Detection method of yak FOXO1 gene single nucleotide polymorphism and kit thereof
A single nucleotide polymorphism and detection method technology, which is applied in the field of the detection method and the kit of the single nucleotide polymorphism of the yak FOXO1 gene, can solve the problem of reducing the tightness of the binding between the probe and the target sequence, and the detection method. The problem of mismatching bases between the needle and the target sequence, affecting the fluorescence release of the probe, etc., achieves the effects of good specificity, high sensitivity and low cost
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Embodiment 1
[0045] Embodiment 1: a method for detecting the single nucleotide polymorphism of the cow-consuming FOXO1 gene, comprising the following steps:
[0046] Preparation of yak FOXO1 gene PCR amplification product: first extract the genomic DNA from the blood of the yak, after dilution, use the FOXO1 gene of the yak whole genome DNA to be tested as a template, and use the specific primer pair A and specific printing B as primers, The yak FOXO1 gene was amplified by PCR, followed by polyacrylamide gel electrophoresis, and then the PCR amplification product was purified with a purification kit, sequenced, and the single nucleotide polymorphism at position 720 of the yak FOXO1 gene was identified according to the sequencing results ( A C-T mutation has occurred).
[0047] Specific steps are as follows:
[0048] Step 1: Preparation of yak FOXO1 gene amplification product: First, extract the genomic DNA from the blood of the cow, dilute it, and use 1% agarose gel electrophoresis and a ...
Embodiment 2
[0071] Embodiment 2: Data statistics
[0072] The genotype and allele frequency were calculated according to the theory of population genetics, and the homozygosity (Ho), heterozygosity (He), effective allele number (Ne) and polymorphism information of the FOXO1 gene polymorphic sites in the yak population were calculated content (PIC). Hardy-Weinberg equilibrium law was used for balance test, and SHEsis software was used for paired linkage disequilibrium analysis. The chi-square test was performed on the genotype distribution of the FOXO1 gene polymorphism site in the yak population by using SPSS17.0 software, and the correlation between different genotypes and body size traits was analyzed.
Embodiment 3
[0073] Embodiment three: result analysis
[0074] PCR amplification product: using yak blood genomic DNA as a template, and using the designed primers for PCR specific amplification, the results are shown in figure 1 , figure 1 middle: figure 1 Among them, 1 and 2 represent primers FOXO1 and FOXO2 respectively; M represents Mark. Depend on figure 1 It can be seen that the PCR amplification products are all single-specific bands, which are basically consistent with the expected size. The above-mentioned specific primer pair A and specific primer pair B are sequenced, and the results show as follows figure 2 As shown, there are 720(C / T)1 polymorphic sites in the partial CDS region sequence of FOXO1 gene.
[0075] Typing of yak FOXO1 gene by HRM method: After sequencing the FOXO1 gene of yak through the constructed DNA pool, the sequence of the spliced CDS region was obtained by analyzing and splicing with Chromas software. The results of genotype analysis of 1 polymorph...
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