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plasmid plus mid kit  (Qiagen)


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    Structured Review

    Qiagen plasmid plus mid kit
    Plasmid Plus Mid Kit, supplied by Qiagen, used in various techniques. Bioz Stars score: 96/100, based on 1415 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/plasmid+mid+kit/QIAGEN+Plasmid+Plus+Maxi+Kit/pm41174277-434-17-16
    Average 96 stars, based on 1415 article reviews
    plasmid plus mid kit - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Plasmid Preparation:

    Article Title: Construction of yellow fever virus subgenomic replicons by yeast-based homologous recombination cloning technique.
    Article Snippet: .. Plasmid DNA was then purified using the QIAGEN Plasmid Mid kit according manufacturer’s instructions. .. IN VITRO TRANSCRIPTION DNA templates for in vitro transcription were produced by PCR amplification of the region containing the T7 promoter and the entire replicon of the relevant plasmids using Klentaq polymerase (Clontech).

    Article Title: Interplay between EZH2/β-catenin in stemness of cisplatin-resistant HNSCC and their role as therapeutic targets.
    Article Snippet: The Wnt/β-catenin signaling pathway is associated with the regulation of cancer stem cells, and it can be driven by epigenetic modifications.. Here, we aim to identify epigenetic modifications involved in the control of the Wnt/β-catenin signaling and investigate the role of this pathway in the accumulation of cancer stem cells (CSC) and chemoresistance of Head and Neck Squamous Cell Carcinoma (HNSCC).. Quantitative-PCR, western blot, shRNA assay, viability assay, flow cytometry assay, spheres formation, xenograft model, and chromatin immunoprecipitation were employed to evaluate the Wnt/β-catenin pathway and EZH2 in wild-type and chemoresistant oral carcinoma cell lines, and in the populations of CSC and non-stem cells.

    Article Title: Production of CETD transgenic mouse line allowing ablation of any type of specific cell population.
    Article Snippet: Diphtheria toxin A-chain (DT-A) is a potent inhibitor of protein synthesis.. As little as a single molecule of DT-A can result in cell death.. DT-A gene driven by a tissue-specific promoter is used to achieve genetic ablation of a particular cell lineage.

    Article Title: Establishment of COS-JC cells persistently producing archetype JC polyomavirus.
    Article Snippet: .. The recombinant plasmids were prepared for a large scale by a QIAGEN Plasmid Mid Kit (Qiagen, Hilden, Germany), and sequenced using ABI PRISM BigDye Terminator v1.1 Cycle Sequencing Kits (Applied Biosystems) and ABI PRISM 310 Genetic Analyzer (Applied Biosystems). ..

    Article Title: A putative multi-replicon plasmid co-harboring beta-lactamase genes bla KPC-2 , bla CTX-M-14 and bla TEM-1 and trimethoprim resistance gene dfrA25 from a Klebsiella pneumoniae sequence type (ST) 11 strain in China
    Article Snippet: .. Plasmid DNA was extracted from K . pneumoniae HS091147 (Qiagen plasmid mid kit; Qiagen, Germany) and transferred by electroporation (Micro-Pulser electroporator; Bio-Rad, USA) into E . coli DH5α. ..

    Article Title: In vivo near-infrared fluorescence imaging of Leishmania amazonensis expressing infrared fluorescence protein (iRFP) for real-time monitoring of cutaneous leishmaniasis in mice.
    Article Snippet: 32 33 The use of Leishmania amazonensis-infected BALB/c mice is an important model 34 for the study of experimental cutaneous leishmaniasis.. Here we report the 35 development of a non-invasive method to directly evaluate and measure parasite 36 burden during the course of the infection, based on the near-infrared fluorescence 37 detection of a recombinant L. amazonensis strain.. So, we generated a L. 38 amazonensis strain that stably expresses the near-infrared protein (iRFP) gene 39 and compared the maintenance of its vitro and in vivo characteristics, such as 40 fitness, pathogenicity and fluorescence emission.

    Purification:

    Article Title: Construction of yellow fever virus subgenomic replicons by yeast-based homologous recombination cloning technique.
    Article Snippet: .. Plasmid DNA was then purified using the QIAGEN Plasmid Mid kit according manufacturer’s instructions. .. IN VITRO TRANSCRIPTION DNA templates for in vitro transcription were produced by PCR amplification of the region containing the T7 promoter and the entire replicon of the relevant plasmids using Klentaq polymerase (Clontech).

    Article Title: Production of CETD transgenic mouse line allowing ablation of any type of specific cell population.
    Article Snippet: Diphtheria toxin A-chain (DT-A) is a potent inhibitor of protein synthesis.. As little as a single molecule of DT-A can result in cell death.. DT-A gene driven by a tissue-specific promoter is used to achieve genetic ablation of a particular cell lineage.

    Article Title: In vivo near-infrared fluorescence imaging of Leishmania amazonensis expressing infrared fluorescence protein (iRFP) for real-time monitoring of cutaneous leishmaniasis in mice.
    Article Snippet: 32 33 The use of Leishmania amazonensis-infected BALB/c mice is an important model 34 for the study of experimental cutaneous leishmaniasis.. Here we report the 35 development of a non-invasive method to directly evaluate and measure parasite 36 burden during the course of the infection, based on the near-infrared fluorescence 37 detection of a recombinant L. amazonensis strain.. So, we generated a L. 38 amazonensis strain that stably expresses the near-infrared protein (iRFP) gene 39 and compared the maintenance of its vitro and in vivo characteristics, such as 40 fitness, pathogenicity and fluorescence emission.

    Extraction:

    Article Title: Interplay between EZH2/β-catenin in stemness of cisplatin-resistant HNSCC and their role as therapeutic targets.
    Article Snippet: The Wnt/β-catenin signaling pathway is associated with the regulation of cancer stem cells, and it can be driven by epigenetic modifications.. Here, we aim to identify epigenetic modifications involved in the control of the Wnt/β-catenin signaling and investigate the role of this pathway in the accumulation of cancer stem cells (CSC) and chemoresistance of Head and Neck Squamous Cell Carcinoma (HNSCC).. Quantitative-PCR, western blot, shRNA assay, viability assay, flow cytometry assay, spheres formation, xenograft model, and chromatin immunoprecipitation were employed to evaluate the Wnt/β-catenin pathway and EZH2 in wild-type and chemoresistant oral carcinoma cell lines, and in the populations of CSC and non-stem cells.

    other:

    Article Title: Leishmania major heat shock protein 70 (HSP70) is not protective in murine models of cutaneous leishmaniasis and stimulates strong humoral responses in cutaneous and visceral leishmaniasis patients.
    Article Snippet: Heat shock proteins (HSP) are highly conserved molecules that play important roles in protein folding, assembly of protein complexes and translocation of proteins across cellular compartments, as well as in several immunological processes.. In this study, we first immunized susceptible BALB/c and resistant C57BL/6 mice with the complete open-reading frame of Leishmania HSP-70 (pcDNA-HSP70) and boosted mice with rHSP-70 (amino acid 221-604 cloned in pQE-HSP70 and referred to as rHSP70) mixed with Montanide 720.. When we evaluated the effects of HSP70 in both mouse strains, we found that the entire fragment (amino acids 221-604) and rCT-HSP70 (amino acids 491-604 cloned in pQE-CT), but not rNT-HSP70 (amino acids 221-291 cloned pQE-NT), contained the highest immunogenicity.

    Article Title: Fluorescent Leishmania species: development of stable GFP expression and its application for in vitro and in vivo studies.
    Article Snippet: Reporter genes have proved to be an excellent tool for studying disease progression.. Recently, the green fluorescent protein (GFP) ability to quantitatively monitor gene expression has been demonstrated in different organisms.. This report describes the use of Leishmania tarentolae (L. tarentolae) expression system (LEXSY) for high and stable levels of GFP production in different Leishmania species including L. tarentolae, L. major and L. infantum.

    Recombinant:

    Article Title: Establishment of COS-JC cells persistently producing archetype JC polyomavirus.
    Article Snippet: .. The recombinant plasmids were prepared for a large scale by a QIAGEN Plasmid Mid Kit (Qiagen, Hilden, Germany), and sequenced using ABI PRISM BigDye Terminator v1.1 Cycle Sequencing Kits (Applied Biosystems) and ABI PRISM 310 Genetic Analyzer (Applied Biosystems). ..

    Sequencing:

    Article Title: Establishment of COS-JC cells persistently producing archetype JC polyomavirus.
    Article Snippet: .. The recombinant plasmids were prepared for a large scale by a QIAGEN Plasmid Mid Kit (Qiagen, Hilden, Germany), and sequenced using ABI PRISM BigDye Terminator v1.1 Cycle Sequencing Kits (Applied Biosystems) and ABI PRISM 310 Genetic Analyzer (Applied Biosystems). ..

    Electroporation:

    Article Title: A putative multi-replicon plasmid co-harboring beta-lactamase genes bla KPC-2 , bla CTX-M-14 and bla TEM-1 and trimethoprim resistance gene dfrA25 from a Klebsiella pneumoniae sequence type (ST) 11 strain in China
    Article Snippet: .. Plasmid DNA was extracted from K . pneumoniae HS091147 (Qiagen plasmid mid kit; Qiagen, Germany) and transferred by electroporation (Micro-Pulser electroporator; Bio-Rad, USA) into E . coli DH5α. ..



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