نتایج جستجو برای: tol2 transposase

تعداد نتایج: 1705  

2010
Ayako Yoshida Yoshifumi Yamaguchi Keiko Nonomura Koichi Kawakami Yoshiko Takahashi Masayuki Miura

In utero electroporation is widely used to study neuronal development and function by introducing plasmid DNA into neural progenitors during embryogenesis. This is an effective and convenient method of introducing plasmid DNA into neural precursors and is suitable for manipulating gene expression in cells of the CNS. However, the applicability of this technique is comparatively limited to neuro...

2012
N. Ika Mayasari Keiko Mukougawa Toshiaki Shigeoka Koichi Kawakami Masashi Kawaichi Yasumasa Ishida

Among the insertional mutagenesis techniques used in the current international knockout mouse project (KOMP) on the inactivation of all mouse genes in embryonic stem (ES) cells, random gene trapping has been playing a major role. Gene-targeting experiments have also been performed to individually and conditionally knockout the remaining 'difficult-to-trap' genes. Here, we show that transcriptio...

2010
Kazuhiro Yagita Iori Yamanaka Noriaki Emoto Koichi Kawakami Shoichi Shimada

BACKGROUND The circadian rhythm in mammals is orchestrated by a central pacemaker in the brain, but most peripheral tissues contain their own intrinsic circadian oscillators. The circadian rhythm is a fundamental biological system in mammals involved in the regulation of various physiological functions such as behavior, cardiovascular functions and energy metabolism. Thus, it is important to un...

Journal: :Antimicrobial agents and chemotherapy 2015
Yan-yan Hu Dan-xia Gu Jia-chang Cai Hong-wei Zhou Rong Zhang

Thirty-nine Klebsiella pneumoniae carbapenemase (KPC)-producing Pseudomonas aeruginosa isolates, all exhibiting high-level resistance to carbapenems and other β-lactam antibiotics, were isolated in Hangzhou, China. Molecular epidemiology analysis indicated the presence of two dominant clones, namely, clones A and B, both of which belong to sequence type 463 (ST463). A genetic environment analys...

Journal: :Genetics 2008
Valérie J Robert M Wayne Davis Erik M Jorgensen Jean-Louis Bessereau

Excision of a Mos1 transposon in the germline of Caenorhabditis elegans generates a double-strand break in the chromosome. We demonstrate that breaks are most prominently repaired by gene conversion from the homolog, but also rarely by nonhomologous end-joining. In some cases, gene conversion events are resolved by crossing over. Surprisingly, expression of the transposase using an intestine-sp...

Journal: :Current protocols in molecular biology 2015
Jason D Buenrostro Beijing Wu Howard Y Chang William J Greenleaf

This unit describes Assay for Transposase-Accessible Chromatin with high-throughput sequencing (ATAC-seq), a method for mapping chromatin accessibility genome-wide. This method probes DNA accessibility with hyperactive Tn5 transposase, which inserts sequencing adapters into accessible regions of chromatin. Sequencing reads can then be used to infer regions of increased accessibility, as well as...

Journal: :Genetics 2004
Marina Karakozova Ekaterina Savitskaya Larisa Melnikova Aleksandr Parshikov Pavel Georgiev

Transposable element P of Drosophila melanogaster is one of the best-characterized eukaryotic transposons. Successful transposition requires the interaction between transposase complexes at both termini of the P element. Here we found that insertion of one or two copies of the Su(Hw) insulator in the P transposon reduces the frequency of its transposition. Inactivation of a Mod(mdg4) component ...

Journal: :The Journal of biological chemistry 2002
Todd A Naumann William S Reznikoff

Tn5 transposase (Tnp) is a 53.3-kDa protein that is encoded by and facilitates movement of transposon Tn5. Tnp monomers contain a single active site that is responsible for catalyzing a series of four DNA breaking/joining reactions at one transposon end. Based on primary sequence homology and protein structural information, we designed and constructed a series of plasmids that encode for Tnps c...

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