qiagen rneasy midi kit (Qiagen)
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Qiagen Rneasy Midi Kit, supplied by Qiagen, used in various techniques. Bioz Stars score: 98/100, based on 5289 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Sequencing:Article Title: In vivo mitochondrial base editing restores genotype and visual function in a mouse model of LHON. Article Snippet: For MEF cell 519 AR TI CL E IN P RE SS ARTICLE IN PRESS 22 transfections, cells were seeded onto 24-well plates (SPL) with density of 1*104 cells, and were 520 transfected with 500 ng/μl left, right sTALED-V28R and pAAV-sTALED-V28R using 3.5 μl of 521 Lipofectamine 3000 after 24 h. For UDC transfections, the electroporation method (NEON, 522 Thermo Fisher, Lonza nucleofector X unit, Lonza) was used. .. Specifically, the sTALED plasmids 523 confirmed by sanger sequencing were extracted using a Article Title: Optogenetics-enabled discovery of integrated stress response modulators. Article Snippet: Article Optogenetics-enabled discovery of integrated stress response modulators Graphical abstract Highlights • An optogenetics platform specifically induces the integrated stress response • This platform enables a high-throughput screen of 370,830 compounds • Identified compounds selectively eliminate ISR-high cells across diverse stressors • These compounds demonstrate broad-spectrum antiviral activity in vitro and in mice Authors Felix Wong, Alicia Li, Satotaka Omori, ..., Hahn Kim, James J. Collins, Maxwell Z. Wilson Correspondence felix@integratedbiosciences.com (F.W.), jimjc@mit.edu (J.J.C.), max@integratedbiosciences.com (M.Z.. W.) In brief An optogenetics-enabled drug screening platform facilitates targeting of the integrated stress response, leading to the identification of compounds that selectively potentiate ISR signaling across diverse stressors and exhibit broad-spectrum antiviral activity.. Wong et al., 2025, Cell 188, 4950–4967 September 4, 2025 © 2025 Elsevier Inc. All rights are reserved, including those for text and data mining, AI training, and similar technologies. https://doi.org/10.1016/j.cell.2025.06.024 ll Article Title: In vivo mitochondrial base editing restores genotype and visual function in a mouse model of LHON Article Snippet: Cells were transfected with 500 ng/μl left, right DddA11, Hifi-DdCBE, sTALED-V28R, using 1.5 μl of Lipofectamine 3000 (Invitrogen) after 24 h. For MEF cell transfections, cells were seeded onto 24-well plates (SPL) with density of 1 x 10 4 cells, and were transfected with 500 ng/μl left, right sTALED-V28R and pAAV-sTALED-V28R using 3.5 μl of Lipofectamine 3000 after 24 h. For UDC transfections, the electroporation method (NEON, Thermo Fisher, Lonza nucleofector X unit, Lonza) was used. .. Specifically, the sTALED plasmids confirmed by sanger sequencing were extracted using a Plasmid Preparation:Article Title: In vivo mitochondrial base editing restores genotype and visual function in a mouse model of LHON. Article Snippet: For MEF cell 519 AR TI CL E IN P RE SS ARTICLE IN PRESS 22 transfections, cells were seeded onto 24-well plates (SPL) with density of 1*104 cells, and were 520 transfected with 500 ng/μl left, right sTALED-V28R and pAAV-sTALED-V28R using 3.5 μl of 521 Lipofectamine 3000 after 24 h. For UDC transfections, the electroporation method (NEON, 522 Thermo Fisher, Lonza nucleofector X unit, Lonza) was used. .. Specifically, the sTALED plasmids 523 confirmed by sanger sequencing were extracted using a Article Title: Pathways and products of base excision DNA repair in Xenopus laevis eggs: contrast with human cell pathways. Article Snippet: To precipitate the plasmid, 0.1 volume of 3 M sodium acetate and 0.7 t w a 1 S t p t D s W d u 3 s p ( w F p a μ i E t d s a w s 6 μ 9 l a t t 0 t t t h t S Z e a fl p A t i o C w l a s D ow nloaded from https://academ ic.oup.com /nar/article/53/22/gkaf1326/8376686 by guest on 12 D ecem ber 2025 otal volume of isopropanol were added to the supernatant, hich was then stored at −20 ◦C for 1 h. After centrifugation t 17 900 × g at 4 ◦C for 30 min, the pellet was dissolved in ml TE buffer on a 65 ◦C heat block with constant pipetting. ubsequently, 9 ml of buffer QBT (Qiagen, 12143) was added o the solution with constant shaking. .. The plasmid was then urified using a Article Title: Optogenetics-enabled discovery of integrated stress response modulators. Article Snippet: Article Optogenetics-enabled discovery of integrated stress response modulators Graphical abstract Highlights • An optogenetics platform specifically induces the integrated stress response • This platform enables a high-throughput screen of 370,830 compounds • Identified compounds selectively eliminate ISR-high cells across diverse stressors • These compounds demonstrate broad-spectrum antiviral activity in vitro and in mice Authors Felix Wong, Alicia Li, Satotaka Omori, ..., Hahn Kim, James J. Collins, Maxwell Z. Wilson Correspondence felix@integratedbiosciences.com (F.W.), jimjc@mit.edu (J.J.C.), max@integratedbiosciences.com (M.Z.. W.) In brief An optogenetics-enabled drug screening platform facilitates targeting of the integrated stress response, leading to the identification of compounds that selectively potentiate ISR signaling across diverse stressors and exhibit broad-spectrum antiviral activity.. Wong et al., 2025, Cell 188, 4950–4967 September 4, 2025 © 2025 Elsevier Inc. All rights are reserved, including those for text and data mining, AI training, and similar technologies. https://doi.org/10.1016/j.cell.2025.06.024 ll Article Title: STAMPS: Signal-peptide Transformer for Augmenting Mammalian Protein Secretion Article Snippet: .. The culture was then Article Title: In vivo mitochondrial base editing restores genotype and visual function in a mouse model of LHON Article Snippet: Cells were transfected with 500 ng/μl left, right DddA11, Hifi-DdCBE, sTALED-V28R, using 1.5 μl of Lipofectamine 3000 (Invitrogen) after 24 h. For MEF cell transfections, cells were seeded onto 24-well plates (SPL) with density of 1 x 10 4 cells, and were transfected with 500 ng/μl left, right sTALED-V28R and pAAV-sTALED-V28R using 3.5 μl of Lipofectamine 3000 after 24 h. For UDC transfections, the electroporation method (NEON, Thermo Fisher, Lonza nucleofector X unit, Lonza) was used. .. Specifically, the sTALED plasmids confirmed by sanger sequencing were extracted using a Article Title: Pathways and products of base excision DNA repair in Xenopus laevis eggs: contrast with human cell pathways Article Snippet: Subsequently, 9 ml of buffer QBT (Qiagen, 12143) was added to the solution with constant shaking. .. The plasmid was then purified using a Article Title: Mast cell-specific CysLT2 receptor signaling inhibits cysteinyl leukotriene-dependent mast cell activation and type 2 allergic lung inflammation Article Snippet: RT2 First Strand Kit , QIAGEN , Cat No./ID: 330404. .. QIAGEN Plasmid Plus Kit, Transfection:Article Title: In vivo mitochondrial base editing restores genotype and visual function in a mouse model of LHON. Article Snippet: For MEF cell 519 AR TI CL E IN P RE SS ARTICLE IN PRESS 22 transfections, cells were seeded onto 24-well plates (SPL) with density of 1*104 cells, and were 520 transfected with 500 ng/μl left, right sTALED-V28R and pAAV-sTALED-V28R using 3.5 μl of 521 Lipofectamine 3000 after 24 h. For UDC transfections, the electroporation method (NEON, 522 Thermo Fisher, Lonza nucleofector X unit, Lonza) was used. .. Specifically, the sTALED plasmids 523 confirmed by sanger sequencing were extracted using a Article Title: STAMPS: Signal-peptide Transformer for Augmenting Mammalian Protein Secretion Article Snippet: .. The culture was then Article Title: In vivo mitochondrial base editing restores genotype and visual function in a mouse model of LHON Article Snippet: Cells were transfected with 500 ng/μl left, right DddA11, Hifi-DdCBE, sTALED-V28R, using 1.5 μl of Lipofectamine 3000 (Invitrogen) after 24 h. For MEF cell transfections, cells were seeded onto 24-well plates (SPL) with density of 1 x 10 4 cells, and were transfected with 500 ng/μl left, right sTALED-V28R and pAAV-sTALED-V28R using 3.5 μl of Lipofectamine 3000 after 24 h. For UDC transfections, the electroporation method (NEON, Thermo Fisher, Lonza nucleofector X unit, Lonza) was used. .. Specifically, the sTALED plasmids confirmed by sanger sequencing were extracted using a Isolation:Article Title: Optogenetics-enabled discovery of integrated stress response modulators. Article Snippet: Article Optogenetics-enabled discovery of integrated stress response modulators Graphical abstract Highlights • An optogenetics platform specifically induces the integrated stress response • This platform enables a high-throughput screen of 370,830 compounds • Identified compounds selectively eliminate ISR-high cells across diverse stressors • These compounds demonstrate broad-spectrum antiviral activity in vitro and in mice Authors Felix Wong, Alicia Li, Satotaka Omori, ..., Hahn Kim, James J. Collins, Maxwell Z. Wilson Correspondence felix@integratedbiosciences.com (F.W.), jimjc@mit.edu (J.J.C.), max@integratedbiosciences.com (M.Z.. W.) In brief An optogenetics-enabled drug screening platform facilitates targeting of the integrated stress response, leading to the identification of compounds that selectively potentiate ISR signaling across diverse stressors and exhibit broad-spectrum antiviral activity.. Wong et al., 2025, Cell 188, 4950–4967 September 4, 2025 © 2025 Elsevier Inc. All rights are reserved, including those for text and data mining, AI training, and similar technologies. https://doi.org/10.1016/j.cell.2025.06.024 ll Amplification:Article Title: Optogenetics-enabled discovery of integrated stress response modulators. Article Snippet: Article Optogenetics-enabled discovery of integrated stress response modulators Graphical abstract Highlights • An optogenetics platform specifically induces the integrated stress response • This platform enables a high-throughput screen of 370,830 compounds • Identified compounds selectively eliminate ISR-high cells across diverse stressors • These compounds demonstrate broad-spectrum antiviral activity in vitro and in mice Authors Felix Wong, Alicia Li, Satotaka Omori, ..., Hahn Kim, James J. Collins, Maxwell Z. Wilson Correspondence felix@integratedbiosciences.com (F.W.), jimjc@mit.edu (J.J.C.), max@integratedbiosciences.com (M.Z.. W.) In brief An optogenetics-enabled drug screening platform facilitates targeting of the integrated stress response, leading to the identification of compounds that selectively potentiate ISR signaling across diverse stressors and exhibit broad-spectrum antiviral activity.. Wong et al., 2025, Cell 188, 4950–4967 September 4, 2025 © 2025 Elsevier Inc. All rights are reserved, including those for text and data mining, AI training, and similar technologies. https://doi.org/10.1016/j.cell.2025.06.024 ll Polymerase Chain Reaction:Article Title: Optogenetics-enabled discovery of integrated stress response modulators. Article Snippet: Article Optogenetics-enabled discovery of integrated stress response modulators Graphical abstract Highlights • An optogenetics platform specifically induces the integrated stress response • This platform enables a high-throughput screen of 370,830 compounds • Identified compounds selectively eliminate ISR-high cells across diverse stressors • These compounds demonstrate broad-spectrum antiviral activity in vitro and in mice Authors Felix Wong, Alicia Li, Satotaka Omori, ..., Hahn Kim, James J. Collins, Maxwell Z. Wilson Correspondence felix@integratedbiosciences.com (F.W.), jimjc@mit.edu (J.J.C.), max@integratedbiosciences.com (M.Z.. W.) In brief An optogenetics-enabled drug screening platform facilitates targeting of the integrated stress response, leading to the identification of compounds that selectively potentiate ISR signaling across diverse stressors and exhibit broad-spectrum antiviral activity.. Wong et al., 2025, Cell 188, 4950–4967 September 4, 2025 © 2025 Elsevier Inc. All rights are reserved, including those for text and data mining, AI training, and similar technologies. https://doi.org/10.1016/j.cell.2025.06.024 ll Cloning:Article Title: Optogenetics-enabled discovery of integrated stress response modulators. Article Snippet: Article Optogenetics-enabled discovery of integrated stress response modulators Graphical abstract Highlights • An optogenetics platform specifically induces the integrated stress response • This platform enables a high-throughput screen of 370,830 compounds • Identified compounds selectively eliminate ISR-high cells across diverse stressors • These compounds demonstrate broad-spectrum antiviral activity in vitro and in mice Authors Felix Wong, Alicia Li, Satotaka Omori, ..., Hahn Kim, James J. Collins, Maxwell Z. Wilson Correspondence felix@integratedbiosciences.com (F.W.), jimjc@mit.edu (J.J.C.), max@integratedbiosciences.com (M.Z.. W.) In brief An optogenetics-enabled drug screening platform facilitates targeting of the integrated stress response, leading to the identification of compounds that selectively potentiate ISR signaling across diverse stressors and exhibit broad-spectrum antiviral activity.. Wong et al., 2025, Cell 188, 4950–4967 September 4, 2025 © 2025 Elsevier Inc. All rights are reserved, including those for text and data mining, AI training, and similar technologies. https://doi.org/10.1016/j.cell.2025.06.024 ll Purification:Article Title: Pathways and products of base excision DNA repair in Xenopus laevis eggs: contrast with human cell pathways Article Snippet: Subsequently, 9 ml of buffer QBT (Qiagen, 12143) was added to the solution with constant shaking. .. The plasmid was then purified using a Article Title: Overexpression of Interleukin-17 Modulates Responses to Marek's Disease Virus Infection and Tumor Formation in Chickens. Article Snippet: .. In brief, DH5α-competent bacterial cells were transformed with the pCDNA3.1/ V5-HIS TOPO and pCDNA3.1/rchIL-17A-V5-HIS TOPO plasmids to propagate the respective plasmids for purification with a Transformation Assay:Article Title: Overexpression of Interleukin-17 Modulates Responses to Marek's Disease Virus Infection and Tumor Formation in Chickens. Article Snippet: .. In brief, DH5α-competent bacterial cells were transformed with the pCDNA3.1/ V5-HIS TOPO and pCDNA3.1/rchIL-17A-V5-HIS TOPO plasmids to propagate the respective plasmids for purification with a |
