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ERCC5 Kit CLIA

ERCC5 Reactivité: Humain Chemiluminescent Sandwich ELISA 156.25 pg/mL - 10000 pg/mL Tissue Homogenate
N° du produit ABIN5660071
  • Antigène Voir toutes ERCC5 Kits CLIA
    ERCC5 (DNA Repair Protein Complementing XP-G Cells (ERCC5))
    Reactivité
    • 3
    • 1
    Humain
    Méthode de détection
    Chemiluminescent
    Type de méthode
    Sandwich ELISA
    Gamme de detection
    156.25 pg/mL - 10000 pg/mL
    Seuil minimal de détection
    156.25 pg/mL
    Application
    ELISA
    Type d'échantillon
    Tissue Homogenate
    Analytical Method
    Quantitative
    Specificité
    This assay has high sensitivity and excellent specificity for detection of Xeroderma Pigmentosum, Complementation Group G (XPG). No significant cross-reactivity or interference between Xeroderma Pigmentosum, Complementation Group G (XPG) and analogues was observed.
    Sensibilité
    5.51 pg/mL
    Top Product
    Discover our top product ERCC5 Kit ELISA
  • Commentaires

    The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5 % within the expiration date under appropriate storage condition. To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.

    Durée du test
    2 - 3 h
    Plaque
    Pre-coated
    Protocole
    The microplate provided in this kit has been pre-coated with an antibody specific to Xeroderma Pigmentosum, Complementation Group G (XPG). Standards or samples are then added to the appropriate microplate wells with a biotin-conjugated antibody specific to Xeroderma Pigmentosum, Complementation Group G (XPG). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then the mixture of substrate A and B is added to generate glow light emission kinetics. Upon plate development, the intensity of the emitted light is proportional to the Xeroderma Pigmentosum, Complementation Group G (XPG) level in the sample or standard.,
    Précision du teste
    Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Xeroderma Pigmentosum, Complementation Group G (XPG) were tested 20 times on one plate, respectively
    Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Xeroderma Pigmentosum, Complementation Group G (XPG) were tested on 3 different plates, 8 replicates in each plate. CV(%) = SD/meanX100
    Intra-Assay: CV<10%
    Inter-Assay: CV<12%
    Restrictions
    For Research Use only
  • Conseil sur la manipulation
    Do not allow to contact skin or eyes. Calibrators, controls and specimen samples should be assayed in duplicate. Once the procedure has been started, all steps should be completed without interruption.
    Stock
    4 °C,-20 °C
    Stockage commentaire
    -20°C. Bring all reagents to room temperature before beginning test. The kit may be stored at 4°C for immediate use within two days upon arrival. Reseal any unused strips with desiccant pack. Minimize freeze/thaw cycles.
    Date de péremption
    4-8 months
  • Antigène Voir toutes ERCC5 Kits CLIA
    ERCC5 (DNA Repair Protein Complementing XP-G Cells (ERCC5))
    Autre désignation
    Xeroderma Pigmentosum, Complementation Group G (ERCC5 Produits)
    Synonymes
    COFS3 Kit CLIA, ERCM2 Kit CLIA, UVDR Kit CLIA, XPG Kit CLIA, XPGC Kit CLIA, cofs3 Kit CLIA, ercm2 Kit CLIA, uvdr Kit CLIA, xpg Kit CLIA, xpgc Kit CLIA, Xpg Kit CLIA, ERCC excision repair 5, endonuclease Kit CLIA, excision repair cross-complementation group 5 L homeolog Kit CLIA, excision repair cross-complementing rodent repair deficiency, complementation group 5 Kit CLIA, ERCC5 Kit CLIA, ercc5.L Kit CLIA, Ercc5 Kit CLIA
    Sujet

    Gene Name: Xeroderma Pigmentosum, Complementation Group G

    Gene Aliases: ERCM2, ERCC5, UVDR, XPGC, Excision Repair Cross-Complementing Rodent Repair Deficiency 5, Cockayne Syndrome, DNA repair protein complementing XP-G cells

    ID gène
    2073
    UniProt
    P28715
    Pathways
    Réparation de l'ADN
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