A kit for rapid detection of il28b SNP rs12979860 polymorphism
A kit and polymorphic technology, applied in the biological field, achieve the effect of short detection process, high degree of automation, and easy operation
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Embodiment 1
[0038] The preparation of embodiment 1 kit of the present invention
[0039] (1) The composition of peripheral blood genomic DNA extraction reagents is as follows: deionized water, 6M NaI, chloroform / isoamyl alcohol (24:1, v / v) mixture, isopropanol and absolute ethanol.
[0040] (2) Primers:
[0041] TT genotype upstream amplification primer sequence is:
[0042] 5'-TCGCCAGGGCCCCTAACCTC-3' (SEQ ID No.1)
[0043] TT genotype downstream amplification primer sequence is:
[0044] 5'-GGAGTGCAATTCAACCCTGGTTCA-3' (SEQ ID No.2)
[0045] CC genotype upstream amplification primer sequence is:
[0046] 5'-GAGGATCCCTCCTGGGGCGG-3' (SEQ ID No.3)
[0047] The downstream amplification primer sequence of CC genotype is:
[0048] 5'-GGAGTGCAATTCAACCCTGGTTCG-3' (SEQ ID No.4)
[0049] Internal reference gene upstream amplification primers:
[0050] 5'-TTATCGCATACGGCTAGGC-3' (SEQ ID No.5)
[0051] Internal reference gene downstream amplification primers:
[0052] 5'-CACAATTCCCACCACGAGA-3'...
Embodiment 3
[0069] Embodiment 3 kit detection capability evaluation:
[0070] Preliminary experiments show that there is no difference between the sensitivity, specificity and sensitivity of this kit compared with the sequencing method, which fully meets the practical requirements of current clinical diagnosis and treatment:
[0071] Table 1 Comparison of two methods for detecting rs12979860 polymorphism
[0072]
[0073]
[0074] in:
[0075] ① Specificity: 100%;
[0076] ②Sensitivity: 100%;
[0077] ③ Positive predictive value: the positive predictive value reaches 100%;
[0078] ④ Negative predictive value: the negative predictive value reaches 100%;
[0079] ⑤Repeatability: The results of repeated experiments are consistent;
[0080] ⑥ Time-consuming: The detection time of a clinical specimen is about 2 to 3 hours, which is short.
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