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Assaying of organisms for the presence of restriction endonucleases.

作者信息

Schleif R

出版信息

Methods Enzymol. 1980;65(1):19-23. doi: 10.1016/s0076-6879(80)65004-6.

DOI:10.1016/s0076-6879(80)65004-6
PMID:6246341
Abstract
摘要

相似文献

1
Assaying of organisms for the presence of restriction endonucleases.检测生物体中是否存在限制性内切酶。
Methods Enzymol. 1980;65(1):19-23. doi: 10.1016/s0076-6879(80)65004-6.
2
A simple electrophoresis system for multiple agarose slab gels.
Anal Biochem. 1980 Oct;108(1):207-11. doi: 10.1016/0003-2697(80)90714-9.
3
Polynucleotide kinase exchange as an assay for class II restriction endonucleases.多核苷酸激酶交换作为II类限制性内切核酸酶的一种检测方法。
Methods Enzymol. 1980;65(1):28-36. doi: 10.1016/s0076-6879(80)65007-1.
4
[The search for strains producing new restriction endonucleases].
Zh Mikrobiol Epidemiol Immunobiol. 1988 Sep(9):86-9.
5
A general assay for restriction endonucleases and other DNA-modifying enzymes with plasmid substrates.
Mol Biotechnol. 1995 Dec;4(3):259-68. doi: 10.1007/BF02779019.
6
[A method for detecting restriction endonucleases in bacterial colonies].
Prikl Biokhim Mikrobiol. 1988 Jan-Feb;24(1):121-4.
7
Identification of a new restriction endonuclease, EagI, from Enterobacter agglomerans.从聚团肠杆菌中鉴定出一种新的限制性内切酶EagI。
Acta Microbiol Pol. 1986;35(3-4):317-20.
8
[Distribution of specific endodeoxyribonucleases in different strains of Citrobacter freundii].
Dokl Akad Nauk SSSR. 1983;271(2):483-5.
9
Construction of restriction fragment maps of 50- to 100-kilobase DNA.50至100千碱基DNA限制性片段图谱的构建
Methods Enzymol. 1993;218:651-71. doi: 10.1016/0076-6879(93)18048-h.
10
A simple and rapid method for the isolation of plasmid and lambda phage DNAs.一种分离质粒和λ噬菌体DNA的简单快速方法。
Nucleic Acids Res. 1989 Dec 11;17(23):10129. doi: 10.1093/nar/17.23.10129.

引用本文的文献

1
Evidence for horizontal transfer of SsuDAT1I restriction-modification genes to the Streptococcus suis genome.SsuDAT1I限制修饰基因向猪链球菌基因组水平转移的证据。
J Bacteriol. 2001 Jan;183(2):500-11. doi: 10.1128/JB.183.2.500-511.2001.
2
Characterization of a restriction-modification system of the thermotolerant methylotroph Bacillus methanolicus.嗜热甲基营养型甲醇芽孢杆菌限制修饰系统的特性分析
Appl Environ Microbiol. 1996 Mar;62(3):1107-11. doi: 10.1128/aem.62.3.1107-1111.1996.
3
Characterization of a restriction endonuclease, PhaI, from Pasteurella haemolytica serotype A1 and protection of heterologous DNA by a cloned PhaI methyltransferase gene.
来自溶血巴斯德氏菌A1血清型的限制性内切酶PhaI的特性以及克隆的PhaI甲基转移酶基因对异源DNA的保护作用。
Appl Environ Microbiol. 1994 Jun;60(6):2006-10. doi: 10.1128/aem.60.6.2006-2010.1994.
4
Gene transfer between Escherichia coli and Enterobacter aerogenes.大肠杆菌与产气肠杆菌之间的基因转移。
Mol Gen Genet. 1983;190(1):179-81. doi: 10.1007/BF00330344.
5
Isolation and characterisation of DraI, a type II restriction endonuclease recognising a sequence containing only A:T basepairs, and inhibition of its activity by uv irradiation of substrate DNA.DraI的分离与鉴定,DraI是一种II型限制性内切核酸酶,识别仅含A:T碱基对的序列,以及通过对底物DNA进行紫外线照射来抑制其活性。
Nucleic Acids Res. 1983 Aug 25;11(16):5467-74. doi: 10.1093/nar/11.16.5467.
6
A site-specific single strand endonuclease activity induced by NYs-1 virus infection of a Chlorella-like green alga.由类小球藻绿藻感染 NYs - 1 病毒诱导的位点特异性单链内切核酸酶活性。
Nucleic Acids Res. 1988 Oct 25;16(20):9477-87. doi: 10.1093/nar/16.20.9477.
7
Restriction endonuclease activity induced by PBCV-1 virus infection of a Chlorella-like green alga.由PBCV-1病毒感染一种类小球藻绿藻诱导产生的限制性内切酶活性。
Mol Cell Biol. 1986 May;6(5):1430-9. doi: 10.1128/mcb.6.5.1430-1439.1986.
8
Restriction endonuclease activity induced by NC-1A virus infection of a Chlorella-like green alga.由类小球藻绿藻的NC - 1A病毒感染诱导的限制性内切酶活性
Nucleic Acids Res. 1986 Aug 11;14(15):6017-30. doi: 10.1093/nar/14.15.6017.
9
IL-3A virus infection of a Chlorella-like green alga induces a DNA restriction endonuclease with novel sequence specificity.一种类似小球藻的绿藻的IL-3A病毒感染会诱导产生一种具有新序列特异性的DNA限制性内切酶。
Nucleic Acids Res. 1987 Aug 11;15(15):6075-90. doi: 10.1093/nar/15.15.6075.
10
Isolation of a Legionella pneumophila restriction mutant with increased ability to act as a recipient in heterospecific matings.分离出一株嗜肺军团菌限制突变体,其在异种交配中作为受体的能力增强。
J Bacteriol. 1989 Apr;171(4):2238-40. doi: 10.1128/jb.171.4.2238-2240.1989.