梁晓岚,杨丛林,王荷花,杨静波,孙乐静,韩明哲,邱录贵,HLA-C_W基因分型在造血干细胞移植中的意义探讨 T)中的作用,对HLA-CW基因位点相合与不相合造血干细胞移植的效果进行分析。方法采用聚合酶链反应-序列特异性引物扩增(polymerasechainreaction-sequencespecificprimers,PCR-SSP)方法对HSCT供、受体共42个样本进行HLA-CW位点等位基因分析。结果HLA-CW基因全相合者9例
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分别设计MSX1、PAX9基因特异性引物，聚合酶链反应扩增全部外显子编码区和内含子-外显子剪接序列，产物纯化后直接测序。
Specific primers were designed for MSX1 and PAX9 respectively. Mutation analysis was performed by direct sequencing of all the coding exons and intron-exon boundaries.
该研究通过设计合成hla基因序列特异性引物，建立了HLA - DR基因分型的套式扩增和直接扩增pcr - SSP技术，并在骨髓移植配型中进行了应用。
In this study, a nested PCR SSP and a direct amplification PCR SSP protocols for HLA DR genotyping were developed and were used in the selection of matched donor for sibling BMT.
方法设计出针对各片段的特异性引物，用P CR方法从Z 37病毒感染的细胞提取细胞总rna，逆转录扩增、产物克隆t载体，纯化后测序，测定的序列应用DNASTAR软件比较分析。
Methods the total RNA was extracted from Z37 virus infected cells and the RT-PCR products were cloned into t vector, sequenced and analyzed by DNASTAR software.
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