62kDa (Reducing)
Store at -25 ~ -15℃ for 2 years
[1] Sun G , Yu X , Bao C ,et al. Identification and characterization of a novel prokaryotic peptide: N-glycosidase from Elizabethkingia meningoseptica.[J].Journal of Biological Chemistry, 2015, 290.
[2] Wang T ,Cai, Zhi P ,et al. Discovery and characterization of a novel extremely acidic bacterial N-glycanase with combined advantages of PNGase F and A.[J].Bioscience Reports, 2014.
N-glycoprotein deglycosylase (peptide∶N-glycanase, abbreviated PNGase), widely distributed in prokaryotes and eukaryotes, hydrolyzes asparagine (Asn)-linked oligosaccharides on polypeptides and releases intact oligosaccharide chains. Prokaryotic PNGases are found only in Elisabethella meningitidis septica, and there are two PNGases in total, named PNGase F and PNGase F-II. PNGase F-II, while having the function of PNGase F, hydrolyzes and releases intact glycan chains containing α-1,3-core fucoidan glycosylated N-glycoproteins of plant and insect origin, and functions in the same way as PNGase A.
Storage Solution: 5U/μL PNGase FII in 20 mM Tris-HCl, 50 mM NaCl, 5 mM EDTA, 50% Glycerol (pH 7.5 @ 25°C)
10* PBS: 136 mM NaCl, 2.6mM KCl, 10 mM Na₂HPO₄, 2 mM KH₂PO₄ (pH 7.4 @ 25°C)
Denaturing Reaction Conditions:
1. Combine 1-5 µg of glycoprotein, 1µl of 10*PBS and H2O (if necessary) in a total reaction volume of 10 µl.
2. Denature glycoprotein by heating reaction at 100°C for 10 minutes.
3. Chill denatured glycoprotein on ice and centrifuge 10 seconds.
4. Make a total reaction volume of 20 µl by adding1-2 µl PNGase F II,1 µl of PBS(10X)and 7-8µl H2O.
5. Incubate reaction at 37°C for 12-16 hour.
1.Reactions may be scaled-up linearly to accommodate larger reaction volumes.
2. Avoid repeated freezing and thawing.
3. We suggest using recombinant Avidin from maize, or horseradish peroxidase (HRP) as positive controls.
4. Glycoprotein denaturation must not contain SDS, which completely inhibits the enzymatic activity of PNGase F II.
1. 1µL of 10mg/ml Horseradish Peroxidase (HRP) was taken, 9µL of PBS was added to the blank group and 8µL of PBS was added to the experimental group, which were placed in a 100°C water bath for 10 minutes for boiling denaturation;
2.After denaturation, remove and place on ice for 3 minutes;
3. 1µL of different concentrations of PNGase F II was added within the experimental group, and both the experimental group and the blank control group were put into 37℃ for overnight reaction;
4. Perform SDS-PAGE detection.
2μg (R: reducing condition, N: non-reducing condition).
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