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Protein deglycosylation kit

Manufactured by Merck Group

The Protein Deglycosylation kit is a laboratory tool designed to remove glycosylation from proteins. It contains reagents and enzymes that facilitate the deglycosylation process, which can be useful for various research and analytical applications.

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3 protocols using protein deglycosylation kit

1

Deglycosylation of Recombinant Pneumolysin

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PLY was deglycosylated under native conditions using the Protein Deglycosylation kit (Sigma) following the instructions of the kit. Briefly, 10 μg of recombinant PLY was incubated with 1 μl each of Peptide:N-glycosidase F, O-Glycosidase, Sialidase A, ß-(1-4)-Galactosidase and ß-N-acetylglucosaminidase in 50 μl reaction buffer for 3 days at 37°C. The extent of deglycosylation was assessed by mobility shifts on SDS-PAGE gels.
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2

Integrin β1 Activation and Glycosylation

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Antibodies against total integrin β1 and activated integrin β1 (HUTS-21) were purchased from BD Biosciences (Lincoln Park, NJ). Integrin β1 blocking antibody (P4C10) was purchased from Millipore (Billerica, MA). Antibodies against C1GALT1, GAPDH, and focal adhesion kinase (FAK) were purchased from Santa Cruz Biotechnology, Inc. (Santa Cruz, CA). Antibody against phospho (p)-FAK was purchased from Cell Signaling Technology Inc. (Beverly, MA). Antibody against actin was purchased from GeneTex Inc. (Irvine, CA). Vicia villosa agglutinin (VVA) and peanut agglutinin (PNA) lectins were purchased from Vector Laboratories (Burlingame, CA). Human collagen IV, human fibronectin, murine laminin, bovine serum albumin (BSA), and protein de-glycosylation kit were purchased from Sigma (St Louis, MO).
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3

Deglycosylation of Recombinant Pneumolysin

Check if the same lab product or an alternative is used in the 5 most similar protocols
PLY was deglycosylated under native conditions using the Protein Deglycosylation kit (Sigma) following the instructions of the kit. Briefly, 10 μg of recombinant PLY was incubated with 1 μl each of Peptide:N-glycosidase F, O-Glycosidase, Sialidase A, ß-(1-4)-Galactosidase and ß-N-acetylglucosaminidase in 50 μl reaction buffer for 3 days at 37°C. The extent of deglycosylation was assessed by mobility shifts on SDS-PAGE gels.
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