D'Amato M, Sorrentino R
Institute of Cell Biology, CNR, Rome, Italy.
Tissue Antigens. 1994 May;43(5):295-301. doi: 10.1111/j.1399-0039.1994.tb02343.x.
A new procedure for HLA-DRB1 typing is proposed. The method combines six group-specific amplifications with heteroduplex analysis and, in some cases, enzyme restriction analysis. This technique, which is as discriminative as oligotyping, is simple, economical and does not require probes. These characteristics make this approach a valid alternative to other HLA genomic typing procedures, especially in those cases such as donor-recipient pairs matching where a small number of samples has to be managed at once.
本文提出了一种新的HLA-DRB1分型方法。该方法将六组特异性扩增与异源双链分析相结合,在某些情况下还结合酶切分析。这项技术与寡核苷酸分型一样具有鉴别力,操作简单、经济且无需探针。这些特性使该方法成为其他HLA基因分型方法的有效替代方案,尤其适用于供体-受体配对等情况,即需要一次性处理少量样本的情况。