Typical reaction conditions (P0709)
- Combine 1–20 μg of glycoprotein, 1 μl of 10X Glycoprotein Denaturing Buffer and H2O (if necessary) to make a 10 μl total reaction volume.
- Denature glycoprotein by heating reaction at 100°C for 10 minutes.
- Make a total reaction volume of 20 μl by adding 2 μl 10X G7 Reaction Buffer, 2 μl 10% NP40, H2O and 1–2 μl PNGase F (Glycerol Free), Recombinant.
- Incubate reaction at 37°C for 1 hour.
- Reaction may be scaled up linearly to accommodate large
amounts of PNGase F and larger reaction volumes.
- Several exo- and endo-glycosidases can be used together
in one digest. For buffer recommendations, please reference the Glycosidases
Double Digest Chart .
- For a more detailed characterization of several
glycosidase enzymes, please reference the Detailed
Characterization of Several Glycosidase Enzymes page.
- For unit conversion between different suppliers, please
reference the Glycobiology
Unit Conversion Chart page.
