Preparation method and system for energy imbalance type obese gene individual intervention drink
A technology of obesity genes and beverages, applied in biochemical equipment and methods, microbe measurement/testing, food science, etc., can solve problems affecting energy metabolism, diversity changes, etc.
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Embodiment 1
[0075] Example 1 Establishment of Joint Genotype Risk Level 1
[0076] The polymorphic site detected in the present embodiment is: rs1800592 ( UCP1 ), rs660339 ( UCP2 ) and rs1042713 ( ADRB2 ), mark them as a, b, and c respectively, and their subtype risks are shown in Table 8 below:
[0077] Table 8
[0078] genetic polymorphism site genotype Risk (OR) a 1(AA) 1
[0079] The risk grades calculated according to the single gene risk listed in Table 8 are shown in Table 4 above.
Embodiment 2
[0080] Example 2 Establishment of Joint Genotype Risk Level II
[0081] The polymorphic site detected in the present embodiment is: rs1800592 ( UCP1 ), rs660339 ( UCP2 ), rs1042713 ( ADRB2 ) and rs1042714 ( ADRB2 ), mark them as a, b, c, and d respectively, and their subtype risks are shown in Table 9 below:
[0082] Table 9
[0083] genetic polymorphism site genotype Risk (OR) a 1(AA) 1
2(AG) 2.63
3(GG) 2.63 b 1(CC) 1
2(CT) 1
3(TT) 2.22 c 1(AA) 1
2(AG) 1
3(GG) 4.12 d 1(CC) 1
2 (CG) 2.66
3(GG) 2.66
[0084] The risk level calculated based on the single gene risk listed in the above table is shown in Table 10 below:
[0085] Table 10
[0086]
Embodiment 3
[0087] Embodiment 3 Individual gene detection one
[0088] The 3 polymorphic sites in Example 1 were used for individual gene detection.
[0089] Individual oral epithelial cell samples were collected, and genomic DNA was extracted by silica gel adsorption method. After electrophoresis detection and verification, fluorescent quantitative PCR reaction was performed.
[0090] Put individual samples into 3 reaction wells respectively, and detect 3 sites at the same time, namely rs1800592( UCP1 ), rs660339 ( UCP2 ), rs1042713 ( ADRB2 ), and additional NTC blank control wells without DNA templates were added according to the experimental needs;
[0091] Add reagents to each reaction well as a fluorescent quantitative PCR reaction system with a total volume of 10 μL, that is, 2 μL of DNA template with a concentration of 20 ng / μL, 10× fluorescent quantitative PCR reaction buffer ABITaqman ? MGB 1 μL, 25mM dNTP four deoxynucleotide substrates for DNA synthesis 0.1 μL, 25mM MgCl ...
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