pc version 6 1 bio rad n a maxquant (Bio-Rad)
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pc version 6 1 bio rad n a maxquant
Pc Version 6 1 Bio Rad N A Maxquant, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 99/100, based on 1326 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/pc+version+6+1+bio+rad+n+a+maxquant/Image+Lab+Software+for+PC+Version+6%2E0%2E1/pm40578345-292-217-220
Average 99 stars, based on 1326 article reviews
Pc Version 6 1 Bio Rad N A Maxquant, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 99/100, based on 1326 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/pc+version+6+1+bio+rad+n+a+maxquant/Image+Lab+Software+for+PC+Version+6%2E0%2E1/pm40578345-292-217-220
Average 99 stars, based on 1326 article reviews
pc version 6 1 bio rad n a maxquant - by Bioz Stars,
2026-09
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Reverse Transcription:Article Title: Microprotein SMIM26 drives oxidative metabolism via serine-responsive mitochondrial translation. Article Snippet: Article Microprotein SMIM26 drives oxidative metabolism via serine-responsive mitochondrial translation Graphical abstract Highlights • CRISPR screen identifies SMIM26 as linking the folate cycle to complex I biogenesis • SMIM26-SFXN1/2-mitoribosome triad promotes serinedependent mt-ND5 translation • SMIM26 loss disrupts mitochondrial tRNA modifications and impairs complex I assembly • SMIM26 is essential for embryonic development and tumor growth in folate-dependent AML Authors Jiemin Nah, Sreya Mahendran, Baptiste Kerouanton, ..., Gregory S. Ducker, David A. Stroud, Lena Ho Correspondence lena@ho-lab.org In brief Nah et al. identify the microprotein SMIM26 as a critical link between mitochondrial serine metabolism and complex I biogenesis.. By scaffolding serine transporters and mitoribosomes, SMIM26 enables nutrient-responsive translation of mt-ND5, revealing a metabolite-gated mechanism for respiratory complex assembly with implications for development and cancer metabolism.. Nah et al., 2025, Molecular Cell 85, 1–17 July 17, 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.molcel.2025.05.033 ll Molecular Cell 85, 1, July 17, 2025 © 2025 Elsevier Inc. 1 All rights are reserved, including those for text and data mining, AI training, and similar technologies. Quantitative RT-PCR:Article Title: Microprotein SMIM26 drives oxidative metabolism via serine-responsive mitochondrial translation. Article Snippet: Article Microprotein SMIM26 drives oxidative metabolism via serine-responsive mitochondrial translation Graphical abstract Highlights • CRISPR screen identifies SMIM26 as linking the folate cycle to complex I biogenesis • SMIM26-SFXN1/2-mitoribosome triad promotes serinedependent mt-ND5 translation • SMIM26 loss disrupts mitochondrial tRNA modifications and impairs complex I assembly • SMIM26 is essential for embryonic development and tumor growth in folate-dependent AML Authors Jiemin Nah, Sreya Mahendran, Baptiste Kerouanton, ..., Gregory S. Ducker, David A. Stroud, Lena Ho Correspondence lena@ho-lab.org In brief Nah et al. identify the microprotein SMIM26 as a critical link between mitochondrial serine metabolism and complex I biogenesis.. By scaffolding serine transporters and mitoribosomes, SMIM26 enables nutrient-responsive translation of mt-ND5, revealing a metabolite-gated mechanism for respiratory complex assembly with implications for development and cancer metabolism.. Nah et al., 2025, Molecular Cell 85, 1–17 July 17, 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.molcel.2025.05.033 ll Molecular Cell 85, 1, July 17, 2025 © 2025 Elsevier Inc. 1 All rights are reserved, including those for text and data mining, AI training, and similar technologies. SYBR Green Assay:Article Title: Microprotein SMIM26 drives oxidative metabolism via serine-responsive mitochondrial translation. Article Snippet: Article Microprotein SMIM26 drives oxidative metabolism via serine-responsive mitochondrial translation Graphical abstract Highlights • CRISPR screen identifies SMIM26 as linking the folate cycle to complex I biogenesis • SMIM26-SFXN1/2-mitoribosome triad promotes serinedependent mt-ND5 translation • SMIM26 loss disrupts mitochondrial tRNA modifications and impairs complex I assembly • SMIM26 is essential for embryonic development and tumor growth in folate-dependent AML Authors Jiemin Nah, Sreya Mahendran, Baptiste Kerouanton, ..., Gregory S. Ducker, David A. Stroud, Lena Ho Correspondence lena@ho-lab.org In brief Nah et al. identify the microprotein SMIM26 as a critical link between mitochondrial serine metabolism and complex I biogenesis.. By scaffolding serine transporters and mitoribosomes, SMIM26 enables nutrient-responsive translation of mt-ND5, revealing a metabolite-gated mechanism for respiratory complex assembly with implications for development and cancer metabolism.. Nah et al., 2025, Molecular Cell 85, 1–17 July 17, 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.molcel.2025.05.033 ll Molecular Cell 85, 1, July 17, 2025 © 2025 Elsevier Inc. 1 All rights are reserved, including those for text and data mining, AI training, and similar technologies. GSH Assay:Article Title: Microprotein SMIM26 drives oxidative metabolism via serine-responsive mitochondrial translation. Article Snippet: Article Microprotein SMIM26 drives oxidative metabolism via serine-responsive mitochondrial translation Graphical abstract Highlights • CRISPR screen identifies SMIM26 as linking the folate cycle to complex I biogenesis • SMIM26-SFXN1/2-mitoribosome triad promotes serinedependent mt-ND5 translation • SMIM26 loss disrupts mitochondrial tRNA modifications and impairs complex I assembly • SMIM26 is essential for embryonic development and tumor growth in folate-dependent AML Authors Jiemin Nah, Sreya Mahendran, Baptiste Kerouanton, ..., Gregory S. Ducker, David A. Stroud, Lena Ho Correspondence lena@ho-lab.org In brief Nah et al. identify the microprotein SMIM26 as a critical link between mitochondrial serine metabolism and complex I biogenesis.. By scaffolding serine transporters and mitoribosomes, SMIM26 enables nutrient-responsive translation of mt-ND5, revealing a metabolite-gated mechanism for respiratory complex assembly with implications for development and cancer metabolism.. Nah et al., 2025, Molecular Cell 85, 1–17 July 17, 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.molcel.2025.05.033 ll Molecular Cell 85, 1, July 17, 2025 © 2025 Elsevier Inc. 1 All rights are reserved, including those for text and data mining, AI training, and similar technologies. Polymerase Chain Reaction:Article Title: Microprotein SMIM26 drives oxidative metabolism via serine-responsive mitochondrial translation. Article Snippet: Article Microprotein SMIM26 drives oxidative metabolism via serine-responsive mitochondrial translation Graphical abstract Highlights • CRISPR screen identifies SMIM26 as linking the folate cycle to complex I biogenesis • SMIM26-SFXN1/2-mitoribosome triad promotes serinedependent mt-ND5 translation • SMIM26 loss disrupts mitochondrial tRNA modifications and impairs complex I assembly • SMIM26 is essential for embryonic development and tumor growth in folate-dependent AML Authors Jiemin Nah, Sreya Mahendran, Baptiste Kerouanton, ..., Gregory S. Ducker, David A. Stroud, Lena Ho Correspondence lena@ho-lab.org In brief Nah et al. identify the microprotein SMIM26 as a critical link between mitochondrial serine metabolism and complex I biogenesis.. By scaffolding serine transporters and mitoribosomes, SMIM26 enables nutrient-responsive translation of mt-ND5, revealing a metabolite-gated mechanism for respiratory complex assembly with implications for development and cancer metabolism.. Nah et al., 2025, Molecular Cell 85, 1–17 July 17, 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.molcel.2025.05.033 ll Molecular Cell 85, 1, July 17, 2025 © 2025 Elsevier Inc. 1 All rights are reserved, including those for text and data mining, AI training, and similar technologies. CRISPR:Article Title: Microprotein SMIM26 drives oxidative metabolism via serine-responsive mitochondrial translation. Article Snippet: Article Microprotein SMIM26 drives oxidative metabolism via serine-responsive mitochondrial translation Graphical abstract Highlights • CRISPR screen identifies SMIM26 as linking the folate cycle to complex I biogenesis • SMIM26-SFXN1/2-mitoribosome triad promotes serinedependent mt-ND5 translation • SMIM26 loss disrupts mitochondrial tRNA modifications and impairs complex I assembly • SMIM26 is essential for embryonic development and tumor growth in folate-dependent AML Authors Jiemin Nah, Sreya Mahendran, Baptiste Kerouanton, ..., Gregory S. Ducker, David A. Stroud, Lena Ho Correspondence lena@ho-lab.org In brief Nah et al. identify the microprotein SMIM26 as a critical link between mitochondrial serine metabolism and complex I biogenesis.. By scaffolding serine transporters and mitoribosomes, SMIM26 enables nutrient-responsive translation of mt-ND5, revealing a metabolite-gated mechanism for respiratory complex assembly with implications for development and cancer metabolism.. Nah et al., 2025, Molecular Cell 85, 1–17 July 17, 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.molcel.2025.05.033 ll Molecular Cell 85, 1, July 17, 2025 © 2025 Elsevier Inc. 1 All rights are reserved, including those for text and data mining, AI training, and similar technologies. Sequencing:Article Title: Microprotein SMIM26 drives oxidative metabolism via serine-responsive mitochondrial translation. Article Snippet: Article Microprotein SMIM26 drives oxidative metabolism via serine-responsive mitochondrial translation Graphical abstract Highlights • CRISPR screen identifies SMIM26 as linking the folate cycle to complex I biogenesis • SMIM26-SFXN1/2-mitoribosome triad promotes serinedependent mt-ND5 translation • SMIM26 loss disrupts mitochondrial tRNA modifications and impairs complex I assembly • SMIM26 is essential for embryonic development and tumor growth in folate-dependent AML Authors Jiemin Nah, Sreya Mahendran, Baptiste Kerouanton, ..., Gregory S. Ducker, David A. Stroud, Lena Ho Correspondence lena@ho-lab.org In brief Nah et al. identify the microprotein SMIM26 as a critical link between mitochondrial serine metabolism and complex I biogenesis.. By scaffolding serine transporters and mitoribosomes, SMIM26 enables nutrient-responsive translation of mt-ND5, revealing a metabolite-gated mechanism for respiratory complex assembly with implications for development and cancer metabolism.. Nah et al., 2025, Molecular Cell 85, 1–17 July 17, 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.molcel.2025.05.033 ll Molecular Cell 85, 1, July 17, 2025 © 2025 Elsevier Inc. 1 All rights are reserved, including those for text and data mining, AI training, and similar technologies. Mass Spectrometry:Article Title: Microprotein SMIM26 drives oxidative metabolism via serine-responsive mitochondrial translation. Article Snippet: Article Microprotein SMIM26 drives oxidative metabolism via serine-responsive mitochondrial translation Graphical abstract Highlights • CRISPR screen identifies SMIM26 as linking the folate cycle to complex I biogenesis • SMIM26-SFXN1/2-mitoribosome triad promotes serinedependent mt-ND5 translation • SMIM26 loss disrupts mitochondrial tRNA modifications and impairs complex I assembly • SMIM26 is essential for embryonic development and tumor growth in folate-dependent AML Authors Jiemin Nah, Sreya Mahendran, Baptiste Kerouanton, ..., Gregory S. Ducker, David A. Stroud, Lena Ho Correspondence lena@ho-lab.org In brief Nah et al. identify the microprotein SMIM26 as a critical link between mitochondrial serine metabolism and complex I biogenesis.. By scaffolding serine transporters and mitoribosomes, SMIM26 enables nutrient-responsive translation of mt-ND5, revealing a metabolite-gated mechanism for respiratory complex assembly with implications for development and cancer metabolism.. Nah et al., 2025, Molecular Cell 85, 1–17 July 17, 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.molcel.2025.05.033 ll Molecular Cell 85, 1, July 17, 2025 © 2025 Elsevier Inc. 1 All rights are reserved, including those for text and data mining, AI training, and similar technologies. Western Blot:Article Title: Microprotein SMIM26 drives oxidative metabolism via serine-responsive mitochondrial translation. Article Snippet: Article Microprotein SMIM26 drives oxidative metabolism via serine-responsive mitochondrial translation Graphical abstract Highlights • CRISPR screen identifies SMIM26 as linking the folate cycle to complex I biogenesis • SMIM26-SFXN1/2-mitoribosome triad promotes serinedependent mt-ND5 translation • SMIM26 loss disrupts mitochondrial tRNA modifications and impairs complex I assembly • SMIM26 is essential for embryonic development and tumor growth in folate-dependent AML Authors Jiemin Nah, Sreya Mahendran, Baptiste Kerouanton, ..., Gregory S. Ducker, David A. Stroud, Lena Ho Correspondence lena@ho-lab.org In brief Nah et al. identify the microprotein SMIM26 as a critical link between mitochondrial serine metabolism and complex I biogenesis.. By scaffolding serine transporters and mitoribosomes, SMIM26 enables nutrient-responsive translation of mt-ND5, revealing a metabolite-gated mechanism for respiratory complex assembly with implications for development and cancer metabolism.. Nah et al., 2025, Molecular Cell 85, 1–17 July 17, 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.molcel.2025.05.033 ll Molecular Cell 85, 1, July 17, 2025 © 2025 Elsevier Inc. 1 All rights are reserved, including those for text and data mining, AI training, and similar technologies. Software:Article Title: Microprotein SMIM26 drives oxidative metabolism via serine-responsive mitochondrial translation. Article Snippet: Article Microprotein SMIM26 drives oxidative metabolism via serine-responsive mitochondrial translation Graphical abstract Highlights • CRISPR screen identifies SMIM26 as linking the folate cycle to complex I biogenesis • SMIM26-SFXN1/2-mitoribosome triad promotes serinedependent mt-ND5 translation • SMIM26 loss disrupts mitochondrial tRNA modifications and impairs complex I assembly • SMIM26 is essential for embryonic development and tumor growth in folate-dependent AML Authors Jiemin Nah, Sreya Mahendran, Baptiste Kerouanton, ..., Gregory S. Ducker, David A. Stroud, Lena Ho Correspondence lena@ho-lab.org In brief Nah et al. identify the microprotein SMIM26 as a critical link between mitochondrial serine metabolism and complex I biogenesis.. By scaffolding serine transporters and mitoribosomes, SMIM26 enables nutrient-responsive translation of mt-ND5, revealing a metabolite-gated mechanism for respiratory complex assembly with implications for development and cancer metabolism.. Nah et al., 2025, Molecular Cell 85, 1–17 July 17, 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.molcel.2025.05.033 ll Molecular Cell 85, 1, July 17, 2025 © 2025 Elsevier Inc. 1 All rights are reserved, including those for text and data mining, AI training, and similar technologies. |