Method for separating and authenticating erythroblast of blood

A technology for nucleating red blood cells and blood, applied in the field of blood separation, identification and detection, can solve the problems of easy pollution, complicated operation and high cost

Inactive Publication Date: 2008-02-13
孙艳萍
View PDF0 Cites 20 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The direct acquisition method is costly, or the specificity is not strong, easy to be polluted, or the operation is cumbersome, t

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
  • Method for separating and authenticating erythroblast of blood

Examples

Experimental program
Comparison scheme
Effect test

Embodiment Construction

[0090] (1) Preparation of main reagents

[0091] 1. Polylysine working solution: fully mix polylysine stock solution with double distilled water 1:10, and wait for the bubbles to disappear for later use;

[0092] 2. 0.01mol / L PBS (PH7.4) containing 0.5% BSA

[0093] Sodium chloride 6.5g

[0094] Na 2 HPO 4 12H 2 O 4g

[0095] NaH 2 PO 4 2H 2 O 0.35g

[0096] Add 800ml of double distilled water, adjust the pH value to 7.4, and make up to 1000ml with double distilled water. 0.01mol / L PBS, after autoclaving, add 5g BSA, store at 40°C.

[0097] 3. Alkaline cell lysate (containing KOH 200mmol / L, DTT 50mmol / L)

[0098] 400mmol / L KOH 1ml

[0099] 1mol / L DTT 100ul

[0100] Sterile water for injection is 850-900ul, mixed thoroughly, filtered through a 0.22μm microporous filter, subpackaged, and stored at -20°C for later use.

[0101] (2) Anti-degumming slide preparation

[0102] 1. Pretreatment of slides

[0103] Wash the ordinary glass slide with hot soapy water, clean...

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 method for separating and appraising nucleated red blood cells in blood, including the following steps: (1) confecting reagent; (2) preparing anti-degumming slide; (3) selecting the staining method for nucleated red blood cells; (4) getting nucleated red blood cells from blood through microoperation. The method for separating and appraising nucleated red blood cells in blood can effectively identify nucleated red blood cells. Nucleated blood cell can be detected in 40 samples and the detection rate is 100 percent. Each sample is detected to have 2*106 to 6*106 /ml nucleated blood cell. In the invention, after the aniline being stained, the nucleated red blood cell is easy to be identified and skilled microoperation can quickly obtain the single nucleated red blood cell, so that the invention lays a good primary foundation to apply the single red blood cell in gene analysis.

Description

technical field [0001] The invention relates to the technical field of blood separation, identification and detection, in particular to a method for separating and identifying nucleated red blood cells in blood. Background technique [0002] Separation of blood samples into various cellular components requires adjustment of blood sample handling / processing techniques accordingly. A conventional method of separating a whole blood sample into its various cellular components is by centrifugation. While effective, this method is labor intensive, relatively inefficient and requires manual control of the cellular fraction of the blood sample. [0003] The separation of nucleated red blood cells is the beginning of genetic analysis, and it is also one of the more difficult steps. Scholars from various countries have tried various methods to separate nucleated red blood cells, but have not found a direct, reliable and efficient way to separate them. [0004] Attempts to carry out...

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): G01N33/49G01N1/30G01N1/34G01N21/25
Inventor 孙艳萍
Owner 孙艳萍
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

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

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap