نتایج جستجو برای: iptg

تعداد نتایج: 1235  

2017
Chao Liu Yuehua Zhao Shuxian Yin Shufeng Liu Huanling Zhang Xiufang Wang Zhanjun Lv

BACKGROUND Exogenous RNAs can specifically up-regulate or down-regulate gene expression after they enter into cells. Alu RNAs are the main constituent of human transcriptome and participate in gene expression regulation. AluY elements belong to a subfamily of Alus and are the youngest Alus. In this paper, we established the technology method of preparing genetically engineered humanized AluY RN...

2012
Aaron R. Haeusler Kathy A. Goodson Todd D. Lillian Xiaoyu Wang Sachin Goyal Noel C. Perkins Jason D. Kahn

DNA looping mediated by the Lac repressor is an archetypal test case for modeling protein and DNA flexibility. Understanding looping is fundamental to quantitative descriptions of gene expression. Systematic analysis of LacI•DNA looping was carried out using a landscape of DNA constructs with lac operators bracketing an A-tract bend, produced by varying helical phasings between operators and th...

Journal: :Infection and immunity 2003
Cynthia D Long Deborah M Tobiason Matthew P Lazio Kimberly A Kline H Steven Seifert

The gonococcal pilus is a major virulence factor that has well-established roles in mediating epithelial cell adherence and DNA transformation. Gonococci expressing four gonococcal pilin variants with distinct piliation properties under control of the lac regulatory system were grown in different levels of the inducer isopropyl-beta-D-thiogalactopyranoside (IPTG). These pilin variants expressed...

Journal: :Bioscience, biotechnology, and biochemistry 1999
L Jiang Y Yang S Chatterjee B Seidel G Wolf S Yang

The expression of the proUK gene was improved by the coexpression of the argU gene cloned in a moderate copy number vector. As the proUK gene contains 2% AGG/AGA codons, which is much higher than the normal frequency in E. coli, about 0.14%-0.21%, the argU gene cloned in a multicopy plasmid was coexpressed with the proUK expression vector in our experiments. In E. coli strain BL21(DE3), IPTG is...

Journal: :BioTechniques 1996
P Trudel S Provost B Massie P Chartrand L Wall

The transcription factor GATA-1 is a zinc finger DNA-binding protein essential for the development of red blood cells. When we expressed different regions of the zinc finger domain in bacteria using an isopropyl-beta-D-thiogalactoside (IPTG) inducible system, growth of bacteria harboring the active DNA-binding domain of GATA-1 was rapidly inhibited upon IPTG induction. The growth inhibition pat...

Journal: :Nucleic Acids Research 2006
Xiao-Zhou Zhang Xin Yan Zhong-Li Cui Qing Hong Shun-Peng Li

Here, we present a novel method for the directed genetic manipulation of the Bacillus subtilis chromosome free of any selection marker. Our new approach employed the Escherichia coli toxin gene mazF as a counter-selectable marker. The mazF gene was placed under the control of an isopropyl-beta-D-thiogalactopyranoside (IPTG)-inducible expression system and associated with a spectomycin-resistanc...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2012
Tara L Deans Anirudha Singh Matthew Gibson Jennifer H Elisseeff

Combining synthetic biology and materials science will enable more advanced studies of cellular regulatory processes, in addition to facilitating therapeutic applications of engineered gene networks. One approach is to couple genetic inducers into biomaterials, thereby generating 3D microenvironments that are capable of controlling intrinsic and extrinsic cellular events. Here, we have engineer...

Journal: :Journal of bacteriology 2005
Lotte Jelsbak Dale Kaiser

An isopropyl-beta-D-thiogalactopyranoside (IPTG)-inducible promoter was constructed in Myxococcus xanthus. The single-copy pilA gene encodes pilin, the monomer unit of M. xanthus type IV pili. To vary the level of pilA expression, we cloned its promoter in front of the lac operator, and a plasmid containing the construct was inserted into the chromosome of a DeltapilA strain. Induction of pilin...

Journal: :Nucleic acids research 1992
A Dayn S Malkhosyan S M Mirkin

We studied the formation of d(A-T)n cruciforms in E.coli cells by probing intracellular plasmid DNA with chloroacetaldehyde followed by fine analysis of modified DNA bases. d(A-T)16 sequences were inserted into specifically designed plasmids either upstream of a single trc promoter, or between two divergent trc promoters. We found that in both cases, induction of transcription by IPTG leads to ...

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