Method for rapidly identifying genders of macrobrachium rosenbergii
A technology of Macrobrachium rosenbergii and sex, applied in the field of aquaculture, can solve the problems of inability to distinguish ZW and WW genotypes, difficult to accurately judge gender, etc., and achieve the effect of high detection sensitivity
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Embodiment 1
[0057] Amplified length polymorphism amplification of the Macrobrachium rosenbergii genome was performed at a lower annealing temperature (Jiang et al., 2013), and the sex-specific genome fragments of the Macrobrachium rosenbergii were obtained.
[0058] 1. Extraction of Macrobrachium rosenbergii Genomic DNA
[0059] Cut the tentacles of Macrobrachium rosenbergii, and extract the genomic DNA by the phenol-chloroform method:
[0060] Take 4 giant giant macrobrachium rosenbergii female shrimp (ZW). Disinfect the tweezers, cut about 2-3 tentacles, and digest with tissue lysate and proteinase K (600 μL in total) until the tissue is completely dissolved. Add an equal volume of phenol: chloroform: isoamyl alcohol (25:24:1) solution, mix well and centrifuge. Transfer the supernatant to a new centrifuge tube and add an equal volume of pre-cooled absolute ethanol, mix well and centrifuge, discard the supernatant. Wash the precipitate with 70% ethanol, discard the ethanol and air dry...
Embodiment 2
[0067] This embodiment provides a method for quickly identifying the sex of Macrobrachium rosenbergii, comprising the following steps:
[0068] 1. Extraction of Macrobrachium rosenbergii Genomic DNA
[0069] Cut the tentacles of Macrobrachium rosenbergii, and extract the genomic DNA by the phenol-chloroform method:
[0070] Four male Macrobrachium rosenbergii males (ZZ), four females (ZW) and super females (WW) were taken respectively. Disinfect the tweezers, cut about 2-3 tentacles, and digest with tissue lysate and proteinase K (600 μL in total) until the tissue is completely dissolved. Add an equal volume of phenol: chloroform: isoamyl alcohol (25:24:1) solution, mix well and centrifuge. Transfer the supernatant to a new centrifuge tube and add an equal volume of pre-cooled absolute ethanol, mix well and centrifuge, discard the supernatant. Wash the precipitate with 70% ethanol, discard the ethanol and air dry the precipitate; add 20-50 μL TE buffer to detect the DNA con...
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