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Human Monoclonal POLD1 Primary Antibody for WB - ABIN151923
Kundu, Balusu, Jaiswal, Narayan: Adenomatous polyposis coli-mediated hypersensitivity of mouse embryonic fibroblast cell lines to methylmethane sulfonate treatment: implication of base excision repair pathways. in Carcinogenesis 2007
Show all 3 Pubmed References
in Drosophila the alternative TRF1/BRF complex appears responsible for the initiation of all known classes of Pol III transcription
DNA polymerase delta catalytic subunit controls noncentrosomal gammaTuRC activity and regulates the organization of Golgi-derived microtubules.
POLH (show POLH Antibodies) & POLK (show PAPD7 Antibodies) are both able to exchange with PolD1 stalled at repetitive CFS (common fragile sites) sequences. POLD1 synthesis was inhibited by replication stress caused by aphidicolin, preventing any replication past CFS. Importantly, POLH (show POLH Antibodies) & POLK (show PAPD7 Antibodies) were still proficient in rescuing this stalled POLD1 synthesis. POLD1 stalling at CFSs allows for free exchange with specialized polymerase that is not driven by PCNA (show PCNA Antibodies).
To our knowledge, the four Valencian families included in the present study are the only families where the POLD1 Leu474Pro mutation has been found.
We demonstrated an association between six previously published single nucleotide polymorphisms (rs15869 [ BRCA2 (show BRCA2 Antibodies)], rs1805389 [ LIG4 (show LIG4 Antibodies)], rs8079544 [ TP53 (show TP53 Antibodies)], rs25489 [ XRCC1 (show XRCC1 Antibodies)], rs1673041 [ POLD1], and rs11615 [ ERCC1 (show ERCC1 Antibodies)]) and subsequent CNS tumors in survivors of childhood cancer treated by radiation therapy.
The proofreading activity of DNA polymerase delta plays a role in shunting DNA mismatch repair to an EXO1 (show EXO1 Antibodies)-dependent excision pathway as opposed to directly participating in gap formation via its 3'-5' exonuclease (show EXOSC10 Antibodies) activity.
Frameshift mutation in POLD1 gene is associated with mismatch repair-deficiency and Lynch syndrome.
the pathogenic role of the POLD1-R689W mutation in the development of the human tumor and emphasize the need to experimentally determine the significance of Poldelta variants present in sporadic tumors.
Our work highlights that mutations in different POLD1 domains can lead to phenotypic variability, ranging from dominantly inherited cancer predisposition syndromes, to mild MDPL phenotypes
Germline or somatic variants in the POLE/POLD1 were identified in unresolved suspected Lynch syndrome cancers with mismatch repair defect.
WRN (show RECQL2 Antibodies) or the Bloom syndrome helicase (BLM (show BLM Antibodies)) stimulates DNA polymerase delta progression across telomeric G-rich repeats, only WRN (show RECQL2 Antibodies) promotes sequential strand displacement synthesis and FEN1 (show FEN1 Antibodies) cleavage.
reducing expression of individual PRMT7 (show PRMT7 Antibodies) target DNA repair genes showed that only the catalytic subunit of DNA polymerase (show POLB Antibodies), POLD1, was able to resensitize PRMT7 (show PRMT7 Antibodies) knock-down cells to DNA-damaging agents.
A point mutation (D400A) in the proofreading domain of DNA polymerase delta, encoded by the Pold1 gene, inactivates the 3' --> 5' exonuclease (show EXOSC10 Antibodies) of poldelta and causes a mutator and epithelial cancer phenotype in a recessive manner.
Heterozygous mutation at L604 in the polymerase active site of DNA polymerase delta reduces life span, increases genomic instability, and accelerates tumorigenesis in an allele-specific manner, novel findings that have implications for human cancer.
DNA polymerase delta is essential for mammalian early embryogenesis, and the 3'-5' exonuclease (show EXOSC10 Antibodies) activity of DNA polymerase delta is dispensable for normal development but necessary to suppress tumorigenesis
This gene encodes the 125-kDa catalytic subunit of DNA polymerase delta. DNA polymerase delta possesses both polymerase and 3' to 5' exonuclease activity and plays a critical role in DNA replication and repair. Alternatively spliced transcript variants have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 6.
, DNA polymerase delta
, DNA polymerase-delta
, lethal (3) 72Ac
, DNA polymerase delta catalytic subunit
, DNA-dependent DNA polymerase
, DNA polymerase delta subunit 3
, polymerase (DNA directed), delta 3
, polymerase (DNA-directed), delta 3, accessory subunit
, DNA-directed DNA polymerase delta 3
, DNA polymerase subunit delta 3
, polymerase (DNA directed), delta 1, catalytic subunit 125kDa
, DNA-directed DNA polymerase delta 1
, DNA polymerase delta catalytic subunit-like
, CDC2 homolog
, DNA polymerase subunit delta p125
, DNA polymerase delta 1, catalytic domain
, DNA polymerase delta, catalytic subunit