Vesicular stomatitis virus recombinant N protein antigen, and preparation method thereof
A technology of vesicular stomatitis and protein antigen, which is applied in the field of genetic engineering, can solve the problems of poor specificity and achieve the effect of simple operation, good effect and small amount of detection samples
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0021] Example 1: Expression of truncated VSVN protein
[0022] 1. VSVN protein epitope analysis and codon optimization: By searching the VSVN gene sequence and corresponding amino acid sequence (GenBank: J02428.1) in the NCBI database, using online software to analyze its main epitope, determine the selected epitope Located at the 88th to 374th amino acid in the N protein, its amino acid sequence is SEQIDNo.1 in the sequence listing, and its corresponding nucleotide sequence (GenBank: J02428.1) is the 325th to 1185nt nucleotide, see the sequence listing SEQIDNo .5.
[0023] 2. VSVN gene codon optimization and artificial synthesis: codon optimization, that is, redesign the gene sequence according to the preference of the expression system for amino acid codons, and modify the codons with low utilization or rare codons in the gene sequence to the expression system Frequent use of codons ensures that the amino acid sequence of the expressed protein remains unchanged. According...
Embodiment 2
[0037] Example 2: Establishment and evaluation of VSV antibody indirect ELISA method
[0038] 1. Indirect ELISA to evaluate the immunological activity of VSVN protein. The ELISA plate was coated with gene-expressed VSV recombinant N protein, and an indirect ELISA antibody detection method was established. The specific operation method is as follows:
[0039] ①. Dilute the purified recombinant protein to 5 μ / mL with a coating solution (carbonic acid buffer solution at pH 9.6), coat a 96-well ELISA plate at 50 μL / well, and place it at 4°C for overnight.
[0040] ②. Discard the coating, and wash 3 times with PBST (20mmol / LPBS+0.5% Tween 20). Add BSA solution with a concentration of 10 g / L, 250 μL / well, and block at 37° C. for 2 h. Discard the blocking solution and wash 3 times with PBST.
[0041] ③. Add positive serum, negative serum and serum to be tested to the ELISA plate, 50μL / well, 37°C, react for 30min.
[0042] ④ Wash 3 times with PBST, add 1:5000 dilution of HRP-labe...
Embodiment 3
[0048] Embodiment 3: Preparation and evaluation of colloidal gold immunochromatography test strip
[0049] 1. The vesicular stomatitis virus recombinant N protein antigen of embodiment 1 is used as the detection line reagent, and the rabbit anti-SPGIgG is used as the contrast reagent simultaneously to make colloidal gold immunochromatography test strips, detection line and control line reagent coating amount They are 0.175μg / bar and 0.35μg / bar respectively.
[0050] 2, the specificity of test strip: detect respectively VSV standard positive serum sample, other relevant virus comprise O type, A type and Asian I type foot-and-mouth disease virus (FMDV), Akabane disease virus (AKV) with the test strip among the embodiment 2 ), bluetongue virus (BTV), bovine viral diarrhea virus (BVDV) and sheeppox virus (CPV) positive serum samples and negative control samples. The results showed that the test strip was positive when detecting VSV-positive serum samples, and was negative when de...
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