A kind of anti-phosphatase 2cm monoclonal antibody and its application
A technology of monoclonal antibody and phosphatase, which is applied in the direction of anti-enzyme immunoglobulin, instruments, biochemical equipment and methods, etc., can solve the problems of incomplete research on molecular mechanism of action, no specific detection of monoclonal antibody, etc., and achieve the goal of preparing The method is simple and efficient, highly specific, and has strong specific effects
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0024] Example 1 Preparation and Purification of Recombinant Rat PP2Cm Protein
[0026] Using the existing template plasmid PP2Cm, the source gene is on the T vector, and the plasmid information comes from the literature: A novelmitochondrial matrix serine / threonine protein phosphatase regulates themitochondria permeability transition pore and is essential for cellular survival and development. Genes Dev 2007;21:784– 96. [PMC free article] [PubMed] (provided by Dong Bing, China Agricultural University), selected a partial gene fragment 377-1405bp for cloning and recombination. Ncol and UTR restriction enzyme sites were added at the 5' and 3' ends of the gene, respectively, and 3'Xhol cloned the gene into the vector pET28a (Kan) by cutting the 5'Ncol and 3'Xhol, and handed it over to Suzhou Jin Synthesized by Weizhi Biotechnology Co., Ltd., the primer sequence is as follows:
[0027] Upstream primer (5'-3'): TAATACGACTCACTATAGG;
[0028] Downstream p...
Embodiment 2
[0032] The establishment of embodiment 2 hybridoma cell lines
[0033] 1. Immunity
[0034]The protein purified in Example 1 was emulsified with complete Freund's adjuvant (Sigma Company), and immunized with 4-6 week-old female Balb / c mice (purchased from Beijing Weitong Lihua Experimental Animal Technology Co., Ltd.) by intraperitoneal injection of each Mice were immunized with 50 μg of protein every 14 days, and the second immunization antigen was emulsified with Freund’s incomplete adjuvant (Sigma Company), and then directly immunized with the antigen at a dose of 50 μg / mouse. Three days after the third booster immunization, indirect ELISA (wavelength 450nm) was used to detect the multi-antibody titer of the anti-immunogen in the mouse serum. 50μg / piece. Serum titer detection of 5 mice after the third immunization see image 3 . The antigen used for immunizing mice is recombinant PP2Cm antigenic protein, which is encoded by the nucleotide sequence in Sequence Table 1 an...
Embodiment 3
[0041] Example 3 Cell line establishment and ascites induction method to prepare monoclonal antibody
[0042] 1. Establishment of cell lines
[0043] After routine ELISA detection, 5 positive reaction cell lines were obtained. After 5 times of subcloning, one of them was found to have a higher reaction value. It was named 7P3 and expanded for culture. It was used for liquid nitrogen cryopreservation and preparation of monoclonal antibody ascites. . The 7P3 hybridoma cell line was collected on March 30, 2017 in the General Microbiology Center of the China Committee for Microbial Culture Collection (Address: No. 3, Yard 1, Beichen West Road, Chaoyang District, Beijing, Institute of Microbiology, Chinese Academy of Sciences, CGMCC for short, zip code 100101), classified as mouse hybridoma cell line, and its deposit number is CGMCCNo.13818.
[0044] 2. Ascites preparation
[0045] Cells in the logarithmic growth phase were washed with serum-free medium and suspended, counting 5...
PUM
Property | Measurement | Unit |
---|---|---|
concentration | aaaaa | aaaaa |
purity | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
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