Microsatellite marker, primer and identification method for genetic sex identification of hucho taimen and application of microsatellite marker and primer for genetic sex identification of hucho taimen
A technology of microsatellite markers and salmonids, applied in the fields of microsatellite markers and primers and applications, can solve the problems of identifying sex by marriage color, failing to fully understand the sex ratio, and inconspicuous marriage color of broodstock, so as to save the sequencing step. Effect
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Embodiment 1
[0029] Example 1 A Microsatellite Marker and Primers for Accurately Identifying the Genetic Sex of Salmon
[0030] A microsatellite marker for accurately identifying the genetic sex of salmon salmon, the nucleotide sequence of the microsatellite marker is shown in SEQ ID NO:1. The repeating unit is GGGTTA, and the core sequence is (GGGTTA) 16 GGTTA (GGGTTA) 5 GGTTA (GGGTTA) 7 .
[0031] A microsatellite marker primer for accurately identifying the genetic sex of salmon salmon, the upstream primer of the microsatellite marker is: 1F 5'-CACTGGGGTACAAAAAGAGCAA-3' (SEQ ID NO: 2);
[0032] The downstream primer is: 1R 5'-ACGGGCCTTTTTAAGCACT-3' (SEQ ID NO: 3).
Embodiment 2
[0033] Embodiment 2 utilizes microsatellite markers to identify the method for the genetic sex of jellyfish
[0034] A method for accurately identifying the genetic sex of jellyfish, comprising the following steps:
[0035] (1) Collect samples of female and male salmon, cut the fin rays and store them in ethanol with a volume content of 95%, replace the ethanol every 24 hours, store at -20°C, and store them for later use;
[0036] (2) extract the genomic DNA of the female and male fin ray samples of jellyfish, measure the DNA concentration with an ultraviolet spectrophotometer, dilute the DNA concentration to 50ng / L, and set aside;
[0037] (3) performing PCR amplification with the genomic DNA obtained in step (2) as a template;
[0038] The reaction system for PCR amplification was 25 μL, and 4 concentration gradients (1 μmol / L, 2 μmol / L, 5 μmol / L, and 10 μmol / L) were set for 18s with reference to the primers for PCR amplification; the 25 μL amplification system included 2×P...
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