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The role of XLF in NHEJ is summarized.
XLF has an important role during V(D)J recombination.
using dual- and quadruple-trap optical tweezers combined with fluorescence microscopy, we show how human XRCC4 (show XRCC4 ELISA Kits), XLF and XRCC4 (show XRCC4 ELISA Kits)-XLF complexes interact with DNA in real time
The data suggest that XLF has multiple functions in DNA repair, and they offer potential explanations for the pleiotropic phenotypes associated with XLF deficiency.
PC4 (show IFRD1 ELISA Kits) protects esophageal squamous cell carcinoma cells from IR-induced death by enhancing the nonhomologous end joining-promoting activity of XLF.
Phosphorylation of XLF impairs non-homologous end-joining DNA repair.
Werner syndrome protein positively regulates XRCC4-like factor transcription.
Human XLF is a non-essential, but critical, classic non-homologous end-joining -repair factor.
An induced pluripotent stem cell (iPSC) model of XLF deficiency, which accurately replicates the double-strand break repair deficiency observed in XLF syndrome patients, is reported.
Data indicate that Ku70 (show XRCC6 ELISA Kits)/Ku80 (show XRCC5 ELISA Kits) facilitates the cooperative binding of multiple XRCC4 (show XRCC4 ELISA Kits)/Ligase IV (XL) and XLF molecules to DNA.
PAXX and XLF proteins may have redundant functions during Non-homologous end joining.
Paxx/Xlf double-knockout mice display embryonic lethality associated with genomic instability, cell death in the central nervous system, and an almost complete block in lymphogenesis
These results reveal an unanticipated functional interplay between the RAG complex and XLF in repairing RAG-induced DNA breaks and maintaining genome integrity during antigen receptor gene assembly.
XLF-deficient mice recapitulate the age-dependent lymphocytopenia of patients.
XLF functionally overlaps with DNA-PKcs in normal development, promotion of genomic stability in fibroblasts, and in IgH class switch recombination in mature B cells.
Cernunnos deficiency results in chronic activation of the DNA damage response, P53 (show TP53 ELISA Kits)-driven upregulation of proapoptotic factors, leading to decreased thymocyte viability and a qualitative alteration of the T cell repertoire in both humans and mice.
XLF repair protein and 53BP1 (show TP53BP1 ELISA Kits) DNA damage response factor have overlapping functions in end joining and lymphocyte development
find that combined XLF/53BP1 (show TP53BP1 ELISA Kits) deficiency in mice severely impairs C-NHEJ, V(D)J recombination, and lymphocyte development while also leading to general genomic instability and growth defects
XLF, ATM and H2AX all have fundamental roles in processing and joining DNA ends during V(D)J recombination, but that these roles have been masked by unanticipated functional redundancies
Double-strand breaks in DNA result from genotoxic stresses and are among the most damaging of DNA lesions. This gene encodes a DNA repair factor essential for the nonhomologous end-joining pathway, which preferentially mediates repair of double-stranded breaks. Mutations in this gene cause different kinds of severe combined immunodeficiency disorders.
nonhomologous end-joining factor 1
, non-homologous end-joining factor 1
, XRCC4-like factor
, protein cernunnos