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PD CEN/TS 16826-2:2015

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

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Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for snap frozen tissue Isolated proteins

Available format(s)

Hardcopy , PDF

Superseded date

22-02-2019

Superseded by

BS EN ISO 20184-2:2018

Language(s)

English

Published date

31-08-2015

£142.00
Excluding VAT

European foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 General considerations
5 Outside the laboratory
6 Inside the laboratory
Annex A (informative) - Quantitative protein analysis
        demonstrates changes of protein amounts
        during cold ischemia
Bibliography

Recommends the handling, documentation and processing of frozen tissue specimens intended for the analysis of extracted proteins during the pre-analytical phase before a molecular assay is performed.

Committee
CH/212
DocumentType
Standard
Pages
22
PublisherName
British Standards Institution
Status
Superseded
SupersededBy

This Technical Specification recommends the handling, documentation and processing of frozen tissue specimens intended for the analysis of extracted proteins during the preanalytical phase before a molecular assay is performed. This Technical Specification is applicable to molecular in vitro diagnostic examinations (e.g., in vitro diagnostic laboratories, laboratory customers, in vitro diagnostics developers and manufacturers, institutions and commercial organisations performing biomedical research, biobanks, and regulatory authorities). Protein profiles and protein-protein interactions in tissues can change drastically before and after collection (due to e.g., gene induction, gene down regulation, protein degradation). Protein species amounts can change differently in different donors’ / patients’ tissues. The expression of genes can be influenced by the given treatment or intervention (surgery, biopsy), or drugs administered for anaesthesia or even treatment of concomitant disease as well as by the different environment conditions after the tissue removal from the body. Therefore, it is essential to take special measures to minimize the described profile changes and modifications within the tissue for subsequent protein analysis. Tissues that have undergone chemical stabilization pre-treatment before freezing are not covered in this document. In addition this document is not applicable for protein analysis by immunohistochemistry.

Standards Relationship
CEN/TS 16826-2:2015 Identical

ISO 15189:2012 Medical laboratories — Requirements for quality and competence
ISO 15190:2003 Medical laboratories Requirements for safety
ISO Guide 30:2015 Reference materials — Selected terms and definitions

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