Fig. 2.
Fig. 2. Gel filtration chromatography of HS oligosaccharides following nitrous acid digestion. HS in HPLC peaks A and B from the nonsupportive cell PG (A and B) and in peak A from the supportive cell peak A PG (C) were subjected to low pH nitrous acid digestion and separated on a Sephadex G-25 column, as described in Materials and Methods. Fractions of 0.3 mL were collected and incorporated3H and 35S radioactivity was monitored.

Gel filtration chromatography of HS oligosaccharides following nitrous acid digestion. HS in HPLC peaks A and B from the nonsupportive cell PG (A and B) and in peak A from the supportive cell peak A PG (C) were subjected to low pH nitrous acid digestion and separated on a Sephadex G-25 column, as described in Materials and Methods. Fractions of 0.3 mL were collected and incorporated3H and 35S radioactivity was monitored.

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