Gexp rapid detection primer set, kit and application for simultaneous identification of three h5 subtype avian influenza virus combinations infecting humans
A technology of avian influenza virus and detection kit, which is applied in the direction of microbial determination/inspection, recombinant DNA technology, biochemical equipment and methods, etc., and can solve problems such as difficult typing and determination, unfavorable prevention and control, and formulation of emergency measures , to achieve the effect of ensuring healthy and sustainable development, fast sensitivity and high sensitivity
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Embodiment 1
[0025] Example 1 : Multiplex RT-PCR Primer Design for Avian Influenza Virus
[0026] Refer to relevant literature to download the sequences of five genes of avian influenza virus M, H5, N1, N2 and N6 from the GenBank database, use DNAStar to analyze and compare the nucleotide sequences of each gene, and find out the conserved genes suitable for designing specific primers. region, utilize the GeXP express profiler tool to design specific primers for 5 genes of avian influenza virus (see Table 1), the designed primers are analyzed and screened using Primer Premier 5.0, NCBI PrimerBlast and Oligo7.0, and then in all forward A non-homologous unique sequence was added to the 5' ends of the primer and reverse primer respectively as a universal primer (Uni-Primer), and the 5' end of the upstream universal primer was labeled with a fluorescent dye Cy5, namely Cy5-Tag-F, which was synthesized by Shanghai Invitrogen Company , HPLC purification.
[0027] Table 1 Primer Information
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Embodiment 2
[0031] Example 2: Establishment of multiplex PCR detection system
[0032] 2.1 Preparation of template and monoclonal plasmid standard containing target gene
[0033] According to the instructions of TaKaRa Company MiniBEST Viral RNA / DNA Extraction Kit Ver.5.0 (catalogue number DV819A), extract nucleic acids of different subtypes (H 1-16 and N 1-9) of avian influenza virus and other poultry viruses, and obtain 50 μL of nucleic acid samples , and stored at -80°C. The RT reaction system was carried out according to the instructions of TaKaRa reverse transcriptase (catalogue number D2639A), and the obtained RNA samples were reverse-transcribed according to the following reaction system and reaction conditions to obtain cDNA; DEPC water was used as the control of total RNA.
[0034] The reverse transcription RT reaction solution is 9 μL per tube: 5 μL of 5×Reverse Transcriptase Buffer, 1 μL of 50 pmol Random Primer (12mer), 2 μL of 10 mM dNTP Mixture, 0.5 μL of 40U Ribonuclease...
Embodiment 3
[0050] Example 3: GeXP system multiple detection system specific detection
[0051] According to the instructions of MiniBEST Viral RNA / DNA Extraction Kit Ver.5.0, extract HA(1-16) and NA(1-9) subtype avian influenza virus nucleic acid from allantoic fluid, and simultaneously extract IBV, NDV and ILTV and other common poultry viruses Nucleic acids were added to the GeXP multiple detection system established in Example 2 to detect the specificity of the method. After the multiplex PCR was completed, the PCR products were analyzed by GeXP capillary electrophoresis, and the results showed that only specific signals appeared in each reaction, and there was no cross-reaction. HA gene except H5 subtype, NA gene except N1, N2 and N6 subtypes, and other NA subtypes, as well as NDV, IBV, ILTV and blank control had no reaction signal, suggesting that the established method has strong specificity and is different from other detection methods. Subjects had no cross-reactivity.
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