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data further suggest that ARTD2 would function in double strand break repair as a dimeric module, while in single strand break repair it would function as a monomer.
Report a requirement for PARP2 in stabilizing replication forks that encounter base excision repair (BER) intermediates through Fbh1-dependent regulation of Rad51 (zeige RAD51 Proteine). Whereas PARP2 is dispensable for tolerance of cells to single stranded breaks or homologous recombination dysfunction, it is redundant with PARP1 (zeige PARP1 Proteine) in BER.
PARP2 specifically limits the accumulation of the resection barrier factor 53BP1 (zeige TP53BP1 Proteine) at DNA damage sites, allowing efficient CtIP (zeige RBBP8 Proteine)-dependent DNA end-resection
either PARP1 (zeige PARP1 Proteine) or PARP2 are sufficient for near-normal XRCC1 (zeige XRCC1 Proteine) recruitment at oxidative single-strand breaks
Studies indicate that poly(ADP-ribose) polymerase 2 (PARP2) is involved in the differentiation of several cell types, including erythrocytes, T cells and adipocytes.
Findings indicate that Increased poly(ADP-ribose) polymerase-2 (PARP-2) expression and loss of micrRNA miR (zeige MLXIP Proteine)-149 expression are involved in the pathogenesis of hepatocellular carcinomas (HCC (zeige FAM126A Proteine)) and are poor prognosis factors in patients with HCC (zeige FAM126A Proteine).
Data show that E7449 represents a dual Poly(ADP-ribose) Polymerase 1 (zeige PARP1 Proteine)/2 and tankyrase 1 (zeige TNKS Proteine)/2 inhibitor which has the advantage of targeting Wnt (zeige WNT2 Proteine)/beta-catenin (zeige CTNNB1 Proteine) signaling addicted tumors.
The initial affinity between the PARP1 (zeige PARP1 Proteine), PARP2 and the DNA damaged site appears to influence both the size of the Poly(ADP-Ribose) synthesized and the time of residence of PARylated PARP1 (zeige PARP1 Proteine) and PARP2 on DNA damages.
Our data suggest for the first time that a SNP in PARP2, rs878156, may together with other genetic variants modulate cancer specific survival in breast cancer patients depending on chemotherapy
Our study differentiates the functions of PARP-2 domains from those of PARP-1 (zeige PARP1 Proteine), the other major DDR (zeige DDR1 Proteine)-PARP, and highlights the specialization of the multi-domain architectures of DDR (zeige DDR1 Proteine)-PARPs.
PARP2 protein deficiency protected mice from Concanavalin A -induced Liver Damage.
Activation of either PARP-1 (zeige PARP1 Proteine) or -2 is likely to play a role in muscle protein catabolism via oxidative stress, NF-kappaB (zeige NFKB1 Proteine) signaling, and enhanced proteasomal degradation in cancer-induced cachexia.
PARP1 (zeige PARP1 Proteine)/2 inhibitor simmiparib causes growth inhibition in cancer cell- or tissue-derived xenografts in nude mice.
The findings highlight specific non-overlapping functions of PARP1 (zeige PARP1 Proteine) and PARP2 at H2AX (zeige H2AFX Proteine)-deficient chromatin during replicative phases of the cell cycle and uncover a unique requirement for PARP1 (zeige PARP1 Proteine) in nonhomologous end-joining-deficient cells.
Data show reduced tumor burden through increased oxidative stress in lung adenocarcinoma cells of PARP-1 (zeige PARP1 Proteine) and PARP-2 knockout mice.
PARP-2 has an essential role in erythropoiesis by limiting replicative stress in erythroid progenitors.
PARP-1 (zeige PARP1 Proteine) and -2 play a role in cancer-induced cachexia, thus selective pharmacological inhibition of PARP-1 (zeige PARP1 Proteine) and -2 may be of interest in clinical settings
the depletion of PARP-2 leads to lower HDL (zeige HSD11B1 Proteine) levels which represent a risk factor to cardiovascular diseases.
This study represents the first description of a significant role for PARP-2 in neuroinflammation and neurological dysfunction in Experimental autoimmune encephalomyelitis
our data show that PARP-2 can directly regulate base excision repair proteins
We found that larger deletions of >20 bp predominated after DSB repair in ku80 (zeige XRCC5 Proteine) and ku80 (zeige XRCC5 Proteine) parp1 parp2 mutants, corroborating with a role of KU in preventing DSB end resection. Deletion lengths did not significantly differ between ku80 (zeige XRCC5 Proteine) and ku80 (zeige XRCC5 Proteine) parp1 parp2 mutants, suggesting that a KU- and PARP (zeige PARP1 Proteine)-independent b-NHEJ mechanism becomes active in these mutants.
we have found that although plant PARPs and PARGs have partially overlapping functions Arabidopsis PARP2 and PARG1 play the predominant roles in plant poly(ADP-ribosyl)ation during DNA damage and immune responses.
whilst all isoforms of PARP (zeige PARP1 Proteine) were localized to the nucleus they are also present in non-nuclear locations with parp1 and parp3 (zeige PARP3 Proteine) also localised in the cytosol, and parp2 also present in the mitochondria
Studies indicate that a massive and rapid accumulation of a massive and rapid accumulation poly(ADP-ribose) polymerases AtPARP1 and AtPARP2 transcripts was observed upon treatment with ionizing radiation and reactive oxigen species (ROS (zeige ROS1 Proteine)).
Poly(ADP-ribose)polymerase (zeige PARP1 Proteine) activity controls plant growth by promoting leaf cell number.
Evidence suggests a link between the glutathione pool and PARP (zeige PARP1 Proteine) expression and activity that is perhaps related to the distribution of intracellular glutathione between the cytoplasm and the nucleus. [PARP2]
This gene encodes poly(ADP-ribosyl)transferase-like 2 protein, which contains a catalytic domain and is capable of catalyzing a poly(ADP-ribosyl)ation reaction. This protein has a catalytic domain which is homologous to that of poly (ADP-ribosyl) transferase, but lacks an N-terminal DNA binding domain which activates the C-terminal catalytic domain of poly (ADP-ribosyl) transferase. The basic residues within the N-terminal region of this protein may bear potential DNA-binding properties, and may be involved in the nuclear and/or nucleolar targeting of the protein. Two alternatively spliced transcript variants encoding distinct isoforms have been found.
ADP-ribosyltransferase (NAD+; poly(ADP-ribose) polymerase)-like 2
, ADP-ribosyltransferase diphtheria toxin-like 2
, NAD(+) ADP-ribosyltransferase 2
, poly (ADP-ribose) polymerase family, member 2
, poly (ADP-ribosyl) transferase-like 2
, poly [ADP-ribose] polymerase 2
, poly(ADP-ribose) synthetase
, poly[ADP-ribose] synthase 2
, poly[ADP-ribose] synthetase 2
, ADP-ribosyltransferase (NAD+, poly(ADP-ribose) polymerase)-like 2
, ADP-ribosyltransferase (NAD+; poly (ADP-ribose) polymerase) 2
, poly (ADP-ribose) polymerase 2
, poly [ADP-ribose] polymerase 2-like
, Poly[ADP-ribose] synthase 2