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Method for detecting high-density lipoprotein in serum

A high-density lipoprotein and serum technology, applied in the preparation of test samples, measuring devices, instruments, etc., can solve the problems of lack of HDL subclass analysis methods and lack of unified understanding, so as to improve efficiency, shorten electrophoresis time, Guaranteed accurate detection results

Pending Publication Date: 2021-04-16
安徽佳创生物科技有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the relative importance of subclasses HDL2 and HDL3 has been divided clinically, and there is still no unified understanding in the world. The main reason is the lack of simple and accurate methods for analyzing HDL subclasses.

Method used

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  • Method for detecting high-density lipoprotein in serum
  • Method for detecting high-density lipoprotein in serum
  • Method for detecting high-density lipoprotein in serum

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0031]A method of detecting high-density lipoprotein in serum, including the steps of:

[0032]Step 1, the sample preparation: 40 ul serum is prepared, and the centrifugation was carried out by the addition of an 8 ul phosphate tungsungnic acid solution, centrifugation was 8 min, the rotation speed was 2500 rpm, and the supernatant was placed in a new centrifuge tube;

[0033]Step 2, dyeing: 20 ul 0.1% (w / v) Sandan black b dyeing liquid and 10 ul40% sucrose solution were sequentially added in step 1, and mixed well and mixed.

[0034]Step 3, preparing an electrophoresis medium: The electrophoresis medium is used with a tubular gel system, and the upper layer employs a concentrated glue, the lower layer adopts a uniform concentration separation glue;

[0035]Step 4, electrophoresis: Put the electrophoresis medium into the disc-shaped electrophoresis instrument, add an electrophoretic buffer, and then slowly add the detection sample obtained by 35 ul step 2, first in electrophoresis at a curren...

Embodiment 2

[0050]A method of detecting high-density lipoprotein in serum, including the steps of:

[0051]Step 1, the sample preparation: 50 ul serum, centrifuged by adding 10 ul of phosphate tungsungstic acid solution for 10 min, centrifugal time is 10 min, the rotation speed is 2500 rpm, and the suction supernatant is placed in a new centrifuge tube;

[0052]Step 2, staining: 25 ul 0.5% (w / v) Sandan black B dyeing liquid and 15 ul40% sucrose solution were sequentially added in step 1, and mixed well and mixed.

[0053]Step 3, preparing an electrophoresis medium: The electrophoresis medium is used with a tubular gel system, and the upper layer employs a concentrated glue, the lower layer adopts a uniform concentration separation glue;

[0054]Step 4, electrophoresis: Put the electrophoretic medium into the disc-shaped electrophoresis instrument, add an electrophoretic buffer, and then slowly add the detection sample obtained by the 40 ul step 2, first in electrophoresis at a 2mA current, to be detected...

Embodiment 3

[0069]A method of detecting high-density lipoprotein in serum, including the steps of:

[0070]Step 1, the sample preparation: 60 ul serum is prepared, and the centrifugation is carried out by adding 12 ul phosphorite acid tungsionic acid solution, centrifugation is 12 min, the rotation speed is 2500 rpm, and the suction supernatant is placed in a new centrifuge tube;

[0071]Step 2, dyeing: 30 ul 0.1% (w / v) Sudanese black b dyeing liquid and 20 ul40% sucrose solution were sequentially added in step 1, and mixed well and mixed, and obtained the sample;

[0072]Step 3, preparing an electrophoresis medium: The electrophoresis medium is used with a tubular gel system, and the upper layer employs a concentrated glue, the lower layer adopts a uniform concentration separation glue;

[0073]Step 4, electrophoresis: Put the electrophoretic medium into the disc-shaped electrophoresis instrument, add an electrophoretic buffer, and then slowly add the detection sample obtained by 45 ul step 2, first in ...

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Abstract

The invention provides a method for detecting high-density lipoprotein in serum. The method comprises four steps of sample preparation, dyeing, electrophoresis medium preparation and electrophoresis, and the sample preparation comprises the following steps: preparing serum, adding a phosphotungstic acid solution, standing, centrifuging, sucking out the supernatant, and putting into a new centrifuge tube. The serum is precipitated, chyle particles, low-density lipoprotein, extremely low-density lipoprotein and lipoprotein in the serum can be precipitated, and the centrifuged supernatant only contains one kind of HDL lipoprotein, so that the HDL in the serum can be conveniently detected, the detection accuracy is ensured, the detection efficiency is improved, the electrophoresis medium is easy to prepare, a special glue pouring device is not needed, the electrophoresis time required by detection is short, and the detection efficiency is improved while the detection accuracy is ensured.

Description

Technical field[0001]The present invention relates to the technical field of detection methods, and more particularly to a method of detecting high density lipoprotein in serum.Background technique[0002]High-densityLipoprotein, HDL is one of the serum proteins, is a composite lipoprotein consisting of lipid and protein and the regulatory factor thereof. It is capable of transporting cholesterol in the tissue, converting it to bile acid. Or directly discharge from the intestinal tract, arterial angiography demonstrate that high-density lipoprotein cholesterol content is significantly negative with arterial stenosis. High-density lipoprotein is known as "blood vessel cleavage", is a kind of protective factor of anti-pharmaceuticallyhamous concentrated plasma fat protein, coronary heart disease, has a role in resisting human atherosclerosis. Therefore, in-depth study of high-density lipoprotein on the resistance of atherosclerosis and its mechanisms have important theoretical significa...

Claims

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Application Information

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IPC IPC(8): G01N1/28G01N1/34G01N27/447
Inventor 吴瑶瑶邓结飞唐红艳汪培
Owner 安徽佳创生物科技有限公司