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Glucagon Kit ELISA

GCG Reactivité: Poulet Colorimetric Competition ELISA 18.52 pg/mL - 1500 pg/mL Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Homogenate
N° du produit ABIN5654583
  • Antigène Voir toutes Glucagon (GCG) Kits ELISA
    Glucagon (GCG)
    Reactivité
    • 10
    • 6
    • 6
    • 5
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Poulet
    Méthode de détection
    Colorimetric
    Type de méthode
    Competition ELISA
    Gamme de detection
    18.52 pg/mL - 1500 pg/mL
    Seuil minimal de détection
    18.52 pg/mL
    Application
    ELISA
    Type d'échantillon
    Cell Culture Supernatant, Cell Lysate, Plasma, Serum, Tissue Homogenate
    Analytical Method
    Quantitative
    Specificité
    This assay has high sensitivity and excellent specificity for detection of Glucagon (GC). No significant cross-reactivity or interference between Glucagon (GC) and analogues was observed.
    Sensibilité
    7.59 pg/mL
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  • 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 h
    Plaque
    Pre-coated
    Protocole
    This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to Glucagon (GC) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled Glucagon (GC) and unlabeled Glucagon (GC) (Standards or samples) with the pre-coated antibody specific to Glucagon (GC). After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of Glucagon (GC) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of Glucagon (GC) in the sample.
    Précision du teste
    Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Glucagon (GC) were tested 20 times on one plate, respectively
    Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Glucagon (GC) 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
    The Stop Solution is acidic. 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 Glucagon (GCG) Kits ELISA
    Glucagon (GCG)
    Autre désignation
    Glucagon (GCG Produits)
    Synonymes
    GLP1 Kit ELISA, GLP2 Kit ELISA, GRPP Kit ELISA, GLP-1 Kit ELISA, Glu Kit ELISA, PPG Kit ELISA, GCG Kit ELISA, gcg-A Kit ELISA, gcg1 Kit ELISA, glucagon Kit ELISA, glucagon L homeolog Kit ELISA, GCG Kit ELISA, Gcg Kit ELISA, gcg.L Kit ELISA
    Sujet

    Gene Name: Glucagon

    Gene Aliases: GCG, GLP1, GLP2, GRPP, Glicentin-Related Polypeptide, Glucagen, Oxyntomodulin, Incretin hormone

    Pathways
    Positive Regulation of Peptide Hormone Secretion, Peptide Hormone Metabolism, cAMP Metabolic Process, Regulation of Carbohydrate Metabolic Process, Feeding Behaviour, Negative Regulation of intrinsic apoptotic Signaling
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