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Certified pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to in-house working standards.

Produit utilisé pour la dénaturation des protéines et comme agent de solubilisation doux pour les protéines insolubles ou dénaturées. Permet de renaturer les protéines des échantillons dénaturés au chlorure de guanidine 6 M, comme les corps d'inclusion. Peut être utilisé en association avec du chlorhydrate de guanidine et du dithiothréitol (DTT) pour replier les protéines dénaturées dans leur forme native active.

These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.

These secondary standards offer multi-traceability to the USP and EP primary standards, where they are available.

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

To see an example of a Certificate of Analysis for this material enter LRAC1664 in the slot below. This is an example certificate only and may not be the lot that you receive.