Author

Ruth M. Kluck

The University of MelbourneORCID 0000-0002-7101-1925Unclaimed ORCID profile · follow to get notified of new preprints

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Ruth M. Kluck1 paper

Biology Disciplines

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Bioinformatics· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:cell signaling & trafficking· 1 Assay:long-read sequencing· 1 Organism:mouse· 1 Organism:rat· 1

Frequent Co-Authors

Matthew E. RitchieiD· 2 shared Rachel T. UreniD· 2 shared Agnes W. WongiD· 1 shared David Peter De SouzaiD· 1 shared Dmitri SviridoviD· 1 shared Etsuko Uno· 1 shared Hema Preethi Subas SatishiD· 1 shared Justin P. Ludeman· 1 shared

Activity by Year

2022-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 30 mutual co-author links

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2 shared papersCell Biology

Matthew E. RitchieORCID

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2 papers

Recent·Most cited

A lipid signature of BAK-driven apoptotic pore formation

Rachel T. Uren, Matthew E. Ritchie, Agnes W. Wong, Justin P. Ludeman, Etsuko Uno, Vinod K. Narayana, David Peter De Souza, Dmitri Sviridov, Ruth M. Kluck

The paper identifies a lipid signature associated with BAK-driven apoptotic pore formation and shows cholesterol inhibits pore formation by preventing BAK clustering.

bioRxiv · Oct 16, 2024 · PreprintCell Biology

NAb-seq: an accurate, rapid and cost-effective method for antibody long-read sequencing in hybridoma cell lines and single B cells

Hema Preethi Subas Satish, Kathleen Zeglinski, Rachel T. Uren, Stephen L. Nutt, Matthew E. Ritchie, Quentin A. Gouil, Ruth M. Kluck

NAb-seq provides a rapid, cost-effective, and species-independent method for sequencing full-length antibody genes from hybridoma cell lines and single B cells, outperforming Sanger sequencing in accuracy and throughput.

mAbs · Aug 13, 2022Peer-reviewedBioinformatics