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Method for trace, fast and accurate detection of human erythrocyte antigen and antibodies in serum

A technology for detecting human body and red blood cells, applied in the field of trace amounts, can solve the problems of time consumption, low efficiency, and high consumption of reagents, and achieve the effect of improving safety, reducing accuracy and promoting development.

Inactive Publication Date: 2011-09-07
周胜利
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The method of using glass slides is simple and fast, but it consumes a lot of reagents and is not very accurate; it consumes time and is inefficient; the test tube method is accurate, but it is time-consuming, consumes reagents, has low efficiency, and the results cannot be preserved; the gel method is accurate and the results can be preserved. But time-consuming, reagent-consuming, and low efficiency; the results of the check-board method can be saved, fast, and can be conveniently automated. The efficiency is high, but the reagents are expensive, the results cannot be saved, the operation is troublesome, it is not intuitive, and sometimes errors occur, and manual review is required.

Method used

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  • Method for trace, fast and accurate detection of human erythrocyte antigen and antibodies in serum
  • Method for trace, fast and accurate detection of human erythrocyte antigen and antibodies in serum
  • Method for trace, fast and accurate detection of human erythrocyte antigen and antibodies in serum

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0034]Example 1, the microplate detects red blood cell A, B, O and Rh antigens.

[0035] In this example, the 30, 60, or 72-well microplate assay contains anti-A, anti-B and anti-D antibodies, or A, B, O red blood cells, adding human red blood cells and serum to detect red blood cells A, B and D antigens and antibodies, Table 1 is the antibodies and red blood cells included in each well of the matching plate.

[0036] Table 1: Erythrocyte I-A, -B, -D Antigen, Antibody Detection Panel

[0037]

[0038]

[0039] The microplates employed are 30, 60 or 72 well plates, each well containing 1 to 2 microliters of monoclonal or polyclonal antibodies against known erythrocyte antigens, overlaid with 5 microliters of mineral oil. There are positive and negative controls in each matching plate, and the first line of quality control tests the matching reliability of the microplate. Anti-A; Anti-B; and Anti-D antibodies were added to the remaining wells, and these wells are used fo...

example 2

[0041] Example 2, microplate detection of erythrocyte phenotype antigen (Phenotype).

[0042] In this example, the 30, 60, or 72-well microplate assay contains antibodies other than the anti-ABO system, and the red blood cells of the person to be tested are added to detect the antigens other than the red blood cell ABO system. Table 2 is the matching plate. Antibodies included in wells.

[0043] Table 2: Red blood cell phenotype detection panel

[0044]

1

2

3

4

5

6

A

Anti-E

Anti-e

Anti-C

Anti-c

Anti-K

Anti-k

B

Anti-E

Anti-e

Anti-C

Anti-c

Anti-K

Anti-k

C

Anti-Fya

Anti-Fyb

Anti-JKa

Anti-JKb

Anti-Lea

Anti-Leb

D

Anti-Fya

Anti-Fyb

Anti-JKa

Anti-JKb

Anti-Lea

Anti-Leb

E

Anti-M

Anti-N

Anti-S

Anti-s

Anti-P

F

Anti-M

Anti-N

Anti-S

Anti-s

Anti-P

[0045]...

example 3

[0048] Example 3, microplate screening of antibodies against erythrocyte phenotype antigens.

[0049] In the following example, 30, 60, or 72-well microplates detect fresh or frozen erythrocytes containing known erythrocyte antigens, add the serum of the person to be tested, and screen the anti-erythrocyte antibodies contained in the serum. Table 3 is the matching plate Each well contains red blood cells.

[0050] Table 3: Serum Antibody Screening Panel

[0051]

[0052]

[0053] The microplates employed are 30, 60 or 72 well plates, each well containing 1 to 2 microliters of fresh or frozen red blood cells of known erythrocyte antigens, overlaid with 5 microliters of mineral oil. Like the detection of ABO system antibodies, this invention uses fresh or frozen red blood cells from known red blood cell antigens containing various red blood cell phenotypes (Phenotype) to detect Rh, P, MNS, Kell, Luthern, Kell, Duffy and Kidd and other red blood cells Antibodies present i...

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PUM

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Abstract

The invention relates to a method for trace, fast and accurate detection of human erythrocyte antigens and antibodies in serum. Tiny known antibodies for resisting erythrocyte antigens are allocated on a trace detection board by the principle of immunohematology, and tiny unknown erythrocytes to be detected are added for detecting the antigens at the surface of the erythrocyte membrane; or the erythrocytes of the tiny known erythrocyte antigens are added into the tiny unknown serum to be detected, so as to detect the antibody for resisting erythrocyte membrane surface antigens in human blood to be detected. The reaction characteristic is erythrocyte aggregation; if the aggregation exists, the reaction is a positive reaction, and otherwise the reaction is a negative reaction; and a centrifugal machine, a spectrophotometer, a microscope and a computer program are cooperated, so that the erythrocyte antigens and antibodies in serum can be detected fast, accurately and automatically. The use of the trace detection board kit prepared by the method in medical field can greatly improve the safety, efficiency and accuracy of clinical erythrocyte matching, reduce the detection expenses, and promote the development of clinical blood application.

Description

technical field [0001] The invention relates to a method for rapidly and accurately detecting human red blood cell antigens and antibodies in serum by using the principle of immunohematology, in particular to a trace, fast and accurate method for detecting human red blood cell antigens and antibodies in serum. Background technique [0002] In 1901, Kaul Landsteiner proved that when blood is transfused between groups of people, the different blood types of red blood cells can cause fever and jaundice in the transfused person, so he divided the blood types into A, B, and O types, and also explained in practical applications There will be no transfusion reactions between people whose blood types match. In 1902 A.Decastrello and A.Sturli discovered the AB blood type. The Rh blood type was discovered by Levine and Stetson in 1940, which is based on the presence or absence of this antigen on the red blood cell membrane. does not contain this antigen. It is now clear that more t...

Claims

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Application Information

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IPC IPC(8): G01N33/80G01N33/577G01N33/543
Inventor 胡当玉周凝周胜利
Owner 周胜利
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