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

Application of leucocythemia related to gene ASH2L in leukemia molecule classification diagnosis

A technology for molecular typing and leukemia, applied in the fields of application, genetic engineering, plant gene improvement, etc., can solve the problems of uncertain expression characteristics of ASH2L, limitations of ASH2L in molecular typing diagnosis, unclear expression characteristics, etc.

Inactive Publication Date: 2006-11-29
THE INST OF BASIC MEDICAL SCI OF CHINESE ACAD OF MEDICAL SCI
View PDF0 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, in the absence of an in-depth understanding of the mechanism of action of ASH2L, it remains unclear whether functionally related molecules of ASH2L have similar expression characteristics during PMA-stimulated K562 differentiation, in other words, whether the expression characteristics of ASH2L is specific, not sure yet
Until these details are clarified, the application of ASH2L in molecular typing diagnosis will be limited

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
  • Application of leucocythemia related to gene ASH2L in leukemia molecule classification diagnosis
  • Application of leucocythemia related to gene ASH2L in leukemia molecule classification diagnosis
  • Application of leucocythemia related to gene ASH2L in leukemia molecule classification diagnosis

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0025] Primer name

Embodiment 2

[0027] Cloning of ASH2L, DPY-30-like and WDR5 genes

[0028] K562 cells were cultured on a 10cm dish with R1640 containing 10% FBS at 37 degrees, 5% CO 2 Cultured until the number of cells reached 2×10 7 Above, cells were harvested to extract total RNA and subjected to reverse transcription. Reverse transcription was carried out using a kit from PROMEGA, and the method is shown in the kit instructions. Using the cDNA as a template, three genes ASH2L, DPY-30-like and WDR5 were amplified. The primers used were ASH2L-1 / 2, DPY-1 / 2 and WDR5-1 / 2 (see Example 1 for the sequence). The conditions of the PCR reaction are: ASH2L, annealing temperature 64 degrees, extension 7 minutes; DPY-30-like, annealing temperature 60 degrees, extension 1 minute; WDR5 annealing temperature 60 degrees, extension 1.5 minutes; other conditions are the same Common PCR conditions, using Pfu enzyme.

[0029]After the PCR product was tailed with Taq enzyme at 72 degrees for 10 minutes, it was directly c...

Embodiment 3

[0031] Preparation of anti-ASH2L, DPY-30-like specific antibodies:

[0032] Antigen preparation: ASH2L and DPY-30-like cDNA template PCR amplification required fragments, primers are ASH2L-6P-UP / ASH2L-6P-DOWN and DPY-6P-UP / DPY-6P-DOWN two Right (see Example 1 for the sequence). The target fragment on ASH2L is the N-terminal 1-99aa coding region, and DPY-30-like is its full length. Both ends of the PCR fragment contain restriction enzyme sites EcoR I and Xho I, so these two enzymes were used to digest the PCR product and vector plasmid pGEX-6P-1. Then use T4 ligase to ligate the digested PCR fragment and the vector to form a recombinant plasmid (see figure 1 ).

[0033] PCR conditions: the annealing temperature is 65 degrees, the extension time is 1 minute, and other conditions are the same as ordinary PCR reactions. PCR reaction product 50ul (approximately 5ug) and vector plasmid (pGEX-6P-1) 6-10ug were digested with EcoR I and Xho I respectively, and DNA fragments were re...

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 ASH2L expression would be specific decrease in the PMA exciting K562 differentiation process. And the DPY-30-like and WDR5 have no such alteration. Thus, ASH2L could be used as the alternate mark material to diagnose leukaemia. It constructs the N-end albumen of ASH2L and DPY-30-like full length albumen plasmid to transform to bacilluscoli expression corresponding albumen. It could be used to diagnose bacilluscoli diagnose.

Description

technical field [0001] The invention belongs to the fields of gene recombination, antibody preparation and clinical diagnosis. Specifically, the present invention relates to a recombinant genetic engineering and protein purification process of the N-terminal part of the leukemia-related gene ASH2L, to the recombinant genetic engineering and protein purification process of the full-length ASH2L interacting protein DPY-30-like, and to the use of The preparation of highly specific antibodies from these two purified proteins involves the specific downregulation of ASH2L during the differentiation process of K562 cells stimulated by PMA, the recombinant plasmids containing part of the ASH2L gene and the recombinant strains expressing the protein and their use in the molecular typing diagnosis of leukemia Applications. Background technique [0002] Accurate classification of leukemia is an important prerequisite for the treatment of leukemia. At present, the diagnosis and typing...

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): C12N15/12C12N15/63C12N1/21C12N15/70C07K16/18G01N33/53C12Q1/68C12N15/09
Inventor 彭勇汪俊华袁建刚彭小忠强伯勤
Owner THE INST OF BASIC MEDICAL SCI OF CHINESE ACAD OF MEDICAL SCI
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