Kawasaki E, Saiki R, Erlich H
Procept Inc., Cambridge, Massachusetts 02139.
Methods Enzymol. 1993;218:369-81. doi: 10.1016/0076-6879(93)18029-c.
The reverse dot-blot method is a simple and rapid diagnostic procedure that allows screening of sample for a variety of mutations/polymorphisms in a single hybridization reaction. Several methods of immobilizing the oligonucleotide probes are discussed. The reverse dot-blot method has several unique properties that are valuable in a diagnostic setting: (1) the typing results from a single sample can be located on a single strip. This facilitates scanning and interpretation of the probe reactivity patterns and minimizes the potential for user error. (2) The test can utilize premade typing strips. This minimizes user labor as well as error potential and allows the use of standardized reagents. (3) Unlike dot-blot/oligonucleotide typing, only the PCR product is labeled, eliminating the potential problem of probes labeled to different specific activities. This method has already been used in the areas of forensic genetic typing (the HLA-DQ alpha Amplitype test), tissue typing for transplantation (the HLA-DR beta) test, cystic fibrosis screening, as well as in a variety of research applications.
反向斑点杂交法是一种简单快速的诊断方法,可在一次杂交反应中对样本进行多种突变/多态性的筛查。文中讨论了几种固定寡核苷酸探针的方法。反向斑点杂交法具有一些在诊断环境中很有价值的独特特性:(1)单个样本的分型结果可位于单个条带上。这便于扫描和解读探针反应模式,并将用户错误的可能性降至最低。(2)该检测可使用预制的分型条带。这最大限度地减少了用户的工作量以及出错的可能性,并允许使用标准化试剂。(3)与斑点杂交/寡核苷酸分型不同,只有PCR产物被标记,消除了探针标记到不同比活性的潜在问题。该方法已用于法医基因分型(HLA - DQα扩增型检测)、移植组织分型(HLA - DRβ检测)、囊性纤维化筛查以及各种研究应用领域。