This document gives guidelines on the handling, storage, processing and documentation of venous whole blood specimens intended for cellular RNA examination during the pre-examination phase before a molecular examination is performed. This document covers specimens collected in venous whole blood collection tubes.
This document is applicable to any molecular in vitro diagnostic examination performed by medical laboratories. It is also intended to be used by laboratory customers, in vitro diagnostics developers and manufacturers, biobanks, institutions and commercial organizations performing biomedical research, and regulatory authorities.
Different dedicated measures are taken for stabilizing blood cell free circulating RNA and RNA in exosomes circulating in blood. These are not described in this document.
Different dedicated measures are taken for collecting, stabilizing, transporting and storing capillary blood as well as for collecting and storing blood by paper based technologies or other technologies generating dried blood. These are not described in this document.
This document does not cover the isolation of specific blood cells and subsequent isolation of cellular
RNA therefrom.
RNA in pathogens present in blood is not covered by this document.
Označení | ČSN EN ISO 20186-3 (857030) |
---|---|
Katalogové číslo | 509318 |
Cena | 350 Kč350 |
Datum schválení | 1. 4. 2020 |
Datum účinnosti | 1. 5. 2020 |
Jazyk | angličtina (obsahuje pouze anglický originál) |
Počet stran | 32 stran formátu A4 |
EAN kód | 8596135093182 |
Tato norma nahradila | ČSN P CEN/TS 16835-3 (857030) z ledna 2017 |
Dostupnost | skladem (tisk na počkání) |
ČSN EN ISO 20186-1 (857030)
Molekulární diagnostická vyšetření in vitro - Specifikace předvyšetřovacích postupů pro plnou žilní krev - Část 1: Izolovaná buněčná RNA
ČSN EN ISO 20186-2 (857030)
Molekulární diagnostická vyšetření in vitro - Specifikace předvyšetřovacích postupů pro plnou žilní krev - Část 2: Izolovaná genomická DNA