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聚合酶链反应扩增产物在聚合物网络中的毛细管电泳:肯尼迪病实例

Capillary electrophoresis of polymerase chain reaction-amplified products in polymer networks: the case of Kennedy's disease.

作者信息

Nesi M, Righetti P G, Patrosso M C, Ferlini A, Chiari M

机构信息

Istituto di Chimica degli Ormoni, CNR, Milano, Italy.

出版信息

Electrophoresis. 1994 May;15(5):644-6. doi: 10.1002/elps.1150150190.

Abstract

In Kennedy disease (an X-linked motoneuronal disorder associated with an increase in the number of (CAG)n triplet repeats in the first exon of the Androgen receptor gene; about twice as many as in normal conditions), polymerase chain reaction-amplified genic products exhibit two DNA fragments in the heterozygous female carriers, one with a range between 468 and 495 bp in the normal polymorphic population and a fragment corresponding to the pathological state that reaches 573 bp. These fragments are easily separated by gel-slab electrophoresis and detected by intercalating dye staining (ethidium bromide). As an alternative procedure, capillary zone electrophoresis in polymer networks, consisting of 8% polyacryloylaminoethoxyethanol at 0% cross-linker, offers a simple procedure for separation and on-line detection via UV absorbance at 254 nm, thus avoiding additional staining steps. The capillary column can be repeatedly used for up to 80-100 times and the electropherogram is stored on a magnetic support. Easy comparison among different runs is obtained by aligning all tracings to an internal standard of a 650 bp fragment added as a marker.

摘要

在肯尼迪病(一种X连锁运动神经元疾病,与雄激素受体基因第一外显子中(CAG)n三联体重复序列数量增加有关;约为正常情况的两倍)中,聚合酶链反应扩增的基因产物在杂合子女性携带者中呈现出两个DNA片段,一个在正常多态性群体中长度介于468至495 bp之间,另一个是对应病理状态的片段,长度可达573 bp。这些片段通过凝胶平板电泳很容易分离,并通过嵌入染料染色(溴化乙锭)进行检测。作为另一种方法,在由0%交联剂的8%聚丙烯酰氨基乙氧基乙醇组成的聚合物网络中进行毛细管区带电泳,提供了一种通过在254 nm处的紫外吸光度进行分离和在线检测的简单方法,从而避免了额外的染色步骤。毛细管柱可重复使用多达80 - 100次,电泳图存储在磁性载体上。通过将所有图谱与作为标记添加的650 bp片段的内标对齐,可以轻松地对不同运行结果进行比较。

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