System, method and kit for identifying genders of cows and early embryos of cows
A kit and gender technology, applied in the field of molecular biology, can solve the problems of inconvenient on-site operation, easy pollution, increase identification results, etc., and achieve the effect of reducing identification cost, less sample demand, and reducing dependence.
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Embodiment 1
[0045] The sequences of primers and probes designed according to bovine foldin gene and SRY gene are shown in Table 1.
[0046] Table 1 internal standard and sex site primer and probe sequence
[0047]
[0048] Standard PCR amplification reaction system:
[0049]
[0050] Place the 384-well plate on the thermal cycler, design and run the following program: Step 1: denaturation at 95°C for 5 minutes, step 2: denaturation at 94°C for 10 seconds, step 3 annealing at 58°C for 20 seconds, repeat 2 to 3 times Step 44 times.
[0051]figure 1 It is a single NB2 amplification, and the CT value of the blood DNA and embryo sample results is not much different, and both have CT values;
[0052] figure 2 It is a bull blood and embryo sample, and a cow blood and embryo sample sex locus BOV97M amplification curve;
[0053] image 3 Multiplex amplification for bull embryo samples;
[0054] Figure 4 It is a compound amplification system for cow embryo samples. In addition to the...
Embodiment 2
[0057] Example 2 specificity
[0058] Table 2 Species-specific verification results of internal standard primers and probes and sex site primers and probes
[0059] Sample Name
[0060] After the species-specific verification, many species samples had no amplification, and only cattle samples had amplification. It can be seen that the primers and probes of this system have strong specificity.
Embodiment 3
[0061] Embodiment 3 (detection and verification of known gender samples)
[0062] The following is the verification of the detection and gender identification of 78 bovine embryo samples provided by customers using the present invention
[0063] 1. DNA processing
[0064] Embryo cells are processed by physical high-temperature method, and the processed samples are centrifuged to become templates, and the templates are mixed evenly during operation.
[0065] 2. Fluorescent quantitative PCR detection
[0066] 2.1 Reaction system:
[0067] The samples provided by the customer were sent three times. The first sample sent 32 cases, all of which were bulls. Among them, there were samples that were deliberately not sampled. The second time there were a total of 26 samples of both bulls and cows. There are a total of 20 empty holes, and this time the customer used his own method to test, and the gender was known each time, so the applicant conducted the test according to the operat...
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