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Human Polyclonal LIG4 Primary Antibody pour IHC (p), IHC - ABIN189697
Ducu, Dayaram, Marriott: The HTLV-1 Tax oncoprotein represses Ku80 gene expression. dans Virology 2011
Show all 2 Pubmed References
Human Polyclonal LIG4 Primary Antibody pour ICC, IF - ABIN4305497
Sousa, Zub, Aas, Hanssen-Bauer, Demirovic, Sarno, Tian, Liabakk, Slupphaug: An inverse switch in DNA base excision and strand break repair contributes to melphalan resistance in multiple myeloma cells. dans PLoS ONE 2013
DNA ligase IV (LIG4) is not essential for telomere joining.
study demonstrated that there was an association between DNA ligase 4 Thr9Ile polymorphism and male infertility and suggests CT genotype as a risk factor for male infertility
An increased frequency of binucleated lymphocytes with micronuclei was increased in carriers of the T/T genotype of the LIG4 (rs1805388) gene compared to miners harbouring the C/T genotype.
Cellular NHEJ of diverse ends thus identifies the steps necessary for repair through LIG4-mediated sensing of differences in end structure and consequent dynamic remodeling of aligned ends.
This study shown that both ligase IV and XRCC4 (Montrer XRCC4 Anticorps) may act in concert to modulate the development of glioma.
We demonstrated an association between six previously published single nucleotide polymorphisms (rs15869 [ BRCA2 (Montrer BRCA2 Anticorps)], rs1805389 [ LIG4], rs8079544 [ TP53 (Montrer TP53 Anticorps)], rs25489 [ XRCC1 (Montrer XRCC1 Anticorps)], rs1673041 [ POLD1 (Montrer POLD1 Anticorps)], and rs11615 [ ERCC1 (Montrer ERCC1 Anticorps)]) and subsequent CNS tumors in survivors of childhood cancer treated by radiation therapy.
In a recombinant PNKP (Montrer PNKP Anticorps)-XRCC4 (Montrer XRCC4 Anticorps)-LigIV complex, both the PNKP (Montrer PNKP Anticorps) FHA (Montrer CRY2 Anticorps) and catalytic domains contact the XRCC4 (Montrer XRCC4 Anticorps) coiled-coil and LigIV BRCT repeats. Multipoint contacts between PNKP (Montrer PNKP Anticorps) and XRCC4 (Montrer XRCC4 Anticorps)-LigIV regulate PNKP (Montrer PNKP Anticorps) recruitment and activity within NHEJ.
Data suggest that stimulation of Artemis nuclease/DCLRE1C (Montrer DCLRE1C Anticorps) activity by XRCC4 (Montrer XRCC4 Anticorps)-DNA ligase IV hetero-complex and efficiency of blunt-end ligation are determined by structural configurations at the DNA ends. (XRCC4 (Montrer XRCC4 Anticorps) = X-ray repair cross complementing 4)
found that the rs228593, rs2267437 and rs1805388 functional polymorphisms probably alter the level of expression of the ATM (Montrer ATM Anticorps), XRCC6 (Montrer XRCC6 Anticorps) and LIG4 genes, respectively, being important in the maintenance of genomic instability in MDS (Montrer PAFAH1B1 Anticorps)
marked overlap of dyskeratosis congenita with four other genetic syndromes, confounding accurate diagnosis and subsequent management. Patients with clinical features of dyskeratosis congenita need to have genetic analysis of USB1 (Montrer USB1 Anticorps), LIG4 and GRHL2 (Montrer GRHL2 Anticorps) in addition to the classical dyskeratosis congenita genes and telomere length measurements.
The rs1805388 in LIG4 was associated with increased radioresistance.
The data firmly demonstrate Lig4(R278H) activity renders nonhomologous end-joining (NHEJ) DNA repair to be more error-prone, and predict increased error-prone NHEJ and A-EJ suppression as the cause of defective B lymphopoiesis in Lig4 patients.
To promote homology-directed r at the expense of nonhomologous end joining , we targeted DNA ligase IV, a key enzyme in the NHEJ pathway, using the inhibitor Scr7. This approach should be applicable to other customizable endonucleases
Lig4 and XRCC1 (Montrer XRCC1 Anticorps) double-deficient cells switch as efficiently as Lig4-deficient cells, clearly indicating that XRCC1 (Montrer XRCC1 Anticorps) is dispensable for A-EJ in CH12F3 cells during class switch recombination
These studies provide insight into the interplay between DNA damage responses in the developing brain and the DNA ligase IV plat (Montrer PLAT Anticorps) the role in repairing endogenously arising DNA double-strand breaks.
Lig4-deficient B cells have reduced, but still substantial, immunoglobulins class switch recombination
Homozygous DNA ligase IV R278H mutation in mice leads to leaky SCID (Montrer PRKDC Anticorps) and represents a model for human LIG4 syndrome.
Lig4 and Rad54 (Montrer RAD54L Anticorps) cooperate to support cellular proliferation, dna repair, and prevent chromosome and single chromatid aberrations
LIG4 mutations can result in either a developmental defect with immunological abnormalities or a severe combined immunodeficiency (Montrer PRKDC Anticorps) picture with normal development.
DNA Ligase IV is engaged in extrachromosomal circular major satellite DNA synthesis
DNA-PK kinase activity results in disassembly of the Ku/DNA ligase IV/Xrcc4 (Montrer XRCC4 Anticorps) complex
The protein encoded by this gene is a DNA ligase that joins single-strand breaks in a double-stranded polydeoxynucleotide in an ATP-dependent reaction. This protein is essential for V(D)J recombination and DNA double-strand break (DSB) repair through nonhomologous end joining (NHEJ). This protein forms a complex with the X-ray repair cross complementing protein 4 (XRCC4), and further interacts with the DNA-dependent protein kinase (DNA-PK). Both XRCC4 and DNA-PK are known to be required for NHEJ. The crystal structure of the complex formed by this protein and XRCC4 has been resolved. Defects in this gene are the cause of LIG4 syndrome. Alternatively spliced transcript variants encoding the same protein have been observed.
DNA ligase 4
, ligase IV, DNA, ATP-dependent
, DNA ligase IV
, DNA ligase (ATP) 4
, ligase4-like protein
, DNA ligase 4-like
, dsDNA break repair ligase
, polydeoxyribonucleotide synthase [ATP] 4
, DNA joinase
, DNA repair enzyme
, polynucleotide ligase