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ADRB1 Kit ELISA

Ce kit ELISA Colorimetric est conçu pour la mesure quantitative de Humain ADRB1.
N° du produit ABIN5651472

Aperçu rapide pour ADRB1 Kit ELISA (ABIN5651472)

Antigène

Voir toutes ADRB1 Kits ELISA
ADRB1 (Adrenergic, beta-1-, Receptor (ADRB1))

Reactivité

  • 2
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  • 1
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  • 1
Humain

Méthode de détection

Colorimetric

Type de méthode

Sandwich ELISA

Gamme de detection

0.312 ng/mL - 20 ng/mL

Application

ELISA

Type d'échantillon

Cell Lysate, Tissue Homogenate
  • Seuil minimal de détection

    0.312 ng/mL

    Analytical Method

    Quantitative

    Specificité

    This assay has high sensitivity and excellent specificity for detection of Adrenergic Receptor Beta 1 (ADRb1). No significant cross-reactivity or interference between Adrenergic Receptor Beta 1 (ADRb1) and analogues was observed.

    Sensibilité

    0.122 ng/mL
  • 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

    3 h

    Plaque

    Pre-coated

    Protocole

    The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Adrenergic Receptor Beta 1 (ADRb1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Adrenergic Receptor Beta 1 (ADRb1). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Adrenergic Receptor Beta 1 (ADRb1), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Adrenergic Receptor Beta 1 (ADRb1) in the samples is then determined by comparing the O.D. of the samples to the standard curve.

    Précision du teste

    Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Adrenergic Receptor Beta 1 (ADRb1) were tested 20 times on one plate, respectively
    Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Adrenergic Receptor Beta 1 (ADRb1) 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 ADRB1 Kits ELISA

    ADRB1 (Adrenergic, beta-1-, Receptor (ADRB1))

    Autre désignation

    Adrenergic Receptor Beta 1

    Sujet

    Gene Name: Adrenergic Receptor Beta 1

    Gene Aliases: ADR-B1, ADRB1R, B1AR, BETA1AR, RHR, Beta 1 Adrenoreceptor, Beta-1 adrenoceptor

    Pathways

    cAMP Metabolic Process, Cellular Glucan Metabolic Process, Regulation of Muscle Cell Differentiation, Synaptic Membrane, Regulation of G-Protein Coupled Receptor Protein Signaling, G-protein mediated Events, Interaction of EGFR with phospholipase C-gamma, Brown Fat Cell Differentiation
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