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A simple method for generating single-stranded DNA probes labeled to high activities.一种生成高活性标记单链DNA探针的简单方法。
Nucleic Acids Res. 1990 Oct 25;18(20):6157-8. doi: 10.1093/nar/18.20.6157.
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Simple and effective method for generating single-stranded DNA targets and probes.
Biotechniques. 2006 Jun;40(6):759-63. doi: 10.2144/000112154.
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Efficient synthesis of 32P-labeled single-stranded DNA probes using linear PCR; application of the method for analysis of strand-specific DNA repair.利用线性PCR高效合成32P标记的单链DNA探针；该方法在链特异性DNA修复分析中的应用。
Mutat Res. 1994 Sep;315(2):189-95. doi: 10.1016/0921-8777(94)90018-3.
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Producing single-stranded DNA probes with the Taq DNA polymerase: a high yield protocol.利用Taq DNA聚合酶制备单链DNA探针：一种高产方案。
Biotechniques. 1991 Jan;10(1):35-6, 38-9.
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An improved protocol to generate high-efficiency single-stranded DNA probes by PCR.
Biotechniques. 1993 Jun;14(6):905-6.
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Generation of high efficiency ssDNA hybridization probes by linear polymerase chain reaction (LPCR).通过线性聚合酶链反应（LPCR）生成高效单链DNA杂交探针。
Scanning Microsc Suppl. 1996;10:57-60.
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Use of polymerase chain reaction for rapid detection of gene insertions in whole yeast cells.利用聚合酶链反应快速检测全酵母细胞中的基因插入情况。
Nucleic Acids Res. 1991 Sep 11;19(17):4775. doi: 10.1093/nar/19.17.4775.
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Preparation of single-stranded antisense cDNA probes by asymmetric PCR.
Methods Mol Biol. 1998;105:337-50. doi: 10.1385/0-89603-491-7:337.
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Hybridization and competition hybridization of Southern blots.
Methods Mol Biol. 1996;58:31-9. doi: 10.1385/0-89603-402-X:31.
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Expression, purification, and in vitro assays of mitochondrial single-stranded DNA-binding protein.线粒体单链DNA结合蛋白的表达、纯化及体外分析
Methods Mol Biol. 2002;197:295-302. doi: 10.1385/1-59259-284-8:295.
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Recent Advances in Micro/Nanomaterial-Based Aptamer Selection Strategies.基于微/纳米材料的适体筛选策略的最新进展
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Advances in Screening and Development of Therapeutic Aptamers Against Cancer Cells.针对癌细胞的治疗性适配体的筛选与开发进展
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Displacement of the transcription factor B reader domain during transcription initiation.转录起始时转录因子 B 阅读器结构域的位移。
Nucleic Acids Res. 2018 Nov 2;46(19):10066-10081. doi: 10.1093/nar/gky699.
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Isolating single stranded DNA using a microfluidic dialysis device.使用微流控透析装置分离单链 DNA。
Analyst. 2014 Jan 7;139(1):215-24. doi: 10.1039/c3an01880f. Epub 2013 Nov 8.
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α,β-D-constrained nucleic acids are strong terminators of thermostable DNA polymerases in polymerase chain reaction.α,β-D-约束核酸是热稳定 DNA 聚合酶在聚合酶链反应中的强终止子。
PLoS One. 2011;6(10):e25510. doi: 10.1371/journal.pone.0025510. Epub 2011 Oct 3.
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Time-resolved measurements of intracellular ATP in the yeast Saccharomyces cerevisiae using a new type of nanobiosensor.使用新型纳米生物传感器对酵母酿酒酵母细胞内 ATP 的时间分辨测量。
J Biol Chem. 2010 Nov 26;285(48):37579-88. doi: 10.1074/jbc.M110.155119. Epub 2010 Sep 29.
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Upgrading SELEX technology by using lambda exonuclease digestion for single-stranded DNA generation.利用λ核酸外切酶消化来生成单链 DNA，从而升级 SELEX 技术。
Molecules. 2009 Dec 24;15(1):1-11. doi: 10.3390/molecules15010001.
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Tentacle probe sandwich assay in porous polymer monolith improves specificity, sensitivity and kinetics.多孔聚合物整体柱中的触手探针夹心分析提高了特异性、灵敏度和动力学性能。
Nucleic Acids Res. 2008 Nov;36(19):e129. doi: 10.1093/nar/gkn564. Epub 2008 Sep 12.
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ABI3 mediates expression of the peroxiredoxin antioxidant AtPER1 gene and induction by oxidative stress.ABI3介导过氧化物还原酶抗氧化剂AtPER1基因的表达以及氧化应激诱导。
Plant Mol Biol. 2003 Oct;53(3):313-26. doi: 10.1023/b:plan.0000006937.21343.2a.
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Ten members of the Arabidopsis gene family encoding methyl-CpG-binding domain proteins are transcriptionally active and at least one, AtMBD11, is crucial for normal development.拟南芥中编码甲基化CpG结合结构域蛋白的基因家族的十个成员具有转录活性，并且至少有一个成员AtMBD11对正常发育至关重要。
Nucleic Acids Res. 2003 Sep 15;31(18):5291-304. doi: 10.1093/nar/gkg735.
本文引用的文献
1
"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum.一种将DNA限制性内切酶片段放射性标记至高比活度的技术。附录
Anal Biochem. 1984 Feb;137(1):266-7. doi: 10.1016/0003-2697(84)90381-6.
2
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.一种将DNA限制性内切酶片段放射性标记至高比活度的技术。
Anal Biochem. 1983 Jul 1;132(1):6-13. doi: 10.1016/0003-2697(83)90418-9.
3
Direct solid phase sequencing of genomic and plasmid DNA using magnetic beads as solid support.以磁珠作为固相支持物对基因组DNA和质粒DNA进行直接固相测序。
Nucleic Acids Res. 1989 Jul 11;17(13):4937-46. doi: 10.1093/nar/17.13.4937.
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