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

Colloidal gold chromatography anti-nucleosome antibody detection test paper and preparation method thereof

A technology for nucleosome antibodies and test strips, applied in the field of medical immunity applications, can solve the problem that anti-nucleosome antibodies have not come out.

Active Publication Date: 2012-08-01
SHANGHAI KEXIN BIOTECH
View PDF9 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0016] In terms of autoimmune diseases, there are currently some test strip products for detecting autoimmune diseases in foreign markets, but colloidal gold immune test strips for anti-nucleosome antibodies have not yet come out in domestic and foreign markets

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
  • Colloidal gold chromatography anti-nucleosome antibody detection test paper and preparation method thereof
  • Colloidal gold chromatography anti-nucleosome antibody detection test paper and preparation method thereof
  • Colloidal gold chromatography anti-nucleosome antibody detection test paper and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0075] Embodiment 1 Nucleosome antigen protein preparation

[0076] The nucleosome antigen protein used in this test paper is a recombinant gene constructed by gene cloning technology, and then the prokaryotic expression technology is used to successfully express all human nucleosome antigen protein. Wherein, the nucleosome antigen protein is derived from purified genetic engineering antigen protein.

Embodiment 2

[0077] Example 2 Antibody Preparation

[0078] Antibody A, Antibody C, and Antibody B were prepared by the following method. Anti-human IgG in Antibody A, Antibody C and Antibody B can generally be produced by multiple subcutaneous (sc) or intraperitoneal (ip) injections of purified immunogens and adjuvants on animals.

[0079] The injection solution was obtained by mixing 0.05mg~1mg of immune preparations (respectively for goats or mice) with 3 times the volume of Freund's complete adjuvant, and injected the injection solution into multiple parts of the animal skin. 5 to 1 / 10 of the original amount of human IgG in Freund's complete adjuvant mixture was injected subcutaneously into multiple sites to boost the immunization. After 7-14 days, the animals were bled, and the serum anti-human IgG titer was measured. Animals were boosted until titers plateaued. Methods for producing polyclonal antibodies are described in many immunology textbooks, for example, "Common Experimental...

Embodiment 3

[0082] Colloidal gold solution preparation

[0083] 0.01% HAuCl 4 Heat the solution to boiling, quickly add every 100mL HAuCl 4 Add an appropriate amount of reducing agent solution to the solution, and the color changes from blue, then light blue, to blue, then red after heating, and transparent orange-red after boiling for 7-10 minutes. Then filter with ultrafiltration or microporous membrane (0.45μm) to remove the polymer and other impurities that may be mixed therein. The prepared colloidal gold should be pure, translucent, free of sediment and floating matter, and discard when oily matter and a large amount of black granular precipitate appear on the liquid surface.

[0084] Wherein the reducing agent used can be trisodium citrate (Frens 1973), tannic acid-trisodium citrate (Slot and Gueeze 1985), white phosphorus, preferably use trisodium citrate, more preferably use 1% trisodium citrate sodium.

[0085] The glass containers used should be absolutely clean, and must b...

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 discloses a colloidal gold chromatography anti-nucleosome antibody detection test paper and a preparation method thereof. The colloidal gold chromatography anti-nucleosome antibody detection test paper comprises a sample pad, a combination pad, a cellulose nitrate coated film and a water absorption pad, and the sample pad, the combination pad, the cellulose nitrate coated film and the water absorption pad are pasted on a base plate sequentially from one side of the base plate to the other side of the base plate, wherein the combination pad is coated with a gold-labeled antibody a and a gold-labeled antibody b; and the cellulose nitrate coated film is provided with a detection line and a quality control line, the detection line is coated with a nucleosome antigen protein, and the quality control line is coated with a gold-labeled antibody c. By adopting indirect immunoassay to introduce the nucleosome antigen protein in the invention to carry out process optimization on the combination pad and the sample pad, so high sensitivity, high specificity and high accuracy detection performances of the anti-nucleosome antibody are realized, and a reference basis is provided for the auxiliary diagnosis of systemic lupus erythematosus.

Description

technical field [0001] The invention belongs to the field of medical immunization applications, and in particular relates to a test paper for detecting anti-nucleosome antibodies by colloidal gold immunochromatography technology and a preparation method thereof. Background technique [0002] Nucleosome is the basic structural unit of chromosome, composed of DNA and histones. There are five types of histone molecules, called H1, H2A, H2B, H3, and H4. Two molecules each of histone H2A, H2B, H3 and H4 together constitute the core of the nucleosome, called histone octamer, also known as core histone. [0003] The only source of nucleosomes in living organisms is the apoptotic cell; when the cell undergoes apoptosis, the DNA in the nucleus of the apoptotic cell makes the nucleosome The connecting region of the DNA is cut into oligonucleotide fragments of 180-200 bp or multiples thereof: these DNA fragments and oligonucleosomes form apoptotic bodies; under normal physiological c...

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
IPC IPC(8): G01N33/577G01N33/558G01N33/532
Inventor 韩永俊高成秀张玥葛文斌孙宏彬钱杰
Owner SHANGHAI KEXIN BIOTECH
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