Monopterus albus rhabdovirus Cr-ERV and RT-PCR detection primer and application thereof
A rhabdovirus, detection primer technology, applied in the application, virus, antiviral agent and other directions, can solve the problem of no detection method, and achieve the effect of ensuring high specificity, fast and simple method, and improving detection efficiency
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Embodiment 1
[0026] A kind of eel rhabdovirus CrERV, its isolation process is as follows:
[0027] 1) After taking out and grinding the eel spleen and kidneys carrying the virus, the culture medium was diluted 100 times, centrifuged at 2000rpm, and the supernatant was filtered, inoculated into a monolayer of crucian carp brain cell line (GibelCarpBrain, GiCB), cultured at 25°C for 7 On the next day, the cytopathic effect (CPE) occurred, and it could be seen that the GiCB cells shrank and became round, the refractive index increased, some cells began to fall off, and the cell monolayer began to rupture.
[0028] Medium: M199, 10% fetal bovine serum, pH 7.0-7.2
[0029] 2) Collect the diseased cells, and use transmission electron microscopy for morphological identification.
[0030] 3) The virus is collected, and its whole genome is sequenced, and the sequence is shown in SEQ ID NO.1.
[0031] Morphological characteristics of eel rhabdovirus: the virus is bullet-shaped or spindle-shaped, a...
Embodiment 2
[0034] Primers designed based on the difference between the full sequence of eel rhabdovirus CrERV (shown in SEQ ID NO.1) and the full sequence of other viruses:
[0035]A kind of eel rhabdovirus CrERV RT-PCR detection primers, including F1: 5'-GAGATGAAGGAAGGACTGAGGAGAA-3', R1: 5'-CCCGACACCACTAAAGTATAAAA-3'; F2: 5'-GAGGAGCATTAGTTACTTAAGGGTC-3', R2: 5'-TCACAATTTGAATCGTCATGACATA -3'.
Embodiment 3
[0037] Utilize the eel rhabdovirus CrERV RT-PCR detection primers to detect the eel rhabdovirus, the method includes:
[0038] 1. Extraction of total RNA from eel tissue or infected cells and synthesis of cDNA: using Extract the total RNA of the sample to be tested. Configure the reverse transcription reaction system: 3 μL of total RNA, 1 μL of Oligo(dT)18 primer, 8 μL of sterilized double-distilled water, mix well at 65°C for 5 minutes, and immediately put it on ice; add 4 μl of 5×Reaction Buffer, 1 μl of RNase inhibitor, 2 μL of 5mM dNTPs, Add 1 μL of M-MLV reverse transcriptase to the reaction solution in an ice bath, mix well, store at 42°C for 1 hour and 95°C for 5 minutes, and store the obtained cDNA template at -20°C for later use.
[0039] 2. Polymerase chain reaction amplification:
[0040] Use 25μl reaction system: add 10μM primers F1 and R1, add 1μL each to the PCR reaction tube, then add 2.5mMdNTPs 2μL, 25mM MgCl 2 1.5 μL, 0.5 μL of 5U Taq polymerase, 1 μl of t...
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