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单细胞中酶活性的定量测定:遗传性疾病的早期产前诊断。

Quantitative assays of enzyme activity in single cells: early prenatal diagnosis of genetic disorders.

作者信息

Hösli P

出版信息

Clin Chem. 1977 Aug;23(8):1476-84.

PMID:872408
Abstract

The combined use of special cell culture techniques and biochemical ultramicromethods permits one to handle very small amounts of materials, to reduce the costs of chemicals, and more accurately to assess gene dosage effects by expressing enzyme activities per cell instead of per total cell protein. An alkaline phosphatase induction test has been developed which allows one to screen small numbers of fibroblasts for lysosomal storage diseases, cystic fibrosis, and chromosomal disorders. A successful attempt has been made to automate the microtechniques. Combining the alkaline phosphatase induction with the ultramicro automatization should eventually permit one to screen all pregnancies for major possible fetal genetic defects. Automated ultramicro enzyme assays should contribute to the general development of clinical chemistry.

摘要

特殊细胞培养技术与生化超微量方法的联合应用,使人们能够处理极少量的材料,降低化学试剂成本,并通过以每个细胞而非每总细胞蛋白来表达酶活性,更准确地评估基因剂量效应。已开发出一种碱性磷酸酶诱导试验,可用于筛选少量成纤维细胞是否患有溶酶体贮积病、囊性纤维化和染色体疾病。已成功尝试将这些微技术自动化。将碱性磷酸酶诱导与超微量自动化相结合,最终应能使人们对所有妊娠进行主要可能胎儿遗传缺陷的筛查。自动化超微量酶测定应为临床化学的总体发展做出贡献。

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