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> Kits ELISA pour la détection des cytokines
Rapide et facile à utiliser: Le test prend 2 heures avec seulement 7 étapes requises.
Cohérent: Calibré selon les normes NIBSC/OMS pour garantir la cohérence entre les lots.
Contrôle strict de la qualité: Sensibilité, spécificité, exactitude, linéarité et précision inter/intra élevées.
Méthode validée: Validation complète avec protocole disponible et assistance technique professionnelle 24h.
Interférence matricielle minimale: Faible interférence de la matrice vérifiée dans le surnageant de culture cellulaire et le sérum.
| Cat. No. | Product Description |
|---|
| RUO | PRO | ||
|---|---|---|---|
| Temps de détection | 2-3h | 2h | |
| Type d'échantillon | Cell Culture Supernates, Serum , Plasma | Cell Culture Supernates, Serum , Plasma | |
| Système de gestion de la qualité | ISO13485 | ||
| Guide de validation | ICH M10 | ||
| Expérience de validation | Effet de crochet | √ | √ |
| Effet de matrice | Bilirubin, Hemoglobin, Triglyceride | ||
| Effet anticoagulant | EDTA, Heparin, Sodium citrate | ||
| Influence des conditions de stockage des échantillons | 3 Freeze–thaw Cycles | ||
| Spécificité | IL-2, IL-4, IL-6, IL-7, IL-10, IL-15, IL-21, IL-1β, TNF-alpha, GM-CSF | IL-1β, IL-2, IL-4, IL-5, IL-6, IL-7, IL-8, IL-10, IL-12 p70, IL-13, IL-15, IL-17, GM-CSF, TNF-alpha, IFN-gamma, etc. | |
The sensitivity of ClinMax™ Human Interferon-γ (IFN-γ) ELISA Kit (Cat. No. CRS-A017) is 5.309 pg/Ml.
ClinMax™ Human Interferon-γ (IFN-γ) ELISA Kit (Cat. No. CRS-A017) was verified to have an intra/inter-precision of less than 10%.
The sensitivity of ClinMax™ Human IFN-γ ELISA Kit, PRO (Cat. No. CEA-C006) is 3.25 pg/mL.
ClinMax™ Human IFN-γ ELISA Kit, PRO (Cat. No. CEA-C006) was verified to have an intra/inter-precision of less than 10%.
Diseases that are commonly present during sample collection such as jaundice (elevated bilirubin), hemolysis (elevated hemoglobin), and lipemia (elevated triglyceride) were simulated. Bilirubin, hemoglobin, and triglycerides were individually spiked into the sample matrix at a concentration of 20 mg/dL, 3500 g/dL, 2.0 g/L, respectively to evaluate matrix effect on our (XXX) kits.
Anticoagulant effect was tested by spiking the sample with either heparin, EDTA, or sodium citrate at a concentration of 40U/mL, 4mg/mL, and 40mg/mL, respectively.
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