Fluorogenic quantitative PCR kit for detecting novel astrovirus of geese and application of kit
A fluorescent quantitative and astrovirus technology, applied in the field of poultry virus detection, can solve the problems of low sensitivity, inability to quantify, and detection blanks, etc., and achieve the effects of high sensitivity, reduced losses, and efficient detection
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Embodiment 1
[0056] Embodiment 1: the design of fluorescence quantitative PCR primer and probe
[0057] The whole genome sequence of the new goose Astrovirus (preservation number CCTCC NO: V201808) was obtained according to the next-generation sequencing technology, and the whole genome sequence is shown in SEQ ID NO.4. Specific primer sequences and fluorescent probe sequences were designed for the sequence conservation region of the ORF2 gene, and the sequence design was as follows:
[0058] Forward primer: ORF2-F: 5'-CCAGGTCAAGATACAATG-3'; (SEQ ID NO.1)
[0059] Reverse primer: ORF2-R; 5'-GTGTGTTCCAAGTGTAAA-3'; (SEQ ID NO.2)
[0060] Fluorescent probe: ORF2-tag: 5'-FAM-AGTCCTTCCACGATAGCCAACAT-BHQ1-3'; (SEQID NO.3)
[0061] The 5' end of the fluorescent probe is labeled with a fluorescent reporter group FAM, and the 3' end is labeled with a fluorescent quencher group BHQ1; the length of the amplified fragment is 83bp (shown in SEQ ID NO.5).
Embodiment 2
[0062] Example 2: Establishment of Fluorescent Quantitative PCR Detection Method
[0063] (1) Extraction of viral RNA:
[0064] Take 30 mg of suspected diseased gosling kidney and liver homogenate tissue, and use the classic Trizol method or a commercial kit to extract total RNA.
[0065] (2) Establishment of fluorescent PCR reaction system:
[0066] The one-step fluorescence quantification kit used adopts the One StepPrimerScript from Takara Company whose article number is RR064A TM RT-PCR Kit, add 2×One Step RT-PCR BufferⅢ~10μL, 1×TaKaRa Ex Taq HS(5U / μL)~0.4μL, PrimeScript RT Enzyme MixⅡ~0.4μL, PCR Forward Primer in 200μL PCR reaction tube (10μM)~0.4μL, PCR Reverse Primer(10μM)~0.4μL, Probe~0.8μL, ROX Reference Dye or DyeⅡ(50×)~0.4μL, Total RNA of the sample to be tested extracted in step (1)~2μL, Using RNase Free dH 2 O supplemented to 20μL system. Placed in ABI 7300Fast fluorescent quantitative PCR instrument for reaction, the reaction conditions were 42°C for 5min; 9...
Embodiment 3
[0074] Example 3: The composition of the kit, the optimization of experimental parameters and the investigation of specificity, sensitivity and repeatability
[0075] 1. The composition of the kit:
[0076] The kit in this example is a fluorescent quantitative PCR kit, which is used to detect the new goose astrovirus (preservation number is CCTCC NO: V201808). The kit contains: the forward primer (10 μM) shown in SEQ ID NO.1 designed in Example 1, the reverse primer (10 μM) shown in SEQ ID NO.2 designed in Example 1, and the reverse primer (10 μM) shown in SEQ ID NO.2 designed in Example 1 The probe shown in SEQ ID NO.3, the standard product and the fluorescent quantitative PCR reaction reagent.
[0077] Standards were prepared as follows:
[0078] The primers shown in SEQ ID NO.1-SEQ ID NO.2 were used to amplify the genome of the Goose Astrovirus whose preservation number was CCTCC NO: V201808, and an 83bp amplification product (shown in SEQ ID NO.5) was obtained. The ampl...
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