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PARP1 Protéine

Protéine Recombinant PARP1 exprimée dans Insect cells (Sf9).
N° du produit ABIN925018

Aperçu rapide pour PARP1 Protéine (ABIN925018)

Antigène

Voir toutes PARP1 Protéines
PARP1 (Poly (ADP-Ribose) Polymerase 1 (PARP1))

Type de proteíne

Recombinant

Origine

  • 11
  • 3
Humain

Source

  • 7
  • 2
  • 2
  • 1
  • 1
  • 1
Insect cells (Sf9)

Pureté

> 99 % as determined by SDS-PAGE.
  • Attributs du produit

    ~1,018 U/mg protein. One unit synthesizes 1 nmole of poly(ADP-ribose) per min. at 25°C, pH 7.5.

    Purification

    Affinity purified
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  • Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    20 µg at 1 mg/mL affinity-purified liquid human recombinant PARP-1 in 100 mM Tris-HCl (pH 7.5) containing 14 mM -mercaptoethanol, 0.5 mM EDTA, 0.5 mM PMSF and 10% glycerol.

    Stock

    -80 °C
  • Antigène

    PARP1 (Poly (ADP-Ribose) Polymerase 1 (PARP1))

    Autre désignation

    PARP-1

    Sujet

    The cDNA encoding human poly(ADP-ribose) polymerase (PARP) was cloned by several groups simultaneously. With the discovery of new members (homologs) of the PARP family, PARP is referred to as PARP-1. An isolated cDNA from mouse and human encoded a protein with considerable homology to the catalytic domain of PARP-1. This protein, termed PARP-2, is a 64 kDa protein that contains a nuclear localization signal (NLS) and is activated by DNA breaks, although its DNA- binding domain is very different from that of PARP-1. Evidence has accumulated that PARP plays a role in DNA repair and a substantial effort has been invested to elucidate the physiological function of the PARP pathway in cellular recovery from DNA damage. PARP has been found in the base excision repair (BER) complex with DNA polymerase-, ligase III and x-ray repair cross-complementing 1 (XRCC1). PARP- 1 and PARP-2, even though lacking the zinc- finger domains, bind to single and double strand breaks during oxidative stress. In general, it appears that an early enzymatic activation of PARP occurs upon DNA-strand break formation. Binding of PARP to a DNA nick may then cause a transient halt to cellular activity and protect the DNA from sister chromatid associated proteins such as histones. Nicotinamide is cleaved in this step from the substrate NAD+ by PARP and the so synthesized poly(ADP)-ribose (PAR) is then used to generate ATP.

    Pathways

    Apoptose, Caspase Cascade in Apoptosis, Réparation de l'ADN, Production of Molecular Mediator of Immune Response, Maintenance of Protein Location
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