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- Detection of keratin 5 gene point mutation in a family with Weber Cockayne EBS by PCR and direct DNA sequencing. PCR-DNA直接测序检测1例单纯型大疱性表皮松解症Weber-Cockayne亚型(WC-EBS)患者角蛋白K5基因点突变
- In contrast, direct DNA sequencing requires only a single sample from the proband. 相比之下，直接测序只需要被检测者的血样 。
- Methods:ABO blood groups were identified by serological tests. B(A) alleles were determined by PCR-SSP and direct DNA sequencing at exons 6 and 7 of ABO gene. 方法:用血清学血型方法、PCR-SSP法和ABO基因第6及第7外显子直接测序的方法对B(A)血型和B(A)型等位基因进行检测。
- The family was blood-grouped serologically as AB phenotypes,while PCR-SSP assay showed as O/O phenotypes,but direct DNA sequencing at exons 6 and 7 of ABO gene indicated that they were B(A)/O phenotypes. 该家系中血型血清学定型为AB型的成员DNA序列分析测定基因型为B(A)/O型,而PCR-SSP法检测AB型成员的基因型为O/O型。
- Method: PCR amplification,DNA sequencing and cladistic analysis. 方法:PCR扩增、DNA序列测定、分支分析。
- HBeBP4A gene was successfully amplified and identified by DNA sequencing. 成功扩增出HBeBP4A基因,测序结果符合GenBank报告序列。
- Laboratory diagnosis of Hgb Hekinan using HPLC and DNA sequencing methods? 施浤彰(Hung-Chang Shih);施木青(Mu-Chin Shih);张煜昌(Yu-Chang Chang);林惠茹(Hui-Ju Lin);林彩秀(Tsai-Hsiu Lin);彭庆添(Ching-Tien Peng);张天杰(Tien-Jye Chang);张建国(Jan-Gowth Chang)*?
- The methylation specific PCR (MSP) and bisulfite DNA sequencing were performed to examine the methylation status of SLIT2 gene promoter. 亚硫酸氢钠处理DNA,用MSP和测序法检测SLIT2启动子甲基化状态。
- New primers were designed for hot - start PCR reaction according to the results of DNA sequencing. 根据测序结果设计新的引物以进行热启动PCR反应；
- It was proved that the E2 genes were integrated stably into chromosome of P.Pastoris by Dot blot and DNA sequencing. Pastotis进行整合，经G418筛选得到25个高拷贝转化子，经DNA斑点试验和DNA测序证明外源基因E2稳定地整合到P.;Pastoris染色体中。
- The methods include using Agr obacterium-mediated transformation, electroporation, gene gun bombardme nt and polyethyleneglycol (PEG)-mediated direct DNA transfer. 果树基因转化方法主要包括农杆菌介导法、电激法、基因枪法、PEG转化法等。
- The mutations were detected by direct DNA sequencing. Results All samples examined carried mtDNA A1555G mutation in 12SrRNA gene and G7444A mutation in COI/tRNASer(UCN) gene. 结果测序结果表明,此家系线粒体DNA12SrRNA基因中存在着A1555G突变,COI/tRNASer(UCN)基因中存在着G7444A突变。
- A deletion mutation with frameshift of neurofibromatosis type 2 gene was detected by DNA sequencing. 以DNA序列分析出，在第二型纤维细胞瘤基因上发生染色体缺失造成移码突变。
- Authentication,PCR and DNA sequencing showed the recombinant plasmid of human MIA/CD-RAP was successfully constructed. 酶切电泳和DNA测序结果表明,成功地克隆了人黑素瘤M IA/CD-RAP cDNA。
- B7 1(CD80) cDNA was cloned by RT PCR from human B lymphma Raji cell line and confirmed by DNA sequencing. 应用RT－PCR技术从人B淋巴瘤细胞系Raji中克隆到B7－1（CD80）cDNA，并经测序证实。
- Methods STK 11 germline mutation was analysed by DNA sequencing in 18 unrelation patients with PJS. 方法 用 DNA直接测序方法 ,对 18个家系的 PJ综合征患者 STK1 1 基因 9个外显子进行研究。
- The more varied the organisms, the more varied the DNA sequences. 生物变化越多，DNA序列的变化也就越多。
- Methods:PCR,denatur ing gradient gel electrophoresis (DGGE) atd DNA sequencing were used. 方法：采用多聚酶链反应（PCR），变性梯度凝胶电泳（DGGE）和DNA测序等方法对上海地区血友病甲基因突变进行检测。
- The more varied the organisms,the more varied the DNA sequences. 生物变化越多，DNA序列的变化也就越多。
- DNA microarray has been applied to DNA sequencing,pharmaceuticals analysis,gene expression and so on. DNA微集阵列已广泛用于DNA测序、药物分析、基因表达等研究领域。
