Fig. 3.
TLC-immunostaining with anti-Lc4Cer antibodies of the products of the reaction with Lc3Cer β-galactosyltransferase. The enzyme reaction was carried out with 10 nmol of Lc3Cer, 5 μg of Triton CF54, 0.2 M KCl, 20 μM MnCl2, 1.56 mM UDP-Gal, 50 mM cacodylate-HCl buffer (pH 6.8), and 100 μg of microsomes at 37°C for 2 h, and the products were developed on a TLC plate with chloroform/methanol/0.5% CaCl2 (55:45:10, by vol.). The heat-denatured microsomal preparation was used as a control. 1, KFr13; 2, KFr13TX; 3, KF28; 4, KF28TX.

TLC-immunostaining with anti-Lc4Cer antibodies of the products of the reaction with Lc3Cer β-galactosyltransferase. The enzyme reaction was carried out with 10 nmol of Lc3Cer, 5 μg of Triton CF54, 0.2 M KCl, 20 μM MnCl2, 1.56 mM UDP-Gal, 50 mM cacodylate-HCl buffer (pH 6.8), and 100 μg of microsomes at 37°C for 2 h, and the products were developed on a TLC plate with chloroform/methanol/0.5% CaCl2 (55:45:10, by vol.). The heat-denatured microsomal preparation was used as a control. 1, KFr13; 2, KFr13TX; 3, KF28; 4, KF28TX.

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