A high-throughput, flow cytometry-based method to quantify DNA-end resection in mammalian cells

Cytometry Part A

Volumn 81 A, Issue 10, 2012, Pages 922-928

  Forment, Josep V ^a   Walker, Rachael V ^b   Jackson, Stephen P ^a  

^a UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^b UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

DNA damage; DNA repair; DNA replication; DNA end resection; Flow cytometry; Homologous recombination; Replication protein A

Indexed keywords

CAMPTOTHECIN; ETOPOSIDE; REPLICATION FACTOR A; SINGLE STRANDED DNA;

ARTICLE; CELL PROLIFERATION; DNA DAMAGE; DNA REPAIR; DOUBLE STRANDED DNA BREAK; DRUG EFFECT; FLOW CYTOMETRY; GENETICS; HIGH THROUGHPUT SCREENING; HOMOLOGOUS RECOMBINATION; HUMAN; METABOLISM; METHODOLOGY; STAINING; TUMOR CELL LINE;

CAMPTOTHECIN; CELL LINE, TUMOR; CELL PROLIFERATION; DNA BREAKS, DOUBLE-STRANDED; DNA DAMAGE; DNA REPAIR; DNA, SINGLE-STRANDED; ETOPOSIDE; FLOW CYTOMETRY; HIGH-THROUGHPUT SCREENING ASSAYS; HOMOLOGOUS RECOMBINATION; HUMANS; REPLICATION PROTEIN A; STAINING AND LABELING;

EID: 84866627047     PISSN: 15524922     EISSN: 15524930     Source Type: Journal    
DOI: 10.1002/cyto.a.22155     Document Type: Article

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