CEN/TS 16826-2:2015
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
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Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for snap frozen tissue - Part 2: Isolated proteins
09-03-2023
12-08-2015
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
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.
Committee |
CEN/TC 140
|
DocumentType |
Technical Specification
|
PublisherName |
Comite Europeen de Normalisation
|
Status |
Withdrawn
|
SupersededBy |
Standards | Relationship |
DIN SPEC 13226-2 : 2015 | Identical |
DIN CEN/TS 16826-2;DIN SPEC 13226-2:2015-12 | Identical |
NEN NVN CEN/TS 16826-2 : 2015 | Identical |
S.R. CEN/TS 16826-2:2015 | Identical |
XP CEN/TS 16826-2 : 2015 XP | Identical |
UNI CEN/TS 16826-2 : 2015 | Identical |
SIS-CEN/TS 16826-2:2015 | Identical |
PD 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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