Fig. 1.
Fig. 1. TC phenotypes revealed by PAGE. / Serum (25 μL) saturated with 10 μL of radioactive B12(57Co-B12; 200mCi/mg, 1 μCi/mL [7.4 GBq/mg, 37 kBq/mL]; Amersham Pharmacia Biotech “CT2” diluted 1:5 N-saline) was incubated with 25 μL of neuraminidase (0.2 IU/mL) in 25 μL of buffer (0.05 M sodium acetate, 0.1% CaCl2, and 0.95% NaCl, pH 5.5) at 37°C for 30 minutes. Twenty-five μL was replaced with buffer (65% [wt/vol] sucrose) and bromophenol blue as an albumin- and front-marker. PAGE was performed in a 10% polyacrylamide gel (1.5 mm × 7.0 cm × 12.5 cm) with 3.5% concentrating top gel (1.5 cm high) and Tris-glycine electrode buffer at pH 8.3 and electrophoresed at 250 V.

TC phenotypes revealed by PAGE.

Serum (25 μL) saturated with 10 μL of radioactive B12(57Co-B12; 200mCi/mg, 1 μCi/mL [7.4 GBq/mg, 37 kBq/mL]; Amersham Pharmacia Biotech “CT2” diluted 1:5 N-saline) was incubated with 25 μL of neuraminidase (0.2 IU/mL) in 25 μL of buffer (0.05 M sodium acetate, 0.1% CaCl2, and 0.95% NaCl, pH 5.5) at 37°C for 30 minutes. Twenty-five μL was replaced with buffer (65% [wt/vol] sucrose) and bromophenol blue as an albumin- and front-marker. PAGE was performed in a 10% polyacrylamide gel (1.5 mm × 7.0 cm × 12.5 cm) with 3.5% concentrating top gel (1.5 cm high) and Tris-glycine electrode buffer at pH 8.3 and electrophoresed at 250 V.

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