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RAD1 Protein (AA 1-282) (His tag)

RAD1 Origine: Humain Hôte: Escherichia coli (E. coli) Recombinant > 90 % by SDS - PAGE SDS
N° du produit ABIN7279094
  • Antigène Voir toutes RAD1 Protéines
    RAD1 (Cell Cycle Checkpoint Protein RAD1 (RAD1))
    Type de proteíne
    Recombinant
    Attributs du protein
    AA 1-282
    Origine
    • 5
    • 1
    Humain
    Source
    • 2
    • 2
    • 1
    • 1
    Escherichia coli (E. coli)
    Purification/Conjugué
    Cette RAD1 protéine est marqué à la His tag.
    Application
    SDS-PAGE (SDS)
    Attributs du produit
    RAD1, 1-282aa, Human, His tag, E.coli
    Pureté
    > 90 % by SDS - PAGE
    Top Product
    Discover our top product RAD1 Protéine
  • Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.5 mg/ml (determined by Bradford assay)
    Buffer
    Liquid. In 20 mM Tris-HCl buffer (pH8.0) containing 0.2M Nacl, 1mM DTT, 10% glycerol
    Stock
    4 °C
  • Antigène
    RAD1 (Cell Cycle Checkpoint Protein RAD1 (RAD1))
    Autre désignation
    RAD1 (RAD1 Produits)
    Synonymes
    HRAD1 Protein, REC1 Protein, zgc:56502 Protein, zgc:77779 Protein, RAD1 Protein, xrad1 Protein, DKFZp459H1127 Protein, RAD1 checkpoint DNA exonuclease Protein, RAD1 homolog (S. pombe) Protein, RAD1 Protein, Rad1 Protein, rad1 Protein
    Sujet
    RAD1 is a component of a heterotrimeric cell cycle checkpoint complex, known as the 9-1-1 complex, that is activated to stop cell cycle progression in response to DNA damage or incomplete DNA replication. This complex also contains the Rad9 and Hus1 proteins and is believed to be involved in cellular responses to DNA damage, possibly by associating with Rad17 and several components of the PCNA-loading heteropentamer, replication factor C. Recombinant human RAD1 protein, fused to His-tag at N-terminus, was expressed in E.coli and purified by using conventional chromatography techniques. Synonyms: HRAD1, REC1, Cell cycle checkpoint protein RAD1. NCBI no.: NP_002844
    Poids moléculaire
    33.9 kDa (302aa) confirmed by MALDI-TOF
    Pathways
    M Phase
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