Method for quantification of cholesterol in small dense low-density lipoprotein
A cholesterol and lipoprotein technology, applied in the field of quantification of cholesterol in small and dense low-density lipoprotein, can solve problems such as time required
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example 1
[0091] Buffer, such as MOPS (pH7.0)
[0092] Cholesterol esterases such as LPL3
[0093] Cholesterol oxidase, such as CHO-PEL
[0094] Reagents for the determination of hydrogen peroxide, such as peroxidase, N-ethyl-N-(3-methylphenyl)-N'-succinylethylenediamide (EMSE) and 4-aminoantipyrine (4- AA)
[0095] Surfactants to study
example 2
[0097] Buffer, such as MOPS (pH7.0)
[0098] Cholesterol esterases such as LPL3
[0099] Cholesterol dehydrogenases such as CHDH5
[0100] Oxidized coenzymes such as NAD
[0101] [The reduced coenzyme assay reagent selected according to the needs, such as 2-(4-iodophenyl)-3-(2,4-dinitrophenyl)-5-(2,4-disulfophenyl)-2H - tetrazole monosodium salt (WST-3)]
[0102] Surfactants to study
example 3
[0104] Buffer, such as MOPS (pH7.0)
[0105] Cholesterol esterases such as LPL3
[0106] Cholesterol dehydrogenases such as CHDH5
[0107] Oxidized coenzymes such as NAD
[0108] Reduced coenzyme oxidases such as NADH oxidase
[0109] Hydrogen peroxide assay reagents such as peroxidase, EMSE and 4-AA
[0110] Surfactants to study
[0111] In addition, each of the above-mentioned reagents may contain an aqueous medium, a stabilizer, a preservative, an interfering substance eliminating agent, a reaction accelerator, and the like, which will be described later, if necessary.
[0112] 3) Judgment method of surfactant A
[0113] Add each lipoprotein fraction as a sample to the reaction cell (2 μL), then add the reagent (0.15 mL) described in the above 2) to start the reaction, heat at 37°C for 5 minutes, and measure the absorbance of the reaction solution to form a straight line Increased time, for example, the change in absorbance of the reaction solution after 5 minutes of ...
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