Freshwater shrimp molt-inhibiting hormone gene and application thereof in accelerating molting and growing of freshwater shrimps
A technology of molting inhibitory hormone and freshwater shrimp, applied in the field of biotechnology and developmental regulation
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Embodiment 1
[0021] Example 1: Obtaining the full-length cDNA of the MIH gene of freshwater shrimp
[0022] Total RNA extraction: Select two mature freshwater shrimps, remove the eye stalk tissue with sterile dissecting scissors, clip the eye stalk pigment part in RNA preservation solution (TaKaRa Bio Inc. Japan), rinse and pre-treat the freshwater shrimp eye stalk For total RNA extraction, refer to the Takara Trizol kit for specific steps.
[0023] First-strand cDNA synthesis: The first-strand cDNA was obtained after reverse transcription with reference to the Takara M-MLV reverse transcription kit with the above total RNA.
[0024] Obtaining the full-length cDNA of MIH gene in freshwater shrimp:
[0025] According to Macrobrachium rosenbergii ( Macrobrachium rosenbergii , KC990939.1) the conserved region of MIH cDNA, two pairs of intermediate primers were designed, see SEQ ID NO: 6~9,
[0026] (middle F1: 5′-CCGGCATTCCTTTGTTTACCTG-3, middle R1: 5′-ATATTCTGGCGTGTGGTCCTG-3′;
[00...
Embodiment 2
[0032] Embodiment 2: Obtaining of dsRNA of the freshwater shrimp MIH gene
[0033] According to the cloned freshwater shrimp MIH gene (Accession number: KF878973), the NCBI online sequence analysis software ( http: / / www.ncbi.nlm.nih.gov / gorf / gorf.html ) to determine the position of the open reading frame of the MIH gene as 436-795bp. According to the above results, the online dsRNA primer design software ( http: / / www.flyrnai.org / cgi-bin / RNAi_find_primers.pl ), design dsRNA primers in the MIH open reading frame of freshwater shrimp, and add the T7 promoter sequence 5'-TAATACGACTCACTATAGGG-3' in front of each primer to form dsRNA synthesis primers, and the primer sequences are the upstream primers SEQ ID NO:2 and downstream primer SEQ ID NO:3. All primers were synthesized at Bosun Biotechnology (Shanghai) Co., Ltd.
[0034] Using the above-mentioned green shrimp dsRNA primers to carry out PCR amplification on the total cDNA of green shrimp (the conditions are the same as i...
Embodiment 3
[0035] Example 3: Injection of the dsRNA of the green shrimp MIH gene on the development of the green shrimp molting
[0036] 1. Selection of Shrimp for Experiment
[0037] In order to study the silencing effect of the dsMIH gene, this study first conducted a one-time RNAi experiment to select 50 adult female shrimp with strong vitality, uniform individuals, and a body weight of about 1.50±0.35g, and divided them into two groups on average. One group was the dsRNA injection group, The other group is the DEPC water injection group (control group). Before the experiment, the snails were inflated in a 500L polyethylene plastic white bucket for 72 hours to adapt to the laboratory breeding environment, and the snails were fed once a day in the morning and evening.
[0038] The continuous RNAi experiment was designed according to the results of the one-time RNAi experiment. The shrimps used in the continuous RNAi experiment were the same batch of hatched juvenile shrimp hatched in ...
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