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Division 4 The reagents of the tests shall consist of:F1F2

United Kingdom

Original text. Later amendments are not shown.

  1. (a)

    antigen: the antigen shall contain specific glycoprotein of enzootic bovine leukosis virus which has been standardised against the E05 serum;

  2. (b)

    the test serum;

  3. (c)

    known positive control serum;

  4. (d)

    agar gel:

    • 0,8 % agar,

    • 8,5 % NaCl,

    • 0,05 M Tris-buffer pH 7,2,

    • 15 ml of this agar shall be introduced into a petri dish of 85 mm diameter, resulting in a depth of 2,6 mm of agar.

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.