PARP-3 [ARTD3] (human) (rec.) (His) (high purity)

AdipoGen Life Sciences

PARP-3 [ARTD3] (human) (rec.) (His) (high purity)

10

Research Use Only

0.2-1 mg/ml

>98%

PARP3

poly(ADP-ribose) polymerase family member 3

ADPRT3, ADPRTL2, ADPRTL3, ARTD3, IRT1, PADPRT-3, protein mono-ADP-ribosyltransferase PARP3, ADP-ribosyltransferase (NAD+; poly (ADP-ribose) polymerase)-like 2, ADP-ribosyltransferase (NAD+; poly (ADP-ribose) polymerase)-like 3, ADP-ribosyltransferase diphtheria toxin-like 3, ADPRT-3, DNA ADP-ribosyltransferase PARP3, NAD(+) ADP-ribosyltransferase 3, NAD+ ADP-ribosyltransferase 3, poly [ADP-ribose] polymerase 3, poly(ADP-ribose) synthetase-3, poly[ADP-ribose] synthase 3, poly[ADP-ribose] synthetase 3

Protein mono-ADP-ribosyltransferase PARP3

PARP-3 [ARTD3] is involved in the base excision repair (BER) pathway, by catalyzing the poly(ADP-ribosyl)ation of a limited number of acceptor proteins involved in chromatin architecture and in DNA metabolism. This modification follows DNA damages and appears as an obligatory step in a detection/signaling pathway leading to the reparation of DNA strand breaks. May link the DNA damage surveillance network to the mitotic fidelity checkpoint. Negatively influences the G1/S cell cycle progression without interfering with centrosome duplication. May be involved in the regulation of PRC2 and PRC3 complex-dependent gene silencing. - Protein. Human full-length PARP-3 [ARTD3] is fused to a HA-tag and a His-tag. Source: Sf21 cells. Liquid. In 50mM TRIS-HCl, pH 7.5, containing 100mM sodium chloride and 50mM imidazole, 0.2% NP-40 and 10% glycerol. Purity: >98% (SDS-PAGE). PARP-3 is involved in the base excision repair (BER) pathway, by catalyzing the poly(ADP-ribosyl)ation of a limited number of acceptor proteins involved in chromatin architecture and in DNA metabolism. This modification follows DNA damages and appears as an obligatory step in a detection/signaling pathway leading to the reparation of DNA strand breaks. May link the DNA damage surveillance network to the mitotic fidelity checkpoint. Negatively influences the G1/S cell cycle progression without interfering with centrosome duplication. May be involved in the regulation of PRC2 and PRC3 complex-dependent gene silencing.

-20°C,-80°C

41116100

Human