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

Reagents and analytical methods for permeabilizing and fixing blood cells

A blood cell and reagent technology, applied in the field of cell molecular analysis, can solve problems such as complicated steps, large changes in cell shape, and destruction of epitopes on the cell surface

Active Publication Date: 2021-10-01
GENERAL HOSPITAL OF NUCLEAR IND
View PDF8 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The previous permeabilization method for cells in slides or suspension was to treat the cells by diluting them with alcohol at low temperature (-20°C). Cell morphology changes greatly, destroying cell surface epitopes

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
  • Reagents and analytical methods for permeabilizing and fixing blood cells
  • Reagents and analytical methods for permeabilizing and fixing blood cells
  • Reagents and analytical methods for permeabilizing and fixing blood cells

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0051] Example 1, non-fixed cells and fixed cell surface antigen labeling

[0052] Table 1 provides 18 cases of whole blood cell membrane surface markers of healthy subjects treated with the reagent of the present invention. The results show that the non-specific binding of antibodies to fixed cells is slightly higher than that of non-fixed cells, but does not produce a large amount of non-specific Fluorescence (negative control) is not enough to interfere with the detection of cell surface marker antigens, and the cells treated with the reagents of the present invention can also maintain sufficient light scattering properties so that lymphocytes, monocytes and granulocytes can be distinguished, and the cell membrane antigens remain Complete and specific. However, when using 10% formaldehyde to fix cells in the prior art, it will increase the non-specific binding of cells (negative control), and change the binding of CD2 epitopes on lymphocytes (decrease in positive expression...

Embodiment 2

[0055] Example 2, Unfixed Cells and Fixed Infiltrated Cell Target Intraantigen Labeling

[0056] The experimental method was operated according to the above-mentioned steps, and 18 healthy subjects were labeled with whole blood cells. The results in the table are the average positive expression and signal-to-noise ratio (P / N) of some representative cell target antigens. The P / N is calculated by using the ratio of the special expression of the molecule in the target cell labeled with the monoclonal antibody to the mean fluorescence intensity (MFI) ratio of the corresponding molecule treated with the isotype control antibody. The internal protein is fixed and retained in place, and the fluorescently labeled macromolecular antibody can penetrate into the cell and bind to the corresponding protein antigen. Dimethyl sulfoxide helps to improve the detection of the intracellular antigen. Intracellular antigen labeling can increase the sensitivity of detection.

[0057] Table 2

[0...

Embodiment 3

[0060]Example 3, evaluating the effects of different concentrations of anionic surfactant BX, amino acid Glycine and different pH conditions on the expression of MPO and Lysozyme in neutrophil cells, the data show that Glycine can reduce the formaldehyde released by diazolidinyl urea The resulting fluorescence quenching of the labeled antibody conjugate improves the signal-to-noise ratio of the detection, and at the same time, the 1.2% BX concentration and the acidic condition of PH5.5 are more sensitive to cell staining.

[0061] table 3

[0062]

[0063]

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 reagent and an analysis method for infiltrating and fixing blood cells. The reagent includes a fixing solution, a permeating solution and a cleaning solution; / ml~10mg / ml sugar compound, the fixed solution also includes aliphatic aldehyde compounds, imine compounds, urea compounds and oxazolidines with a concentration of 0.3mol / L~12.3mol / L One or more of the compounds; the infiltration solution includes a surfactant with a mass concentration of 0.01%-10%, and a protein or amino acid with a mass concentration of 0.2%-15%. The reagent can effectively lyse red blood cells and permeabilize white blood cell membranes, but will not substantially destroy cell characteristics such as surface markers, morphology and light scattering properties of white blood cell membranes, and allow antibodies or other components of interest to enter cells, and the cell contents are well preserved , Analyze intracellular proteins, nucleic acids, enzymes, cytokines, virus particles, etc. by flow cytometry.

Description

technical field [0001] The invention relates to the technical field of cell molecule analysis, more specifically, it relates to reagents and analysis methods for infiltrating and fixing blood cells. Background technique [0002] The analysis of blood cell differentiation phenotype is used to assess the disease state and other health conditions of organisms is the latest development trend in the field of cell molecular analysis, and foreign countries have been able to provide commercial kits for detailed analysis of intracellular and cell surface targets. analyze. Staining of cell surface target antigens is readily accomplished using existing monoclonal antibody labeling techniques, such as by using specific cell surface markers to identify specific subpopulations of leukocytes, using flow cytometry, and determining the specificity Binder-labeled cells are analyzed to detect and differentiate multiple markers and physical characteristics of the cells, such as cell size and g...

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): G01N1/30G01N1/34G01N15/14
CPCG01N1/30G01N1/34G01N15/14G01N2001/305
Inventor 俞秋兴张海方
Owner GENERAL HOSPITAL OF NUCLEAR IND
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

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com