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Promega fugene hd
Fugene Hd, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/fugene+hd/fugene+hd/pmc12221515-180-6-8
Average 90 stars, based on 1 article reviews
fugene hd - by Bioz Stars, 2026-09
90/100 stars

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Generated:

Article Title: A proximity-labeling-based approach to directly detect mRNA delivery to specific subcellular locations
Article Snippet: HEK293T and A549 cells were maintained in high-glucose DMEM (Sigma) supplemented with 10% fetal bovine serum (FBS; Gibco). .. Lentiviral stocks were generated by transfection of HEK293T cells with the packaging vectors pMD2.9 (Addgene 12259) and psPAX2 (Addgene 12260), with either ERM-APEX2 (Addgene 79055) or APEX2-NES (Addgene 92158) included to target APEX2 to the endoplasmic reticulum or cytoplasm, respectively, using Fugene HD (Promega). ..

Transfection:

Article Title: A proximity-labeling-based approach to directly detect mRNA delivery to specific subcellular locations
Article Snippet: HEK293T and A549 cells were maintained in high-glucose DMEM (Sigma) supplemented with 10% fetal bovine serum (FBS; Gibco). .. Lentiviral stocks were generated by transfection of HEK293T cells with the packaging vectors pMD2.9 (Addgene 12259) and psPAX2 (Addgene 12260), with either ERM-APEX2 (Addgene 79055) or APEX2-NES (Addgene 92158) included to target APEX2 to the endoplasmic reticulum or cytoplasm, respectively, using Fugene HD (Promega). ..

Article Title: Compositions and methods for the diagnosis and treatment of lymphatic system disorders
Article Snippet: The S214P mutation was introduced by site-directed mutagenesis using the Q5 mutagenesis kit from NEB following the manufacturer's instructions. .. Transfections in HEK293T and HeLa were performed using Fugene HD (Promega), with 3 μg DNA (empty vector, WT ARAF (ARAF-WT) or ARAF mutant (ARAF-S214P)) and 9 μl of the transfection reagent, according to the manufacturer's protocols. .. At 36-48 h after transfection, cells were washed twice with ice-cold phosphate-buffered saline (PBS) and lysed on ice using a freshly prepared ice-cold cell lysis buffer containing 50 mM Tris-HCl, pH 7.4, 100 mM NaCl, 50 mM β-glycerophosphate, 10% glycerol (w/v), 1% NP-40 (w/v), 1 mM EDTA, 2 mM NaVO4 and a complete, EDTA-free protease inhibitor cocktail (Roche Applied Science) at 20 μl per millilitre of lysis buffer.

Article Title: Activation of bioluminescence by structural complementation
Article Snippet: On day 1, a transfection mixture of 2 ng NLPoly156, NLPoly11S or NanoLuc® luciferase (Nluc) DNA, 1 ug pGEM3Zf(+) carrier DNA, 4 ul Fugene HD (Promega Corporation) and Phenol red-free OptiMEM to 100 ul was made and incubated at RT for 10 minutes. .. On day 1, a transfection mixture of 2 ng NLPoly156, NLPoly11S or NanoLuc® luciferase (Nluc) DNA, 1 ug pGEM3Zf(+) carrier DNA, 4 ul Fugene HD (Promega Corporation) and Phenol red-free OptiMEM to 100 ul was made and incubated at RT for 10 minutes. ..

Article Title: Development of an inhalable dry powder formulation for inhibition of SARS-CoV-2
Article Snippet: .. Transfection: transfection mix was prepared using Fugene HD (Promega GmbH, Walldorf, Germany) and 8 μg Spike protein expression plasmid (pCG1-SARS-CoV-2-S, kindly provided by Stefan Pöhlmann (German Primate Center GmbH – Leibniz Institute for Primate Research, Göttingen, Germany) and incubated to allow complex formation for 30 min at room temperature. .. Cell culture medium was removed, and transfection complex was added to the cells followed by 6 h incubation at +37 °C with 5% CO 2 .

Article Title:
Article Snippet: .. To generate stable cell line, HEK293 EBNA cells were transfected with the expression vector using Fugene HD (Promega, France). .. 48 hrs after transfection, the medium was replaced with DMEM/F12 medium with 10% FCS containing 0.5 μg/ml puromycin (Sigma-Aldrich, France) for selection.

Mutagenesis:

Article Title: Compositions and methods for the diagnosis and treatment of lymphatic system disorders
Article Snippet: The S214P mutation was introduced by site-directed mutagenesis using the Q5 mutagenesis kit from NEB following the manufacturer's instructions. .. Transfections in HEK293T and HeLa were performed using Fugene HD (Promega), with 3 μg DNA (empty vector, WT ARAF (ARAF-WT) or ARAF mutant (ARAF-S214P)) and 9 μl of the transfection reagent, according to the manufacturer's protocols. .. At 36-48 h after transfection, cells were washed twice with ice-cold phosphate-buffered saline (PBS) and lysed on ice using a freshly prepared ice-cold cell lysis buffer containing 50 mM Tris-HCl, pH 7.4, 100 mM NaCl, 50 mM β-glycerophosphate, 10% glycerol (w/v), 1% NP-40 (w/v), 1 mM EDTA, 2 mM NaVO4 and a complete, EDTA-free protease inhibitor cocktail (Roche Applied Science) at 20 μl per millilitre of lysis buffer.

Luciferase:

Article Title: Activation of bioluminescence by structural complementation
Article Snippet: On day 1, a transfection mixture of 2 ng NLPoly156, NLPoly11S or NanoLuc® luciferase (Nluc) DNA, 1 ug pGEM3Zf(+) carrier DNA, 4 ul Fugene HD (Promega Corporation) and Phenol red-free OptiMEM to 100 ul was made and incubated at RT for 10 minutes. .. On day 1, a transfection mixture of 2 ng NLPoly156, NLPoly11S or NanoLuc® luciferase (Nluc) DNA, 1 ug pGEM3Zf(+) carrier DNA, 4 ul Fugene HD (Promega Corporation) and Phenol red-free OptiMEM to 100 ul was made and incubated at RT for 10 minutes. ..

Incubation:

Article Title: Activation of bioluminescence by structural complementation
Article Snippet: On day 1, a transfection mixture of 2 ng NLPoly156, NLPoly11S or NanoLuc® luciferase (Nluc) DNA, 1 ug pGEM3Zf(+) carrier DNA, 4 ul Fugene HD (Promega Corporation) and Phenol red-free OptiMEM to 100 ul was made and incubated at RT for 10 minutes. .. On day 1, a transfection mixture of 2 ng NLPoly156, NLPoly11S or NanoLuc® luciferase (Nluc) DNA, 1 ug pGEM3Zf(+) carrier DNA, 4 ul Fugene HD (Promega Corporation) and Phenol red-free OptiMEM to 100 ul was made and incubated at RT for 10 minutes. ..

Article Title: Development of an inhalable dry powder formulation for inhibition of SARS-CoV-2
Article Snippet: .. Transfection: transfection mix was prepared using Fugene HD (Promega GmbH, Walldorf, Germany) and 8 μg Spike protein expression plasmid (pCG1-SARS-CoV-2-S, kindly provided by Stefan Pöhlmann (German Primate Center GmbH – Leibniz Institute for Primate Research, Göttingen, Germany) and incubated to allow complex formation for 30 min at room temperature. .. Cell culture medium was removed, and transfection complex was added to the cells followed by 6 h incubation at +37 °C with 5% CO 2 .

Article Title: Activation of bioluminescence by structural complementation
Article Snippet: 1 ug plasmid DNA containing a non-luminescent polypeptide mutant was mixed with OptiMEM (Life Technologies) to a final volume of 52 ul. .. 3.3 μl of Fugene HD (Promega Corporation) was added, and samples incubated for 15 minutes at room temperature. ..

Expressing:

Article Title: Development of an inhalable dry powder formulation for inhibition of SARS-CoV-2
Article Snippet: .. Transfection: transfection mix was prepared using Fugene HD (Promega GmbH, Walldorf, Germany) and 8 μg Spike protein expression plasmid (pCG1-SARS-CoV-2-S, kindly provided by Stefan Pöhlmann (German Primate Center GmbH – Leibniz Institute for Primate Research, Göttingen, Germany) and incubated to allow complex formation for 30 min at room temperature. .. Cell culture medium was removed, and transfection complex was added to the cells followed by 6 h incubation at +37 °C with 5% CO 2 .

Article Title:
Article Snippet: .. To generate stable cell line, HEK293 EBNA cells were transfected with the expression vector using Fugene HD (Promega, France). .. 48 hrs after transfection, the medium was replaced with DMEM/F12 medium with 10% FCS containing 0.5 μg/ml puromycin (Sigma-Aldrich, France) for selection.

Plasmid Preparation:

Article Title: Development of an inhalable dry powder formulation for inhibition of SARS-CoV-2
Article Snippet: .. Transfection: transfection mix was prepared using Fugene HD (Promega GmbH, Walldorf, Germany) and 8 μg Spike protein expression plasmid (pCG1-SARS-CoV-2-S, kindly provided by Stefan Pöhlmann (German Primate Center GmbH – Leibniz Institute for Primate Research, Göttingen, Germany) and incubated to allow complex formation for 30 min at room temperature. .. Cell culture medium was removed, and transfection complex was added to the cells followed by 6 h incubation at +37 °C with 5% CO 2 .

Article Title:
Article Snippet: .. To generate stable cell line, HEK293 EBNA cells were transfected with the expression vector using Fugene HD (Promega, France). .. 48 hrs after transfection, the medium was replaced with DMEM/F12 medium with 10% FCS containing 0.5 μg/ml puromycin (Sigma-Aldrich, France) for selection.

other:

Article Title: Chimeric PD-1 receptor redirects primary T cells against childhood solid tumors but not to PD-1 ligand-positive CD80-coexpressing cells
Article Snippet: To generate RD114-pseudotyped retroviruses, lipofection was used to transfect 293T cells (Fugene HD, Promega, Madison, WI, USA).

Transduction:

Article Title: Compositions and methods for making epigenetic modifications
Article Snippet: Media was replaced with fresh media supplemented with ViralBoost (Alstem, NC0966705) 6 hours post-transfection. .. Lentiviral Packaging and Transduction Lentiviral particles were produced by co-transfecting lentiviral transfer plasmids with standard packaging vectors psPAX2 (Addgene #12260) and pMD2.G (Addgene #12259) into HEK293T using FuGENE HD (Promega, PAE2311) or PEI. .. Media was replaced with fresh media supplemented with ViralBoost (Alstem, NC0966705) 6 hours post-transfection.

Produced:

Article Title: Compositions and methods for making epigenetic modifications
Article Snippet: Media was replaced with fresh media supplemented with ViralBoost (Alstem, NC0966705) 6 hours post-transfection. .. Lentiviral Packaging and Transduction Lentiviral particles were produced by co-transfecting lentiviral transfer plasmids with standard packaging vectors psPAX2 (Addgene #12260) and pMD2.G (Addgene #12259) into HEK293T using FuGENE HD (Promega, PAE2311) or PEI. .. Media was replaced with fresh media supplemented with ViralBoost (Alstem, NC0966705) 6 hours post-transfection.

Stable Transfection:

Article Title:
Article Snippet: .. To generate stable cell line, HEK293 EBNA cells were transfected with the expression vector using Fugene HD (Promega, France). .. 48 hrs after transfection, the medium was replaced with DMEM/F12 medium with 10% FCS containing 0.5 μg/ml puromycin (Sigma-Aldrich, France) for selection.



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