OpenLegislation

Division 1 Solutions and materials required:F1F2

United Kingdom

Original text. Later amendments are not shown.

  1. (a)

    40 ml of 1,6 % agarose in 0,05 M Tris/HCl buffer, pH 7,2 with 8,5 % NaCl;

  2. (b)

    15 ml of a bovine leukosis serum, having antibody only to bovine leukosis virus glycoproteins, diluted 1:10 in 0,05 M Tris/HCl buffer, pH 7,2 with 8,5 % NaCl;

  3. (c)

    15 ml of a bovine leukosis serum, having antibody only to bovine leukosis virus glycoproteins, diluted 1:5 in 0,05 M Tris/HCl buffer, pH 7,2 with 8,5 % NaCl;

  4. (d)

    four plastic petri dishes with a diameter of 85 mm;

  5. (e)

    a punch with a diameter of 4 to 6 mm;

  6. (f)

    a reference antigen;

  7. (g)

    the antigen which is to be standardised;

  8. (h)

    a water bath (56 °C).

Annotations

Textual amendments

F1

Substituted by Council Directive 97/12/EC of 17 March 1997 amending and updating Directive 64/432/EEC on health problems affecting intra-Community trade in bovine animals and swine.

F2

Substituted by Commission Decision of 15 December 2009 amending Annex D to Council Directive 64/432/EEC as regards diagnostic tests for enzootic bovine leukosis (notified under document C(2009) 9951) (Text with EEA relevance) (2009/976/EU).

Notes on Annex D

Textual amendments

F2

Substituted by Council Directive 98/46/EC of 24 June 1998 amending Annexes A, D (Chapter I) and F to Directive 64/432/EEC on health problems affecting intra-Community trade in bovine animals and swine.