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Example of leaflet Europese Overeenkomst betreffende de uitwisseling van testsera voor bloedgroepenonderzoek

COUNCIL OF EUROPE

European Agreement on the exchange of blood-grouping reagents

1. Central Blood Transfusion Laboratory, 1 Main Street, Metropolis, Westland

2. Anti-E (anti-rh”) serum (human)

3. 10 ml

4. Date du dernier co test: 30th May 1961

5. Expiry Date, 30th May 1962

6. No. 5432

7. The red blood cells to be tested are washed one or more times with a NaCl solution of 9 g/1. An erythrocyte suspension with a volume fraction of approximately 0.03 is prepared by mixing one volume or drop of packed red cells with 30 volumes or drops of isotonic NaCl-solution. With practice the strength of a suspension can be judged adequately by inspection.

A small drop of serum is delivered into a precipitin tube (6 mm x 30 mm) from a Pasteur pipette, and a similar drop of red corpuscle suspension is added. (With practice considerable economy can be achieved by delivering the serum and cell suspension from pipettes marked at a volume of 10 µl). The contents of the tube are mixed and incubated at 37° C for two hours. The contents of the tube are then cautiously transferred to a microscope slide and gently spread upon it. Unless agglutination is unmistakable to the unaided eye the slide is examined for the presence and degree of agglutination under the microscope.

8. Store at -20° C or below. If to be used after day of opening, add 0.1 ml of a solution containing 100 gram sodium azide per litre.

9. Human anti-E („anti-rh”) serum: 5 ml; solution containing 300 gram bovine albumin per litre: 5 ml

10. This product contains material of human origin.

Regeling
Europese Overeenkomst betreffende de uitwisseling van testsera voor bloedgroepenonderzoek
Soort
Verdrag
Geldend vanaf
07-04-1978
BWB-id
BWBV0004573
Versie
1978-04-07_0

In de hele regeling · Officiële tekst op wetten.overheid.nl