Anti-human neutrophil gelatinase-associated lipocalin antibodies and use thereof
A technology of lipocalin and neutrophils, applied in the fields of biotechnology and immunology, can solve the problems of inability to timely and accurately reflect glomerular filtration rate, low specificity and sensitivity, and reduced clinical effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0055] In an example of the present invention, the monoclonal antibody can be prepared by the following preparation method, which includes the steps of: (1) providing mice pretreated with adjuvant; (2) intraperitoneally inoculating the mouse with the said hybridoma cells and secrete monoclonal antibody; (3) extract ascites and separate and obtain said monoclonal antibody. As a preferred method, the method for isolating monoclonal antibody from ascites is as follows: collect ascites, precipitate with ammonium sulfate and octanoic acid, and then purify with Protein G prepacked chromatography column to obtain high-purity PSA monoclonal antibody.
[0056] In addition, the hybridoma cells can also be cultured and expanded in vitro according to conventional animal cell culture methods, so as to secrete the monoclonal antibody.
[0057] Reagent test kit
[0058] The present invention utilizes monoclonal antibody and polyclonal antibody specifically recognizing NGAL protein, and acco...
Embodiment 1
[0075] Embodiment 1, the preparation of hybridoma cell line
[0076] 1. Construction of DNA antigen for immunization
[0077] pBudCE4.1 was used to construct the pBud-Dse dual-promoter secretory expression vector as follows: the coding sequence of human IgE heavy chain signal peptide (Ig E-leader peptide) was codon-optimized to improve expression. The eukaryotic cell ribosome recognition site Kozak sequence GCCGCCACC was introduced before the start codon ATG; the signal peptide sequence was followed by a multiple cloning site, and two optimized signal peptides and multiple cloning site sequences were synthesized in the whole gene, and one segment was used in a restriction internal Dicer NotI and BglII were digested, and then connected to the multiple cloning site behind the hEF1α promoter of the pBudCE4.1 vector, and the other nucleotide sequence was digested with restriction endonucleases BamHI and HindIII, and connected to the previously constructed In the vector, the isola...
Embodiment 2
[0116] Embodiment 2, mammalian cell recombinant NGAL protein
[0117] In order to evaluate the affinity of the monoclonal antibody and provide a standard for the assembly of the detection kit, the present invention uses the FreeStyle MAX CHO expression system provided by Invitrogen to express and purify the secretable NGAL protein. The protein is a fusion protein with a 6×His tag at the C-terminus and a size of 28kD. The pBud-Dse-NGAL plasmid was transiently transfected into CHO-S cells (Invitrogen) according to the instructions provided by Invitrogen. After 72 hours of suspension culture, the cell culture supernatant was collected, centrifuged at 4°C and 6000rpm for half an hour, and the cell debris was removed. Purifier UPC100 fast protein purification system (FPLC), through Ni Sepharose High Performance chromatography column (GE), the C-terminal NGAL protein with 6×His tag secreted by cells in the cell culture supernatant is efficiently bound, and finally 300mM imidazole is...
PUM
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