300 mM NaOH, 1.0 mM Na₂EDTA.

ready to use

2,5 M NaCl, 100 mM Na₂EDTA, 10 mM TRIS, 0,97% Sarkosyl, 1% Triton X-100, pH = 10.0.

TRIS Buffer pH = 7,50.

ready for use

0.4% neutral red (C.I. 50040).

Zur Fluoreszenz-Färbung von DNA.
Propidiumiodid 1mg/ml.

10x concentrated electrophoresis running buffer.
0.4 M Tris, 0.2 M acetic acid, 10 mM EDTA-Na₂, pH = 8.5 ± 0.2, microfiltered.

10x concentrated electrophoresis running buffer.
0.4 M Tris, 0.2 M acetic acid, 1 mM EDTA-Na₂, pH = 8.5 ± 0.2, microfiltered.
TAE buffer for electrophoresis with reduced EDTA concentration.

10x concentrated electrophoresis running buffer.
0.89 M Tris, 0.89 M boric acid, 20 mM EDTA-Na₂, pH = 8.3 ± 0.2, microfiltered.
TBE buffer for the preparation of sequencing gels and as a running buffer in electrophoresis.

10x concentrated TRIS-Glycine gel electrophoresis running buffer.
0.25 M TRIS, 1.92 M Glycine, pH = 8.3 ± 0.2, microfiltered.

10x concentrated TRIS-Glycin-SDS gel electrophoresis running buffer (SDS-PAGE).
0.25 M TRIS, 1.92 M Glycine, 1 % SDS, pH = 8.6 ± 0.2, microfiltered.