Glycogen Determination from Tissues
From Bridges Lab Protocols
Materials and Buffers
- Screw Capped Vials
- 30% KOH, prepared fresh
- 1M Sodium Sulfate
- Ethanol
- 50 mM Sodium Acetate, pH 4.8
- Amyloglucosidease
Protocol
- Weight out 30-90 mg tissue into screw cap vial and record weights.
- Add 300 uL 30% KOH and place on 95C heat block for 30 min with occasional mixing.
- Cool and then add 100 uL Sodium Sulfate and 800 uL Ethanol.
- Boil for 5 min.
- Centrifuge at 13 000 RPM for 5 min.
- Resuspend pellet in 200 uL water then add 400 uL ethanol. Boil 5 min, spin 5 min and Repeat wash steps twice more.
- Dry pellet
- Resuspend pellet in 200 uL of 50 mM Sodium Acetate, pH 4.8
- Add 0.3 mg/mL amyloglucosidase and place at 37C for 3h
- Quantify glucose
Reference: