present invention, the detection method of the high-performance small and dense low-density lipoprotein cholesterol detection kit specifically comprises the following steps:
[0025] S1. Elimination of non-sdLDL-C: take serum or plasma samples, add reagent A to the serum or plasma samples, and remove non-sdLDL-C components first under the action of cholesterol lipase, cholesterol oxidase, phospholipase and catalas...
Embodiment 2
[0028] The raw materials of a high-performance small and dense low-density lipoprotein cholesterol detection kit include: Reagent A: Good's buffer 100mmol / L, cholesterol esterase 2ku / L, cholesterol oxidase 1.5ku / L, phospholipase 0.8 ku / L, catalase 500ku / L and N-ethyl-N-(2-hydroxy-3-sulfopropyl)-3-methylaniline sodium salt (TOOS) 2mmol / L; Reagent B: Good's buffer solution 100mmol / L, peroxidase 2.5ku / L, 4-aminoantipyrine 4mmol / L and sodium azide 0.05%, the pH value of Good's buffer is 7.2, phospholipase is sphingomyelinase, peroxide The pH of the enzyme is 7.0.
[0029] In the present invention, the detection method of the high-performance small and dense low-density lipoprotein cholesterol detection kit specifically comprises the following steps:
[0030]S1. Removal of non-sdLDL-C: Take serum or plasma samples, add reagent A to the serum or plasma samples, and remove non-sdLDL-C components first under the action of cholesterol lipase, cholesterol oxidase, phospholipase and cat...
Embodiment 3
[0033] The raw materials of a high-performance small and dense low-density lipoprotein cholesterol detection kit include by weight: Reagent A: Good's buffer 110mmol / L, cholesterol esterase 3ku / L, cholesterol oxidase 2ku / L, phospholipase 0.9ku / L, catalase 600ku / L and N-ethyl-N-(2-hydroxy-3-sulfopropyl)-3-methylaniline sodium salt (TOOS) 3mmol / L; Reagent B: Good's buffer 110mmol / L, peroxidase 3ku / L, 4-aminoantipyrine 5mmol / L and sodium azide 0.06%, the pH value of Good's buffer is 7.4, the phospholipase is sphingomyelinase, the peroxidase The pH value is 7.2.
[0034] In the present invention, the detection method of the high-performance small and dense low-density lipoprotein cholesterol detection kit specifically comprises the following steps:
[0035] S1. Removal of non-sdLDL-C: Take serum or plasma samples, add reagent A to the serum or plasma samples, and remove non-sdLDL-C components first under the action of cholesterol lipase, cholesterol oxidase, phospholipase and cat...
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