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

m 6 a recombinant rabbit monoclonal antibody and its preparation method

A monoclonal antibody and heavy chain technology, applied in the field of molecular biology, can solve problems such as low sensitivity, difficult enrichment, difficult IF experiments, etc., and achieve the effect of improving screening efficiency, high gene diversity, and easy screening

Active Publication Date: 2022-03-15
WUHAN AIBO TAIKE BIOTECH CO LTD
View PDF4 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The enrichment of specific antibodies is a commonly used method, however, the currently used m 6 Antibody A still has the defect of low sensitivity, and it is difficult to perform IF experiments; at the same time, in the presence of a large amount of interfering RNA, m 6 Enrichment of A-modified RNAs is very difficult

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
  • m <sup>6</sup> a recombinant rabbit monoclonal antibody and its preparation method
  • m <sup>6</sup> a recombinant rabbit monoclonal antibody and its preparation method
  • m <sup>6</sup> a recombinant rabbit monoclonal antibody and its preparation method

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0034] The present invention provides a kind of by m 6 A method for synthesizing an antigen from a hapten, the specific steps are as follows:

[0035] 1. Weigh m 6 A small molecule 40mg, add to a 50ml test tube, then add 0.1M NaIO drop by drop 4 Solution until 5ml, shake while adding, react at room temperature for 30 minutes. Add 1ml ethylene glycol to neutralize excess NaIO 4 , react at room temperature for 5 minutes.

[0036] 2. Take 10ml of KLH carrier protein (Merck, product number: 374805) with a concentration of 6.15mg / ml, add it to a new 50ml test tube, and use 2M K 2 CO 3 The pH value of the solution was adjusted to be between pH 9.0 and 9.5.

[0037] 3. Then slowly add the carrier protein in step 2 to the solution in step 1 and react for 45 minutes. Use 5% K during the period 2 CO 3 The pH of the solution was adjusted to maintain the pH between 9 and 9.5.

[0038] 4. Weigh 37.5mg NaBH 4 Dissolve in 2.5ml of water, add dropwise to the reaction solution in st...

Embodiment 2

[0042] This example provides a method for immunizing animals with the antigen synthesized in Example 1 and screening for positive clones. The specific steps are as follows:

[0043] 1. Multi-point injections on the back and abdomen of rabbits (750ug antigen per rabbit for the first time, 350ug antigen per rabbit after that), repeated immunization every 2 weeks, repeated 3 times, the rabbits used in this example were New Zealand white rabbits, the first time Complete adjuvant (Sigma, product number: F5881) was used for immunization, and incomplete adjuvant (Beijing Boaolong, product number: KX0210047Q-10) was used for subsequent immunization.

[0044] 2. One week after the end of immunization, take rabbit serum for ELASA for polyantibody detection, and synthesize the following primers:

[0045] M6A-1: m 6A-CUGGUAACGAAUGGCUG-Biotin

[0046] M6A-2: A-CUGGUAACGAAUGGCUG-Biotin

[0047] M6A-3: AAAAAAAAAAAAA-Biotin

[0048] The M6A-1 primer is a positive control containing m 6 A...

Embodiment 3

[0054] This example provides a method for expressing and purifying the antibody from the B cells screened in Example 2. The specific steps are as follows:

[0055] 1. After the cells of positive clones were collected and lysed, RNA was extracted by conventional methods and reverse transcribed into cDNA. The PCR method is adopted, and the heavy chain amplification primers are shown in SEQ.NO.13~SEQ.NO.14.

[0056] Light chain amplification primers are shown in SEQ.NO.15~SEQ.NO.16.

[0057] In SEQ.NO.15, Y is C or T; in SEQ.NO.16, R is G or A). The PCR reaction system is: 95°C for 2min, then carry out 25 cycle reactions according to the following conditions, 95°C for 1min, 56°C for 1min, 72°C for 0.5min; finally 95°C for 10min.

[0058] The heavy and light chain genes (VH and VL) of the natural paired rabbit monoclonal antibody were amplified from the cDNA of the corresponding positive clone, and the sequence was determined by sequencing. The gene sequence of the variable regi...

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 present invention provides m 6 A recombinant rabbit monoclonal antibody and its preparation method, the amino acid sequence of its heavy chain CDR1 is shown in SEQ.NO.1, the amino acid sequence of CDR2 is shown in SEQ.NO.2, and the amino acid sequence of heavy chain CDR3 is shown in SEQ.NO. 3; the amino acid sequence of its light chain CDR1 is shown in SEQ.NO.4, the amino acid sequence of CDR2 is shown in SEQ.NO.5, and the amino acid sequence of CDR3 is shown in SEQ.NO.6. m provided by the present invention 6 A recombinant rabbit monoclonal antibody against m 6 A-modified RNA has a good enrichment ability, and in the DNA damage repair living cell model, the detection of m6A-modified RNA has a good sensitivity.

Description

technical field [0001] The invention belongs to the field of molecular biology, in particular to m 6 A recombinant rabbit monoclonal antibody and its preparation method. Background technique [0002] N6-Methyladenine (m 6 A) is the most abundant chemical modification found on eukaryotic mRNA, and it is also widely present in various bacteria and RNA viruses. In animals or plants, m 6 A can be modified, demodified and recognized by a series of methyltransferases, demethylases and binding proteins. m 6 A can regulate a variety of biological functions by affecting RNA processing and metabolism. Related studies have also found that RNA m6A modification plays an important role in UV-induced DNA damage response, and RNA m6A 6 A modification is mainly to guide cells to quickly and accurately recruit Polκ to the damage site and accelerate DNA damage repair to promote cell survival. Therefore, the m 6 A modification is an important reference factor for related disease mechani...

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): C07K16/00C12N15/13C12N15/10
CPCC07K16/00C12N15/1003C07K2317/565C07K2317/56
Inventor 陈亮张云程瑶李博吴知才
Owner WUHAN AIBO TAIKE 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

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