Nano antibody for HDAC6-cat 1 region and application thereof
A nanobody and domain technology, applied in the field of biotechnology or biomedicine, can solve the problem of lack of selective inhibitors
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0073] Example 1: Construction of a Nanobody library for the HDAC6-cat1 region:
[0074] (1) 200 μg HDAC6-cat1 antigen ( figure 1 ) mixed with Freund's adjuvant in equal volume, immunized a Xinjiang Bactrian camel, once a week, a total of 6 consecutive immunizations, during the immunization process stimulated B cells to express specific nanobodies, and the antibody titer ended at the end of 6 immunizations After the determination, the result is 10 4 ( figure 2 ); (2) After 6 times of immunization, extract 100ml of camel peripheral blood lymphocytes and extract total RNA; (3) Synthesize cDNA and amplify VHH by nested PCR; (4) Use restriction enzymes PstI and NotI Cut 20 μg pMECS phage display vector and 10 μg VHH and connect the two fragments; (5) Transform the ligated product into electroporation competent cell TG1, construct HDAC6-cat1 region nanobody phage display library and measure the storage capacity, the size of the storage capacity is about 1.2 ×10 8 At the same t...
Embodiment 2
[0075] Example 2: Nanobody screening process for the HDAC6-cat1 region:
[0076] (1) Take 200 μL of recombinant TG1 cells and culture them in 2×TY medium, add 40 μL of helper phage VCSM13 to infect TG1 cells, and culture overnight to amplify the phages, use PEG / NaCl to precipitate the phages the next day, and centrifuge to collect the amplified phages ; (2) 200 μg of HDAC6-cat1 recombinant protein dissolved in 100 mM pH 8.4 NaHCO3 was coupled to a microtiter plate, placed overnight at 4 ° C, and a negative control was set up at the same time; (3) 100 μl of 3% BSA was added the next day, Block at room temperature for 2 h; (4) After 2 h, add 100 μl of amplified phage (2×10 11 tfu immunized camel nanobody phage display gene library), and acted at room temperature for 1h; (5) washed off the bound phage with PBS+0.05% Tween-20; (6) combined with HDAC6-cat1 with trypsin at a final concentration of 25mg / ml Under the dissociation of specific binding phage, infect E. coli TG1 cells in...
Embodiment 3
[0077] Embodiment 3: Screen specific positive clone ( Figure 4 ):
[0078] (1) Select 175 single colonies from the cell culture plates after the above three rounds of screening and inoculate them in 96 deep-well plates containing 100ug / mL ampicillin in TB medium, and set up a blank control, and culture at 37°C until logarithmic After the period, add IPTG with a final concentration of 1mM and incubate overnight at 28°C; (2) Obtain the crude antibody by osmotic bursting method, transfer the antibody to an antigen-coated ELISA plate, and place it at room temperature for 1 hour; (3) Wash off unbound antibody with PBST, add 100ul of Mouse anti-HA tag antibody (mouse anti-HA antibody) diluted 1:2000, and let stand at room temperature for 1h; (4) wash off unbound antibody with PBST, add 100ul Anti-mouse alkaline phosphatase conjugate (goat anti-mouse alkaline phosphatase-labeled antibody) diluted at 1:2000, placed at room temperature for 1 hour; (5) Wash unbound antibody with PBST,...
PUM
Property | Measurement | Unit |
---|---|---|
molecular weight | 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