Kit for testing and identifying genetic cardiac hypertrophy related gene mutation
A technology of cardiac hypertrophy and heredity, applied in the field of molecular biology, can solve the problems of large differences in the occurrence time of ventricular hypertrophy, numerous factors of ventricular hypertrophy, and difficulty in identifying hypertension, etc., to meet the clinical detection requirements, improve detection accuracy and Stability, the effect of reducing the link of repeated operations
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[0032]1. Probe design: According to the genes MYH7, MYH6, MYBPC3, TNNT2, TNNI3, TNNC1, ACTC1, TPM1, TTN, CSRP3, DES, DMD, LDB3, VCL, TCAP, PLN, NEXN, ACTN2, FKTN published in the Human Genome Database , MYPN, TMPO, ANKRD1, PSEN1, PSEN2, ABCC9, SGCD, DSG2, EYA4, DSP, SCN5A, LMNA, MURC exon sequence design and synthetic probes, the probe is RNA, designed in a shingled manner in the target segment, The length of the probe is 20bp, the overlapping region is 5bp, and the coverage reaches 15bp at both ends of the target segment. Agilent's SureSelect buffer system is adopted.
[0033] 2. Genome extraction: Qiagen FlexiGene DNA Kit (Code No: 51204) was used to extract the genomes of 96 samples to be tested. The OD value reached 1.8-2.0, and 5ug was used as the starting template.
[0034] 3. Sample preparation before sequencing
[0035] 1) Fragmentation of the target gene: take 96 parts of genomic DNA that have been quantified, and dilute to contain 5 μg of genomic DNA per 100 μL, th...
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