摘要
用地高辛标记引物酶显色法,检测了63例e抗原阴性慢性肝炎HBV基因多态性。结果突变率为53.9%(34/63)。前C/C区1896位突变率最高为49.2%(31/63),1814位38.1%(24/63);BCP区1762位、1764位均为39.7%(25/63),552位突变率为14.3%(9/63)。该检测方法灵敏度高,简便易行。严格控制杂交温度及显色温度是检测操作的关键。
Detection of HBV gene polymorphism was carried out by using of enzyme coloration with digoxin-labeled primers in 63 cases of eAg ( - ) chronic HBV infections. And the detected mutation rate was 53.9% ( 34/63 ). The mutation rate in 1896th position of pre-c/c region was the highest as 49.2% (31/63) ; in 1814th was 38.1% (24/63) ;the mutation rate in 1762th and 1764th in BCP region were the same as 39.7% (25/63). The mutation rate in 552th position in P region was 14.3% ( 9/63 ). The method is more sensitive and easily operated in clinical practice. The key points are strictly control of temperature both in the hybridization and colour development in the detection.
出处
《微生物学免疫学进展》
2006年第4期52-53,共2页
Progress In Microbiology and Immunology
关键词
寡核苷酸芯片
乙型肝炎病毒
基因多态性
杂交
Oligonucleotide array
Hepatitis B virus ( HBV )
Gene polymorphism
Hybridization