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single-stranded break repair by human DNA ligase III isoforms reveal biochemical differences from DNA ligase I (zeige LIG1 ELISA Kits)
The g.29661G>A and g.29059C>T polymorphisms of LIG3 may play a role in the keratoconus and Fuchs endothelial corneal dystrophy pathogenesis and can be considered as markers in these diseases.
A computational approach to determine susceptibility to cancer by evaluating the deleterious effect of nsSNP in XRCC1 (zeige XRCC1 ELISA Kits) gene on binding interaction of XRCC1 (zeige XRCC1 ELISA Kits) protein with ligase III.
In the context of tyrosine kinase (zeige TXK ELISA Kits)-activated leukemias, c-MYC (zeige MYC ELISA Kits) contributes to aberrant DNA repair through downstream targets LIG3 and PARP1 (zeige PARP1 ELISA Kits) up-regulation.
there is an absolute requirement for fully functional DNA ligase III (LIG3), but not ligase IV (LIG4 (zeige LIG4 ELISA Kits)), to facilitate the escape from a telomere-driven crisis.
Results show that overexpression of DNA ligase III in mitochondria improves mitochondrial base excision repair and enhances cell survival after oxidative stress.
data confirm previous work showing that Lig3 is required to maintain mtDNA integrity and function, and highlight a new function of ATM (zeige ATM ELISA Kits) in regulating DNA Lig3 stability and consequently mtDNA repair
Human Mre11 (zeige MRE11A ELISA Kits)/human Rad50 (zeige RAD50 ELISA Kits)/Nbs1 (zeige NBN ELISA Kits) and DNA ligase IIIalpha/XRCC1 (zeige XRCC1 ELISA Kits) protein complexes act together in an alternative nonhomologous end joining pathway.
Using our cohort of 480 breast cancer patients, we provide replicated evidence that a polymorphism near the LIG3 gene is associated with acute skin toxicity following radiotherapy.
results establish a role for Lig3 in mitochondria, but distinguish it from its interacting protein Xrcc1 (zeige XRCC1 ELISA Kits)
Telomere-internal double-strand breaks (DSBs) are also repaired by a PARP1- and Ligase3-dependent reaction, suggesting alternative non-homologous end-joining (alt-NHEJ), which relies on microhomology at DSBs.
Lig3 has an essential role in mtDNA maintenance but is dispensable for the viability of cultured cells
data reveal that the critical biological role of Lig3 is to maintain mtDNA integrity and not Xrcc1 (zeige XRCC1 ELISA Kits)-dependent DNA repair
Early embryonic lethality is due to targeted inactivation of DNA ligase III.
This gene is a member of the DNA ligase family. Each member of this family encodes a protein that catalyzes the joining of DNA ends but they each have a distinct role in DNA metabolism. The protein encoded by this gene is involved in excision repair and is located in both the mitochondria and nucleus, with translation initiation from the upstream start codon allowing for transport to the mitochondria and translation initiation from a downstream start codon allowing for transport to the nucleus. Additionally, alternate transcriptional splice variants, encoding different isoforms, have been characterized.
DNA ligase III
, ligase III, DNA, ATP-dependent
, DNA ligase (ATP) 3
, DNA ligase 3
, ligase II, DNA, ATP-dependent
, polydeoxyribonucleotide synthase [ATP] 3
, DNA ligase 3 isoform alpha
, DNA ligase 3-like
, DNA ligase III isoform alpha
, ligase III, DNA, ATP-dependent L homeolog