Relativity of voltage controlling sodium pass 7 type alpha subunit gene with primary hypertension
A technology of voltage regulation and hypertension, applied in the fields of molecular biology and medicine, can solve problems such as uncertainty
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Embodiment 1
[0145] 1 Objects and methods
[0146] 1.1 Research object
[0147] 1.1.1 Chinese SNP discovery and confirmation samples
[0148] In order to improve the representativeness and effectiveness of SNP detection, DNA samples were taken from 30 subjects from different regions of my country (Shandong, Shaanxi, Fujian, Guangdong, Guangxi, Shanghai, Lhasa, Yunnan, Jilin, Inner Mongolia, Guizhou, Sichuan and Xinjiang, etc. ) of different nationalities (Han, Zhuang, Tibetan, Brown, Korean, Dai, Mongolian, Miao, Yi, Uighur, etc.).
[0149] 1.1.2 Preliminary research samples of SNP typing and association analysis
[0150] All subjects were of Han nationality. The essential hypertension group (EH group) and the normotensive group (NT group) had 96 cases each, both from Shanghai, China, and had no relationship with each other. The EH group consisted of hypertensive patients who were diagnosed in the Hypertension Department of Shanghai Ruijin Hospital or in the general survey in Shanghai, ...
Embodiment 2
[0191] Essential Hypertension Susceptibility Detection Kit
[0192] A kit is prepared which contains:
[0193] Name Sequence (5′→3′) Number Concentration
[0194] Forward primer cct gga gcc tac aat ctc tga SEQ ID NO: 47 dry powder 2 OD
[0195] Reverse primer gaa agg tgt cat gta cca aca atg SEQ ID NO: 48 dry powder 2 OD
[0196] PCR reaction solution PCR reaction buffer containing Taq enzyme, dNTP, magnesium ion
[0197] Enzyme Reaction Solution BclI Endonuclease and Reaction Solution
[0198] Take 3ml of blood from the patient to be tested, and use a conventional method (or use a specific kit) to extract DNA from the blood. Dilute the PCR primers in the hypertension detection kit to 1 μmol / μl, and use the extracted DNA as a template to carry out PCR reaction with the provided primers. The PCR product was digested with BclI endonuclease. The amplification product containing T at the 153rd position can be cut by BclI, while the PCR product containing G at the 153rd positi...
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