Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

A kind of immunoturbidity kit and detection method

An immunoturbidimetric and kit technology, which is applied in the field of medical immunology in vitro diagnosis, can solve the problems of inaccurate test results of reagents, inability to meet the requirements of use, and the coefficient of variation becomes large, and achieves good reagent stability, wide versatility, and detection. Accurate results

Active Publication Date: 2019-02-12
SICHUAN MACCURA BIOTECH CO LTD
View PDF8 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0008] Antibodies are prone to flocculent or flaky precipitation during storage, resulting in poor antibody performance, poor repeatability, and large coefficient of variation (CV), directly resulting in inaccurate reagent test results, and additional filtration steps, complicated operation, And filtration may remove antibodies, affect the detection effect, cause certain impact on patients, and cannot meet the requirements for use

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • A kind of immunoturbidity kit and detection method
  • A kind of immunoturbidity kit and detection method
  • A kind of immunoturbidity kit and detection method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0046] Example 1 Apolipoprotein E Detection Kit

[0047] Reagent R1:

[0048] TRIS buffer

20mmol / L

Sodium chloride

1g / L

Sodium azide

0.5g / L

polyethylene glycol 6000

1g / L

Ethylphenyl polyethylene glycol

1g / L

[0049] Reagent R2:

[0050] TRIS buffer

20mmol / L

Sodium chloride

1g / L

Sodium azide

0.5g / L

Goat anti-human apolipoprotein E antibody

10mg / L

Ethylphenyl polyethylene glycol

1g / L

magnesium sulfate

0.01g / L

calcium acetate

0.01g / L

[0051] Calibrator:

[0052] ApoE antigen standard diluent (20mmol / L phosphate buffer, 1g / L sodium chloride, 0.1g / L sodium azide, 0.3g / L dextran, 1g / L trehalose, 1g / L sucrose, 1g / L bovine serum albumin) was dissolved, tested with a commercially available control reagent and adjusted to 120mg / L, and stored in -20°C. Take it out before use, and dilute it into different concentrations of ApoE standard wit...

Embodiment 2

[0053] Example 2 Apolipoprotein A1 detection kit

[0054] Reagent R1:

[0055] Phosphate buffer

30mmol / L

potassium chloride

5g / L

phenol

0.7g / L

polyethylene glycol 6000

20g / L

Ethylphenyl polyethylene glycol

50g / L

[0056] Reagent R2:

[0057] Phosphate buffer

40mmol / L

potassium chloride

5g / L

phenol

0.7g / L

Goat anti-human apolipoprotein A1 antibody

50mg / L

Ethylphenyl polyethylene glycol

50g / L

magnesium sulfate

15g / L

calcium acetate

20g / L

[0058] Calibrator:

[0059] Apolipoprotein A1 antigen standard diluent (40mmol / L glycine buffer, 10g / L sodium chloride, 0.7g / L sodium azide, 20g / L dextran, 25g / L trehalose, 30g / L sucrose , 20g / L bovine serum albumin) was dissolved, tested with a commercially available control reagent and adjusted to 100mg / L, and stored in -20°C. Take it out before use, and dilute it into different concentrations of...

Embodiment 3

[0060] Example 3C-reactive protein detection kit

[0061] Reagent R1:

[0062] acetate buffer

70mmol / L

potassium chloride

15g / L

Sodium azide

0.8g / L

polyethylene glycol 6000

50g / L

Ethylphenyl polyethylene glycol

5g / L

[0063] Reagent R2:

[0064] acetate buffer

80mmol / L

potassium chloride

20g / L

Sodium azide

1g / L

Goat anti-human C-reactive protein antibody

250mg / L

Ethylphenyl polyethylene glycol

5g / L

magnesium sulfate

0.05g / L

calcium acetate

0.05g / L

[0065] Calibrator:

[0066] C-reactive protein antigen standard diluent (80mmol / L TRIS buffer, 20g / L sodium chloride, 1g / L sodium azide, 55g / L dextran, 50g / L trehalose, 60g / L sucrose, 70g / L bovine serum albumin) was dissolved, tested with a commercially available control reagent and adjusted to 200mg / L, and stored in -20°C in aliquots. Take it out before use, and dilute it into differ...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention provides an immunonephelometry detection kit. The immunonephelometry detection kit comprises a reagent R1 and a reagent R2, wherein the reagent R1 contains 1-50 g / L of octylphenoxy polyethoxyethanol, the reagent R2 contains 1-50 g / L of octylphenoxy polyethoxyethanol, 0.01-15 g / L of magnesium salt, 0.01-20 g / L of calcium acetate and an antibody. The detection kit has the advantages of good performance, good repeatability, and accurate reagent detection result, and can satisfy the usage requirement.

Description

technical field [0001] The invention relates to the field of medical immune in vitro diagnosis, in particular to an immune turbidimetric kit and a detection method. Background technique [0002] Turbidimetry has been widely used in clinical testing. Now the most common application is immunoturbidimetry. [0003] Most of the early immunoassay techniques analyzed the presence and content of specific proteins in the sample to be tested by observing the formation of precipitates, the occurrence of agglutination and hemolysis, and measuring the light scattering caused by aggregates, such as immunodiffusion, Immunoelectrophoresis, direct and brief hemagglutination, passive hemagglutination, complement fixation test, etc. These detection methods are low in cost, easy to judge the results, easy to master technically, and can be widely used to detect various types of clinical samples. However, the above method tends to be eliminated due to its cumbersome operation, time-consuming a...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): G01N33/53G01N33/68
CPCG01N33/53G01N33/6803G01N33/6854
Inventor 耿英利罗湘宇甘萍萍黎明龙腾镶
Owner SICHUAN MACCURA BIOTECH CO LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products