ENO2/NSE Kit ELISA

N° du produit ABIN2648800

Kit ELISA Humain ENO2/NSE, test Colorimetric pour la quantification de Humain ENO2/NSE.

Aperçu rapide pour ENO2/NSE Kit ELISA (ABIN2648800)

Antigène: ENO2/NSE (ENO2) (Enolase 2 (Gamma, Neuronal) (ENO2))

Reactivité: Humain

Méthode de détection: Colorimetric

Application: ELISA

Type d'échantillon: Serum

Détail du produit ENO2/NSE Kit ELISA

Sensibilité: 1.2 ng/ml

Attributs du produit: Human Neuron Specific Enolase (NSE) ELISA Assay Kit (enzyme-linked immunoassay kit) is intended for the quantitative determination of human neuron specific enolase (NSE) levels in serum. Human Neuron Specific (NSE) ELISA Assay Kit is for research use only and not to be used in diagnostic procedures.

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Volume d'échantillon: 10 μL

Durée du test: 1 h

Protocole: Human Neuron Specific Enolase (NSE) ELISA Assay Kit is designed, developed and produced for the quantitative measurement of human NSE in serum sample. The assay utilizes the two-site "sandwich" technique with two selected monoclonal antibodies that bind to different epitopes of the γ-subunit of the enzyme. Assay standards, controls and patient samples are added directly to wells of microplate that is coated with a streptavidin. Subsequently, a mixture of a biotinylated NSE specific monoclonal antibody and a horseradish peroxidase (HRP) labeled NSE specific monoclonal antibody is added to each microtiter well. After the first incubation a "sandwich" immunocomplex of "streptavidin-biotin-monoclonal antibody - human NSE - monoclonal antibody-HRP" is formed. The unbound monoclonal antibodies are removed in the subsequent washing step. For the detection of this immunocomplex, the well is then incubated with a substrate solution in a timed reaction and then measured in a spectrophotometric microplate reader. The enzymatic activity of the immunocomplex bound to the NSE on the wall of the microtiter well is directly proportional to the amount of NSE in the sample. A standard curve is generated by plotting the absorbance versus the respective human NSE concentration for each standard on point-to-point, cubical scales or 4 parameter curve fit. The concentration of human NSE in test samples is determined directly from this standard curve.

Restrictions: For Research Use only

Stockage

Stock: 4 °C

Détail du antigène

Antigène: ENO2/NSE (ENO2) (Enolase 2 (Gamma, Neuronal) (ENO2))

Autre désignation: Neuron Enolase (NSE)