Method for obtaining wire-worm microsome amino peptidase gene and use thereof
A technology of twisting Haemonchus contortus and microsomes, which is applied in the biological field to achieve high stability, biological activity and complete sequence
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Embodiment 1
[0034] This example describes the method for obtaining the cDNA sequence of the H11 gene of H. contortus Zhejiang strain provided by the present invention, and the whole test process of long-distance RT-PCR amplification and cloning of the H11 cDNA.
[0035](1) RT-PCR amplification of the cDNA sequence of H. contortus Zhejiang strain H11
[0036] 1. Refer to the third edition of Molecular Cloning to prepare RNA from tissues with one-step method and extract H. contortus total RNA. After formaldehyde gel electrophoresis confirms that there is no degradation, store at -80°C.
[0037] 2. Primer design: according to the sequence published by Smith (1997), according to the sequence characteristics of its reading frame, the two ends were respectively added with Sal I and HindIII restriction sites and protected bases to design primers P1 / P2 (refer to SEQ NO 1 and SEQ NO 2), the primers were synthesized by Shanghai Boya Biotechnology Co., Ltd.
[0038] 3. Synthesis of cDNA of H. conto...
Embodiment 2
[0046] This example describes the process of obtaining the genome sequence of the H11 gene mainly by using the gene walking technology in the present invention.
[0047] (1) Acquisition of H11 partial genome sequence: Take 50 mg of H. contortus washed with PBS buffer and transfer it to a Collection Tube in an ice bath, quickly grind it into a paste with a grinding rod, and extract it according to the method of TaKaRa Universal Genomic DNA Extraction Kit Genomic DNA, stored at -20°C.
[0048] Using the extracted H. contortus genomic DNA sequence as a template, a long-distance PCR reaction was performed using primers Hc-GSF / Hc-GSR (refer to SEQ NO 5 and SEQ NO 6). Reaction system (50μl): TaKaRa LA Taq (5U / μl) 0.5μl, 10×LA PCR Buffer (Mg 2+ Plus) 5 μl, dNTPMixture (2.5 mM each) 8 μl, genomic DNA 0.7 μl, Hc-GSF (20 μM) 1 μl, Hc-GSR (20 μM) 1 μl, ddH 2 O 38 μl. The reaction conditions were pre-denaturation at 94°C for 3min; 94°C for 60s, 58°C for 60s, 72°C for 6min; 72°C for 10m...
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