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XPA Protein (AA 1-273) (His tag)

Protéine Recombinant XPA exprimée dans Escherichia coli (E. coli).
N° du produit ABIN1098757

Aperçu rapide pour XPA Protein (AA 1-273) (His tag) (ABIN1098757)

Antigène

Voir toutes XPA Protéines
XPA (Xeroderma Pigmentosum, Complementation Group A (XPA))

Type de proteíne

Recombinant

Origine

  • 3
  • 1
  • 1
Humain

Source

  • 2
  • 2
  • 1
Escherichia coli (E. coli)

Application

SDS-PAGE (SDS)

Pureté

> 85 %
  • Attributs du protein

    AA 1-273

    Purification/Conjugué

    Cette XPA protéine est marqué à la His tag.

    Séquence

    MAAADGA LPEAAALEQP AELPASVRAS IERKRQRALM LRQARLAARP YSATAAAATG GMANVKAAPK IIDTGGGFIL EEEEEEEQKI GKVVHQPGPV MEFDYVICEE CGKEFMDSYL MNHFDLPTCD NCRDADDKHK LITKTEAKQE YLLKDCDLEK REPPLKFIVK KNPHHSQWGD MKLYLKLQIV KRSLEVWGSQ EALEEAKEVR QENREKMKQK KFDKKVKELR RAVRSSVWKR ETIVHQHEYG PEENLEDDMY RKTCTMCGHE LTYEKM

    Purification

    > 85% by SDS-PAGE
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  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Commentaires

    Synonyms: DNA repair protein complementing XP-A cells, XP1, XPAC

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    20 mM Tris-HCl buffer ( pH 8.0) containing 0.4M urea, 10 % glycerol

    Stock

    4 °C,-20 °C,-80 °C

    Stockage commentaire

    Can be stored at +2C to +8C for 1 week. For long term storage, aliquot and store at -20C to -80C. Avoid repeated freezing and thawing cycles.
  • Antigène

    XPA (Xeroderma Pigmentosum, Complementation Group A (XPA))

    Autre désignation

    XPA

    Sujet

    XPA, also known as DNA repair protein complementing XP-A cells, belong to the XPA family. This protein is involved in DNA excision repair. It Initiates repair by binding to damaged sites with various affinities, depending on the photoproduct and the transcriptional state of the region. Defects in XPA are a cause of xeroderma pigmentosum complementation group A (XP-A), which is a rare human autosomal recessive disease characterized by solar sensitivity, high predisposition for developing cancers on areas exposed to sunlight and, in some cases, neurological abnormalities. Recombinant human XPA protein, fused to His-tag at N-terminus, was expressed in E. coli.

    Poids moléculaire

    33.8 kDa (296aa)

    NCBI Accession

    NP_000371

    Pathways

    Réparation de l'ADN
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