Infliximab Kit ELISA
Aperçu rapide pour Infliximab Kit ELISA (ABIN4886393)
Antigène
Tous les produits InfliximabReactivité
Méthode de détection
Type de méthode
Gamme de detection
Application
Type d'échantillon
-
-
Seuil minimal de détection
- 0.78 ng/mL
-
Fonction
- Quantification of Infliximab in biological matrices
-
Analytical Method
- Quantitative
-
Specificité
- Infliximab (Remicade)
-
Réactivité croisée (Details)
- hIgG1 and Infliximab prepared at 250 ng/ mL were assayed and exhibited no cross-reactivity or interference.
-
Ingrédients
-
- Coated microtiter plate, 96 wells
- Calibrator diluent. - 1.8ml
- Calibrator 12ul 10X wash buffer - 25ml
- Assay buffer - 50ml
- 1000X detection reagent - 17ul TMB - 12ml
- TMB stop solution - 12ml
- Plate sealers - 3
-
Matériel non inclus
-
- Precision pipettes calibrated to deliver 5-1000μL
- Multi-channel pipette calibrated to deliver 50-200μL
- Plate shaker
- Disposable tips
- Vortex-Mixe
- Distilled or de-ionized water
- Microplate reader capable of reading 450nm with background subtraction
-
-
-
-
Indications d'application
- Optimal working dilution should be determined by the investigator.
-
Volume d'échantillon
- 15 μL
-
Durée du test
- 2.5 h
-
Plaque
- Pre-coated
-
Protocole
- The Infliximab ELISA kit is designed to measure free Infliximab with high specificity and sensitivity . This assay employs the sandwich enzyme immunoassay technique. A precoated anti-Infliximab 96 well plate is provided. Calibrator, quality control samples and test samples are pipetted into the appropriate wells. Infliximab present in biological matrices is bound by the immobilized capture antibody. After washing away any unbound substances, enzyme linked detection antibody is added to the wells. The plate is washed to remove any unbound antibody-enzyme reagent and a substrate solution is added to the wells for color development. The color development is proportional to the amount of Infliximab present in test samples and the concentration is calculated from the standard series.
-
Préparation des réactifs
-
Prepare the appropriate amount of required reagent on the day of use. Store all reagents as per instructions stated on the label. 1. Wash Buffer (1X) Preparation: Dilute wash buffer concentrate with ultra-pure water 1/10 before use (for example add 20 mL concentrate to 180 mL ultra-pure water). Mix well. 2. Detection Reagent (1X) Preparation: Dilute detection reagent with assay buffer 1/1000 before use (for example add 11 μL concentrate to 11 mL of assay buffer). Mix well. 3. Preparation of Calibrators: Prepare calibrators with concentrations ranging from 2,500 ng/mL to 78 ng/ mL. The following is an example calibrator curve.
-
Prélèvement de l'échantillon
- This kit is compatible with EDTA-plasma, heparinplasma and serum samples. Samples can be stored at or below -20 °C for up to 1 year.
-
Préparation de l'échantillon
-
Dilute calibrators and test samples 1/100 with assay buffer (for example add 5μL of prepared calibrator or sample to 495μL of assay buffer). Mix well. *Note that test samples may require further dilution when peak values are predicted to exceed 2.5 μg/mL. Do not store diluted samples.
-
Procédure de l'essai
-
This assay employs the sandwich enzyme immunoassay technique. Anti- Infliximab is coated onto a 96 well microplate. Calibrator, quality control samples (if desired) and test samples are pipetted into the appropriate wells. Infliximab present in biological matrices is bound by the immobilized anti- Infliximab antibody. After washing away any unbound substances, enzyme linked anti- Infliximab antibody is added to the wells. This antibody is developed and purified specifically against truncated Remicade® (domain residing in Fc portion of the Remicade® molecule). The plate is washed to remove any unbound antibody-enzyme reagent and a substrate solution is added to the wells for color development. The color development is proportional to the amount of Infliximab present in test samples. The color development is stopped and the intensity of the color is measured.
-
Calcul des résultats
-
- Construct a standard curve by plotting the absorbance obtained from each standard against concentration. Use a 4 or 5 parameter curve fit. Alternatively a log-log curve fit may be used. 2. The concentration of the unknowns can be read directly from this standard curve using the absorbance value for each sample. 3. Any sample undiluted or diluted still reading greater than the highest standard should be diluted appropriately with assay buffer and retested. If the samples have been diluted, the concentration determined from the standard curve must be multiplied by the dilution factor.
-
Précision du teste
-
Intra-assay precision: <10%
Inter-assay precision: <10% -
Restrictions
- For Research Use only
-
-
-
Agent conservateur
- Without preservative
-
Stock
- -20 °C
-
Stockage commentaire
- -20C, 1 year
-
Date de péremption
- 12 months
-
-
- Infliximab
-
Sujet
- Infliximab (Remicade®) is a chimeric monoclonal antibody against tumour necrosis factor alpha (TNF- α). Infliximab neutralizes the biological activity of TNF- α by binding with high affinity to the soluble (free floating in the blood) and transmembrane (located on the outer membranes of T cells and similar immune cells) forms of TNF-α, and inhibits or prevents the effective binding of TNF-α with its receptors.
-
ID gène
- 7124
Antigène Tous les produits Infliximab
-