多核苷酸
噬菌体
核酸
寡核苷酸
化学
DNA
生物化学
磷酸酶
分子生物学
核苷酸
酶
组合化学
生物
基因
大肠杆菌
作者
Michael R. Green,Joseph Sambrook
出处
期刊:CSH Protocols
[Cold Spring Harbor Laboratory]
日期:2021-08-01
卷期号:2021 (8): pdb.prot100677-pdb.prot100677
被引量:6
标识
DOI:10.1101/pdb.prot100677
摘要
The removal of 5' phosphates from nucleic acids with phosphatases and their readdition in radiolabeled form by bacteriophage T4 polynucleotide kinase is a widely used technique for generating 32P-labeled probes. When the reaction is performed efficiently, 40%-50% of the protruding 5' termini in the reaction becomes radiolabeled. However, the specific activity of the resulting probes is not as high as that obtained by other radiolabeling methods because only one radioactive atom is introduced per DNA molecule. Nevertheless, the availability of [γ-32P]ATP with specific activities in the 3000-7000 Ci/mmol range allows the synthesis of probes suitable for many purposes. This protocol includes procedures for labeling the 5' ends of dsDNA and oligonucleotides.
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