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The protein encoded by TDP1 is involved in repairing stalled topoisomerase I-DNA complexes by catalyzing the hydrolysis of the phosphodiester bond between the tyrosine residue of topoisomerase I and the 3-prime phosphate of DNA. Additionally we are shipping TDP1 Proteins (9) and TDP1 Kits (1) and many more products for this protein.
Showing 10 out of 66 products:
Human Polyclonal TDP1 Primary Antibody for ELISA, WB - ABIN565920
Katyal, el-Khamisy, Russell, Li, Ju, Caldecott, McKinnon: TDP1 facilitates chromosomal single-strand break repair in neurons and is neuroprotective in vivo. in The EMBO journal 2007
Show all 5 references for ABIN565920
Human Monoclonal TDP1 Primary Antibody for ELISA, WB - ABIN393275
Dexheimer, Stephen, Fivash, Fisher, Pommier: The DNA binding and 3'-end preferential activity of human tyrosyl-DNA phosphodiesterase. in Nucleic acids research 2010
Show all 5 references for ABIN393275
Human Monoclonal TDP1 Primary Antibody for EIA, IHC (p) - ABIN400858
Dexheimer, Antony, Marchand, Pommier: Tyrosyl-DNA phosphodiesterase as a target for anticancer therapy. in Anti-cancer agents in medicinal chemistry 2008
Show all 2 references for ABIN400858
AtTDP plays a clear role in the repair of topoisomerase I (show TOP1 Antibodies)-DNA complexes.
The data obtained suggest that PARP1 (show PARP1 Antibodies) and TDP1 bind in an antiparallel orientation; the N-terminus of the former protein interacts with the C-terminal domain of the latter.
Tyrosyl-DNA-phosphodiesterase I (TDP1) participates in the removal and repair of stabilized-Top2alpha cleavage complexes in human cells.
varying expression levels of TOP1 (show TOP1 Antibodies) and TDP1 polypeptides in multiple colorectal cancer cell lines and in clinical colorectal cancer samples, are reported.
both TOP1 (show TOP1 Antibodies) and TDP1 were upregulated in the tumor tissue compared to the adjacent non-tumor tissue in non-small cell lung cancer tissue
Density functional theory computations are used to acquire thermodynamic and kinetic data along the catalytic pathway, including the phosphoryl transfers of Tdp1 and subsequent hydrolysis.
TDP1 plays a role during the early stages of mammalian NHEJ. TPD1 stimulated DNA binding by XLF. TDP1 also promoted DNA binding by Ku70/80 and stimulated DNA-PK activity.
These findings suggest that the flexibility of Tdp1 active site residues may impair the resolution of mutant Tdp1 covalent phosphohistidyl intermediates
This article summarizes and compares the biochemistry, functions, and post-translational regulation of TDP1 and TDP2 (show TDP2 Antibodies), as well as the relevance of TDP1 and TDP2 (show TDP2 Antibodies) as determinants of response to anticancer agents
TDP1 and APTX (show APTX Antibodies) take part in the mitochondrial DNA repair and are apparently being transported from the cell nucleus. (Review)
Data provides insights into the possible inactivation of TDP1 in cancers and its relationship to cellular response to Top1 (show TOP1 Antibodies)-targeted drugs.
These findings provide evidence for TDP1 as a novel mitochondrial enzyme.
The interaction with Lig3alpha is promoted by serine 81 that is located within a putative S/TQ site in the N-terminus domain of TDP1.
Data indicate that TDP1 is required for neural homeostasis and reveal a widespread requisite for TDP1 function in response to acutely elevated levels of DNA topoisomerase I (Top1 (show TOP1 Antibodies))-associated DNA strand breaks.
This study provides a direct demonstration that Tdp1 repairs Topo I (show TOP1 Antibodies) covalent lesions in vivo and suggests that spinocerebellar ataxia (show USP14 Antibodies) with axonal neuropathy (SCAN1 (show CANT1 Antibodies)) arises from the recessive neomorphic mutation H493R.
Tdp1(-/-) fibroblasts exhibited deficiencies in processing 3'-phosphotyrosyl single-strand breaks and 3'-phosphoglycolate double-strand breaks, but not 3 (show CNOT3 Antibodies)'-phosphoglycolate single-strand breaks.
The protein encoded by this gene is involved in repairing stalled topoisomerase I-DNA complexes by catalyzing the hydrolysis of the phosphodiester bond between the tyrosine residue of topoisomerase I and the 3-prime phosphate of DNA. This protein may also remove glycolate from single-stranded DNA containing 3-prime phosphoglycolate, suggesting a role in repair of free-radical mediated DNA double-strand breaks. This gene is a member of the phospholipase D family and contains two PLD phosphodiesterase domains. Mutations in this gene are associated with the disease spinocerebellar ataxia with axonal neuropathy (SCAN1). While several transcript variants may exist for this gene, the full-length natures of only two have been described to date. These two represent the major variants of this gene and encode the same isoform.
tyrosyl-DNA Phosphodiesterase (Tdp1)
, tyrosyl-DNA phosphodiesterase (Tdp1)
, tyrosyl-DNA phosphodiesterase 1
, tyrosyl-DNA phosphodiesterase 1-like
, tyr-DNA phosphodiesterase 1
, protein expressed in male leptotene and zygotene spermatocytes 501
, tyrosyl-DNA phodphodiesterase 1